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From the 3/29/2024 release of VAERS data:

Found 2,937 cases where Vaccine is COVID19 and FLU4

Government Disclaimer on use of this data

Table

   
Event Outcome Count Percent
Death 54 1.84%
Life Threatening 61 2.08%
Permanent Disability 64 2.18%
Hospitalized 316 10.76%
Emergency Doctor/Room 465 15.83%
Emergency Room 1 0.03%
Office Visit 727 24.75%
Recovered 1,129 38.44%
None of the Above 942 32.07%
TOTAL † 3,759 † 127.99%
† Because VAERS cases can have multiple vaccinations, symptoms, and event outcomes, a single case can account for multiple entries in this table. This is why the Total Count is greater than 2,937 (the number of cases found), and the Total Percent is greater than 100.



Case Details (Sorted by State)

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VAERS ID: 2104971 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-13
Onset: 2021-10-11
   Days after vaccination: 28
Submitted: 0000-00-00
Entered: 2022-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 021C21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Upper gastrointestinal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Gastrointestinal haemorrhage (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute upper gastrointestinal bleeding. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2522711 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK LA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS 23E5G / UNK LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient should have received COVID19 PFIZER UPDATED BOOSTER 12+(BIVALENT) and received COVID19 (PRIZER AGE 12+) GRAY CAP.


VAERS ID: 2522720 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient should have received COVID19 PFIZER UPDATED BOOSTER 12+(BIVALENT) and received COVID19 (PRIZER AGE 12+) GRAY CAP.


VAERS ID: 2522721 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-23
Onset: 2022-11-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient should have received COVID19 PFIZER UPDATED BOOSTER 12+(BIVALENT) and received COVID19 (PRIZER AGE 12+) GRAY CAP.


VAERS ID: 2522725 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient should have received COVID19 PFIZER UPDATED BOOSTER 12+(BIVALENT) and received COVID19 (PRIZER AGE 12+) GRAY CAP.


VAERS ID: 2523711 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-22
Onset: 2022-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was expecting to receive COVID19 PFIZER UPDATED BOOSTER 12+, instead received COVID19 (PFIZER AGE 12+) GRAY CAP


VAERS ID: 2523712 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-22
Onset: 2022-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was expecting to receive COVID19 PFIZER UPDATED BOOSTER 12+, instead received COVID19 (PFIZER AGE 12+) GRAY CAP


VAERS ID: 2523714 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-22
Onset: 2022-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was expecting to receive COVID19 PFIZER UPDATED BOOSTER 12+, instead received COVID19 (PFIZER AGE 12+) GRAY CAP


VAERS ID: 2523718 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was expecting to receive COVID19 PFIZER UPDATED BOOSTER 12+, instead received COVID19 (PFIZER AGE 12+) GRAY CAP


VAERS ID: 2118963 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-22
Onset: 2021-12-12
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2022-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Rib fracture
SMQs:, Accidents and injuries (narrow), Osteoporosis/osteopenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Closed fracture of multiple ribs of right side. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2116018 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-01
Onset: 2021-12-06
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-02-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cellulitis
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Cellulitis. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2520518 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-09-09
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ882AB / UNK RA / OT
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Chest X-ray, Pain in extremity, Tuberculin test
SMQs:, Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CORTISONE [CORTISONE ACETATE]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Welts (Twenty-five or thirty years ago she had a TB test with ppd. After that test, her entire arm "blew up" instantly with a giant welt).
Allergies:
Diagnostic Lab Data: Test Name: chest x ray; Test Result: Negative ; Test Name: PPD; Result Unstructured Data: test was contaminated with something
CDC Split Type: USMODERNATX, INC.MOD20226

Write-up: little soreness in her arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (little soreness in her arm) in a 64-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) for COVID-19 prophylaxis. Co-suspect products included non-company products VARICELLA ZOSTER VACCINE RGE (CHO) (SHINGRIX) for an unknown indication and INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) for an unknown indication. The patient''s past medical history included Welts (Twenty-flve or thirty years ago she had a TB test with ppd. After that test, her entire arm "blew up" instantly with a giant welt.). Previously administered products included for Drug use for unknown indication: Flu Shots, TD and Typhoid. Past adverse reactions to the above products included No adverse event with TD and Typhoid; and Pain in extremity with Flu Shots. Concomitant products included CORTISONE ACETATE (CORTISONE [CORTISONE ACETATE]) for an unknown indication. On 09-Sep-2022, the patient received dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) (unknown route) at an unspecified dose. On an unknown date, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and dose of VARICELLA ZOSTER VACCINE RGE (CHO) (SHINGRIX) (unknown route) at an unspecified dose. On an unknown date, the patient experienced PAIN IN EXTREMITY (little soreness in her arm). At the time of the report, PAIN IN EXTREMITY (little soreness in her arm) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Chest X-ray: Negative. On an unknown date, Tuberculin test: test was contaminated with something. Patient dermatologist gave her a shot Of cortisone and she took antihistamines. Both her dermatologist and internist were not sure if the Fluzone HD could be the cause, especially with the 4-day delay Of onset, however the patient could not think of anything else that she might had been exposed to that would have caused the hives. When the hives began, they started in the armpit of her right arm at that same level as the injection site. She discussed her previous experience with other vaccines as to how it was so unusual for her to had hives after Fluzone HD QIV. She received Moderna Covid vaccines. The bivalent Covid booster a week ago caused her to have a little soreness in her arm. All of the other Covid boosters did not cause problems for her. She has taken vaccines against pneumonia without problems. Twenty-five or thirty years ago she had a TB test with ppd. After that test, her entire arm blewed up instantly with a giant welt. She was told at first that she had T B. A follow-up chest x-ray was negative. It was realized that she did not have TB and that instead something was wrong with that test. She later had subsequent ppd tests without reactions. No treatment medications were provided. This case was linked to MOD-2022-679659 (Patient Link).


VAERS ID: 2104731 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-08
Onset: 2022-01-28
   Days after vaccination: 112
Submitted: 0000-00-00
Entered: 2022-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100353153 / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive for COVID-19.


VAERS ID: 2104724 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-22
Onset: 2022-01-26
   Days after vaccination: 65
Submitted: 0000-00-00
Entered: 2022-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100364263 / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive for COVID-19.


VAERS ID: 2530029 (history)  
Form: Version 2.0  
Age: 89.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-18
Onset: 2022-12-11
   Days after vaccination: 54
Submitted: 0000-00-00
Entered: 2022-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ2524 / 5 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ933AA / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Alanine aminotransferase normal, Anaemia, Anion gap, Anticoagulant therapy, Aspartate aminotransferase normal, Asthenia, Bacterial test, Base excess, Basophil count decreased, Basophil percentage decreased, Bilirubin urine, Blood albumin normal, Blood alkaline phosphatase normal, Blood bicarbonate, Blood bilirubin normal, Blood calcium decreased, Blood chloride normal, Blood creatinine increased, Blood culture negative, Blood gases, Blood glucose normal, Blood lactic acid normal, Blood pH normal, Blood potassium normal, Blood sodium normal, Blood urea normal, Brain natriuretic peptide increased, Breath sounds abnormal, Bronchitis, COVID-19, Carbon dioxide normal, Chest X-ray abnormal, Chromaturia, Coma scale, Creatinine renal clearance, Culture positive, Dyspnoea, Dyspnoea exertional, Eosinophil count decreased, Eosinophil percentage decreased, Fatigue, Glomerular filtration rate decreased, Glucose urine absent, Haematocrit decreased, Haemoglobin decreased, Influenza A virus test negative, Influenza B virus test, Influenza virus test negative, Lung infiltration, Lymphocyte count decreased, Lymphocyte percentage decreased, Malaise, Mean cell haemoglobin concentration increased, Mean cell haemoglobin increased, Mean cell volume increased, Mean platelet volume normal, Microbiology test, Monocyte count normal, Monocyte percentage decreased, Neutrophil count normal, Neutrophil percentage increased, Nitrite urine absent, PCO2 normal, Platelet count normal, Pneumonia, Productive cough, Protein total decreased, Protein urine absent, Pyrexia, Rales, Red blood cell count decreased, Red cell distribution width normal, Rhonchi, SARS-CoV-2 test positive, Streptococcus test negative, Troponin I, Urine analysis, Urine ketone body absent, Urine leukocyte esterase, Urobilinogen urine, Viral test, White blood cell count normal, pH urine normal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Cardiac failure (broad), Anaphylactic reaction (broad), Haematopoietic erythropenia (narrow), Haematopoietic leukopenia (narrow), Haemorrhage laboratory terms (broad), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Chronic kidney disease (broad), Tumour lysis syndrome (narrow), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow), Infective pneumonia (narrow), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Molecular Diagnostic Tests COVID 19 Specimen Source Nasopharyngeal Coronavirus SARS-CoV2 Rapid * (A) Detected Microbiology Studies - Bacterial Blood CX NEG In Progress; NEG In Progress Resp CX + Stn NEG In Progress Bacterial L pneumo Urine Ag QL Not Detected L pneumo Urine Ag QL Interp L pneumo Urine Ag QL Interp Strep pneumo Ag Ur Not Detected Strep pneumo Ag Ur Interp Negative Viral FS Rapid Influenza Method PCR - Liat Rapid Influenza A PCR * Not Detected Rapid Influenza B PCR * Not Detected
CDC Split Type:

Write-up: Document Type: History and Physical Document Subject: History & Physical Note Performed By: DO on December 12, 2022 05:10 Verified By: DO on December 12, 2022 05:10 Encounter Info: Hospital, Observation, 12/11/22 - * Final Report * Chief Complaint cough History of Present Illness/Subjective Patient presents via private vehicle due to fatigue, generalized weakness, productive cough, DOE and low grade fever x 4 days. Patient was seen at Clinic on Thursday and diagnosed with bronchitis. She was started on amoxicillin and prednisone at that time. She was negative for Covid and flu at that time. Patient denies chest pain, n/v/d . Associated medical hx includes: Add''l medical hx includes: HTN, HLD, OA, MDD, neuropathy, Social hx: lives at home alone, non smoker CXR shows right sided infiltrate concerning for pneumonia. Patient is also Covid +. She is Covid vaccinated. Flu is negative. No leukocytosis, not septic. Not hypoxic at rest. Discussed discharge to home with antibiotic change to Augmentin and doxy with patient and her daughter to better cover for pneumonia. Also, advised to stop prednisone. Patient and her daughter are not comfortable with discharge at this time due to patient''s general weakness since being ill. She lives at home alone, no one can stay with her. Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.5 (36.5-36.5) Temp (FAHR) 97.7 (97.7-97.7), BP 167/70 (144-212)/(65-89), HR 53 (53-83), RR 16 (16-18), O2Sat 94 (94-94) Neurologic (most recent and range for last 24 hours) GCS 15(15-15) Patient Weight Current Daily Weight: 95 kg 12/11/22 Patient Height Current Height: 152.79 cm 12/11/22 Constitutional: No acute distress, well-nourished Eyes: PERRL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs are coarse, scattered rhonchi, Respirations are labored, RLL Crackles, no wheezes Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect, denies SI or HI Assessment/Plan 1. Weakness R53.1 Will place in observation and have PT OT eval''s to make sure it is safe for patient to go home since she lives alone Likely due to #2 and #3, no focal deficits suggesting CVA or neurologic process 2. Pneumonia J18.9 Will cover for CAP with Rocephin Doxy, collect sputum cultures, Legionella, strep antigen, and continue to monitor 3. COVID-19 U07.1 At present time disease appears to be mild, will start fluticasone inhalation, respiratory assessment, collect inflammatory markers, start famotidine, and continue to monitor, supplemental O2 as needed 4. Anemia D64.9 Noted. Stable, no evidence of acute bleeding, maintain hemoglobin greater than 7 5. HTN (hypertension) I10 6. Hyperlipidemia E78.5 7. OA (osteoarthritis) M19.90 8. Major depression F32.9 9. Neuropathy G62.9 Noted. Continue home medications as appropriate 10. DVT prophylaxis Z29.9 Lovenox subcu and SCDs while in bed Code Status None Recorded Chronic Problem List Anxiety Arthritis Chronic right sacroiliac pain Cystitis cystica DDD (degenerative disc disease), lumbar Depression Essential hypertension Headache History of kidney stones Hyperlipidemia Hypothyroid Idiopathic neuropathy Kidney cysts Leg cramps Lichenoid drug reaction Limb pain LVH (left ventricular hypertrophy) Major depression Morbid obesity OA (osteoarthritis) OG (onychogryphosis) OM (onychomycosis) Onychomycosis of toenail Osteoporosis Peripheral neuropathy, hereditary/idiopathic Recurrent UTI Right hip pain Tremor Vertigo Procedure/Surgical History ?Diabetic retinal eye exam (08/09/2021) ?Eye examination (02/25/2019) ?Repair of bladder (2009) ?Total hysterectomy (2009) ?Cataract surgery ?Tonsillectomy Medications Home Medications (23) Active amoxicillin 500 mg oral capsule 500 mg = 1 Capsule, Orally, TID aspirin 81 mg oral tablet 81 mg = 1 Tablet, Orally, Daily Ativan 0.5 mg oral tablet 0.5 mg = 1 Tablet, PRN, Orally, TID carvedilol 6.25 mg oral tablet 6.25 mg = 1 Tablet, Orally, BID cholestyramine 4 g/5 g oral powder for reconstitution 4 GM, Orally, BID cranberry oral tablet doxazosin 2 mg oral tablet 2 mg = 1 Tablet, Orally, BID Estrace Vaginal Cream 0.1 mg/gm 1 GM, Vaginally, 2x/WK, Apply pea sized amount to outside vaginal area nightly before bed x 2 weeks then 2x/week thereafter. levothyroxine 50 mCg (0.05 mg) oral tablet 75 mCg = 1.5 Tablet, Orally, Daily Lexapro 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily losartan 100 mg oral tablet 100 mg = 1 Tablet, Orally, Daily Misc Med , D-Mannose1 pill BIDOTC Nexium 40 mg oral delayed release capsule 40 mg = 1 Capsule, Orally, Daily predniSONE 10 mg oral tablet See Instructions, 5 tab orally today, then 4 tab x 3 days, then 3 tab x 3 days, then 2 tab x 3 days, then 1 tab x 3 days ProAir HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, Q4H Sarna 0.5%-0.5% topical lotion See Instructions, PRN, Topical TID spironolactone 25 mg oral tablet 25 mg = 1 Tablet, Orally, BID Systane Ultra preserved ophthalmic solution 1 Drop Tessalon Perles 100 mg oral capsule 100 mg = 1 Capsule, Orally, TID Vitamin C 1,000 mg, Orally, Daily Vitamin D3 (cholecalciferol) , Orally Voltaren Topical 1% topical gel 2 GM, Topical, 4 Times Daily, Use dosing card to measure dose Zofran ODT 4 mg oral tablet, disintegrating 4 mg = 1 Tablet, PRN, Orally, Q6H Active Scheduled Inpatient Medications None Reported One-Time Medications Given 12/11/22 00:00:00 TO 12/12/22 05:10:16 benzonatate (Tessalon Perles), Capsule, 200 mg, Orally, ONCE, (1 DOSE 12/12/22 01:25:00) ceftRIAXone, Injection, 2 GM, IVPB, ONCE, (1 DOSE 12/11/22 21:07:00) doxycycline, Injection, 100 mg, IVPB, ONCE, (1 DOSE 12/11/22 21:55:00) guaiFENesin (Mucinex 600 mg oral tablet, extended release), Tab, Extended Rel, 600 mg, Orally, ONCE, (1 DOSE 12/12/22 01:40:00) hydroCODONE-acetaminophen (hydroCODONE-acetaminophen 5 mg-325 mg oral tablet), Tablet, 1 Tablet, Orally, ONCE, (1 DOSE 12/11/22 22:19:00) PRN Medications (0600 - 0559) from 12/11 - 12/12 None Reported Allergies Dyazide (Unknown) Sular (Flushing) Yellow Dye (Sores in mouth, Unknown) Zocor (Unknown) sulfa drugs (Rash) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Widow- 3 children, Lives with Alone. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Congestive heart failure..: Father. Diabetes mellitus type 2: Grandmother. Diabetes...: Brother. Emphysema: Father. Heart disease..: Father. Hypertension..: Mother. Osteoarthritis: Mother. Uterine cancer: Mother. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 6.3 k/cumm (12/11/22 20:18:00) RBC: 3.42 million/cumm Low (12/11/22 20:18:00) Hgb: 11 GM/dL Low (12/11/22 20:18:00) Hct: 32.7 % Low (12/11/22 20:18:00) MCV: 96 fL (12/11/22 20:18:00) MCH: 32.1 pg (12/11/22 20:18:00) MCHC: 33.5 GM/dL (12/11/22 20:18:00) RDW: 12.8 % (12/11/22 20:18:00) Platelet: 250 k/cumm (12/11/22 20:18:00) MPV: 7.8 fL (12/11/22 20:18:00) Neutrophils %: 83 % (12/11/22 20:18:00) Lymphocytes %: 7 % (12/11/22 20:18:00) Monocytes %: 10 % (12/11/22 20:18:00) Eosinophils %: 0 % (12/11/22 20:18:00) Basophils %: 0 % (12/11/22 20:18:00) Absolute Neutrophil: 5.2 k/cumm (12/11/22 20:18:00) Absolute Lymphocyte: 0.4 k/cumm Low (12/11/22 20:18:00) Absolute Monocyte: 0.6 k/cumm (12/11/22 20:18:00) Absolute Eosinophil: 0 k/cumm (12/11/22 20:18:00) Absolute Basophil: 0 k/cumm (12/11/22 20:18:00) Chemistry: Sodium SerPl QN: 140 mmol/L (12/11/22 20:18:00) Potassium SerPl QN: 3.9 mmol/L (12/11/22 20:18:00) Chloride SerPl QN: 103 mmol/L (12/11/22 20:18:00) Carbon Dioxide SerPl QN: 26 mmol/L (12/11/22 20:18:00) Anion Gap: 11 mmol/L (12/11/22 20:18:00) BUN SerPl QN: 17 mg/dL (12/11/22 20:18:00) Creatinine SerPl QN: 1.14 mg/dL (12/11/22 20:18:00) Estimated GFR (CKD-EPI, no race): 46 mL/min/1.73m2 Low (12/11/22 20:18:00) Estimated CRCL (CG): 35 mL/min Low (12/11/22 20:18:00) Glucose SerPl QN: 129 mg/dL High (12/11/22 20:18:00) Calcium Total SerPl QN: 8.8 mg/dL (12/11/22 20:18:00) Alkaline Phos SerPl QN: 48 Units/L (12/11/22 20:18:00) ALT SerPl QN: 14 Units/L (12/11/22 20:18:00) AST SerPl QN: 17 Units/L (12/11/22 20:18:00) Bilirubin Total SerPl QN: 0.3 mg/dL (12/11/22 20:18:00) Total Protein SerPl QN: 6.2 GM/dL Low (12/11/22 20:18:00) Albumin SerPl QN: 3.7 GM/dL (12/11/22 20:18:00) Troponin-I High Sensitivity: 18 ng/L High (12/11/22 22:31:00) BNP Pl QN: 125 pg/mL High (12/11/22 20:18:00) Lactate Venous Pl QN: 1.3 mmol/L (12/11/22 20:18:00) Blood Gas Comment: venous (12/11/22 22:31:00) pH Bld Venous QN: 7.35 (12/11/22 22:31:00) PCO2 Bld Venous QN: 47 mmHg (12/11/22 22:31:00) PO2 Bld Venous QN: 46 mmHg High (12/11/22 22:31:00) Base Excess Bld Venous: 0 mmol/L (12/11/22 22:31:00) Bicarb Bld Venous Calc: 26 mmol/L (12/11/22 22:31:00) O2 Sat Bld Venous Calc: 79 % (12/11/22 22:31:00) Patient Temperature: 37 DegC (12/11/22 22:31:00) Urine Studies: Color: Yellow (12/11/22 22:17:00) Clarity: Clear (12/11/22 22:17:00) Specific Gravity: <=1.005 (12/11/22 22:17:00) pH: 6.5 (12/11/22 22:17:00) Protein: NEGATIVE (12/11/22 22:17:00) Glucose: NEGATIVE (12/11/22 22:17:00) Ketones: NEGATIVE (12/11/22 22:17:00) Bilirubin: NEGATIVE (12/11/22 22:17:00) Hgb Ur: NEGATIVE (12/11/22 22:17:00) Nitrite: NEGATIVE (12/11/22 22:17:00) Urobilinogen: NormalUro (12/11/22 22:17:00) Leukocyte Esterase Ur: NEGATIVE (12/11/22 22:17:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (12/11/22 20:18:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (12/11/22 20:18:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (12/11/22 20:18:00) Rapid Influenza A PCR: Not Detected (12/11/22 20:18:00) Rapid Influenza B PCR: Not Detected (12/11/22 20:18:00) Coronavirus SARS Ag FIA, POC: Negat (12/06/22 11:50:00) Diagnostics Radiology Results - Last 24 hours Across Visits 12/11/2022 20:04 - XR Chest PA or AP IMPRESSION:Focal right basilar airspace disease concerning for pneumoniaThank you for consulting our team of subspecialty radiologists at Radiology. Healthcare providers wishing to discussthis case further can contact the Cardiothoracic Reading Room. For after-hours or emergency department cases, pleasecall. Signature Line Electronically Signed on 12/12/22 05:10 ________________________________________________________ DO


VAERS ID: 2102091 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-03
Onset: 2022-01-31
   Days after vaccination: 89
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6202 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100358553 / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2102073 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-24
Onset: 2021-11-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ778AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Refill for Epi Pen. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2101819 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-01
Onset: 2022-01-24
   Days after vaccination: 84
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 076C21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367237 / N/A LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2542680 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER 4302MF023 / 2 LA / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7701MA / 1 RA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Dizziness, Nausea
SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSA2022SA516805

Write-up: dizziness; lightheaded; nausea; nauseated; Initial information received on 19-Dec-2022 regarding an non-serious case received from via consumer/non-hcp. This case involves a 26 years old male patient who was diagnosed with dizziness; lightheaded and nausea; nauseated after receiving influenza quadrival a-b high dose hv vaccine [Fluzone High-Dose Quadrivalent] and vaccines covid-19 vaccine. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 21-Nov-2022, the patient received a dose suspect influenza quadrival a-b high dose hv vaccine at dose 1 (batch number: UT7701MA) (strength, frequency, formulation, expiry date: unknown) via intramuscular route in the right arm for Influenza immunization. On 21-Nov-2022, the patient received suspect covid-19 vaccine produced by unknown manufacturer at dose 2 in injection form (batch number: 4302MF023) (strength, expiry date: unknown) via intramuscular route in the left arm for COVID-19 immunisation On 21-NOV-2022 the patient diagnosed with a non-serious events of dizziness; lightheaded (dizziness), nausea; nauseated (nausea) (same day latency) following the administration of influenza quadrival a-b high dose hv vaccine and following the administration of covid-19 vaccine. Action taken was not applicable for both suspects. It was not reported if the patient received a corrective treatment for both the events. At time of reporting, the outcome was Unknown for both events.


VAERS ID: 2101815 (history)  
Form: Version 2.0  
Age: 13.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-20
Onset: 2022-01-24
   Days after vaccination: 96
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 95K95 / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2101807 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-06
Onset: 2022-01-24
   Days after vaccination: 110
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P10035153 / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: SARS-CoV-2 test positive, Vaccine breakthrough infection
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 1829282 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-28
Onset: 2021-10-29
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026D21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ726AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Musculoskeletal disorder, Pain in extremity
SMQs:, Rhabdomyolysis/myopathy (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: hypertension, type 2 diabetes
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient woke up at 3am to use the restroom and her legs and arms would not work. She couldn''t sit or stand. She denies numbness or tingling in her limbs. She called 911 which brought her to the ED. She was given a "pain shot" because her arm hurt, and an injection for her blood pressure and diabetes. She was not treated with anything specifically for the loss of function in her limbs. Arm and leg function returned to normal around 11am.


VAERS ID: 2131433 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-29
Onset: 2021-10-10
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 046C21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7336NA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cardioversion, Gastrointestinal tube insertion, Hypothermia, Hypoxia, Intensive care, Postoperative adhesion, Respiratory arrest, Respiratory distress, Resuscitation, Small intestinal obstruction
SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (broad), Gastrointestinal obstruction (narrow), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Accidents and injuries (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 12 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Small bowel obstruction due to postoperative adhesions. Patient developed increased respiratory distress after multiple NG tube placement attempts, he then developed hypoxia and respiratory arrest. Patient received 15 minutes of CPR, 4 doses of epinephrine, and 2 doses of bicarbonate, and 1 cardioversion. Patient initially required ICU support along with a hypothermic protocol and 3 pressor support. Patient slowly stabilized and hypothermia reversal began and support was slowly weaned. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2131171 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-03
Onset: 2021-11-21
   Days after vaccination: 18
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7378JA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Gangrene, Osteomyelitis acute, Skin discolouration
SMQs:, Osteonecrosis (broad), Hypotonic-hyporesponsive episode (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 11 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ER visit on 11/21 - concerns of a blackened right fifth toe. Biotic ointment and Call your podiatrist or surgeon early next week and consider early amputation before spreading infection does occur. 12/3 - hospital admission gangrene. Procedure - Acute osteomyelitis of right foot. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2131136 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-12
Onset: 2021-12-09
   Days after vaccination: 27
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7347LA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Anticoagulant therapy, Cardiopulmonary bypass, Coronary artery bypass
SMQs:, Embolic and thrombotic events, arterial (narrow), Other ischaemic heart disease (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 11 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Coronary artery bypass grafting x3 - left internal mammary artery grafted to LAD and reverse saphenous vein grafts placed to diagonal and right posterior descending coronary arteries on cardiopulmonary bypass. The patient was discharged on ASA, statin and beta blocker therapy. Plavix was added by CT surgery post-op and should be continued for one year (smaller targets). ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2131122 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-20
Onset: 2021-10-25
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8020 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Catheter placement, Fall, Head injury, Incisional drainage, Oedema, Pain, Pyrexia, Skin abrasion, Swelling face, Tenderness
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Accidents and injuries (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient fell and had swelling and a large abrasion to the forehead, extending into the scalp. ED visit; Patient given tramadol for pain with a small prescription for this. Hospital admission for history of progressive left vulvar edema tenderness and febrile sensation. Incision and drainage was performed with placement of a Word catheter. She was deemed to have achieved maximal benefit of inpatient therapy on the third postoperative day and discharged to home care on doxycycline. ED visit and hospital admission were separate and both within 6 weeks of receiving the COVID vaccine.


VAERS ID: 1829667 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-27
Onset: 2021-10-29
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-10-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Rash pruritic
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: allergic type, itchy rash on full body. treated with dexamethasone and vistaril.


VAERS ID: 2507077 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-01-04
Onset: 2022-01-06
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 069H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100372322 / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Alcohol withdrawal syndrome, Suicidal ideation
SMQs:, Suicide/self-injury (narrow), Psychosis and psychotic disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: Patient admitted to the hospital within 30 days of receiving MODERNA COVID-19 vaccine. Patient is admitted for alcohol withdrawal with suicidal ideation.


VAERS ID: 2129453 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-14
Onset: 2021-10-02
   Days after vaccination: 18
Submitted: 0000-00-00
Entered: 2022-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: C-reactive protein abnormal, Pneumonia, Pneumonia bacterial, White blood cell count increased
SMQs:, Neuroleptic malignant syndrome (broad), Eosinophilic pneumonia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit to hospital admission for Community acquired bacterial pneumonia. At the time of admission he was also requiring 4 L supplemental oxygen versus chronic 3 L supplemental oxygen at home to maintain oxygen saturations greater than 90%. On 10/4/2021 WBC remained elevated but stable, CRP continued to trend down, and oxygen requirements returned to baseline 3 L/min. Patient was transition to oral Augmentin and azithromycin, IV steroids were decreased in frequency, and patient continued on scheduled and as needed breathing treatments. He will be discharged on oral azithromycin for 1 additional day to complete a 5-day course, as well as an additional 6 days of oral Augmentin to complete a 7-day course. This visit was within 6 weeks of receivingthe COVID vaccine.


VAERS ID: 2129154 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-08
Onset: 2021-10-28
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2022-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 312845 / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Acute kidney injury, Dehydration, Hypophagia, Urinary tract infection
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 23 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ER admission for dehydration on 10/28/2021. Patient was found to have a urinary tract infection. First dose of nitrofurantoin was given in the emergency department with remaining prescription sent to the pharmacy. ED to hospital admission on 11/9/2021. AKI - resolved with hydration, stable off IV fluids although PO Intake is poor. ER visits and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2122983 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-16
Onset: 2021-11-16
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2022-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 312854 / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Arterial graft, Peripheral artery bypass, Peripheral ischaemia, Vascular stent occlusion
SMQs:, Myocardial infarction (broad), Ischaemic central nervous system vascular conditions (narrow), Embolic and thrombotic events, arterial (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute class IIb right lower extremity ischemia secondary to occluded right superficial to popliteal artery stents s/p right common femoral to above-knee popliteal artery bypass with PTFE. deemed appropriate for discharge after 3 days. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2504453 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-07
Onset: 2022-11-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ875AD / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given a monovalent pfizer vaccine as a booster. Patient should have been given the bivalent pfizer vaccine. No adverse outcomes. PCP consulted. Patient advised per CDC that repeat dose needed in at least two months.


VAERS ID: 2101796 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-09
Onset: 2022-01-21
   Days after vaccination: 43
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100369750 / N/A LA / IM
HEPAB: HEP A + HEP B (TWINRIX) / GLAXOSMITHKLINE BIOLOGICALS 93KF5 / 3 RA / IM
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS J39HG / UNK LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2504464 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-07
Onset: 2022-11-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ875AD / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given a monovalent pfizer vaccine as a booster. Patient should have been given the bivalent pfizer vaccine as a booster. No adverse outcomes. PCP consulted. Patient advised per CDC that repeat dose needed in at least two months.


VAERS ID: 2504468 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-07
Onset: 2022-11-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ875AD / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given a monovalent pfizer vaccine as a booster. Patient should have been given the bivalent pfizer vaccine as a booster. No adverse outcomes. PCP consulted. Patient advised per CDC that repeat dose needed in at least two months.


VAERS ID: 2122957 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-04
Onset: 2021-11-22
   Days after vaccination: 18
Submitted: 0000-00-00
Entered: 2022-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cervical radiculopathy, Intervertebral disc operation, Pain, Spinal osteoarthritis
SMQs:, Arthritis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Admitted with cervical spondylosis and cervical radiculopathy failing medical management. Procedure: Anterior discectomy and fusion. At time of Dc tolerating general diet, ambulating safely in corridors, voiding without difficulty, and pain acceptably controlled with oral pain medications. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2514101 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7137 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS J39G3 / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Covid19 Pfizer 12 and up was given and was expired on 11-7-22. No reaction.


VAERS ID: 2119468 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-14
Onset: 2021-10-21
   Days after vaccination: 37
Submitted: 0000-00-00
Entered: 2022-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Small intestinal obstruction, Surgery
SMQs:, Gastrointestinal obstruction (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Small bowel obstruction. Acute care surgery. Discharged to home. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2119428 (history)  
Form: Version 2.0  
Age: 93.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-20
Onset: 2021-10-14
   Days after vaccination: 24
Submitted: 0000-00-00
Entered: 2022-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cardiac failure acute, Left ventricular failure
SMQs:, Cardiac failure (narrow), Cardiomyopathy (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute on chronic systolic heart failure. Patient was diuresed with an improvement in symptoms. She remains rate controlled on BB therapy. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2515736 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-06
Onset: 2022-10-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9703 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7695JA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product storage error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Bupropion XL, Lisinopril-HCTZ, Dulaglutide, fluticasone propionate, metformin, buspirone, montelukast, albuterol
Current Illness: N/A
Preexisting Conditions: Diabetes Type II, Hypertension, Mixed anxiety and depression, PTSD, Asthma, hyperlipidemia
Allergies: Aspirin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Gave pt a Covid booster vaccine that had been opened more than 12Hrs before administration. Vaccine Opened documenation stated 10/05/2022 13:45 Exp- 10/06/2022 1945. My mistake was that i just verified exp date and time and not opened time and date. Did review this information with Pt pcp and he reviewed the vaccine information and information stated vaccine was good refrigirated for 10 weeks room temperature 12 hrs. Unable to find information for vaccine stability once opened. He stated vaccine should be ok. Manager was also notiifed vial was discarded


VAERS ID: 2515845 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-15
Onset: 2022-11-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GK3724 / 5 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal pain, Headache, Illness, Insomnia, Interchange of vaccine products, Off label use, Product use issue, Pyrexia, SARS-CoV-2 test
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Covid-19 test; Test Result: Negative ; Comments: tested for negative for covid
CDC Split Type: USPFIZER INC202201318613

Write-up: she has been sick since then/She has been sick for 6 days; headache; abdominal pain; difficulty in sleeping/could not sleep properly; fever; she received the vaccine last 15Nov2022, and at the same day, she also received the flu vaccine; she received the vaccine last 15Nov2022, and at the same day, she also received the flu vaccine; Interchange of vaccine products; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP) from medical information team. The reporter is the patient. A 77-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Nov2022 as dose 5 (booster), single (Lot number: GK3724) for covid-19 immunisation; influenza vaccine inact split 4v (FLUZONE HIGH DOSE QUADRIVALENT), on 15Nov2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Moderna covid vaccine (DOSE 4 (Booster), she received 4 doses of the Moderna covid vaccine), administration date: 13May2022, for Covid-19 Immunization; Moderna covid vaccine (DOSE 3 (Booster), she received 4 doses of the Moderna covid vaccine), for Covid-19 Immunization; Moderna covid vaccine (DOSE 2, she received 4 doses of the Moderna covid vaccine), for Covid-19 Immunization; Moderna covid vaccine (DOSE 1, she received 4 doses of the Moderna covid vaccine), for Covid-19 Immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 15Nov2022, outcome "unknown"; OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 15Nov2022, outcome "unknown" and all described as "she received the vaccine last 15Nov2022, and at the same day, she also received the flu vaccine"; ILLNESS (non-serious), outcome "unknown", described as "she has been sick since then/She has been sick for 6 days"; HEADACHE (non-serious), outcome "unknown"; ABDOMINAL PAIN (non-serious), outcome "unknown"; INSOMNIA (non-serious), outcome "unknown", described as "difficulty in sleeping/could not sleep properly"; PYREXIA (non-serious), outcome "unknown", described as "fever". The event "she has been sick since then/she has been sick for 6 days" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: Patient stated that she received the vaccine last 15Nov2022, and at the same day, also received the flu vaccine. Patient was told by the nurse who administered the vaccines that it was okay to receive them together, while some told her that it should not be given together. Patient added that she has been sick since then. Patient had been sick for 6 days and had visited the urgent care last Saturday where patient was tested for negative for covid. Patient further explained that she had been healthy before getting the mentioned vaccines, but she had been experiencing headache, abdominal pain, difficulty in sleeping/could not sleep properly, and fever. Patient added that she frequently used the bathroom due to the abdominal pain. Patient also mentioned that previously, received 4 doses of the Moderna covid vaccine. Patient was worried that she may die due to these SEs and that her son died from Covid, and she does not want to happen to her as well. Consumer stated, "It was good now you could talk to me, before I cannot talk and did not even get up from bed. I just eat my lunch. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1825525 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-25
Onset: 2021-10-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS E9K44 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Inappropriate schedule of product administration, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamin daily
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Given 0.3 ml of Pfizer Covid vaccine at 8 years old .


VAERS ID: 2076172 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-04
Onset: 2021-11-13
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2022-01-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7383LA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Nodal arrhythmia
SMQs:, Disorders of sinus node function (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Junctional bradycardia. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2092421 (history)  
Form: Version 2.0  
Age: 85.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-07
Onset: 2021-10-17
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2022-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chronic obstructive pulmonary disease
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 12 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: COPD, moderate. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2087712 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-12
Onset: 2021-10-20
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2022-02-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 6 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Syncope and collapse. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2087643 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-06
Onset: 2021-11-16
   Days after vaccination: 41
Submitted: 0000-00-00
Entered: 2022-02-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30125BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Colon cancer metastatic, Metastases to liver
SMQs:, Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 14 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Metastatic colon cancer spread to liver. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID-19 vaccine.


VAERS ID: 2635143 (history)  
Form: Version 2.0  
Age: 0.75  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-05-12
Onset: 2023-05-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 214K22A / 2 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 244L3 / UNK LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna yellow cap 0.2mL/10ug given instead of higher dose of Moderna bivalent 0.25vmL/25ug


VAERS ID: 2638412 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-09-12
Onset: 2023-05-29
   Days after vaccination: 259
Submitted: 0000-00-00
Entered: 2023-05-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA A57143C / 4 - / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS G2979 / UNK - / -
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS 3G2C4 / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Anion gap, Base excess, Basophil count decreased, Basophil percentage decreased, Blood bicarbonate increased, Blood calcium decreased, Blood chloride decreased, Blood creatinine normal, Blood gases abnormal, Blood glucose normal, Blood lactic acid normal, Blood pH increased, Blood potassium decreased, Blood sodium decreased, Blood urea normal, Brain natriuretic peptide normal, Carbon dioxide normal, Chest X-ray abnormal, Chronic obstructive pulmonary disease, Computerised tomogram thorax abnormal, Condition aggravated, Creatinine renal clearance normal, Culture, Differential white blood cell count, Dyspnoea, Eosinophil count normal, Eosinophil percentage, Fraction of inspired oxygen, Full blood count, Gastrooesophageal reflux disease, Glomerular filtration rate normal, Haematocrit decreased, Haematology test abnormal, Haemoglobin decreased, Heart rate increased, Hypoxia, Laboratory test, Laboratory test abnormal, Lung disorder, Lymphocyte count, Lymphocyte percentage decreased, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume normal, Metabolic function test, Monocyte count, Monocyte percentage, Neutrophil count increased, Neutrophil percentage increased, Oxygen saturation decreased, PCO2 normal, PO2 normal, Platelet count normal, Pneumonia, Procalcitonin, Productive cough, Pyrexia, Rales, Red blood cell count decreased, Red cell distribution width normal, Renal function test normal, SARS-CoV-2 test negative, Sepsis, Staphylococcus test, Streptococcus test, Troponin, Troponin I, Wheezing, White blood cell count increased
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Haematopoietic erythropenia (narrow), Haematopoietic leukopenia (narrow), Lactic acidosis (broad), Haemorrhage laboratory terms (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific dysfunction (narrow), Hyponatraemia/SIADH (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Chronic kidney disease (broad), Hypersensitivity (broad), Tumour lysis syndrome (broad), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow), Infective pneumonia (narrow), Dehydration (broad), Hypokalaemia (narrow), Sepsis (narrow), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Document Type: History and Physical Document Subject: History & Physical Note Performed By: NP on May 29, 2023 17:25 Verified By: NP on May 29, 2023 17:25 Encounter Info: Inpatient, 05/29/23 - * Final Report * Document Has Been Revised And Contains Addenda History of Present Illness/Subjective 59 year old female w/ a hx of COPD on 2L O2 at baseline presents to the ED via private vehicle for evaluation of worsening SOA, fever, and productive cough over the last 24 hours. Pt was admitted on 5/6/2023 hospital for sepsis, COPD, and pneumonia. She explains that her current systems feel worse than then, and she has had to raise her O2 to 4L last night. Pt had a CT performed on 5/25/2023 which shows evidence of pneumonia, and she was informed of this. Denies vomiting or diarrhea. Denies hx of tobacco use. Upon ER evaluation her room air sat dropped below 88% and he was requiring up to 5 L per nasal cannula. Temperature was 37.4, heart rate was elevated at 118 respiratory rate was 20 and blood pressure was initially 105/73. Lab work obtained white blood cell count was elevated at 12.2, hemoglobin was 10.7, sodium was 135, potassium was 3.3, renal function was at her baseline with GFR greater than 90, glucose was 97, troponin was 27 BN P was 56, lactate was 1.2, VBG obtained with a pH of 7.48 and PCO2 was 40, COVID testing was negative. CXR showed Worsening multifocal airspace disease, likely infectious. Due to failure to improve with outpatient treatment for pneumonia patient will be brought in for further evaluation and management of pneumonia, sepsis. Review of Systems All 13 point review of systems were reviewed with the patient and are negative except as specified in the HPI Physical Exam/Objective Vitals & Measurements most recent past 24 hours Hemodynamics Neurologic Patient Weight Patient Height None Reported Constitutional: No acute distress, well-nourished Eyes: PEERL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs crackles and exp wheezing Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Sepsis A41.9 Sepsis order set in place ? Due to pneumonia failed outpatient treatment ? We will start vancomycin pharmacy dosing, cefepime and doxycycline ? Pending labs respiratory culture, procalcitonin, strep and MRSA PCR ? De-escalate antibiotic therapy as warranted as labs return 2. Pneumonia J18.9 Requiring oxygen at this time at increased flow within baseline. ? Chronic O2 use of 2 to 4 L at home, now on 5l nc ? RT protocol ? See plan above -CXR 5/29 Worsening multifocal airspace disease, likely infectious. 3. Hypoxia R09.02 Continue O2 as needed 4. Failure of outpatient treatment Z78.9 Meets inpatient criteria 5. GERD (gastroesophageal reflux disease) K21.9 Resume PPI 6. SOB (shortness of breath) R06.02 As above pneumonia plus?minus COPD exacerbation 7. Hypokalemia E87.6 replacement protocol Chronic back pain M54.9 Resume home meds COPD exacerbation J44.1 RT protocol continue Breo, Mucinex, doxycycline and IV steroids -Pt does not smoke , no hx of smoking, no work place exposures -Pt is a RT Hypertension I10 resume home meds Sleep apnea G47.30 RT routine evaluation and protocol -pt wears cpap at 8 ???????Patient is a full code ? DVT''s prophylaxis with Lovenox Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 05/29/23 17:25:00 albuterol, 2.5 mg, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q6H, PRN, Shortness of Breath/Wheezing, 05/29/23 17:24:00 RT Care Assessment and Protocol per Policy albuterol, 2.5 mg, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q6H, 05/29/23 19:00:00 RT Care Assessment and Protocol per Policy calcium carbonate, 750 mg, Orally, Tab, Chewable, 4 Times Daily, PRN, Indigestion, 05/29/23 17:25:00 cefePIME, 1 GM, IVPB, Injection, Q8H, Indication: Pneumonia - CAP (MRSA/PSA Risk Factors), 05/29/23 18:00:00 for 5 Days, 06/03/23 10:00:00 EDT, Total Volume (mL) = 50 docusate-senna, 2 Tablet, Orally, Tablet, BID, 05/29/23 21:00:00 doxycycline, 100 mg, Orally, Capsule, BID, Indication: COPD Exacerbation, 05/29/23 22:00:00 for 5 Days, 06/03/23 10:00:00 enoxaparin, 40 mg, Subcutaneous, Injection, Q24H, 05/30/23 6:00:00 guaifenesin, 600 mg, Orally, Tab, Extended Rel, BID, 05/29/23 21:00:00 hydrocodone-acetaminophen, 1 Tablet, Orally, Tablet, Q6H, PRN, Pain, Moderate (4-6 out of 10), 05/29/23 17:25:00 labetalol, 10 mg, IV Push, Injection, Q6H, PRN, Systolic Blood Pressure, 05/29/23 17:25:00 magnesium sulfate, 4 GM, IVPB, Injection, Q12H, PRN, Lab (Details Required), 05/29/23 17:26:00 methylPREDNISolone, 40 mg, IV Push, Injection, Q12H, 05/29/23 18:00:00 ocular lubricant, 1 App, Eyes, Both, Ophthalmic OINT, Q4H, PRN, Dry Eyes, 05/29/23 17:25:00 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 05/29/23 17:25:00 polyethylene glycol 3350, 17 GM, Orally, Powder, Daily, PRN, Constipation - Use First, 05/29/23 17:25:00 potassium chloride, 30 mEq, Orally, Tab, Extended Rel, Unscheduled, PRN, Lab (Details Required), 05/29/23 17:26:00 potassium chloride, 40 mEq, Orally, Tab, Extended Rel, Unscheduled, PRN, Lab (Details Required), 05/29/23 17:26:00 potassium phosphate-sodium phosphate, 1 Packet, Orally, Powder, Unscheduled, PRN, Lab (Details Required), 05/29/23 17:26:00 potassium phosphate-sodium phosphate, 1 Packet, Orally, Powder, Unscheduled, PRN, Lab (Details Required), 05/29/23 17:26:00 umeclidinium-vilanterol, 1 Puff, Inhalation, MDI/DPI Inhaler Treatment, Daily, 05/30/23 9:00:00 vancomycin, 1,750 mg, IVPB, Injection, ONCE, Indication: Pneumonia - HAP/VAP, NOW, 05/29/23 17:25:00 EDT, 05/29/23 17:25:00, 250 mL/hr, Infuse Over 2 Hours, Total Volume (mL) = 500 Admit to Inpatient CAH Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature CBC w/Differential Collect Specimen Collect Specimen Collect Specimen Comp Metabolic Panel COPD Education per Respiratory Care CPAP Nocturnal CPAP Nocturnal with NAPs DC SIRS Alert and Sepsis Screen Do Not (Specify) Heating Pad Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol Level of Care Message to Nursing MRSA PCR Nasal Cannula Notify Provider Notify Provider Notify Provider Notify Provider Peripheral IV Insertion Procalcitonin PT Evaluation and Treatment Regular Diet Resp CX + Stn Resp Evaluation or Assessment Resp Evaluation or Assessment Resuscitation Status Strep pneumoniae Ag Urine Titrate FiO2 to Keep O2 Sat Troponin-I High Sensitivity Vancomycin Pharmacy Dosing Consult Vital Signs Vital Signs Weight Code Status None Recorded Chronic Problem List Anemia B12 deficiency Bariatric surgery status Bilateral shoulder pain Chronic back pain Chronic fatigue COPD exacerbation Depression Encounter for long-term (current) use of medications Failure of outpatient treatment Fibromyalgia GERD (gastroesophageal reflux disease) History of total knee arthroplasty Hypertension Hypoxia IBS (irritable bowel syndrome) Laryngopharyngeal reflux Left knee pain Migraine headache Neuropathy Osteoarthritis of right shoulder Osteoarthritis of shoulders, bilateral Pneumonia Polypharmacy Pre-diabetes Restrictive lung disease Sepsis Sleep apnea SOB (shortness of breath) Total knee replacement status Urinary frequency Vocal cord leukoplakia Vocal cord nodules Wellness examination Procedure/Surgical History nerve block in lower back (03/29/2023) Total knee replacement (11/27/2017) Colonoscopy (2015) EGD (2015) Mammogram (07/07/2014) Cataract Extraction (2012) Hernia repair (2009) Total hysterectomy (1997) Cholecystectomy Laparoscopic (1993) Appendectomy BONE SPUR REMOVAL Carpal tunnel release Laminectomy lap band removal LAP-BAND surgery status left eye Release of trigger finger Scleral buckle procedure Thoracotomy Total replacement of right knee joint TUMOR REMOVED Surgical History Internal 08/31/2018 Retinal Detachment Repair (Left) MD 11/27/2017 Knee Arthroplasty (Left) MD 10/21/2016 Gastric Band Revision Lapscpy MD 01/12/2016 Bronchoscopy Diagnostic w Fluoro MD Medications Home Medications (24) Active Advair Diskus 250 mCg-50 mCg inhalation powder 1 Puff, Inhalation, BID, Refills must be obtained from PCPrinse mouth and throat after use albuterol 2.5 mg/3 mL (0.083%) inhalation solution 2.5 mg = 3 mL, PRN, Inhalation, Q6H albuterol-ipratropium inh soln 2.5 mg-0.5 mg/3 mL 3 mL, Neb Inhal, 4 Times Daily amitriptyline 25 mg oral tablet 25 mg = 1 Tablet, Orally, At Bedtime, for migraine prevention busPIRone 10 mg oral tablet 10 mg = 1 Tablet, Orally, BID cycloBENZaprine 10 mg oral tablet 10 mg = 1 Tablet, Orally, TID Cymbalta 60 mg oral delayed release capsule 60 mg = 1 Capsule, Orally, Daily, (do not crush or chew) Ester-C 1000 mg oral tablet 1,000 mg = 1 Tablet, Orally, Daily famotidine 20 mg oral tablet 20 mg = 1 Tablet, PRN, Orally, Daily ferrous sulfate 325 mg (65 mg elemental iron) oral tablet 325 mg = 1 Tablet, Orally, BID gabapentin 300 mg oral capsule 600 mg = 2 Capsule, Orally, TID hydroCHLOROthiazide 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily hyoscyamine 0.375 mg oral tablet, extended release 0.375 mg = 1 Tablet, PRN, Orally, Q12H ibuprofen 200 mg oral tablet 600 mg = 3 Tablet, Orally, TID Imitrex 100 mg oral tablet 100 mg = 1 Tablet, PRN, Orally, ONCE lansoprazole 15 mg oral delayed release capsule 15 mg = 1 Capsule, Orally, At Bedtime loperamide 2 mg oral tablet 2 mg = 1 Tablet, PRN, Orally, Q4H losartan 100 mg oral tablet 100 mg = 1 Tablet, Orally, Daily lysine 1000 mg oral tablet 1,000 mg = 1 Tablet, Orally, TID Norco 5 mg-325 mg oral tablet 1 Tablet, PRN, Orally, Q4H Os-Cal 500 , Orally Singulair 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily Super B Complex 1 Tablet, Orally, Daily Vitamin D3 10 mCg (400 intl units) oral capsule 10 mCg = 1 Capsule, Orally Active Scheduled Inpatient Medications albuterol (albuterol 2.5 mg/0.5mL (0.5%) inhalation solution), Inhalation SOLN, 2.5 mg, Neb Inhal, Q6H, Start: 05/29/23 19:00:00 One-Time Medications Given 05/28/23 00:00:00 TO 05/29/23 17:25:09 None Reported PRN Medications (0600 - 0559) from 05/28 - 05/29 None Reported Allergies Diflucan (severe itching) Stadol NS (Itching) Ventolin HFA (shortness of breath) Topamax (Tingling in extremities) Social History Alcohol Current, Wine, 1-2 times per week, Previous treatment: None. Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School disability Exercise Exercise duration: 0. Home/Environment MARRIED - two children - disability, Lives with Spouse. Nutrition/Health Diet: Regular. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Alcohol abuse: Aunt. Autoimmune disease..: Mother. Coronary artery disease..: Mother. DM (diabetes mellitus)..: Father. Heart disease..: Father. Hypertension..: Mother. Multiple sclerosis..: Mother and Aunt. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 12.2 k/cumm High (05/29/23 14:27:00) RBC: 3.6 million/cumm Low (05/29/23 14:27:00) Hgb: 10.7 GM/dL Low (05/29/23 14:27:00) Hct: 32.1 % Low (05/29/23 14:27:00) MCV: 89 fL (05/29/23 14:27:00) MCH: 29.7 pg (05/29/23 14:27:00) MCHC: 33.3 GM/dL (05/29/23 14:27:00) RDW: 13.6 % (05/29/23 14:27:00) Platelet: 253 k/cumm (05/29/23 14:27:00) MPV: 8 fL (05/29/23 14:27:00) Neutrophils %: 87 % (05/29/23 14:27:00) Lymphocytes %: 8 % (05/29/23 14:27:00) Monocytes %: 4 % (05/29/23 14:27:00) Eosinophils %: 1 % (05/29/23 14:27:00) Basophils %: 0 % (05/29/23 14:27:00) Absolute Neutrophil: 10.6 k/cumm High (05/29/23 14:27:00) Absolute Lymphocyte: 1 k/cumm (05/29/23 14:27:00) Absolute Monocyte: 0.5 k/cumm (05/29/23 14:27:00) Absolute Eosinophil: 0.1 k/cumm (05/29/23 14:27:00) Absolute Basophil: 0 k/cumm (05/29/23 14:27:00) Chemistry: Sodium SerPl QN: 135 mmol/L (05/29/23 14:27:00) Potassium SerPl QN: 3.3 mmol/L Low (05/29/23 14:27:00) Chloride SerPl QN: 97 mmol/L Low (05/29/23 14:27:00) Carbon Dioxide SerPl QN: 27 mmol/L (05/29/23 14:27:00) Anion Gap: 11 mmol/L (05/29/23 14:27:00) BUN SerPl QN: 12 mg/dL (05/29/23 14:27:00) Creatinine SerPl QN: 0.66 mg/dL (05/29/23 14:27:00) Estimated GFR (CKD-EPI, no race): $g90 (05/29/23 14:27:00) Estimated CRCL (CG): 107 mL/min (05/29/23 14:27:00) Glucose SerPl QN: 97 mg/dL (05/29/23 14:27:00) Calcium Total SerPl QN: 8.6 mg/dL (05/29/23 14:27:00) Troponin-I High Sensitivity: 27 ng/L High (05/29/23 14:27:00) BNP Pl QN: 56 pg/mL (05/29/23 14:27:00) Lactate Venous Pl QN: 1.2 mmol/L (05/29/23 14:27:00) pH Bld Venous QN: 7.48 High (05/29/23 14:27:00) PCO2 Bld Venous QN: 40 mmHg (05/29/23 14:27:00) PO2 Bld Venous QN: 42 mmHg (05/29/23 14:27:00) Base Excess Bld Venous: 6 mmol/L High (05/29/23 14:27:00) Bicarb Bld Venous Calc: 30 mmol/L High (05/29/23 14:27:00) O2 Sat Bld Venous Calc: 82 % (05/29/23 14:27:00) Patient Temperature: 37 DegC (05/29/23 14:27:00) All Other Labs: COVID 19 Specimen Source: Nasal (05/29/23 14:27:00) Coronavirus SARS-CoV2 Rapid: Not Detected (05/29/23 14:27:00) Diagnostics Radiology Results - Last 24 hours Across Visits 05/29/2023 15:16 - XR Chest PA or AP Portable IMPRESSION:Worsening multifocal airspace disease, likely infectious.Thank you for consulting our team of subspecialty radiologists Radiology. Please contact with any questions. Signature Line Electronically Signed on 05/29/23 17:25 ________________________________________________________ NP Electronically Signed on 05/29/23 17:27 ________________________________________________________ NP Addendum by MD on May 29, 2023 17:35:31 (Verified) I saw and evaluated the patient in addition to NP. I provided a substantive portion of the care for this patient. I personally performed in its entirety the history, exam and medical decision making for this encounter. I have reviewed and verified this documentation and it accurately reflects our care. Constitutional: No acute distress, well-nourished Eyes: no scleral icterus ENMT: Moist oral mucosa Respiratory: Increased WOB Cardiovascular: Regular rate and rhythm Gastrointestinal: non-distended Musculoskeletal: intact ROM Integumentary: no rashes Neurologic: no focal deficits Psychiatric: Cooperative, appropriate mood and affect MD, FACP Signature Line Electronically Signed on 05/29/23 17:35 ________________________________________________________ MD


VAERS ID: 2643471 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-28
Onset: 2023-06-05
   Days after vaccination: 220
Submitted: 0000-00-00
Entered: 2023-06-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051D22A / 5 - / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UNK / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal pain lower, Alanine aminotransferase normal, Ammonia, Anion gap, Aspartate aminotransferase normal, Asthenia, Auscultation, Back pain, Bacterial test positive, Basophil count decreased, Basophil percentage decreased, Bilirubin urine, Blood albumin normal, Blood alkaline phosphatase normal, Blood bilirubin increased, Blood calcium normal, Blood chloride normal, Blood creatine phosphokinase normal, Blood creatinine, Blood creatinine normal, Blood glucose normal, Blood lactic acid normal, Blood potassium normal, Blood sodium normal, Blood urea increased, Brain natriuretic peptide normal, Carbon dioxide decreased, Cerebral atrophy, Chest X-ray normal, Chromaturia, Chronic kidney disease, Coagulation test abnormal, Computerised tomogram abdomen abnormal, Computerised tomogram head abnormal, Condition aggravated, Creatinine renal clearance decreased, Eosinophil count decreased, Eosinophil percentage decreased, Fungal test positive, Gait inability, Gastrooesophageal reflux disease, Glomerular filtration rate normal, Glucose urine, Glycosylated haemoglobin normal, Haemangioma of liver, Haematocrit normal, Haematology test abnormal, Haemoglobin normal, Haemoglobin urine present, Headache, Hepatic steatosis, Hyperlipidaemia, Hypertension, International normalised ratio increased, Laboratory test abnormal, Leukocytosis, Lymphocyte count decreased, Lymphocyte percentage decreased, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume normal, Mesenteric arteriosclerosis, Micturition urgency, Monocyte count increased, Monocyte percentage increased, Muscular weakness, Neck pain, Neutrophil count increased, Neutrophil percentage increased, Nitrite urine absent, Percussion test normal, Platelet count normal, Pollakiuria, Protein total normal, Protein urine, Prothrombin time prolonged, Red blood cell count normal, Red blood cells urine positive, Red cell distribution width increased, SARS-CoV-2 test, Scan with contrast abnormal, Specific gravity urine normal, Troponin I, Urinary sediment present, Urinary tract infection, Urine abnormality, Urine analysis abnormal, Urine ketone body present, Urine leukocyte esterase positive, Urobilinogen urine, White blood cell count increased, White blood cells urine positive, pH urine normal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Liver related investigations, signs and symptoms (narrow), Liver neoplasms, benign (incl cysts and polyps) (narrow), Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Liver-related coagulation and bleeding disturbances (narrow), Haemolytic disorders (narrow), Acute pancreatitis (broad), Dyslipidaemia (narrow), Haematopoietic leukopenia (narrow), Peripheral neuropathy (broad), Haemorrhage laboratory terms (broad), Hyperglycaemia/new onset diabetes mellitus (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Embolic and thrombotic events, arterial (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Dystonia (broad), Biliary system related investigations, signs and symptoms (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific dysfunction (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypertension (narrow), Lipodystrophy (broad), Chronic kidney disease (narrow), Arthritis (broad), Tumour lysis syndrome (broad), Proteinuria (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on June 05, 2023 21:34 Verified By: MD on June 05, 2023 21:34 Encounter Info: Hospital, Inpatient, 06/05/23 - * Final Report * Document Has Been Revised History of Present Illness/Subjective Chief complaint: Generalized weakness History of present illness: 82-year-old female with past medical history of hypertension, diabetes mellitus, hyperlipidemia presented with generalized weakness. Family is at bedside assisting with history Patient is fairly active for her age, she works in the garden and is very independent of her ADLs. She was doing fine until the last 2 days when she started to have generalized weakness. Initially she had headache and neck pain and then felt very weak and was not able to walk. Today when family came from outside the found her sitting in the chair and was not able to move or use the bathroom. She was wearing a diaper which is very unusual for her. Patient complains of lower abdominal pain, low back pain without any radiation. This is better now She denies shortness of breath or cough. No fever or chills No vomiting or diarrhea She denies dysuria but has some urgency and frequency In the ED, she was given amlodipine 5 mg for uncontrolled hypertension and ceftriaxone Review of Systems Pertinent positives/negatives as noted in HPI. All other systems were reviewed and are negative. Physical Exam/Objective Vitals & Measurements most recent past 24 hours Hemodynamics Neurologic Patient Weight Patient Height None Reported 06/05/23 16:48 (L) 36.1 DegC 75 bpm 15 br/min 97 % 4 (H) 157 mmHg 67 mmHg 97 mmHg 55 kg Stand up General: Alert, in no acute cardiopulmonary distress. Mental Status: Oriented to person, place and time. Normal affect. Head: Normocephalic. Eyes: Pupils are equal, round and reactive to light. Extraocular muscles intact. Throat: Oropharynx clear, mucous membranes moist. Neck: Supple, Full range of motion. Respiratory: Clear to auscultation and percussion. No wheezing, rales or rhonchi. Cardiovascular: Heart sounds normal. No thrills. Regular rate and rhythm, no murmurs, rubs or gallops. Gastrointestinal: Abdomen soft, non-tender, non-distended. Normal bowel sounds. No pulsatile mass. No hepatosplenomegaly. Genitourinary: No costovertebral angle tenderness. Neurologic: Cranial nerves II-XII grossly intact. No focal neurological deficits. Deep tendon reflexes +2 bilaterally. Flexor plantar response. Moves all extremities spontaneously. Sensation intact bilaterally. Skin: No rashes or lesions. No petechiae or purpura. No edema. Musculoskeletal: No cyanosis or clubbing. No gross deformities. Normal range of motion. Assessment/Plan 82-year-old female with past medical history of hypertension, diabetes mellitus, hyperlipidemia presented with generalized weakness 1. Generalized weakness R53.1 PT/OT -Likely from UTI -Check TSH and B12 -COVID-19 is pending -CT head showed generalized cerebral atrophy without acute intracranial abnormality ? Chest x-ray showed no acute findings ? CT abdomen/pelvis showed no acute findings, liver hemangiomas, proximal SMA atherosclerotic narrowing, mild fatty liver -Her weakness is more in the lower legs but she does not have any weakness in the upper extremities or facial droop/dysphagia or dysarthria. We will hold off on MRI of the brain. She denies having any trauma to her back. Denies any fall 2. Acute UTI N39.0 UA showed WBC of 21-50 and moderate leukocyte esterase -Continue ceftriaxone and follow urine cultures 3. Leukocytosis D72.829 Leukocytosis with WBC of 12.6. Patient does not have sepsis. No tachycardia or tachypnea -Chest x-ray and CT abdomen/pelvis showed no acute issues 4. Chronic kidney disease (CKD) N18.9 stage 3. Baseline creatinine is less than 1. Monitor 5. Diabetes mellitus E11.9 Hold metformin due to recent contrast exposure and start on low sliding scale insulin. Her A1c''s have been less than 7 6. Gastroesophageal reflux disease K21.9 Awaiting reconciliation. Plan to continue Protonix 7. Hypertension I10 On hydralazine as needed. She received amlodipine 5 mg in ED 8. Liver hemangioma D18.03 Noted and stable from previous CT scans 9. Hyperlipidemia E78.5 On statin 10. On deep vein thrombosis (DVT) prophylaxis Z79.899 On Lovenox Orders: Status Order Acknowledgement Code Status None Recorded Chronic Problem List Anxiety Atrophic vaginitis B12 deficiency Chronic kidney disease (CKD) Cognitive decline Dementia Diabetes mellitus Encounter for vitamin deficiency screening Encounter for vitamin deficiency screening Foot pain, left Gastroesophageal reflux disease Hypertension Hypokalemia Insomnia Liver hemangioma Long term use of drug Annual wellness visit, subsequent Pain of left lower leg Procedure/Surgical History ?Diabetic retinal eye exam (11/22/2021) ?colonoscopy (10/12/2016) ?CT of abdomen and pelvis (10/19/2015) ?Appendectomy ?Cesarean section ?Cystocele ?Hysterectomy Surgical History Internal 10/12/2016 Colonscpy Diagnostic/Screen MD Medications Home Medications (12) Active amLODIPine 5 mg oral tablet 5 mg = 1 Tablet, Orally, BID Blood Glucose Test Strips See Instructions, Test Blood Sugar once a day Dx: DM E11.9 Claritin 10 mg oral tablet 10 mg, Orally, Daily lancets See Instructions, use to test blood sugar once daily.Dx: E11.9 Lancets See Instructions, use to check blood sugar once dailywhat brand ins covers dx E11.9 Melatonin 10 mg, Orally, At Bedtime metFORMIN 500 mg oral tablet 500 mg = 1 Tablet, Orally, BID multivitamin , Orally, Daily pravastatin 40 mg oral tablet 40 mg = 1 Tablet, Orally, At Bedtime Protonix 40 mg oral delayed release tablet 40 mg = 1 Tablet, Orally, Daily Strips - Glucose Test See Instructions, use to check blood sugar once daily dx: E11.9 Systane Ultra Preservative Free 1 Drop, Eyes, Both, BID Active Scheduled Inpatient Medications None Reported One-Time Medications Given 06/04/23 00:00:00 TO 06/05/23 21:32:05 None Reported PRN Medications (0600 - 0559) from 06/04 - 06/05 None Reported Allergies Centrum Silver (unknown) Fish (unknown) Premarin (unknown) Tagamet (unknown) aspirin (unknown) penicillins (unknown) terfenadine derivatives (unknown) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Asthma: Mother. Depression: Sister. Diabetes...: Father. Heart disease..: Grandmother (M). Hypertension..: Father. Stroke: Grandmother (M). Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 12.6 k/cumm High (06/05/23 18:04:00) RBC: 4.75 million/cumm (06/05/23 18:04:00) Hgb: 13.4 GM/dL (06/05/23 18:04:00) Hct: 40.7 % (06/05/23 18:04:00) MCV: 86 fL (06/05/23 18:04:00) MCH: 28.3 pg (06/05/23 18:04:00) MCHC: 33 GM/dL (06/05/23 18:04:00) RDW: 14.6 % High (06/05/23 18:04:00) Platelet: 395 k/cumm (06/05/23 18:04:00) MPV: 7.6 fL (06/05/23 18:04:00) Neutrophils %: 83 % (06/05/23 18:04:00) Lymphocytes %: 8 % (06/05/23 18:04:00) Monocytes %: 10 % (06/05/23 18:04:00) Eosinophils %: 0 % (06/05/23 18:04:00) Basophils %: 0 % (06/05/23 18:04:00) Absolute Neutrophil: 10.4 k/cumm High (06/05/23 18:04:00) Absolute Lymphocyte: 0.9 k/cumm Low (06/05/23 18:04:00) Absolute Monocyte: 1.2 k/cumm (06/05/23 18:04:00) Absolute Eosinophil: 0 k/cumm (06/05/23 18:04:00) Absolute Basophil: 0 k/cumm (06/05/23 18:04:00) Chemistry: Sodium SerPl QN: 138 mmol/L (06/05/23 18:04:00) Potassium SerPl QN: 3.6 mmol/L (06/05/23 18:04:00) Chloride SerPl QN: 101 mmol/L (06/05/23 18:04:00) Carbon Dioxide SerPl QN: 22 mmol/L (06/05/23 18:04:00) Anion Gap: 15 mmol/L High (06/05/23 18:04:00) BUN SerPl QN: 30 mg/dL High (06/05/23 18:04:00) Creatinine SerPl QN: 0.92 mg/dL (06/05/23 18:04:00) Estimated GFR (CKD-EPI, no race): 62 mL/min/1.73m2 (06/05/23 18:04:00) Estimated CRCL (CG): 41 mL/min Low (06/05/23 18:04:00) Glucose SerPl QN: 169 mg/dL High (06/05/23 18:04:00) Calcium Total SerPl QN: 10.1 mg/dL (06/05/23 18:04:00) Alkaline Phos SerPl QN: 66 Units/L (06/05/23 18:04:00) ALT SerPl QN: 12 Units/L (06/05/23 18:04:00) AST SerPl QN: 15 Units/L (06/05/23 18:04:00) Bilirubin Total SerPl QN: 1.2 mg/dL High (06/05/23 18:04:00) Total Protein SerPl QN: 8.2 GM/dL High (06/05/23 18:04:00) Albumin SerPl QN: 4.4 GM/dL (06/05/23 18:04:00) CK SerPl QN: 124 Units/L (06/05/23 18:04:00) Troponin-I High Sensitivity: 10 ng/L (06/05/23 18:04:00) BNP Pl QN: 67 pg/mL (06/05/23 18:04:00) Ammonia Pl QN: 32 mCmol/L (06/05/23 18:04:00) Lactate Venous Pl QN: 1.4 mmol/L (06/05/23 18:04:00) Coagulation: PT: 13.1 seconds (06/05/23 18:04:00) INR: 1.14 (06/05/23 18:04:00) Urine Studies: Color: Yellow (06/05/23 18:33:00) Clarity: Slightly Cloudy (06/05/23 18:33:00) Specific Gravity: 1.027 (06/05/23 18:33:00) pH: 5.5 (06/05/23 18:33:00) Protein: 200 Abnormal (06/05/23 18:33:00) Glucose: 50 Abnormal (06/05/23 18:33:00) Ketones: 20 Abnormal (06/05/23 18:33:00) Bilirubin: NEGATIVE (06/05/23 18:33:00) Hgb Ur: Small 1+ Abnormal (06/05/23 18:33:00) Nitrite: NEGATIVE (06/05/23 18:33:00) Urobilinogen: Normal (06/05/23 18:33:00) Leukocyte Esterase Ur: Moderate250 Abnormal (06/05/23 18:33:00) WBC: 21-50 Abnormal (06/05/23 18:33:00) RBC: 6-10 Abnormal (06/05/23 18:33:00) Bacteria: TRACE. (06/05/23 18:33:00) Yeast Ur: PRESENT. Abnormal (06/05/23 18:33:00) Squamous Epithelial: Few (06/05/23 18:33:00) Mucous: PRESENT. (06/05/23 18:33:00) Diagnostics Radiology Results - Last 24 hours Across Visits 06/05/2023 18:08 - XR Chest PA or AP Portable IMPRESSION:1. No acute findings in the chest.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. 06/05/2023 19:58 - CT Abd/Pelvis W/IV Contrast IMPRESSION:1. No acute findings in the abdomen or pelvis.2. Multiple hypoechoic liver lesions are similar to decreased insize from the patient''s prior study and are compatible withhemangiomas.3. Mild to moderate atherosclerotic narrowing of the proximal SMAfor 2.5 cm.4. Mild fatty liver.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. 06/05/2023 19:58 - CT Head W/o IV Contrast IMPRESSION: 1. Stable generalized cerebral atrophy without CT evidence of acuteintracranial abnormalities.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. Signature Line Electronically Signed on 06/05/23 21:34 ________________________________________________________ MD Electronically Signed on 06/05/23 23:19 ________________________________________________________ MD Reviewed by MD


VAERS ID: 2643532 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-11-22
Onset: 2023-06-06
   Days after vaccination: 196
Submitted: 0000-00-00
Entered: 2023-06-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 074B22A / 2 - / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ945AB / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal pain upper, Alanine aminotransferase increased, Alcohol use, Amylase normal, Anion gap, Aspartate aminotransferase increased, Auscultation, Back pain, Bacterial test negative, Bilirubin conjugated normal, Bilirubin urine, Blood albumin normal, Blood alkaline phosphatase normal, Blood bilirubin normal, Blood calcium normal, Blood chloride decreased, Blood creatinine, Blood glucose normal, Blood potassium normal, Blood sodium normal, Blood urea normal, Carbon dioxide normal, Chest X-ray normal, Chromaturia, Cold sweat, Coma scale, Computerised tomogram abdomen abnormal, Creatinine renal clearance, Glomerular filtration rate, Glucose urine absent, Haematocrit increased, Haematology test, Haemoglobin increased, Haemoglobin urine absent, Hepatic steatosis, Laboratory test, Laboratory test abnormal, Lipase increased, Mean cell haemoglobin concentration normal, Mean cell haemoglobin increased, Mean cell volume increased, Mean platelet volume normal, Nausea, Nitrite urine absent, Pain, Pancreatitis, Platelet count normal, Protein total normal, Protein urine present, Red blood cell count normal, Red blood cells urine, Red cell distribution width normal, Sleep disorder, Specific gravity urine normal, Troponin I, Urinary sediment present, Urine analysis abnormal, Urine ketone body absent, Urine leukocyte esterase, Urobilinogen urine, White blood cell count increased, White blood cells urine, pH urine normal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Liver related investigations, signs and symptoms (narrow), Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Acute pancreatitis (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Chronic kidney disease (broad), Proteinuria (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on June 06, 2023 13:27 EDT Verified By: MD on June 06, 2023 16:10 EDT Encounter Info: Hospital, Emergency, 06/06/23 - 06/06/23 * Final Report * History of Present Illness/Subjective Chief complaint: Abdominal pain Patient is a 59-year-old female history CAD hypertension hypothyroid smoker complains of upper abdominal pain x3 days, constant, dull, radiates to her back, nothing makes it better or worse. She has tried tylenol and other otc medications without relief. Woken up in the middle of the night w/ cold sweats. Denies chest pain shortness of breath nausea vomiting or dysuria. Denies any surgical abdominal history. States pancreatitis diagnosed a few years ago but was sent home and does not know etiology of her pancreatitis. Still currently drinks alcoholic beverages 2-3 times a week. Upon evluation in ER found to have mild pancreatitis without abscess. Present on CT imaging. Review of Systems All 13 point review of systems were reviewed with the patient and are negative except as specified in the HPI Physical Exam/Objective Vitals & Measurements most recent past 24 hours T: 36.7 ?C (Oral) BP: 148/100 HR: 96 (Monitored) HR: 97 (Peripheral) RR: 17 SpO2: 95% Oxygen Therapy: Room air WT: 101.20 kg (WFC) Hemodynamics Neurologic Glasgow Coma Score: 15 Patient Weight Current Daily Weight: 101.2 kg 06/06/23 Patient Height Current Height: 172.7 cm 06/06/23 General: Alert and oriented, No Acute distress Eye: Pupils are equal, round and reactive to light HEENT: Normocephalic, atraumatic Neck: Supple, normal range of motion Oropharynx: No erythema or drainage. Respiratory: Lungs are clear to auscultation. No added sounds Cardiovascular: Normal rate, Regular rhythm. s1 s2 positive Gastrointestinal: Soft, Non-tender. BS present all 4 quadrants Musculoskeletal: Normal range of motion, No focal tenderness Integumentary: Warm, Dry, No rash Neurologic: No focal weakness. Sensation intact. Normal mood and affect. cranial nerves grossly intact Assessment/Plan 1. Pancreatitis K85.90 Patient has pancreatitis on the imaging at the time of presentation to the emergency room. -Keep patient n.p.o. start patient on normal saline 125 mill an hour -Nausea control with Zofran and pain control via Dilaudid and Norco. -Reintroduce diet tomorrow if patient is doing better. -Obtain GI consult if needed. -No need to trend lipase. 2. Upper abdominal pain R10.10 See problem #1 3. Alcohol abuse F10.10 Patient is known to have alcohol use disorder. -Check alcohol levels today and monitor for withdrawal. 4. CAD (coronary artery disease) I25.10 Noted. Resume home medications. Patient is chest pain-free. 5. Hypertension I10 Resume home medications. -Withhold lisinopril due to current pancreatitis. 6. Hypothyroidism E03.9 Resume home medications. Code Status None Recorded Chronic Problem List Affective disorder Alcohol abuse Alcohol intoxication Allergic rhinitis Black stools CAD (coronary artery disease) CAD in native artery Cervicalgia Chronic gastritis Dyslipidemia Dyspnea Hypertension Hypokalemia Hypothyroidism Hypovitaminosis D Left ankle pain Low back pain Lumbosacral Spondylosis without Myelopathy Osteoarthrosis, Unspecified Whether Generalized or Localized, Involving Other Specified Sites Polypharmacy Preventive measure Rheumatoid Arthritis Spinal cord stimulator status Tobacco use Tobacco use Procedure/Surgical History ?Appendectomy ?Ear surgery - rebuilt ear drums ?Hysterectomy ?T & A Surgical History Internal 07/31/2012 Spinal Drug Pump Revise Remove MD 06/29/2009 Spinal Drug Pump Revise Remove MD Medications Home Medications (14) Active albuterol-ipratropium , Neb Inhal aspirin 81 mg, Orally, Daily Combivent 103 mcg-18 mcg/inh inhalation aerosol with adapter 2 Puff, Inhalation, Daily DME Compression Stockings Not Applicable, Other, Unscheduled, Dispense 1 pair of stockings; wear as directed. Above the knee DME Shower Chair Not Applicable, Other, Unscheduled GaviLyte-G With Lemon Flavor Pack oral powder for reconstitution See Instructions, as directed. levothyroxine 25 mCg, Orally, Daily Lipitor 10 mg, Orally, Daily lisinopril 2.5 mg oral tablet , TAKE 1 TABLET BY MOUTH ONCE DAILY Lyrica 75 mg oral capsule 75 mg = 1 Capsule, Orally, TID Nexium 40 mg oral delayed release capsule 40 mg = 1 Capsule, Orally, BID oxygen 2 liters Prenatal Multivitamins 1 Tablet, Orally, Daily ProAir HFA , PRN, Inhalation Active Scheduled Inpatient Medications None Reported One-Time Medications Given 06/05/23 00:00:00 TO 06/06/23 13:27:48 HYDROmorphone (Dilaudid), Injection, 0.5 mg, IV Push, ONCE, (1 DOSE 06/06/23 10:34:00) HYDROmorphone (HYDROmorphone Inj ED (1 mg/mL)), Injection, 1 mg, IV Push, ONCE, (1 DOSE 06/06/23 13:16:00) metoCLOPramide, Injection, 10 mg, IV Push, ONCE, (1 DOSE 06/06/23 12:33:00) ondansetron, Injection, 4 mg, IV Push, ONCE, (1 DOSE 06/06/23 09:19:00) ondansetron, Injection, 4 mg, IV Push, ONCE, (1 DOSE 06/06/23 11:12:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 06/06/23 12:22:00) PRN Medications (0600 - 0559) from 06/05 - 06/06 None Reported Allergies sulfa drugs Arthrotec (Numbness) Darvocet (Nausea) Effexor ("feels wierd") Keflex (Rash) Neurontin (Nausea) Paxil (Nausea) Topamax (Nausea) Ultram (Nausea) morphine (Hives) sulfADIAZINE (Rash) Social History Alcohol Current, Liquor, 1-2 times per week Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse - Denies Substance Abuse Current, Marijuana Tobacco Tobacco Use: 10 or more cigarettes (1/2 pack or more)/day in last 30 days. Family History Diabetes mellitus: Mother and Sister. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 15 k/cumm High (06/06/23 09:13:00) RBC: 4.99 million/cumm (06/06/23 09:13:00) Hgb: 16.6 GM/dL High (06/06/23 09:13:00) Hct: 48.9 % (06/06/23 09:13:00) MCV: 98 fL (06/06/23 09:13:00) MCH: 33.3 pg (06/06/23 09:13:00) MCHC: 33.9 GM/dL (06/06/23 09:13:00) RDW: 14.4 % (06/06/23 09:13:00) Platelet: 244 k/cumm (06/06/23 09:13:00) MPV: 7.8 fL (06/06/23 09:13:00) Chemistry: Sodium SerPl QN: 137 mmol/L (06/06/23 09:13:00) Potassium SerPl QN: 3.6 mmol/L (06/06/23 09:13:00) Chloride SerPl QN: 97 mmol/L Low (06/06/23 09:13:00) Carbon Dioxide SerPl QN: 30 mmol/L High (06/06/23 09:13:00) Anion Gap: 10 mmol/L (06/06/23 09:13:00) BUN SerPl QN: 18 mg/dL (06/06/23 09:13:00) Creatinine SerPl QN: 0.72 mg/dL (06/06/23 09:13:00) Estimated GFR (CKD-EPI, no race): $g90 (06/06/23 09:13:00) Estimated CRCL (CG): 105 mL/min (06/06/23 09:13:00) Glucose SerPl QN: 108 mg/dL High (06/06/23 09:13:00) Calcium Total SerPl QN: 9.1 mg/dL (06/06/23 09:13:00) Alkaline Phos SerPl QN: 70 Units/L (06/06/23 09:13:00) ALT SerPl QN: 78 Units/L High (06/06/23 09:13:00) AST SerPl QN: 66 Units/L High (06/06/23 09:13:00) Bilirubin Direct SerPl QN: 0.1 mg/dL (06/06/23 09:13:00) Bilirubin Total SerPl QN: 0.6 mg/dL (06/06/23 09:13:00) Total Protein SerPl QN: 6.9 GM/dL (06/06/23 09:13:00) Albumin SerPl QN: 4.1 GM/dL (06/06/23 09:13:00) Amylase SerPl QN: 69 Units/L (06/06/23 10:44:00) Lipase SerPl QN: 496 Units/L High (06/06/23 09:13:00) Troponin-I High Sensitivity: 10 ng/L (06/06/23 09:13:00) Urine Studies: Color: Yellow (06/06/23 10:43:00) Clarity: Clear (06/06/23 10:43:00) Specific Gravity: 1.026 (06/06/23 10:43:00) pH: 6.5 (06/06/23 10:43:00) Protein: 10 Abnormal (06/06/23 10:43:00) Glucose: Normal (06/06/23 10:43:00) Ketones: NEGATIVE (06/06/23 10:43:00) Bilirubin: NEGATIVE (06/06/23 10:43:00) Hgb Ur: NEGATIVE (06/06/23 10:43:00) Nitrite: NEGATIVE (06/06/23 10:43:00) Urobilinogen: Normal (06/06/23 10:43:00) Leukocyte Esterase Ur: NEGATIVE (06/06/23 10:43:00) WBC: 0-5 (06/06/23 10:43:00) RBC: 0-2 (06/06/23 10:43:00) Bacteria: NONE (06/06/23 10:43:00) Squamous Epithelial: Few (06/06/23 10:43:00) Diagnostics Radiology Results - Last 24 hours Across Visits 06/06/2023 10:19 - XR Chest PA or AP Portable IMPRESSION:Cervical spine stimulator.No acute findings. 06/06/2023 11:51 - CT Abd/Pelvis W/IV Contrast IMPRESSION: Diffuse hepatic steatosis.Subtle inflammation around the head of the pancreas and descendingportion of the duodenum may represent mild pancreatitis versusduodenitis. Correlate clinically.Status post hysterectomy.Retained spine stimulator electrode. Signature Line Electronically Signed on 06/06/23 16:10 EDT ________________________________________________________ MD


VAERS ID: 2685566 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-09-23
Onset: 2023-09-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030368 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U80848A / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Injection site pain, Loss of consciousness, Paraesthesia
SMQs:, Torsade de pointes/QT prolongation (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt said they felt pain in left arm upon needle insertion like it "hit a nerve". She reports that her fingers were tingly but she felt well enough to leave the immunization room. Upon walking to the waiting area, she then felt faint and lowered herself to the ground where her spouse said she lost consciousness for about 5 seconds. She was given a cold pack and cold water and recovered after about 10 minutes.


VAERS ID: 2082306 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-13
Onset: 2021-10-28
   Days after vaccination: 15
Submitted: 0000-00-00
Entered: 2022-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chest pain, Small intestinal obstruction
SMQs:, Gastrointestinal obstruction (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ER - chest pain, ER - small bowel obstruction. Hospital admission. These visits were within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2688103 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-09-27
Onset: 2023-09-28
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 204F232A / UNK AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8130EA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Loss of consciousness, Road traffic accident, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt reported fainting "blackout" 1.5hrs after vaccination. Pt was driving at the time, resulted in minor car accident. No injuries reported.


VAERS ID: 2620356 (history)  
Form: Version 2.0  
Age: 98.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-04-22
Onset: 2023-04-23
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-04-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH - / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dysphagia, Facial paralysis
SMQs:, Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hearing impairment (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lexapro Ferrous sulfate Heparin Lidoderm patch Vit-B-1 Lasix Tylenol Flomax Lipitor
Current Illness:
Preexisting Conditions: ? Aortic atherosclerosis ? Arthritis of knee Prior cortisone injections ? Gastric ulcer 2002 Associated with UGI hemorrhage, syncope; related to NSAID use. ? Insomnia ? Sciatica
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Right facial droop, unable to swallow, steroids given and eyes drops instilled. Patient became better over time.


VAERS ID: 2689593 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-09-27
Onset: 2023-09-29
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH U8041CA / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Stomatitis
SMQs:, Severe cutaneous adverse reactions (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Developed an oral mucositis two days after vaccination. Resolved a few days later.


VAERS ID: 2069127 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-28
Onset: 2021-11-26
   Days after vaccination: 29
Submitted: 0000-00-00
Entered: 2022-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ768AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Hypoaesthesia, Paraesthesia
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Numbness and tingling in both hands. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2062336 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-04
Onset: 2021-11-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 211104-060 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7378JA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Bipolar I disorder, Mania, Psychotic disorder
SMQs:, Systemic lupus erythematosus (broad), Dementia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hostility/aggression (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 40 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Bipolar I disorder, single manic episode, severe, with psychosis. ED visit and hospital admission. This visit was within 6 weeks of receiving COVID vaccine.


VAERS ID: 2692393 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-01
Onset: 2023-10-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031279 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8094BA / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Nausea, Vertigo, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: vertigo, extreme nausea and vomiting


VAERS ID: 2059202 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-01
Onset: 2021-12-12
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2022-01-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Diverticulitis intestinal haemorrhagic
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Gastrointestinal haemorrhage (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Diverticular hemorrhage. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2693455 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-10
Onset: 2023-10-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031279 / 6 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS FJ4XS / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8132DA / N/A LA / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Received 2 doses of seasonal influenza vaccine. One high dose and one standard dose.


VAERS ID: 2695373 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-09-25
Onset: 2023-09-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: School       Purchased by: ?
Symptoms: Visual impairment
SMQs:, Anticholinergic syndrome (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: unknown
Diagnostic Lab Data:
CDC Split Type:

Write-up: A student complaining that he started having vision problems the night of receiving flu and COVID shots on 9/25/23. He has already been checked out in the ER and by an eye doctor. Outcome unknown.


VAERS ID: 1894178 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-19
Onset: 2021-10-20
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS NK45F / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Testicular pain
SMQs:, Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: got booster and next day my testicals felt like i got kicked in them. coincidently after initially receiving my 1st and 2nd dose i had a thrombus in my right spermatic cord which led to me having a denervation of the right groin in june. Initially, my doctors chalked up the first incident to coincidence. after talking with my urologist, he had me do 2 weeks of nsaids, with only an increase in pain. now currently on 600mg gabapentin 3x a day with moderate relief. currently continuing to follow with urologist.


VAERS ID: 2048048 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-08
Onset: 2022-01-06
   Days after vaccination: 90
Submitted: 0000-00-00
Entered: 2022-01-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Infection
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Breakthrough COVID


VAERS ID: 2095993 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-19
Onset: 2022-01-10
   Days after vaccination: 83
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100358553 / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2101764 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-22
Onset: 2022-01-20
   Days after vaccination: 29
Submitted: 0000-00-00
Entered: 2022-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367237 / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2099089 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-22
Onset: 2021-11-10
   Days after vaccination: 19
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026D21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Small intestinal obstruction
SMQs:, Gastrointestinal obstruction (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: SBO (small bowel obstruction). ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2099019 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-05
Onset: 2021-11-12
   Days after vaccination: 38
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025C21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dyspnoea
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: end-stage COPD, coronary artery disease, hypertension and solitary kidney who presented with progressive dyspnea. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2099018 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-23
Onset: 2022-01-13
   Days after vaccination: 21
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367237 / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2568701 (history)  
Form: Version 2.0  
Age: 6.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-01-24
Onset: 2023-01-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GD1857 / 1 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7723LA / 1 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given the Covid 19 Vaccine on 1/24/23 and it best by use date was 1/20/23. Patient had no issue after the shot was given.


VAERS ID: 2098851 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-02
Onset: 2022-01-11
   Days after vaccination: 40
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 95K95 / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 1885141 (history)  
Form: Version 2.0  
Age: 6.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-18
Onset: 2021-11-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7411LA / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vaccine that had been out of fridge for $g12 hrs was administered. No adverse reactions have been reported.


VAERS ID: 2098810 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-09
Onset: 2022-01-11
   Days after vaccination: 33
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029H21B / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367237 / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2098732 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-06
Onset: 2022-01-11
   Days after vaccination: 97
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100353153 / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2096668 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-02-08
Onset: 2022-02-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8094 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / UNK RA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. T028583 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dizziness, Pallor, Presyncope
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: near fainting pale lips dizziness


VAERS ID: 1876626 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-08
Onset: 2021-10-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Chills
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: RIgors starting approximately 15 hours after dose administration and continuing for 3-4 hours


VAERS ID: 2095850 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-01
Onset: 2022-01-10
   Days after vaccination: 70
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 062E21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367238 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19.


VAERS ID: 2571830 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-02
Onset: 2021-11-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367899 / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative:


VAERS ID: 2574866 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-02
Onset: 2021-11-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367899 / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative:


VAERS ID: 2574884 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-16
Onset: 2021-11-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 065F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367900 / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Cardio-respiratory arrest, Death, Mechanical ventilation, Unresponsive to stimuli
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Respiratory failure (broad), Hypoglycaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-11-17
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: Patient received vaccines 11/16/2021. On 11/17/2021 patient was found unresponsive in his yard by his son in law, EMS was called and patient taken to outside emergency facility. Noted to be in cardio/respiratory arrest by EMS while in route to hospital. Patient was placed on a ventilator at the outside facility and expired later that day. ER documents not available at this time.


VAERS ID: 2095624 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-25
Onset: 2022-01-05
   Days after vaccination: 72
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100358553 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Positive COVID-19


VAERS ID: 2095501 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-01
Onset: 2021-11-12
   Days after vaccination: 42
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 034C21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Acute left ventricular failure
SMQs:, Cardiac failure (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Cardiomyopathy (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute diastolic heart failure. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2095461 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-27
Onset: 2021-10-16
   Days after vaccination: 19
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Myasthenia gravis
SMQs:, Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-11-27
   Days after onset: 42
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Myasthenia gravis. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2092838 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-03
Onset: 2021-11-25
   Days after vaccination: 22
Submitted: 0000-00-00
Entered: 2022-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ768AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Acute myocardial infarction
SMQs:, Myocardial infarction (narrow), Embolic and thrombotic events, arterial (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: NSTEMI . ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2092439 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-20
Onset: 2021-10-03
   Days after vaccination: 13
Submitted: 0000-00-00
Entered: 2022-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Major depression
SMQs:, Psychosis and psychotic disorders (broad), Depression (excl suicide and self injury) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 37 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Current severe episode of major depressive disorder without psychotic features without prior episode. Hospital Admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2328828 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-01-05
Onset: 2022-01-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-06-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5Y9FK / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: vaccine administered past beyond use date


VAERS ID: 2192350 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-19
Onset: 2021-10-21
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7315KA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: End stage renal disease, Haemodialysis
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Chronic kidney disease (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ESRD (end stage renal disease) - Patient was started on hemodialysis. Social worker was consulted and arrange for outpatient dialysis. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2192122 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-29
Onset: 2021-11-03
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Bladder catheterisation, Bladder irrigation, Chromaturia, Coagulopathy, Computerised tomogram normal, Haematuria, Urinary tract infection, Urine analysis abnormal
SMQs:, Rhabdomyolysis/myopathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhage laboratory terms (broad), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient in for persistent hematuria. Was discharged last week with hematuria that resolved with bedside irrigations. Foley catheter was removed at the time of his last discharge as urine was clear. Patient redeveloped clot retention. He was treated in the emergency department with CBI and again his urine cleared. CT scan shows no obvious source of bleeding such as large bladder mass. No large quantity of clots within the bladder. UA suggestive of persistent UTI. At the time of discharge his urine is amber. This is with CBI off for approximately 1 hour. Patient will discharge back to memory care unit with the indwelling Foley catheter in place. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2192101 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-07
Onset: 2021-11-01
   Days after vaccination: 25
Submitted: 0000-00-00
Entered: 2022-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Acute respiratory failure, Cardiac failure congestive, Escherichia test positive, Polyuria, Urine analysis abnormal
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Retroperitoneal fibrosis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Cardiomyopathy (broad), Hypersensitivity (broad), Tubulointerstitial diseases (broad), Respiratory failure (narrow), Infective pneumonia (broad), Hypokalaemia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute respiratory failure with hypoxia - Her treatments at outside hospital included dobutamine, nitroglycerin iv, furosemide, metolazone, clindamycin, and azithromycin. Her presentation here seemed most consistent with acute CHF, but she was also treated for possible community acquired pneumonia. She also had E. Coli in her urine and was treated for possible UTI. She was diuresed, and treated with antibiotics, and had gradual improvement. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2190030 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-12
Onset: 2021-10-27
   Days after vaccination: 15
Submitted: 0000-00-00
Entered: 2022-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ760AC / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Aneurysm, Catheterisation cardiac normal, Echocardiogram abnormal, Ejection fraction decreased, Electroencephalogram, Endotracheal intubation, Pneumonia, Seizure, Troponin increased
SMQs:, Torsade de pointes/QT prolongation (broad), Cardiac failure (narrow), Angioedema (broad), Systemic lupus erythematosus (broad), Myocardial infarction (narrow), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (narrow), Eosinophilic pneumonia (broad), Generalised convulsive seizures following immunisation (narrow), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (narrow), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient had a seizure which brought her into the hospital and required intubation following inability to protect her airway. She was resumed on her Keppra, after being seen by Neurology and having an EEG. The seizures were due to an aneurysm that she had coiled years ago. She was also noted to have an elevation in her troponin. She was found to have an echo with an EF of about 40%. She had a Left heart cath which showed no evidence of CAD. While here she was treated for pneumonia which cleared up quickly after 7 days of treatment. She was discharged on the new medications of Keppra, Coreg, ASA, Lasix and her losartan was changed to 25 mg po every day. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2190002 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-12
Onset: 2021-11-12
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2022-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Fall, Hip arthroplasty, Hip fracture
SMQs:, Accidents and injuries (narrow), Osteoporosis/osteopenia (broad), Osteonecrosis (broad), Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient off ladder on day of admission sustaining a left hip fracture. Admitted for management. optimized medically and taken to the operating room where patient underwent a left hip bipolar hemiarthroplasty for fracture. Patient tolerated the procedure well with no apparent complications. Patient was transferred to the floor where patient remained afebrile with stable vitals signs. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2189939 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-07
Onset: 2021-11-11
   Days after vaccination: 35
Submitted: 0000-00-00
Entered: 2022-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ733AC / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Acute respiratory failure, Respiratory failure
SMQs:, Anaphylactic reaction (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Respiratory failure (narrow), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute on chronic hypoxic respiratory failure - She was given Solumedrol in ED and then was continued on with oral prednisone on admission. Her Levaquin was also continued to complete therapy recommended by Pulmonology. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2187559 (history)  
Form: Version 2.0  
Age: 86.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-29
Onset: 2021-11-10
   Days after vaccination: 42
Submitted: 0000-00-00
Entered: 2022-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30145BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Chest X-ray abnormal, Chronic obstructive pulmonary disease, Lung infiltration, Procalcitonin normal
SMQs:, Interstitial lung disease (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: COPD with acute exacerbation - Chest x-ray did not show obvious pneumonia. Patient was given 1 dose of ceftriaxone and azithromycin for questionable right lung infiltrate. Procalcitonin was negative. There was no leukocytosis. Patient was started on IV Solu-Medrol and was admitted to the hospital. The next day, the patient felt much better. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2184360 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-05
Onset: 2021-11-10
   Days after vaccination: 36
Submitted: 0000-00-00
Entered: 2022-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ733AC / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Atrial fibrillation
SMQs:, Supraventricular tachyarrhythmias (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient admitted for scheduled admission for Tikosyn initiation for persistent A fib rvr. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2184350 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-22
Onset: 2021-11-18
   Days after vaccination: 27
Submitted: 0000-00-00
Entered: 2022-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 312835 / 1 - / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Anticoagulant therapy, Biopsy liver abnormal, Hepatic cirrhosis, Pulmonary embolism
SMQs:, Liver related investigations, signs and symptoms (narrow), Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Embolic and thrombotic events, venous (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 6 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was admitted with acute pulmonary embolism moderate load without cor pulmonale. We used heparin and did a biopsy of the liver this lesion here was high suspicion of cancer however came back as nodular cirrhosis. he is to be on Eliquis for 7 days at 10 mg twice daily and then 5 mg twice daily indefinitely he does understand he has a high risk of bleeding bleeding complications otherwise he did well his family was involved many hours were spent in counseling and discussion to the course of this admission. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2184210 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-06
Onset: 2021-10-28
   Days after vaccination: 22
Submitted: 0000-00-00
Entered: 2022-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ733AC / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Atrioventricular block second degree, Cardiac pacemaker insertion
SMQs:, Conduction defects (narrow), Hypokalaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Second degree AV block, Mobitz type II-s/p PPM placement. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2194364 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-19
Onset: 2021-11-24
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-03-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051F21A / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ764AC / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Acute left ventricular failure, Blood creatinine decreased, Echocardiogram, Polyuria
SMQs:, Cardiac failure (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Retroperitoneal fibrosis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Cardiomyopathy (broad), Tubulointerstitial diseases (broad), Hypokalaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute diastolic heart failure - Following admission, he was started on iv diuresis and 2 D Echo was done. Seen by heart failure navigator and plan for outpatient follow-up. IV diuresis changed to p.o. torsemide. Cr as low as 0.81 with diuresis on discharge. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2574831 (history)  
Form: Version 2.0  
Age: 88.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-27
Onset: 2021-11-02
   Days after vaccination: 6
Submitted: 0000-00-00
Entered: 2021-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100350386 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Bruxism, Confusional state, Death, Decreased appetite, Eating disorder, Fatigue, Hyperaesthesia, Hypersomnia, Mouth breathing, Myalgia, Pain, Pyrexia, Screaming, Tremor, Urine output decreased
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Eosinophilic pneumonia (broad), Depression (excl suicide and self injury) (broad), Chronic kidney disease (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-11-03
   Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: covid booster and influenza vaccine administered 10/27/21, patient with baseline dementia and was screening prior to administration of vaccine and was in usual state of health. Fevers presented w/in 24 hours and resolved. Patient continued with fatigue, muscle pain and decreased appetite with difficulties eating (pocketing food) which was new. Confusion increased and developed hand tremors. Five days after vaccine patient had little urine output, was hollering in pain, gritting teeth when touched by caregiver. As patient with dementia at 88 years old, treatment plan did not include returning for further hospitalization. Patient became more sedated and began sleeping almost all day, developed further mouth breathing. Hospice services were ordered, however patient passed prior to starting on 11/3/21. Caregiver denied any other changes to patients routine/medications prior to administration of vaccines.


VAERS ID: 1868331 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-09
Onset: 2021-10-22
   Days after vaccination: 13
Submitted: 0000-00-00
Entered: 2021-11-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Anxiety, Balance disorder, Dizziness, Fatigue, Headache, Myalgia, Neck pain, Pain
SMQs:, Rhabdomyolysis/myopathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: levothyroxine
Current Illness: mild rhinovirus
Preexisting Conditions: CREST
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: also had a flu shot in the other arm - can''t find the paperwork to provide specific flu shot. My spouse and I received the vaccines on the same day. We both had the same symptoms over the last several weeks. Symptoms include: neck muscle pain that radiates up to the head, neck muscle pain that makes it painful to turn head, light headedness upon rising, fatigue. Spouse reports balance problems upon rising at night. Symptoms are decreasing but are worrying.


VAERS ID: 2328834 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-04-20
Onset: 2022-04-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-06-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK9895 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9339N / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: vaccine administered past beyond use date


VAERS ID: 1849451 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-05
Onset: 2021-11-06
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Mental status changes, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Reports of high fever and chills as well as mental status changes within 24 hours of vaccine. Patient was administered ibuprofen at home and seemed to reduce symptoms. Today patient states she is still chilling but has improved


VAERS ID: 2184175 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-07
Onset: 2021-11-11
   Days after vaccination: 35
Submitted: 0000-00-00
Entered: 2022-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30135BA / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR P100358553 / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Pelvic fracture
SMQs:, Accidents and injuries (narrow), Osteoporosis/osteopenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pelvic fracture. Surgical intervention was not recommended. She was cleared for weightbearing as tolerated. It was determined that admission to Rehab was necessary to allow for safe discharge back to home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2182428 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-16
Onset: 2021-11-23
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2022-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Anticoagulant therapy, Pulmonary embolism
SMQs:, Embolic and thrombotic events, venous (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pulmonary embolism - Pt was initiated on coumadin w/ lovenox bridging. This is due to hx of brain bleed and need for readily reversible anticoagulant. With assistance from the clinical pharmacist the pt was arranged for outpatient INR checks and follow up at a coumadin clinic in city. He was taught to self inject lovenox and given a 10 day supply to make sure he has enough supply in case the bridging takes longer. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2435936 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Male  
Location: Unknown  
Vaccinated: 0000-00-00
Onset: 2021-11-11
Submitted: 0000-00-00
Entered: 2022-08-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367897 / UNK - / IM

Administered by: Other       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative:


VAERS ID: 2433362 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Male  
Location: Unknown  
Vaccinated: 0000-00-00
Onset: 2021-11-11
Submitted: 0000-00-00
Entered: 2022-08-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 9100367897 / UNK - / IM

Administered by: Other       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative:


VAERS ID: 2422469 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-13
Onset: 2022-07-06
   Days after vaccination: 296
Submitted: 0000-00-00
Entered: 2022-08-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Delivery, Maternal exposure before pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Tetralogy of Fallot
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient DOB: 10/27/1987 Date of Admission: 7/5/2022 Date of Discharge: 7/8/2022 Diagnosis: Vaginal Delivery Hospital Course OB History Gravida Para Term Preterm AB Living 6 5 5 1 5 SAB IAB Ectopic Multiple Live Births 1 0 1 # Outcome Date GA Lbr Len/2nd Weight Sex Delivery Anes PTL Lv 6 Term 07/06/22 39w3d 3.856 kg (8 lb 8 oz) F Vag-Spont None LIV 5 Term 12/26/13 3.289 kg (7 lb 4 oz) M Vag-Spont 4 Term 07/12/12 2.778 kg (6 lb 2 oz) F Vag-Spont N Birth Comments: cleft palate 3 Term 03/30/10 3.402 kg (7 lb 8 oz) M Vag-Spont 2 Term 08/04/06 3.515 kg (7 lb 12 oz) M VBAC N 1 SAB The patient underwent a Vaginal delivery during this hospitalization. She is now 2 days postpartum. She has not had complications since the delivery. She has not been febrile. She did not have a surgical sterilization at the time of her delivery. At the time of discharge, the patient was afebrile and has been tolerating a regular diet. She has been ambulating and voiding without difficulty. Denies symptoms of orthostasis. Plan She has been given discharge instructions which include the following: No straining, No lifting over 15 pounds, No sex, No tampons, No douche and No tub baths. Follow up for a postpartum exam in 6 weeks. Call for any signs of fever, foul discharge, increased bleeding, wound redness or draining, or signs of postpartum depression. Discharge Medications Motrin 800 mg one every 8 hours #30 Signed: 7/8/2022 8:00 AM


VAERS ID: 2216092 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-01
Onset: 2021-10-31
   Days after vaccination: 30
Submitted: 0000-00-00
Entered: 2022-04-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Acute kidney injury, Blood culture negative, Culture urine negative, Hyperkalaemia, Pyrexia, Renal tubular necrosis
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Renovascular disorders (broad), Chronic kidney disease (broad), Tumour lysis syndrome (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 9 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit for febrile illness; treated and released. 3 Days later admitted for AKI; suspected to be due to ATN vs immunotherapy mediated. Hyperkalemial. Was started on empiric Vanco and Zosyn $g discontinued 2 days later after blood and urine cultures came back negative. Was seen by ID on 11/4 $g recommendation was to stop antibiotics and monitor. Was also seen by oncology on 11/7 $g fever thought to be either neoplastic fever versus Abraxane induced fever. Other hospital problems treated. ED visits and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2204302 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-20
Onset: 2021-10-09
   Days after vaccination: 19
Submitted: 0000-00-00
Entered: 2022-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal discomfort, Abdominal distension, Abdominal pain, Computerised tomogram abdomen abnormal, Nausea, Small intestinal obstruction
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal obstruction (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented to the ED on 10/9/2021 complaining of a three day history of abdominal discomfort/cramping, abdominal distension and nausea. CT scan of the abdomen and pelvis revealed a partial small bowel obstruction with transition point in the RLQ. She was admitted to the Acute Care Surgery Service for bowel rest and IV fluids - symptoms resolved and she began having bowel movements. Discharged to home. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2201777 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-01-13
Onset: 2022-01-31
   Days after vaccination: 18
Submitted: 0000-00-00
Entered: 2022-03-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 033H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Biopsy colon abnormal, Cardiac failure acute, Colitis microscopic, Decreased appetite, Left ventricular failure
SMQs:, Cardiac failure (narrow), Pseudomembranous colitis (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Ischaemic colitis (broad), Cardiomyopathy (broad), Noninfectious diarrhoea (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 12 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit - loss of appetite for 2 weeks, treated and discharged. ED to hospital admission 5 days later - Acute on chronic diastolic heart failure. Continue on IV Lasix 20 mg twice daily, Lopressor 50 mg twice daily, echocardiogram ordered. Biopsy of the colon confirms lymphocytic colitis. Case discussed with Dr. recommend treatment with budesonide, 9 mg daily for 2 weeks and then 6 mg daily for 2 weeks and then 3 mg daily for 1 month. Continued treatment and discharge to skilled nursing facility. ED visits and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2206728 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-16
Onset: 2022-01-05
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2022-03-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ779AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Blood pressure inadequately controlled, Hypoaesthesia, Lacunar infarction, Magnetic resonance imaging head abnormal
SMQs:, Peripheral neuropathy (broad), Ischaemic central nervous system vascular conditions (narrow), Embolic and thrombotic events, arterial (narrow), Guillain-Barre syndrome (broad), Hypertension (narrow), Cardiomyopathy (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient admitted to ED with complaints of numbness in head. MRI head showed acute left lacunar infarct. Per discussion with neuro stroke service, plan for optimal blood pressure control. Patient is being discharged with new blood pressure medication and blood pressure cuff to monitor BP. Patient will continue PTA aspirin and statin on discharge. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2201757 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-15
Onset: 2022-01-10
   Days after vaccination: 26
Submitted: 0000-00-00
Entered: 2022-03-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1620 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Pain, Pulmonary mass
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2022-02-03
   Days after onset: 24
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Right lower lobe lung mass - He will continue Augmentin to complete an antibiotic course for possible pneumonia. On discharge he had adequate pain/symptom control. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2209133 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-26
Onset: 2021-12-07
   Days after vaccination: 42
Submitted: 0000-00-00
Entered: 2022-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 077C21B / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 308475 / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Acute respiratory failure, Cardiac failure congestive, Dyspnoea, Hypoxia, Lung infiltration, Metabolic encephalopathy, Multiple organ dysfunction syndrome, Sepsis, Wheezing
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Interstitial lung disease (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Noninfectious encephalopathy/delirium (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Sepsis (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Severe sepsis with acute organ dysfunction - acute respiratory failure, metabolic encephalopathy;he developed a LLL infiltrate and was treated for possible bacterial pneumonia with Rocephin, doxycycline and continued on Solu-Medrol and nebulizer treatments. He had evidence of CHF so he was given IV Lasix during his hospitalization and his oral dose will be increased from 40 to 60 mg daily until his follow-up appointment to address any further adjustments necessary. He had slow improvement in his symptoms of wheezing, dyspnea and hypoxia and by the time of discharge he only required 1 liter supplemental O2. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2209189 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-20
Onset: 2021-12-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031H21A / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 LA / SYR
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. U021995 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient had ED visit and/or hospitalization within 6 weeks of receiving COVID-19 vaccine.


VAERS ID: 2201496 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-02
Onset: 2022-01-09
   Days after vaccination: 38
Submitted: 0000-00-00
Entered: 2022-03-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 045J21A / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ705AB / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cardiac failure acute, Cardiac failure congestive, Dyspnoea, Hypotension, Imaging procedure, Left ventricular failure, White blood cell count increased
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (narrow), Neuroleptic malignant syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad), Hypokalaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute on chronic systolic congestive heart failure - On the day after admission he was given IV lasix and his work of breathing continued to improve. He was transitioned to his home dose of torsemide, 20mg BID. He did develop a slightly elevated white count, however, his breathing was improved, no consolidation seen on imaging, and he had no fever, so there was little clinical concern for pneumonia. His PTA hypertension medications were held due to low pressures. His breathing was improved and he was stable for discharge. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2211294 (history)  
Form: Version 2.0  
Age: 92.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-14
Onset: 2022-01-25
   Days after vaccination: 42
Submitted: 0000-00-00
Entered: 2022-04-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Aortic stenosis, Aortic valve replacement
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Severe, Symptomatic Aortic Stenosis; procedure - Successful Transcatheter Aortic Valve Replacement. Recovery in hospital; discharged to home. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2213940 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-01-28
Onset: 2022-01-30
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-04-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK9729 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7317MA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Diabetic ketoacidosis, Hyperglycaemia, Immobile, Rhabdomyolysis, Wound
SMQs:, Rhabdomyolysis/myopathy (narrow), Hyperglycaemia/new onset diabetes mellitus (narrow), Neuroleptic malignant syndrome (broad), Accidents and injuries (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Ketosis due to diabetes. He was admitted for correction of the acidosis his hyperglycemia and for appropriate kidney resuscitation. He did do very well with appropriate interventions of insulin IV fluids and wound care. He did need PT and OT as well and they did feel that because of how he was prolonged immobile on the ground he would need additional rehabilitation. Rhabdomyolysis and hyperglycemia did slowly improve acidosis resolved. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2216025 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-19
Onset: 2021-12-19
   Days after vaccination: 30
Submitted: 0000-00-00
Entered: 2022-04-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8027 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ772AC / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abscess drainage, Pain in extremity, Pelvic abscess, Pelvic mass, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit for left leg pain and swelling - treated and released. Admission to the hospital with a left hemipelvic mass. She underwent CT-guided drainage and fortunately the mass was found to be an abscess rather than a malignancy as we were originally concerned. Drainage was uneventful and patient was placed on vancomycin and Zosyn. Treated and discharged. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2580132 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-20
Onset: 2021-09-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039B21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P00355859 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Cardio-respiratory arrest, Cataplexy, Chills, Facial paralysis, Full blood count normal, Glycosylated haemoglobin normal, Hemiparesis, Hypoaesthesia, Hyporesponsive to stimuli, Laboratory test normal
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Acute central respiratory depression (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (narrow), Hearing impairment (broad), Hypotonic-hyporesponsive episode (broad), Respiratory failure (broad), Hypoglycaemia (broad), Sexual dysfunction (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: No relevant lab tests. 8/27/21 :CBC : WNL, Hemoglobin A1C 5.4, Chem 20 WNL.
CDC Split Type:

Write-up: Narrative: Pt at vaccine clinic, received her COVID-19 vaccine (Moderna) and flu shot. While on observation, 15 minutes post vaccine administration, she became limp and minimally responsive. Pt brought to Urgent Care, noted with left sided facial droop. Pt report has numbness/left sided weakness. Pt state she gets (L)side hemiparesis (Todd''s paralysis) when she gets migraines. Vital Signs * Temperature Pulse 81, Respirations 16, Blood Pressure 142/63, Pain scale recorded: 99, Pulse Oximetry 99 Room Air. Code blue called. Responded to Code Blue, pt noted with lips shivering, Code blue called. Responded to Code Blue, pt noted with lips shivering, responding minimally and slowly, but appropriate. Pt brought to room 2, Placed on cardiac and pulse ox monitor. FS 74, #20g IV access placed to (L) AC and secured. MD at bedside evaluating pt. Pt to be sent to non agency Hospital. 911 called and booked. MR arrived for transport. Outcome unknown. No further documentation in patients chart to date regarding this issue. Patient did return to facility on 9/30/21 for a physical therapy appt unrelated to this issue. There was no documentation or reference in the physical therapy note on 9/30/21 regarding the adverse event that occurred on 9/20/21.


VAERS ID: 1859025 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-06
Onset: 2021-11-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 320308D / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100369750 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cough, Injection site vesicles, Pain
SMQs:, Anaphylactic reaction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The following morning after the shot (11/7/21), the patient woke up with a strange blister that popped on his shoulder in the arm where he received the covid shot. The next day (11/8/21), the patient felt radiating pain from his armpit down the side of his body. In addition, he developed a deep cough. Patient went to his doctor''s office on 11/8/21 to determine if these were complications of the shot.


VAERS ID: 2216101 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-30
Onset: 2022-01-03
   Days after vaccination: 34
Submitted: 0000-00-00
Entered: 2022-04-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD0809 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ742AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Asthenia, Bacteriuria, Lymphocytic leukaemia, Pancytopenia, Plasma cell myeloma, Platelet count decreased, Platelet transfusion, Thrombocytopenia, Transfusion, Urine analysis abnormal
SMQs:, Agranulocytosis (narrow), Haematopoietic cytopenias affecting more than one type of blood cell (narrow), Haematopoietic thrombocytopenia (narrow), Systemic lupus erythematosus (broad), Guillain-Barre syndrome (broad), Myelodysplastic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Haematological malignant tumours (narrow), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 10 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient with multimyeloma, B-cell lymphocytic leukemia, with pancytopenia requiring frequent transfusions admitted with weakness above baseline. Patient was found to have moderate bacturia on urinalysis and was treated with Rocephin. In addition, patient had severe thrombocytopenia with a platelet count of 6000. She was given 1 unit of platelets. She was started on prednisone 20 mg twice daily with improvement in her platelets. Discharged to nursing home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2218176 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-06
Onset: 2021-12-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8027 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7347LA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain lower, Fungal infection, Hydronephrosis, Renal colic, Stent placement
SMQs:, Retroperitoneal fibrosis (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED to hospital admission on 1/2 for lower abdominal pain. Acute left renal colic, caused by the above + yeast encrusted left lower pole stent/ left upper and lower pole hydronephrosis, improved post urology intervention, stent replaced, cleared by urology to dc. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2196600 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-08
Onset: 2021-11-30
   Days after vaccination: 22
Submitted: 0000-00-00
Entered: 2022-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Colostomy, Nodule, Proctectomy, Rectal cancer, Splenic flexure mobilisation, Surgery
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 22 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient underwent APR with end colostomy creation, mobilization of splenic flexure and removal of perineal nodule on 11/30/2021 for rectal carcinoma. Treated in hospital and discharged. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2223271 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-30
Onset: 2022-01-05
   Days after vaccination: 36
Submitted: 0000-00-00
Entered: 2022-04-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939903 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 RA / IM
TD: TD ADSORBED (NO BRAND NAME) / SANOFI PASTEUR U7092AA / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chronic obstructive pulmonary disease, Coronavirus infection, Oxygen saturation abnormal, Pneumonia bacterial, Superinfection
SMQs:, Acute central respiratory depression (broad), Respiratory failure (broad), Infective pneumonia (narrow), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit for abnormal pulse oximetry. admitted due to suspected COPD exacerbation secondary to coronavirus OC43 (not SARS-CoV-2) and suspected superimposed bacterial pneumonia. She received steroid, antibiotics and Bronchodilators. She also received IV Lasix 20 mg x1 due to concern for pulmonary edema. Symptoms have improved and patient insists on going home day 2. She is clinically stable for discharge at this time. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2223312 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-26
Onset: 2021-12-06
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2022-04-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1620 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Road traffic accident, Sepsis
SMQs:, Accidents and injuries (narrow), Sepsis (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit for MVA on 12/6. Treated and released. Hospital admission on 1/4/22 for severe sepsis; received IV fluids and stats improved with rest. Discharged home. ED visits and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2228417 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-02
Onset: 2022-01-10
   Days after vaccination: 39
Submitted: 0000-00-00
Entered: 2022-04-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 211202-103 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 7317 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Ewing's sarcoma metastatic, Radiotherapy
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: with metastatic Ewing sarcoma who was admitted for week 3 consolidation after a one-week delay for low counts. Upon admission he received aggressive hydration and anti-emetics prior to daily ETOP/IFOS x 5 days with concurrent radiation tx. Discharged to home. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2236199 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-08-19
Onset: 2022-04-11
   Days after vaccination: 235
Submitted: 0000-00-00
Entered: 2022-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3181 / 1 - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3182 / 2 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9P935 / UNK - / -
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. T036812 / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Chest X-ray normal, Computerised tomogram head normal, Computerised tomogram neck, Imaging procedure, Laboratory test normal, Magnetic resonance imaging head normal, Magnetic resonance imaging spinal normal, Muscular weakness, Pain in extremity, Sensory loss
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Negative workup - including imaging (MRI of brain and entire spine, chest x-ray, brain/neck stroke CT), all labs, etc.
CDC Split Type:

Write-up: Right leg weakness and pain and decreased sensation


VAERS ID: 2196519 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-11
Onset: 2021-12-06
   Days after vaccination: 25
Submitted: 0000-00-00
Entered: 2022-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939903 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal wall operation, Colectomy, Colon cancer, Hepatectomy
SMQs:, Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 12 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Malignant neoplasm of colon, unspecified part of colon. Admission for surgery - Open resection of transverse colon, abdominal wall, and portion left liver. Managed and recovered in hospital. Admission was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2194030 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-02-04
Onset: 2022-02-05
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 022J21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100369750 / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Chills, Headache, Pain
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: 2/4/22: moderna 3rd dose covid booster. Next day Saturday started feeling a headache/chill moving up his neck into the back of his head. Also had chills, woke up with a headache at the base of his skull, acetaminophen no help, a little better with a hot shower but headache returned, though less intense. Woke up Monday again with pain at base of skull and headache, decreased to a dull pain with hot shower. No headache after Wednesday. Headache did NOT wake him from sleep, he woke up as normally then felt a headache.


VAERS ID: 2475178 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-05
Onset: 2022-10-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030G22B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS3620B / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Hypotension, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: 1305: Vaccine administered Afluria/Moderna Bivalent. 1307: Patient experienced syncope and hypotension, Blood pressure 91/59, Heart Rate 69, O2: 100%, Interventions: Oral fluids given 1310: Patient alert and oriented x4 at this time 1325: Blood Pressure 111/74, Heart Rate 74, O2: 100% Patient denies any discomfort or symptoms. 1340: Blood pressure: 116/74, Heart Rate 72, O2: 100% Patient denies any discomfort or symptoms.


VAERS ID: 2475710 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-09-30
Onset: 2022-09-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7682KA / 1 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Inappropriate schedule of product administration
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The patient received this dose of the Covid vaccine approximately 4 weeks early.


VAERS ID: 2151848 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-19
Onset: 2021-10-28
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2022-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8020 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Caecectomy, Laparoscopic surgery, Large intestine polyp
SMQs:, Gastrointestinal premalignant disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: admission for Laparoscopic Cecectomy due to 1 benign colon polyp. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2151823 (history)  
Form: Version 2.0  
Age: 91.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-24
Onset: 2021-12-03
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2022-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Fracture treatment, Hip fracture, Hip surgery
SMQs:, Accidents and injuries (narrow), Osteoporosis/osteopenia (broad), Osteonecrosis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 19 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Closed left hip fracture; underwent a surgical repair. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2151655 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-21
Onset: 2021-10-25
   Days after vaccination: 34
Submitted: 0000-00-00
Entered: 2022-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7317MA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Fatigue, Head injury, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: On day of admission patient was feeling fatigued and was at work when she had a syncopal episode. She hit the back of her head. It is recommended that she stop her Plavix and warfarin until she follow-ups with neurosurgery in 2 weeks with a head CT previous. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2151646 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-17
Onset: 2021-12-07
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2022-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051F21A / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 312865 / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Anticoagulant therapy, Hypoxia, Pulmonary embolism
SMQs:, Asthma/bronchospasm (broad), Embolic and thrombotic events, venous (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Eosinophilic pneumonia (broad), Respiratory failure (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient admitted with hypoxia and pulmonary emboli. She was started on heparin, has now obtained Eliquis, and home O2 has been arranged. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2481468 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-12
Onset: 2022-10-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9697 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS3620B / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Hyperhidrosis, Thirst, Tinnitus, Vision blurred
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Hearing impairment (narrow), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: BlurredVision diaphoresis, thirsty, tinnitus Narrative: Reaction occurred within 5 minutes post vaccination and employee was taken to the ED, later discharged to home.


VAERS ID: 1837080 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-08
Onset: 2021-10-09
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 020F21A / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Foaming at mouth, Loss of consciousness, Nausea, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received Moderna booster vaccine and high dose flu vaccine on the same day. The day after she felt very nauseous and had to vomit. The patient had passed out after vomiting and had a lot of fluid in their mouth when they woke up. She claims it appeared she was foaming at the mouth.


VAERS ID: 2194048 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-27
Onset: 2021-10-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8735 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367899 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Dizziness, Palpitations, Vision blurred
SMQs:, Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Glaucoma (broad), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: Patient received flu shot and Covid vaccine today. she instructed to sit in the monitor room to wait for 15 minutes. but the patient left early and waiting in front of clinic to see by Doctor. during that time she had palpitation and dizziness. (Privacy) find her and inform me I went there and the time I reach there she said she is fine her HR was 90 on her smart watch and she said she is hungry need some juice and crackers. she refused to go to ER in the first place. patient provided with water and then she said she is having blurred vision for a minute. CVC staff assisted her to the ER. Patient transported to ER by 2 RNS without any complications


VAERS ID: 1873914 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-07
Onset: 2021-11-10
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Aphonia, Cough, Dyspnoea, Fatigue, Oropharyngeal pain, Pyrexia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Three days following vaccines fever began and then the next day she had a sore throat, and lost her voice. A week following vaccines she had difficulty breathing, increased respiration?s, little voice, and increased fatigue. Her cough sounded like a croup cough. Physician was able to prescribe oral steroids. Two doses were taken, first dose was day 2 of symptoms and then Inhaled steroids and another dose of oral steroids 4 days after the symptoms began. She started to improve after the second dose of steroids and the inhaled steroids.


VAERS ID: 2154590 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-26
Onset: 2021-10-28
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8020 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Acute myocardial infarction, Catheterisation cardiac abnormal, Chest pain, Electrocardiogram abnormal, Myocardial infarction
SMQs:, Myocardial infarction (narrow), Arrhythmia related investigations, signs and symptoms (broad), Embolic and thrombotic events, arterial (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute STEMI presentation - initial cath with no culprit lesion identified. with history of type 2 diabetes, permanent atrial fibrillation with intrinsically controlled heart rates, and long term anticoagulation with Xarelto, Obesity, hypertension , hyperlipidemia, DVT and right sided carotid endarterectomy admitted for further evaluation of chest pain progressively worsening since receiving COVID vaccine booster 2 days prior. ECG was consistent with anterior STEMI. Initial emergent LHC was felt to show TIMI 3 flow in all vessels and moderate diffuse disease - the films were reviewed by multiple interventionalists and the consensus was that no culprit vessel could be identified. ED and hospital admission was within 2 days of receiving the COVID vaccine.


VAERS ID: 2134404 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-07
Onset: 2021-11-04
   Days after vaccination: 28
Submitted: 0000-00-00
Entered: 2022-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7378JA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Brain abscess, Craniotomy, Drainage
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 14 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Brain abscess, status post craniotomy and drainage. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2134297 (history)  
Form: Version 2.0  
Age: 86.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-12
Onset: 2021-11-07
   Days after vaccination: 26
Submitted: 0000-00-00
Entered: 2022-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Femur fracture, Periprosthetic fracture, Surgery
SMQs:, Accidents and injuries (narrow), Osteoporosis/osteopenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Periprosthetic supracondylar fracture of femur -surgical procedure without complications and was hospitalized for a total of 8 nights following the surgical procedure. Hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2131532 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-03
Onset: 2021-12-12
   Days after vaccination: 39
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Anticoagulant therapy, Carotid angioplasty, Carotid artery stent insertion, Cerebral small vessel ischaemic disease, Dysarthria, Hypertension, Hypoaesthesia, Magnetic resonance imaging head abnormal
SMQs:, Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Ischaemic central nervous system vascular conditions (narrow), Embolic and thrombotic events, arterial (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hypertension (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The patient has recently underwent extensive cardiac interventions. On the night of admission, patient was watching TV with his wife when she noted that he was not speaking clearly. She described his speech is slurred and difficult to understand. Patient had also been reporting intermittent right hand numbness. Brain MRI 12/13/2021 revealed diffuse punctate areas throughout the left cerebral hemisphere indicative of small ischemic insults concerning for thromboembolic disease. As per stroke neurology, patient is likely unresponsive to Plavix. Stroke neurology recommended switching Plavix to Brilinta and permissive hypertension. Left internal carotid artery angioplasty and stent completed on 12/14/2021. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2131529 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-29
Onset: 2021-11-03
   Days after vaccination: 35
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Open reduction of fracture, Tibia fracture
SMQs:, Accidents and injuries (narrow), Osteoporosis/osteopenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 16 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient admitted to Medical Center for a principle and pre-operative diagnosis of closed displaced fracture of lateral condyle of right tibia. Patient underwent open reduction internal fixation and was hospitalized post-op. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2131458 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-13
Onset: 2021-11-07
   Days after vaccination: 25
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Anticoagulant therapy, Chronic obstructive pulmonary disease, Condition aggravated, Dyspnoea, Troponin increased
SMQs:, Anaphylactic reaction (broad), Myocardial infarction (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented to ED this evening with shortness of breath, troponin elevated at 0.154 and transferred to local hospital to start heparin bolus with drip. Started on 5 day prednisone course for COPD exacerbation, reports improvement of SOB but not back to baseline. Had RN perform walking saturations, 95% on room air therefore not meeting criteria for home O2. Prescribed Spiriva on discharge to add to her Qvar, albuterol, DuoNeb. Recommend Pulmonology consultation, outpatient PFTs, and close follow up with PCP. Patient hemodynamically and clinically stable and ready for discharge home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 1832412 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-29
Onset: 2021-10-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Injection site pain, Lymphadenopathy
SMQs:, Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lexapro 20mg
Current Illness: None
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pain at injection sites, swollen lymph node in right armpit lasting several days. Extreme tiredness.


VAERS ID: 2489824 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-19
Onset: 2022-10-21
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ6739 / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ895AB / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Rash, Rash pruritic, Varicella zoster virus infection
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 2 days after vaccine the patient developed a rash which was itchy and then painful. On evaluation in clinic the rash was consistent with varicella zoster. Notably she has had both of her shingrix vaccines.


VAERS ID: 2490892 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-09-09
Onset: 2022-09-13
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2022-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ882AB / UNK RA / OT
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Depressed level of consciousness, Tenderness, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CORTISONE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSA2022SA424546

Write-up: kind of knocked me out a little bit; she came down with a severe case of hives. The hives covered from her chest down to her ankles, and part of her back.; little soreness in her arm; Initial information received on 14-Oct-2022 regarding an unsolicited valid serious case received from a consumer/non-hcp. This case involves a 64 years old female patient who experienced kind of knocked me out a little bit, she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back. and little soreness in her arm while receiving vaccines moderna covid-19 vaccine, shingrix and influenza quadrival a-b high dose hv vaccine [fluzone high-dose quadrivalent]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included CORTISONE (CORTISONE). On 09-Sep-2022, the patient received a dose of suspect influenza quadrival a-b high dose hv lot UJ882AB via unknown route in the right arm. from prophylactic vaccination. On an unknown date, the patient received a dose of suspect shingrix not produced by Sanofi Pasteur lot number not reported via unknown route in unknown administration site from prophylactic vaccination. On an unknown date, the patient received a Booster dose of suspect moderna covid-19 vaccine not produced by Sanofi Pasteur lot number not reported via unknown route in unknown administration site from prophylactic vaccination. On an unknown date the patient developed a serious kind of knocked me out a little bit (depressed level of consciousness) (unknown latency) following the administration of influenza quadrival a-b high dose hv, shingrix, moderna covid-19 vaccine. This event was assessed as medically significant. On 13-Sep-2022 the patient developed a non-serious she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back. (urticaria) and little soreness in her arm (tenderness) 4 days following the administration of quadrival a-b high dose hv, shingrix, moderna covid-19 vaccine. It was reported "She received Fluzone HD QIV for the first time on 09Sep2022. She has received flu shots for many years in the past without any problems other than a sore arm. This year, four days after the Fluzone HD QIV was administered in her right arm, she came down with a severe case of hives. The hives covered from her chest down to her ankles, and part of her back. They were so severe that she could not function. Her dermatologist gave her a shot of cortisone and she took antihistamines. Both her dermatologist and internist were not sure if the Fluzone HD QIV could be the cause, especially with the 4-day delay of onset, however the patient cannot think of anything else that she might have been exposed to that would have caused the hives. When the hives began, they started in the armpit of her right arm at that same level as the injection site. She discussed her previous experience with other vaccines as to how it is so unusual for her to have hives after Fluzone HD QIV. She received Moderna Covid vaccines. The bivalent Covid booster a week ago caused her to have a little soreness in her arm. When she received the second full dose of the initial series of Moderna Covid vaccine, that dose "knocked me off my feet and I could not get out of bed for 24 hours". All of the other Covid boosters did not cause problems for her. She has taken vaccines against typhoid, Td, and pneumonia without problems. The Shingrix vaccine "kind of knocked me out a little bit. I was told by other people that Shingrix really hurts." (see #01322462 for report for "other people"). Twenty-five or thirty years ago she had a TB test with ppd. After that test, her entire arm "blew up" instantly with a giant welt. She was told at first that she had TB. A follow-up chest x-ray was negative. It was realized that she did not have TB and that instead something was wrong with that test. She later had subsequent ppd tests without reactions. She says, "I suspect that test was contaminated with something". Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events (she came down with a severe case of hives. The hives covered from her chest down to her ankles, and part of her back., little soreness in her arm, kind of knocked me out a little bit). At time of reporting, the outcome was Recovering / Resolving for the event she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back., was Recovering / Resolving for the event little soreness in her arm and was Unknown for the event kind of knocked me out a little bit.; Sender''s Comments: Sanofi company comment dated 24-Oct-2022: This case concerns 64 years old female patient who experienced kind of knocked me out a little bit, she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back. and little soreness in her arm while receiving vaccines moderna covid-19 vaccine, shingrix and influenza quadrival a-b high dose hv vaccine [fluzone high-dose quadrivalent]. Based on information provided, the causal role of company suspect cannot excluded. Case will be re-evaluated post further update on information regarding underlying disease, risk precipitating factor, past medical history and patient lifestyle which will preclude a comprehensive assessment of this case. Based upon the reported information, the role of the suspect vaccine cannot be assessed.


VAERS ID: 2492691 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-25
Onset: 2022-10-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ917AA / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Amlodipine, atorvastatin, glimepiride, Novolin, lisinopril, metformin
Current Illness: Unknown.
Preexisting Conditions: Hypertension, T2DM, osteoarthritis, hyperlipidemia
Allergies: Not on file.
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was scheduled to receive their second COVID-19 booster dose. The patient was supposed to receive the bivalent formulation but was inadvertently administered the monovalent formulation. Patient waited in waiting room for 15 minutes without incident.


VAERS ID: 2168122 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-11
Onset: 2021-11-16
   Days after vaccination: 36
Submitted: 0000-00-00
Entered: 2022-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Anaemia, Cardiac telemetry, Transfusion
SMQs:, Haematopoietic erythropenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute on chronic anemia - Patient was admitted on telemetry started on Protonix drip and patient was given 3 unit blood transfusions. She has remained hemodynamically stable even at arrival, no further acute loss identified. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2579525 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-29
Onset: 2021-09-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 009C21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100358553 / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: Patient received Pfizer covid vaccine dose #1 Feb 6, 2021 and 2nd dose on Feb 27,2021 at an outside facility. Patient''s vaccine history was documented in the pt''s record by LPN while viewing the patient''s vaccine card on 4/28/21. The patient presented to the facility on 9/29 for a covid booster and was given Moderna dose by RN. The patient has not reported any adverse effects at this time to any of the COVID vaccine doses. Will update this report in the future if patient has any adverse effects from the booster dose. Patient has not tested positive for COVID and is also considered immunocompromised due to prednisone taken chronically for COPD.


VAERS ID: 2179894 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-10
Onset: 2021-12-10
   Days after vaccination: 30
Submitted: 0000-00-00
Entered: 2022-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Aortic stenosis, Aortic valve replacement, Catheterisation cardiac abnormal, Chest discomfort, Chest tube insertion, Coronary artery bypass, Coronary artery disease, Drainage, Endotracheal intubation, Intensive care
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Embolic and thrombotic events, arterial (narrow), Other ischaemic heart disease (narrow), Respiratory failure (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented for outpatient left heart cath on 12/8/21 to assess worsening exertional chest pressure/discomfort. The workup revealed multi-vessel coronary artery disease with left main involvement and severe aortic stenosis. On December 10 the patient was admitted and underwent CABG and AVR. The patient was extubated shortly following surgery in the ICU. The mediastinal chest tubes were removed on POD #1 when the drainage was sufficiently low. The patient was weaned off vasoactive drips as tolerated. Hospital admission was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2179877 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-16
Onset: 2021-10-10
   Days after vaccination: 24
Submitted: 0000-00-00
Entered: 2022-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ212AA / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Chemotherapy, Constipation, Culture, Fatigue, Malaise, Pyrexia, Radiotherapy
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented to the ED 10/10/21 with fevers, fatigue/malaise and constipation since 10/8. He underwent week #4 chemotherapy with carboplatin and Taxol on 10/7. He was admitted for IV antibiotics and continued close monitoring while awaiting culture results. Since admission, he has demonstrated overall clinical improvement, though did have ongoing low grade fevers overnight. He was able to continue radiation therapy during his hospital stay. ED Visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2173254 (history)  
Form: Version 2.0  
Age: 91.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-16
Onset: 2021-10-19
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2022-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Affective disorder, Atrial fibrillation, Cognitive disorder, Conversion disorder, Crying, Screaming, Somatic symptom disorder
SMQs:, Supraventricular tachyarrhythmias (narrow), Dementia (broad), Psychosis and psychotic disorders (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hostility/aggression (broad), Depression (excl suicide and self injury) (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient with history of depression, anxiety, hypertension, osteoarthritis and gout longstanding challenges with poorly controlled anxiety and panic presents with 2 weeks of multitude of somatic symptoms in addition to functional impairment from after mentioned suboptimally controlled mood. Upon seeing her in ED she was quite hysterical, crying out/calling out. Admitted her, discontinued benzodiazepines and BuSpar, scheduled low-dose Risperdal and continued paroxetine. During her short hospital course she improved back to baseline status. Additional ED visit for atrial fin wtih RVR; treated and released. ED visits and hospital admission were within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2173237 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-09
Onset: 2021-12-10
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 058H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Brain stem haemorrhage, Cerebrovascular accident, Hemiparesis
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Noninfectious encephalitis (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Left pontine stroke with right hemiparesis. Treated and discharged. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2171053 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-08
Onset: 2021-11-16
   Days after vaccination: 39
Submitted: 0000-00-00
Entered: 2022-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Aortic stenosis, Aortic valve replacement, Cardiac valve prosthesis user
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Aortic stenosis, severe - operation: Transfemoral Transcutaneous Aortic Valve Replacement with aortic valve prosthesis of a 29 mm Evolut Pro+. Post procedure the patient did very well. Admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2170981 (history)  
Form: Version 2.0  
Age: 90.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-21
Onset: 2021-10-22
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Atrial fibrillation
SMQs:, Supraventricular tachyarrhythmias (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Atrial fibrillation with RVR, admitted to the telemetry floor for further management and continued on a diltiazem drip overnight with good control of heart rate. The morning of 10/23/21, the diltiazem drip was weaned off. Toprol XL 150 mg daily was restarted. Cardiologist recommended the addition of digoxin 0.125 mg daily for treatment of atrial fibrillation as well as the addition of aspirin 81 mg twice weekly for secondary prevention of stroke. The patient was stable for discharge and felt comfortable with this plan. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2170970 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-13
Onset: 2021-11-23
   Days after vaccination: 41
Submitted: 0000-00-00
Entered: 2022-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AB / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acute respiratory failure, Pneumonia streptococcal, Streptococcus test positive, Urine antigen test
SMQs:, Anaphylactic reaction (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Hypersensitivity (broad), Respiratory failure (narrow), Infective pneumonia (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Streptococcal pneumonia with acute hypoxic respiratory failure -Urine antigen positive for strep pneumo, patient needed supplemental persistent oxygen to maintain saturations above 90%, patient initially treated with IV Rocephin, her oxygen requirement decreased with time and now she has not qualified for home oxygen. Will give a week of Augmentin post discharge. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2168334 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-29
Onset: 2021-10-31
   Days after vaccination: 32
Submitted: 0000-00-00
Entered: 2022-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30135BA / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ741AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Bladder catheterisation, Bladder irrigation, Dysuria, Haematuria, Trial of void, Urinary retention
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Hematuria, gross, with urinary retention. Recent instrumentation as above.. CBI discontinued on 10/31, failed voiding trial, Foley replaced on 10/31 and patient discharged home with Foley catheter, per urology recommendations. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2168284 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-14
Onset: 2021-10-28
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2022-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Coronary artery bypass
SMQs:, Embolic and thrombotic events, arterial (narrow), Other ischaemic heart disease (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Coronary artery bypass grafting x4 on pump. The patient''s oxygen was weaned to room air. He progressed well with physical and occupational therapy and was stable to be discharged to home with family support on POD #3. Hospital admission was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2095465 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-12
Onset: 2021-10-16
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7378JA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Biliary obstruction, Fatigue, Malaise, Neoplasm malignant
SMQs:, Retroperitoneal fibrosis (broad), Biliary tract disorders (narrow), Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Malaise and fatigue - ED visit and then Biliary obstruction due to malignant neoplasm, ED visit to hospital admission. These visits were within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2453472 (history)  
Form: Version 2.0  
Age: 2.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2022-09-20
Onset: 2022-09-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Fatigue, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vomited twice within 1 hour. Seems tired day after receiving vaccines


VAERS ID: 2168017 (history)  
Form: Version 2.0  
Age: 92.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-27
Onset: 2021-11-10
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2022-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Bradycardia, Diverticulum intestinal, Rectal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal haemorrhage (narrow), Gastrointestinal nonspecific dysfunction (broad), Ischaemic colitis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit for reported bradycardia - treated and released. Hospital admission after 3 episodes of bright red blood per rectum . Severe diverticulosis in the sigmoid and distal descending colon. Treated and discharged. ED visits and hospital admissions within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2165652 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-28
Onset: 2021-10-06
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2022-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ741AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hip fracture, Internal fixation of fracture, Pelvic venous thrombosis, Peripheral swelling, Thrombosis
SMQs:, Cardiac failure (broad), Angioedema (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad), Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Osteoporosis/osteopenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Left hip fracture -post left hip gamma nail, discharged from hospital and then ED visit 12 days later for left leg swelling. Patient has evidence of extensive thrombosis extending from the left common iliac vein to peroneal veins of mid calf. Order for interventional radiology thrombectomy of the left leg, Order for interventional radiology thrombectomy of the left leg. Hospital admission and ED visit were both within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2157679 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-28
Onset: 2021-10-11
   Days after vaccination: 13
Submitted: 0000-00-00
Entered: 2022-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3183 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7336LA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Death, Dehydration, Lung cancer metastatic, Lung neoplasm malignant, Sepsis
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Non-haematological malignant tumours (narrow), Dehydration (narrow), Sepsis (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-11-07
   Days after onset: 27
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 14 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: ED visit for dehydration, treated and discharged. ED to hospital for Severe sepsis; Primary malignant neoplasm of left lung metastatic to other site Treated and discharged to skilled nursing facility. Patient died on 11/7/2021. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 1870013 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-13
Onset: 2021-11-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0170 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7377JA / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received pfizer covid vaccine that was past its BUD. BUD was 11/12/21 @ 1738. Patient received vaccine on 11/13/21 @ 1706.


VAERS ID: 2157662 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-29
Onset: 2021-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD0809 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7319NA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Medication refills at adult well check. Same day as 3rd COVID vaccine.


VAERS ID: 2597299 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-21
Onset: 2021-10-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8736 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367238 / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Feeling hot, Pruritus
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: Patient came came in for an appointment to receive pfizer booster and flu vaccine today. Pfizer booster was administered to left deltoid and influenza was administered to right deltoid. During the 15 minute post vaccination monitoring, patient complained of feeling hot and itching to all over her body. V/S 168/98, 75,100%. Patient denies resp. distress. Resp. even and unlabored. Informed patient that she will be escorted to the ER for further evaluation, patient agreed. Offered to take patient via w/c she refused and requested she wanted to talk to the ER. Endorsed to the ER triage nurse to continue with patient care.


VAERS ID: 2155004 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-20
Onset: 2021-11-21
   Days after vaccination: 32
Submitted: 0000-00-00
Entered: 2022-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745ABF8211312 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acute respiratory failure
SMQs:, Anaphylactic reaction (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Hypersensitivity (broad), Respiratory failure (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute respiratory failure with hypoxia Plan to discharge with steroid burst to be completed in 3 more days. Also ordered Spiriva and albuterol inhaler. Recommend he follow-up with primary care or pulmonary clinic for further evaluation including pulmonary function testing. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2469919 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-10-04
Onset: 2022-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7138 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 93CP5 / N/A LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The intended COVID-19 vaccination was the Pfizer Bivalent booster for the patient''s 4th dose. However, the administered vaccine was the Pfizer monovalent primary series product. The patient did not experience any adverse events due to this error.


VAERS ID: 2702501 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-16
Onset: 2023-10-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030339 / 6 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8137DA / UNK LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS G2MG3 / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received 2 doses of RSV vaccine (Arexvy) on 08/19/2023 and 10/16/2023. Patient has not experience any side effects/adverse events.


VAERS ID: 2738849 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2024-01-02
Onset: 2024-01-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AV3833C / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8162EA / 1 LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS FN2FD / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Headache, Neuralgia
SMQs:, Peripheral neuropathy (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient reported headache and nerves pain developed 20 minutes after the above vaccines which lead to a doctor''s visit two days later.


VAERS ID: 2741165 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2024-01-26
Onset: 2024-01-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: PT was given a covid vaccine that had already had one on 12/23. As well as a Flu vaccine that had already received on 10/23. no adverse signs or symptoms


VAERS ID: 2025193 (history)  
Form: Version 2.0  
Age: 88.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-27
Onset: 2021-11-07
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2022-01-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cardiac failure acute, Cardiac failure congestive, Left ventricular failure
SMQs:, Cardiac failure (narrow), Cardiomyopathy (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 12 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute on chronic diastolic congestive heart failure - ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 1967487 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-17
Onset: 2021-12-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 067H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ767AB / N/A LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Fall, Feeling hot, Hyperhidrosis, Loss of consciousness, Seizure like phenomena
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: I first gave the flu shot and then the covid shot in the same arm, at an acceptable distance apart. After the second vaccine she passed out of the chair and fell forward onto the floor. She had some seizure-like movements but woke up in less than 30 seconds. Patient states she has no personal or family history of seizures. We let the patient slowly sit up on the floor and then eventually move to the chair while she waited for a family member to come pick her up. She stated she felt fine other than hot and sweaty. Pharmacists recommended she speak to her primary care provider about this incident to see if they would like her to have any follow-up testing. I called the patient later that evening to see how she was doing and she said good. She said she spoke to her primary care provider, and Doctor does not see a need for any follow up testing.


VAERS ID: 2703998 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-26
Onset: 2023-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031283 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8057BA / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8200CA / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Incorrect dose administered, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient given high dose flu in error.


VAERS ID: 2741960 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2024-01-18
Onset: 2024-01-20
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2024-01-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3032265 / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8130CA / N/A LA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH HE6176 / N/A LA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS J743F / 2 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: On 1/18/24, patient received Prevnar 20, Shingrix (2nd dose), Fluzone HD, and Spikevax at the pharmacy. On 1/28/24, patient returned to the pharmacy and stated she was experiencing an allergic reaction to the vaccines she received. Patient presented with a rash on both of her arms (visible across each arm at the time of consultation) and some of her back (not visible at the time of consultation - covered by shirt). Patient requested a recommendation to help with the rash. Patient stated the rash developed on 1/20/24. She stated the rash was not itchy, and she denied any other potential causes of the rash (ie changes in detergent, body wash, etc.). I recommended the patient take Benadryl, and I advised the patient to seek urgent/emergency care if condition worsens/spreads or signs/symptoms of anaphylaxis develop (difficulty breathing, facial swelling, swelling of the tongue).


VAERS ID: 2708809 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-23
Onset: 2023-10-24
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG5967 / 6 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8156CA / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Confusional state
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient experienced increased confusion several hours after receiving both COVID19 vaccine and high-dose influenza vaccine. Confusion resolved within 24 hours.


VAERS ID: 2727402 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-20
Onset: 2023-10-29
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2023-12-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER 5433MF001 / 2 RA / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 72423 / 1 RA / OT
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. W035042 / 2 RA / OT
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR W1C751M / 2 LA / OT
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. V014623 / 2 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Chest pain, Electrocardiogram, Headache, Laboratory test, Pericarditis, Troponin
SMQs:, Systemic lupus erythematosus (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ALBUTEROL [SALBUTAMOL]; COMPOUND W; DENTA 5000 PLUS
Current Illness: Asthma; Back pain
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20231029; Test Name: Electrocardiogram; Result Unstructured Data: no results reported; Test Date: 20231029; Test Name: Laboratory test; Result Unstructured Data: no results reported; Test Date: 20231029; Test Name: Troponin; Result Unstructured Data: no results reported
CDC Split Type: USSA2023SA394394

Write-up: pericarditis; chest pain; headache; Initial information received from country on 18-Dec-2023 regarding an unsolicited valid serious Courtesy case received from a consumer/non-hcp (non-healthcare professional). This case involves 14 years old male patient who had pericarditis, chest pain and headache after receiving covid-19 vaccine PROT. SUBUNIT (NVX COV 2373) (Novavax Covid-19 Vaccine); Hepatitis B vaccine RHBSAG (YEAST) (Recombivax HB); measles vaccine live (ENDERS-EDMONSTON), mumps vaccine live (jeryl lynn), rubella vaccine live (WISTAR RA 27/3), varicella zoster vaccine live (OKA/MERCK) (Proquad); IPV (VERO) [IPOL] and influenza quadrival A-B vaccine [Fluzone Quadrivalent]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. At the time of the event, the patient had ongoing Back pain and Asthma. The individual had no known allergies. Concomitant medications included SAlbutamol (Albuterol [Salbutamol]); Salicylic Acid (Compound W); and Sodium Fluoride (Denta 5000 Plus). On 20-Oct-2023, the patient received a dose 1 of suspect influenza quadrival A-B vaccine Suspension for injection (lot 72423) via intramuscular route in the right arm; also received a dose 2 of suspect Recombivax HB not produced by Sanofi Pasteur (with an unknown formulation) (lot W035042) via intramuscular route in the right arm; received a dose 2 of suspect Proquad not produced by Sanofi Pasteur (with an unknown formulation) lot V014623 via intramuscular route in the left arm and received a dose 2 of suspect IPV (VERO) Suspension for injection (lot W1C751M) via intramuscular route in the left arm (with an unknown strength and expiry date) for prophylactic vaccination (Immunisation). On 20-Oct-2023, the patient received a dose 2 of suspect novavax covid-19 vaccine Adjuvanted (2023-2024 Formula) not produced by Sanofi Pasteur (with an unknown formulation, strength and expiry date) at a dose of 0.5 ml (lot 5433MF001) via intramuscular route in the right arm for COVID-19 vaccination (COVID-19 immunisation). On 29-OCT-2023 the patient developed pericarditis, chest pain and headache 9 days following the administration of influenza quadrival A-B vaccine, IPV (VERO), Recombivax HB, Proquad and novavax covid-19 vaccine. Reportedly, Sudden onset chest pain and headache, then the individual went to the emergency room, where he was diagnosed with pericarditis. Currently seeing cardiology. The individual had an office visit on an unreported date. Relevant laboratory test results included: Electrocardiogram - On 29-Oct-2023: [no results reported] Laboratory test - On 29-Oct-2023: [no results reported] Troponin - On 29-Oct-2023: [no results reported] Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Unknown for all the events. Seriousness criteria: medically significant for the event pericarditis.; Sender''s Comments: Sanofi company comment dated 26-DEC-2023: This case involves 14 years old male patient who had pericarditis, chest pain and headache after receiving covid-19 vaccine PROT. SUBUNIT (NVX COV 2373) (Novavax Covid-19 Vaccine); Hepatitis B vaccine RHBSAG (YEAST) (Recombivax HB); measles vaccine live (ENDERS-EDMONSTON), mumps vaccine live (jeryl lynn), rubella vaccine live (WISTAR RA 27/3), varicella zoster vaccine live (OKA/MERCK) (Proquad); IPV (VERO) [IPOL] and influenza quadrival A-B vaccine [Fluzone Quadrivalent]. Further information regarding concomitant medication, and tolerance, laboratory investigations excluding alternative etiologies for the reported event are needed to fully assess this case. Based upon the reported information, the role of the suspect vaccine cannot be assessed. Furthermore, medical history of the patient is a confounding factor.


VAERS ID: 2039216 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-10-26
Onset: 2021-11-20
   Days after vaccination: 25
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chronic left ventricular failure, Death
SMQs:, Cardiac failure (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-11-20
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient passed away from chronic combined systolic and diastolic heart failure. This event was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2705388 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-16
Onset: 2023-10-19
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG9498 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8057DA / UNK RA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS 5AN52 / N/A LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Contusion, Injected limb mobility decreased, Pain in extremity
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Accidents and injuries (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: pt experienced pain in the whole arm as well as a bruise on a location other than the injection site lower on the bicep towards the inner elbow a few days after receiving the COMNARTY shot on 10/16/23 . pt experienced the same a few days after given flu and RSV vaccinations in her left arm on 08/29/23 (pain in the whole arm which still exists preventing her from moving her arm and a bruise close to her inner elbow). pt saw the physician about the pain in the arm and was prescribed prednisone for it.


VAERS ID: 2720974 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-11-16
Onset: 2023-11-19
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Back pain, Headache, Hypoaesthesia, Muscle tightness, Pain, Pain in extremity, Paraesthesia
SMQs:, Peripheral neuropathy (broad), Retroperitoneal fibrosis (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline, Singulair, multivitamin, probiotic
Current Illness: None
Preexisting Conditions: None
Allergies: Flagyl
Diagnostic Lab Data: I went to Urgent Care on November 28 and was given muscle relaxers to help with the pain and tightness of the muscles in my back. No tests or Xrays were given.
CDC Split Type:

Write-up: Started experiencing arm pain the next day in my right arm which I considered to be normal. A couple of days later, I started experiencing horrible back pain in the upper right quadrant next to my right shoulder blade. Within a couple of days, the pain began to radiate down my right arm into my fingers as well as upwards to the right side of my head. I began experiencing numbness and tingling in those areas.


VAERS ID: 2039221 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-04
Onset: 2021-11-05
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Anaemia
SMQs:, Haematopoietic erythropenia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute on chronic anemia. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2727177 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated: 2023-10-18
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2023-12-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER HF9300 / 1 LA / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 49281-423-88/U8 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Pain in extremity, Psoriasis
SMQs:, Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSA2023SA397461

Write-up: psoriasis in the scalp, neck and upper back/shoulder blades which has now persisted for 5 weeks; within 12 hrs, extreme pain in the arms and hands, like glass shards poking me; Initial information received on 15-Dec-2023 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This was a courtesy case received from Pfizer. This case involves an unknown age and unknown gender patient who experienced psoriasis in the scalp, neck and upper back/shoulder blades which has now persisted for 5 weeks and within 12 hrs, extreme pain in the arms and hands, like glass shards poking me after receiving Covid-19 vaccine and influenza quadrival a-b vaccine [Fluzone quadrivalent]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 18-Oct-2023, the patient received a dose 1 of suspect covid-19 vaccine not produced by Sanofi Pasteur lot hf9300 via unknown route in the left arm (formulation, strength and expiration date: not provided) for immunisation. On 28-Oct-2023, the patient received a dose 1 of suspect influenza quadrival a-b vaccine Suspension for injection lot 49281-423-88/U8201EA via unknown route in unknown administration site (dose, formulation, strength and expiration date: not provided) for Immunisation. On Oct-2023 the patient developed a non-serious within 12 hrs, extreme pain in the arms and hands, like glass shards poking me (pain in extremity) (latency- 12 hours) following the administration of influenza quadrival a-b vaccine and covid-19 vaccine. On 05-Nov-2023 the patient developed a non-serious psoriasis in the scalp, neck and upper back/shoulder blades which has now persisted for 5 weeks (psoriasis) 8 days following the administration of influenza quadrival a-b vaccine and 18 days following the administration of covid-19 vaccine. Action taken- not applicable. An unknown corrective treatment was received for the events. At time of reporting, the outcome was Unknown for the event within 12 hrs, extreme pain in the arms and hands, like glass shards poking me and was Not Recovered / Not Resolved for the event psoriasis in the scalp, neck and upper back/shoulder blades which has now persisted for 5 weeks.


VAERS ID: 1943190 (history)  
Form: Version 2.0  
Age: 90.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-08
Onset: 2021-09-09
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100358553 / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Narrative: None stated.


VAERS ID: 2014782 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2022-01-03
Onset: 2022-01-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / UNK - / -
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnant patient mistakenly received live vaccines.


VAERS ID: 2039510 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-12
Onset: 2021-11-23
   Days after vaccination: 42
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30125BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ730AA / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Cardiac failure congestive, Condition aggravated
SMQs:, Cardiac failure (narrow), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Acute exacerbation of CHF (congestive heart failure). ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2727067 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-12-21
Onset: 2023-12-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / N/A RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Neuralgia, Pain in jaw, Toothache
SMQs:, Peripheral neuropathy (narrow), Osteonecrosis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: About an hour after the injections, the right side of my jaw started hurting (around a 2 to 3 on the pain scale). The pain subsided then about 6 hours after injection I took a drink of cool water and it caused a very painful spike in my upper and lower right side teeth (around an 8 or 9). It felt like intense nerve pain for a few seconds, only on the right side. This pain occurs every time I take a drink of cool/cold or warm/hot liquid. It still hurts 41 hours after the injections.


VAERS ID: 2701427 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-23
Onset: 2023-10-24
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030535 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U80875EA / UNK LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient signed up to receive the flu and covid shot. We confirmed she was receiving the two vaccinations prior to administering. The following day patient called and stated she received her flu shot five days prior at her MD office. Patient received two doses of high dose flu vaccination within 5 days. We confirmed with our corporate office that Patient will be fine and to reach out with any additional questions or concerns.


VAERS ID: 1943862 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-10
Onset: 2021-12-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 009C21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: NA


VAERS ID: 2025158 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-28
Onset: 2021-11-06
   Days after vaccination: 39
Submitted: 0000-00-00
Entered: 2022-01-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3183 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ741AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acute respiratory failure, Arteriosclerosis coronary artery, Atrial fibrillation
SMQs:, Anaphylactic reaction (broad), Supraventricular tachyarrhythmias (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Other ischaemic heart disease (narrow), Hypersensitivity (broad), Respiratory failure (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Persistent atrial fibrillation, Arteriosclerotic coronary artery disease, Acute respiratory failure with hypoxia. ED Visit and hospital admission. this visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2658661 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-08
Onset: 2021-12-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027H21B / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367237 / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Anal incontinence, Asthenia, Cerebral infarction, Cerebral ischaemia, Condition aggravated, Discomfort, Dizziness, Dizziness postural, Dyspnoea exertional, Electroencephalogram normal, Eye movement disorder, Fatigue, Implantable cardiac monitor insertion, Implantable cardiac monitor removal, Loss of consciousness, Magnetic resonance imaging head abnormal, SARS-CoV-2 test negative, Syncope, Urinary incontinence
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Ischaemic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Ocular motility disorders (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Noninfectious diarrhoea (broad), Hypoglycaemia (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 01/02/2022@14:25:05 COVID-19 PCR (FLUVID) NotDetected 01/03/2022 EEG WNL 01/03/2022 MRI of the brain: Impression: 1. No acute intracranial process. No acute infarct. 2. Mild, age related involutional changes of the brain parenchyma and chronic white matter microvascular ischemic changes. 3. Punctate chronic infarcts of bilateral cerebellar hemispheres.
CDC Split Type:

Write-up: Narrative: 12/08 COVID vaccine dose #3 01/02 pt presents to ED c/o generalized weakness x 3 weeks with SOB with exertion, acute on chronic "passing out" episodes, states multiple w/u in the past for recurrent syncope with no dx given Has had increase in amount of episodes - states 3-4 in the past week, per patient he passed out in the car on the way to ED, admitted to hospital; per med H&P note: PMHx of vasovagal syncopes, Sarcoidosis, CKD3, HTN and dyslipidemia presented with generalized weakness and multiple syncopal episodes during this week. Pt has been very tired and fatigued x 6 weeks per wife. He stated that he has been very debilitated since getting J&J booster on 12/08/21. Pt endorses fatigue and said that last Sunday he became lightheaded while sitting at church and passed out. He was carried to the floor until he regained consciousness. Pt had bladder incontinence which had never happened before. He spent the day sleeping yesterday. Today he was sitting having breakfast and became lightheaded when he stood up, sat down on the floor and lost consciousness. Per wife, he lost control of his bowel and bladder and rolled his eyes to the back of his head. Pt woke up and c/o L sided discomfort prior to passing out again per wife, but pt denied CP, SOB , n/v prior to the episodes and only stated feeling lightheaded before syncopizing. In the car on his way to the hospital pt had another syncopal episode. Denied fever, chill, sob, recent URI, headache or palpitations. Endorses good appetite and denied been outside in sun/being dehydrated. Of note, pt was diagnosed with vasovagal syncope s/p extensive cardiac and neurologic work-up done in home. Had a loop recorder implanted and subsequently removed. 01/05 Discharged from hospital, no abnormal findings during admission, returned home for follow up


VAERS ID: 1963623 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-18
Onset: 2021-12-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS FT779 / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Fatigue, No adverse event, Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: There have been no adverse events, just sore arm and mild fatigue.


VAERS ID: 1775102 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-28
Onset: 2021-09-29
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site swelling, Pain in extremity, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: montelukast 10 mg once dialy
Current Illness: no
Preexisting Conditions: nno
Allergies: azithromycin
Diagnostic Lab Data:
CDC Split Type:

Write-up: swelling of injection site very sore arm after administration giant welt appeared on right arm less than 24 hours after administration only went away after taking Benadryl for2-3 days


VAERS ID: 2717788 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-11-25
Onset: 2023-11-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030339 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8155JA / 1 RA / IM
HEP: HEP B (HEPLISAV-B) / DYNAVAX TECHNOLOGIES CORPORATION 943011 / 1 LA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. X002058 / 1 RA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X006981 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Nausea, Nervousness, Pallor
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt felt nauseous and was looking pale after 2 vaccines were administered. He was extremely nervous and hadn''t eaten lunch. Gave pt water and some chocolate. He started to feel better within minutes, and I was able to administer the rest of the vaccines. He was fine.


VAERS ID: 1963258 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-17
Onset: 2021-12-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 59267-1000-2 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 19515-818-41 / 1 RA / IM
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. 0006-4943-01 / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain upper, Chills, Hyperhidrosis, Mobility decreased, Pyrexia, Urinary retention, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: Diagnosis Sort Priority Severe protein-calorie malnutrition Routine Varicose veins of both lower extremities with complications High History of smoking High Intrinsic asthma, unspecified Routine Reflux esophagitis Routine Irritable bowel syndrome Routine History of gynecomastia Routine Chronic obstructive pulmonary disease (COPD) Routine Melena Routine Thrombocytopenia Routine Macrocytosis Routine Cannabis dependence Routine Arthralgia of hand Routine Hemangioma of skin and subcutaneous tissue Routine Changing nevus Routine Insomnia Routine Polyarthralgia Routine Annual physical exam Routine Erectile dysfunction due to arterial insufficiency Routine External hemorrhoid Routine Esophageal varices Routine History of hepatitis C Routine PHT (portal hypertension) Routine Uncomplicated alcohol withdrawal Routine Leukoplakia of vocal cords Routine Laryngitis, chronic Routine Hyperopia of both eyes with astigmatism and presbyopia Routine Pinguecula of both eyes Routine Alcohol use disorder, severe, dependence Routine Wernicke encephalopathy Routine Alcoholic cirrhosis of liver without ascites Routine Tubular adenoma Routine Alcoholic cirrhosis of liver with ascites Routine Adjustment reaction with anxiety and depression Routine Chronic right-sided low back pain with right-sided sciatica Routine GI bleed
Preexisting Conditions:
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Couldn''t urinate for about 12 hours, fever 102.2, couldn''t move out bed for 36 hours, chills, sweating, stomach ache, vomited.


VAERS ID: 1774939 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-06
Onset: 2021-10-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / SYR

Administered by: Private       Purchased by: ?
Symptoms: Appendicitis, Computerised tomogram abnormal, Laboratory test abnormal
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Wellbutrin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Labs and CT scan showed appendicitis.
CDC Split Type:

Write-up: Appendicitis occurring day after vaccination.


VAERS ID: 2728895 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-19
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2023-12-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4628 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9CE79 / UNK LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Injection site pain, Pain
SMQs:, Extravasation events (injections, infusions and implants) (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: pain still when lifting arm, putting seat belt on across body, and injection spot is still sore.


VAERS ID: 2727980 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-19
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2023-12-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4628 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9CE79 / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Mobility decreased, Pain in extremity
SMQs:, Parkinson-like events (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: patient doesn''t have full rotation of arm, its achy all the time. vaccine seemed higher than normal on the arm


VAERS ID: 2730812 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-26
Onset: 2023-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031279 / 6 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8162CA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Asthenia, Dysstasia, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: amiodarone, amlodipine,, rosuvastatin, losartan, apixaban
Current Illness: afib
Preexisting Conditions: diabetes, hypertensioin, sleep apnea, cervical spondylosis, tinnitus, afib
Allergies: amoxiciliin an dpenicillin -uticaria, lisinopril cough, metformiin mood swings
Diagnostic Lab Data: none
CDC Split Type:

Write-up: weak, trouble standing up, shakey - went away after 24 hours


VAERS ID: 1967501 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-16
Onset: 2021-12-18
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK LA / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Axillary pain, Chills, Lymph node pain, Lymphadenopathy, Pain
SMQs:, Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Daily multi vitamins
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Not sure which influenza vaccine i received, but got it at same time as covid booster (previously vaccinated with J&J vaccine). Following day had body aches and chills. The day after that I had swollen lymph nodes under left arm and swelling in that armpit as well. Still painful and swollen today, but possibly decreasing in both pain and swelling.


VAERS ID: 1708693 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-15
Onset: 2021-09-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-09-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ696AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Chills, Headache, Injection site pain, Pain in extremity
SMQs:, Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: injection site pain left and right arms beginning two hours after injection and worsening over the next 24 hours before gradually decreasing. Pain was worse in left arm versus right. Headache and chills around 3 AM the following morning post injection resolved within 3 hours. Significant right shoulder joint pain at 3 AM approximately 39 hours post injection. Pain was not relieved with 600mg Ibuprofen, stretching or postural changes. Pain eventually resolved spontaneously after about 2 hours.


VAERS ID: 2731203 (history)  
Form: Version 2.0  
Age: 1.25  
Sex: Female  
Location: Unknown  
Vaccinated: 2024-01-09
Onset: 2024-01-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR - / UNK - / -
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Seizure, Status epilepticus
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Seizure with status epilepticus


VAERS ID: 2727489 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-12-23
Onset: 2023-12-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 210F23 2A / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5ME79 / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: right after the administration of the second vaccine, pt fainted briefly. W helped him to the floor on his back and called911. After fainting for about 2 to 3 seconds, he woke up and became alert. he had normal HR and BR. He had clear visio
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient fainted briefly after getting the second shot (spikeVax). we helped him to the floor on his back and called 911. he woke up after 2 to 3 seconds. He was alert. he had clear vision, normal HR and normal RR.


VAERS ID: 1704769 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-14
Onset: 2021-09-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ689AB / N/A LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: severe vomiting and fever


VAERS ID: 2708012 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated: 2023-09-26
Onset: 2023-10-06
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2023-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER NO BATCH NUMBER / UNK RA / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK LA / OT

Administered by: Pharmacy       Purchased by: ?
Symptoms: Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Cabergoline
Current Illness: Prolactinoma
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSEQIRUS202305699

Write-up: Urticaria, across right side of neck, jaw, and torso; This spontaneous case was received on 26-Oct-2023 from other non-healthcare professional (consumer) via Pfizer (reference number 202300323410) and concerned a patient of unknown demographics. The patient''s concurrent conditions included prolactinoma. The patient''s concomitant medications included cabergoline, used for unreported indication. On 26-Sep-2023 the patient was vaccinated with Afluria Quadrivalent (influenza vaccine inact split 4v, anatomical location: left arm, dose, indication and route of administration: not reported). The batch number was not reported. On the same date the patient was vaccinated with non-company, co-suspect Pfizer BioNTech COVID-19 vaccine, Bivalent (active ingredients: not specified; anatomical location: right arm; dose, route of administration and indication: not reported). The batch number was not reported. On 06-Oct-2023, ten days after receiving Afluria Quadrivalent and non-company, co-suspect Pfizer BioNTech COVID-19 vaccine, the patient experienced urticaria, across right side of neck, jaw, and torso. On an unspecified day in Oct-2023, the patient received loratadine and hydrocortisone cream as treatment. At the time of the initial reporting on 26-Oct-2023, the patient had not recovered from the event. The reporter did not provide a causality assessment. The case was assessed as non-serious. Company comment: The event of urticaria is assessed as unassessable to Afluria Quadrivalent due to unsuggestive temporal relationship.; Sender''s Comments: The event of urticaria is assessed as unassessable to Afluria Quadrivalent due to unsuggestive temporal relationship.


VAERS ID: 2021190 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-05
Onset: 2022-01-09
   Days after vaccination: 65
Submitted: 0000-00-00
Entered: 2022-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 2 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Hospitalization of vaccinated COVID patient.


VAERS ID: 1693059 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-08-16
Onset: 2021-08-01
Submitted: 0000-00-00
Entered: 2021-09-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3180 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Inappropriate schedule of product administration, Inflammation, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The patient received her COVID vaccine and flu vaccine in the same arm, an inch apart from each other. The patient went to urgent care due to inflammation in her arm and received prescriptions for Norco and Ibuprofen. The redness and swelling did not resolve so she later went to another urgent care where she was given antibiotics and her symptoms resolved days later.


VAERS ID: 2705666 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-29
Onset: 2023-10-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 6 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Brain fog, Fatigue, Pain in extremity, Sleep disorder
SMQs:, Noninfectious encephalopathy/delirium (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: right arm soreness (COVID vaccine admin location) - began overnight. painful to sleep on. continued in the morning. ongoing as of time of reporting. treating with ice pack on arm. fatigue - began a few hours after vaccination. continued the following morning. brain fog - began morning after vaccination. ongoing.


VAERS ID: 2713257 (history)  
Form: Version 2.0  
Age: 0.5  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-11-07
Onset: 2023-11-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5558B / 1 RL / IM
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS A32BB / 3 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8230AA / 1 LL / IM
PNC15: PNEUMO (VAXNEUVANCE) / MERCK & CO. INC. X020316 / 3 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Full contents of Moderna 2023-2023 formulation vial administered to patient, thought to be $g0.25mL. No adverse events noted following 15 minute monitoring period.


VAERS ID: 2538788 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-12-06
Onset: 2021-12-14
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2021-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367231 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Anaemia, Asthenia, COVID-19, Decreased appetite, Diarrhoea, Dyspnoea, Fluid intake reduced, Gastrointestinal haemorrhage, Nausea, Odynophagia, Productive cough, Pyrexia, Rectal haemorrhage, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Haematopoietic erythropenia (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal haemorrhage (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Cardiomyopathy (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: LAB RESULTS: Date Test Name Result 12/15/2021@02:30:03 SARS-CoV-2 IgG (ABBOT) 0.02 12/14/2021@18:10:04 COVID-1 DIAG (BIOFIRE) DETECTED 11/29/2021@06:00:03 COVID-19 DIA (ORL) NotDetected 07/05/2021@18:33 COVID-19 DIAG (ORL) NotDetected 03/07/2021@11:21COVID-19 PCR (FLUVID) NotDetected
CDC Split Type:

Write-up: Narrative: COVID infection following COVID vaccine series 02/26 COVD vaccine dose #1 03/07 seen in ED c/o pain on swallowing x 1 week, pt declined inpatient admission, rx''d sucralfate, maalox, fluconazole 03/10 pt reports swallowing pain resolved 03/18 COVID vaccine dose #2 07/05 seen in ED c/o difficulty swallowing, unable to eat or drink x 2 days, diarrhea; tx''d with maalox, famotidine, acetaminophen; rx''d maalox and fluconazole 11/29 seen in ED c/o rectal bleeding x 5 days, nausea, fever, weak, SOB on exertion; admitted to inpatient 12/02 pt left hospital AMA 12/06 COVID vaccine dose #3 12/14 pt c/o SOB, weakness, nausea/vomiting, productive cough and loose stools, 1 week s/p hospitalization for anemia/GI blled; COVID positive, no pneumonia 12/17 discharged from hospital


VAERS ID: 1997698 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-10
Onset: 2021-11-12
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-01-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 33030BD / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Fatigue, Heart rate increased, Mental fatigue, Night sweats, Pain, Pyrexia, Respiratory rate increased
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin, doxycycline
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fever, achiness, high mental and physical fatigue, night sweats, elevated respiratory and resting heart rate lasting approximately 10 days after Pfizer booster dose.


VAERS ID: 2700795 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-19
Onset: 2023-10-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030372 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8131BA / 1 LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS 32S4C / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Induration, Injection site induration, Injection site swelling, Oedema peripheral
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Harden and swollen skin between the area of the vaccine and armpit. Size as big as a "golfball." Was counseled to massage it and ice it to bring down the swelling. If it gets any worse, advised to go to emergency room.


VAERS ID: 2043621 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-09-30
Onset: 2021-10-05
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-01-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ704AA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Warfarin (Coumadin). Office/Lab visit within 6 weeks of receiving COVID vaccine.


VAERS ID: 1637626 (history)  
Form: Version 2.0  
Age: 13.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-08-26
Onset: 2021-08-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-08-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0186 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2X295 / N/A RA / SC

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pfizer dose was given after expired date and time, passing the 6 hour threshold.


VAERS ID: 1920644 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-03
Onset: 2021-12-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 035C21A / 3 UN / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / 1 UN / IM

Administered by: Public       Purchased by: ?
Symptoms: Dizziness, Immediate post-injection reaction
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: client stated that she immediately felt dizzy, but states that this always happens to her after vaccines.


VAERS ID: 1782563 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-11
Onset: 2021-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ705AA / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Chest discomfort, Dyspnoea, Inappropriate schedule of product administration
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received COVID-19 booster and flu vaccine, one each arm. Within a few minutes, complained of chest tightness and SOB. (history of asthma) Vitals: Pulse 76, BP 130/80 O2 100%, respirations 16. Patient used her inhaler and was given a drink of water. After 5 more minutes patient vitals remained the same and patient said she was feeling better. Left after wait period with adult son, agreed to watch for further symptoms and seek medical care if necessary.


VAERS ID: 1910012 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-22
Onset: 2021-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0173 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ775AA / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Dizziness
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Medications: albuterol sulfate (PROVENTIL HFA;VENTOLIN HFA) 90 mcg/actuation HFA inhaler Inhale by mouth. citalopram (CELEXA) 10 MG tablet Take 10 mg by mouth daily. DULoxetine (CYMBALTA) 20 MG capsule Take 20 mg by mouth daily. escitalopra
Current Illness:
Preexisting Conditions: PMH: Asthma, Hypothyroidism, DDD (lumbar), hysterectomy, cervical stenosis of spinal canal, depression, chronic pain, anxiety, panic attacks
Allergies: Allergies: Septra (itching, hives, anaphylaxis), Nuts - peanuts, almonds, pecans
Diagnostic Lab Data:
CDC Split Type:

Write-up: 50 mins post vaccination pt reported light headedness Vitals: 157/94, 66, 16 Pt stable and released from the vaccination site


VAERS ID: 1909174 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-11-01
Onset: 2021-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Feeling abnormal, Headache, Muscle spasms, Nausea, Pain, Pyrexia, Respiratory tract congestion, Sensitive skin
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Peptop Bismol, bee stings
Diagnostic Lab Data:
CDC Split Type:

Write-up: Within 2 hours I started feeling similar symptoms to when I had covid. Fever of 100.6, intense body aches and pains, headache, congestion, muscle cramping, brain fog, nausea, and sensitivity to temperature.


VAERS ID: 1979549 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: No adverse event, Therapeutic response unexpected
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Got Pfizer COVID booster dose. Then two weeks later got High dose flu vaccine. No adverse event but instead a good one: long standing warts on hands and feet,that have been so resistant to treatment that I had stopped.treatng them 6 months before, immediately started shrinking. Gone in a week and have stayed gone for more than, 6mo.


VAERS ID: 2713274 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-11-08
Onset: 2023-11-09
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031419 / 7+ LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8055MA / UNK LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site pain, Injection site pruritus, Injection site rash, Injection site warmth
SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Allergies, migraines, chronic widespread pain and neuropathy, IBS
Allergies: Gluten, some topical adhesives, grasses, dust mites, pet dander, cockroaches, mold, wasps
Diagnostic Lab Data:
CDC Split Type:

Write-up: Painful, itchy rash that''s hot to the touch, on upper left arm at the injection site, has persisted for several days


VAERS ID: 2719374 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-11-27
Onset: 2023-11-29
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 4 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest pain, Headache, Palpitations, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Headache,fever on second day,chest pain on third and forth day,heart palpitations


VAERS ID: 2720186 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-19
Onset: 2023-10-20
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Dizziness, Electric shock sensation
SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CYMBALTA
Current Illness: Fibromyalgia (patient has Fibromyalgia)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USGSKUS2023AMR164793

Write-up: Dizziness; Electric shock sensation; This non-serious case was reported by a consumer via other manufacturer and described the occurrence of dizziness in a 44-year-old female patient who received Flu Seasonal QIV Dresden (Fluarix Quadrivalent 2023-2024 season) for prophylaxis. Co-suspect products included COVID-19 vaccine for prophylaxis. Concurrent medical conditions included fibromyalgia (patient has Fibromyalgia). Concomitant products included duloxetine hydrochloride (Cymbalta). On 19-OCT-2023, the patient received Fluarix Quadrivalent 2023-2024 season (intramuscular, left arm) and COVID-19 vaccine (intramuscular, right arm) .5 ml. On 20-OCT-2023, 1 days after receiving Fluarix Quadrivalent 2023-2024 season, the patient experienced dizziness (Verbatim: Dizziness) and electric shock sensation (Verbatim: Electric shock sensation). The outcome of the dizziness and electric shock sensation were not resolved. It was unknown if the reporter considered the dizziness and electric shock sensation to be related to Fluarix Quadrivalent 2023-2024 season and Fluarix Tetra Pre-Filled Syringe Device. It was unknown if the company considered the dizziness and electric shock sensation to be related to Fluarix Quadrivalent 2023-2024 season and Fluarix Tetra Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date-21-NOV-2023 The reporter reported that the patient experienced electric shock sensation and dizziness after 1 days of vaccination. The patient received Fluarix Quadrivalent vaccine and COVID-19 vaccine at same time. The reporter considered the electric shock sensation and dizziness possible related to Covid19 vaccine. The consent to follow up requested.


VAERS ID: 2753466 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated: 2023-11-01
Onset: 2023-11-30
   Days after vaccination: 29
Submitted: 0000-00-00
Entered: 2024-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 5 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8201FA / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Chills, Cough, Fatigue, Myalgia, Pyrexia, Rhinorrhoea
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ROSUVASTATIN; OMEPRAZOLE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSA2024SA077089

Write-up: myalgia; low grade fever; chills; fatigue; runny nose; coughing; Initial information received on 05-Mar-2024 regarding an unsolicited valid non-serious courtesy case received via consumer/non-healthcare professional. This case involves Adult and unknown gender patient who had runny nose, coughing, myalgia, low grade fever, chills and fatigue while receiving elasomeran [Spikevax] and influenza quadrival A-B vaccine [Fluzone Quadrivalent]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included rosuvastatin; and omeprazole. On an unknown date in Nov-2023, the patient received a 1 DF (dosage form) dose of suspect influenza quadrival A-B vaccine, Suspension for injection (strength, expiry date: unknown) (lot: U8201FA) via unknown route in unknown administration site for prophylactic vaccination (immunization) and dose 5 of an unknown dose of suspect SPIKEVAX injection not produced by Sanofi Pasteur (strength, lot number, expiry date: unknown) via intramuscular route in unknown administration site for covid-19 prophylaxis. On 30-Nov-2023 the patient had events of runny nose (rhinorrhoea) and coughing (cough) (unknown latency) following the administration of influenza quadrival A-B vaccine and spikevax. On 30-Nov-2023 at 07:00 hours, the patient had events of myalgia and low grade fever (pyrexia), chills and fatigue (unknown latency) following the administration of INFLUENZA QUADRIVAL A-B VACCINE and (SPIKEVAX. Action taken: not applicable. The patient was treated with Paracetamol (Tylenol) from 30-Nov-2023 to 02-Dec-2023 for Fever and Myalgia, at a dose of UNK UNK, prn. It was not reported if the patient received a corrective treatment for the events runny nose, coughing, chills, fatigue. Outcome: Recovering / Resolving for the events runny nose, coughing, was Recovered / Resolved on 03-Dec-2023 for the events myalgia, low grade fever, chills and fatigue.


VAERS ID: 1926071 (history)  
Form: Version 2.0  
Age: 21.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-04
Onset: 2021-12-05
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site pain, Injection site pruritus, Injection site rash
SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft Oral birth control pill
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Itchy and tender rash about 1 inch below vaccination site. Rash about 1 inch in diameter


VAERS ID: 2043663 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-30
Onset: 2021-12-08
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2022-01-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ766AB / 1 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Rectal cancer
SMQs:, Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Rectal cancer - hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2715011 (history)  
Form: Version 2.0  
Age: 100.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-19
Onset: 2023-11-15
   Days after vaccination: 27
Submitted: 0000-00-00
Entered: 2023-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030340 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8150DA / N/A RA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH HA2259 / N/A LA / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Aortic valve incompetence, Aortic valve thickening, Aspartate aminotransferase increased, Blood alkaline phosphatase increased, Blood creatinine increased, Blood urea increased, Bundle branch block left, Central nervous system lesion, Cerebral atrophy, Cerebral calcification, Cerebral small vessel ischaemic disease, Cerebrovascular accident, Computerised tomogram head abnormal, Diastolic dysfunction, Dysphagia, Echocardiogram abnormal, Ejection fraction decreased, Electrocardiogram abnormal, Facial paralysis, Glomerular filtration rate decreased, Hemiparesis, Left atrial dilatation, Left ventricular dysfunction, Meningioma, Mitral valve incompetence, Mitral valve thickening, Monocyte count increased, Platelet count increased, Pulmonary valve incompetence, QRS axis abnormal, Right atrial dilatation, Sinus bradycardia, Speech disorder, Tricuspid valve incompetence, Troponin I normal, Ultrasound Doppler, Unresponsive to stimuli, Ventricular hypokinesia, Visual tracking test abnormal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Cardiac failure (narrow), Liver related investigations, signs and symptoms (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Disorders of sinus node function (narrow), Conduction defects (narrow), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Retroperitoneal fibrosis (broad), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Psychosis and psychotic disorders (broad), Biliary system related investigations, signs and symptoms (broad), Pulmonary hypertension (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (narrow), Hearing impairment (broad), Hypotonic-hyporesponsive episode (broad), Chronic kidney disease (broad), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: -potassium chloride (K-TAB) 10 mEq CR tablet -pantoprazole (PROTONIX) 20 mg enteric coated tablet -lisinopril (PRINIVIL, ZESTRIL) 5 mg tablet -carVEDilol (COREG) 12.5 mg tablet -furosemide (LASIX) 20 mg tablet -polyethylene glycol
Current Illness: No acute illnesses
Preexisting Conditions: Essential hypertension [I10] Disorder of bone and cartilage [M89.9, M94.9 Open-angle glaucoma, moderate stage Bilateral senile cataracts Exudative age-related macular degeneration Pure hypercholesterolemia [E78.00 Hypothyroidism (acquired) [E03.9 Chronic systolic congestive heart failure Nursing home resident [Z59.3] CHF (congestive heart failure) [I50.9] Bronchitis [J40] Heart failure with reduced ejection fraction
Allergies: No allergies
Diagnostic Lab Data: LAB 11/15/23 Troponin I: 0.026 BUN: 23 Creatinine: 1.16 Alkaline Phosphatase: 192 AST - SGOT: 36 eGFRcr(AS): 42 Low Platelet Count: 416 High Monocytes Absolute: 1.1 High EXAM: CT HEAD WITHOUT CONTRAST 11/15/23 INDICATION: Stroke TECHNIQUE: CT of the brain performed without IV contrast. COMPARISON(S): 3/23/2023 FINDINGS: There is no acute intra or extra axial fluid collection. There is stable generalized cerebral atrophy. The ventricles are symmetric in size, shape, and position. There are mild areas of hyper bowel attenuation within the cerebral white matter consistent with chronic small vessel disease. No mass effect or midline shift is present. The gray-white matter differentiation is maintained. There is a stable calcified dural based extra-axial lesion near the vertex overlying the parietal convexity which likely represents meningioma. There is no significant mass effect upon the adjacent cerebral sulci. The visualized portions of the orbits, paranasal sinuses, and mastoids are normal. No fractures are identified. IMPRESSION: No acute intracranial process. EKG 11/15/23 WAVEFORM Sinus bradycardia Left axis deviation Left bundle branch block Abnormal ECG Echocardiogram 11/15/23 Left Ventricle The left ventricle appears normal in size. Wall thickness is normal. The EF is visually estimated to be 30-35%. The mid inferior, apical septal and apical inferior wall segments are akinetic. Global hypokinesis of the left ventricular wall segments. Apical tabeculae noted. Grade II diastolic dysfunction and left ventricular filling pressure is elevated. There is no thrombus. Right Ventricle The right ventricle appears normal in size. Systolic function is normal. Wall thickness is normal. The RVSP measures 24 mmHg. There is no evidence of pulmonary hypertension. Left Atrium The left atrium is dilated by visual assessment. Interatrial Septum No evidence of an atrial shunt by color Doppler. Right Atrium The right atrium is dilated by visual assessment. Aortic Valve The aortic valve is tricuspid. Normal valve mobility. The cusps are mildly thickened. There is mild regurgitation. Aortic regurgitation pressure half-time is 506 msec. There is no evidence of aortic valve stenosis. Mitral Valve Mitral valve structure is normal. The leaflets are mildly thickened. There is moderate regurgitation. There is no evidence of mitral valve stenosis. Tricuspid Valve Tricuspid valve structure is normal. There is mild regurgitation. Pulmonic Valve Pulmonic valve structure is normal. There is mild regurgitation. There is no evidence of pulmonic valve stenosis. Aorta The sinus of Valsalva is normal. The sinotubular junction is within normal limits. The ascending aorta is normal. Pulmonary Artery The estimated pulmonary artery systolic pressure is 24 mmHg.There is no pulmonary hypertension. IVC/SVC Normal IVC size with normal respirophasic changes. Pericardium There is no pericardial effusion.
CDC Split Type:

Write-up: Resident was checked on at 1515 to give 1500 med, resident was noticed to be unresponsive at that time. TMA called this nurse into room, assessment started, eye not tracking, mumbled speech noted, right side mouth droop, not following commands. 911 called. VS taken and charted. Resident was to lunch at noon walked with walker to dining room, received ride in wc back to room which is her normal routine, last checked on at 1300, no concerns at that time. Assessment / Plan Active Problems: *CVA left-sided with right-sided paresis -Not a candidate for thrombolytic given significant comorbidities as well as age -Patient will be admitted We will repeat CT scan in the morning She will have a 2D echo She will be given aspirin 325 per rectum Patient is not able to swallow


VAERS ID: 1905937 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-15
Onset: 2021-11-22
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ702AB / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Acute kidney injury, Acute respiratory distress syndrome, Atrial fibrillation, COVID-19 pneumonia, Cerebrovascular accident, Deep vein thrombosis, Illness, Intensive care, Laboratory test, Mechanical ventilation
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Interstitial lung disease (broad), Supraventricular tachyarrhythmias (narrow), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad), Acute central respiratory depression (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Tumour lysis syndrome (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (narrow), Dehydration (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data: extensive
CDC Split Type:

Write-up: 1. Subactue large right MCA stroke. 2. AKI 3. Atrial fibrillation 4. ARDS 5. Multiple DVTs 6. COVID-19 PNA on the ventilator Currently very sick in ICU and still on the ventilator.


VAERS ID: 1759054 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-02
Onset: 2021-09-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Colitis ischaemic, Fatigue, Rectal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Gastrointestinal haemorrhage (narrow), Ischaemic colitis (narrow), Noninfectious diarrhoea (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Trulicity, metformin, celexa, wellbutrin
Current Illness: T2DM
Preexisting Conditions: T2DM
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Ischemic colitis, rectal bleeding, fatigue


VAERS ID: 2014092 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-06
Onset: 2021-10-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301558A / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Atrial fibrillation
SMQs:, Supraventricular tachyarrhythmias (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Atrial fibrillation with RVR now controlled. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2039516 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-09-03
Onset: 2021-09-23
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3183 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Neoplasm, Pathological fracture
SMQs:, Osteoporosis/osteopenia (broad), Non-haematological tumours of unspecified malignancy (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pathological fracture of right hip due to neoplastic disease with routine healing, subsequent encounter. Hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.


VAERS ID: 2709863 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-26
Onset: 2023-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9300*SE-VFC / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS A2L45*SE-VFC / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: No adverse event, Product administered to patient of inappropriate age, Product administration error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: No known adverse event. Vaccine administration error: Comirnaty (recommended starting at age 12 years ) administered to a child 3 weeks short of the 12th birthday.


VAERS ID: 1988191 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Unknown  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Loss of consciousness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ENZALUTAMIDE; ELIGARD
Current Illness: Malignant neoplasm of prostate
Preexisting Conditions: Medical History/Concurrent Conditions: Stent placement
Allergies:
Diagnostic Lab Data:
CDC Split Type: USGLAXOSMITHKLINEUS2021AM

Write-up: Knocked out, could not function; This case was reported by a consumer via other manufacturer and described the occurrence of unconscious in a 70-year-old male patient who received Flu Seasonal QIV Dresden (Flu Seasonal QIV Dresden) for prophylaxis. Co-suspect products included COVID-19 VACCINE for prophylaxis and leuprorelin acetate (Eligard) for product used for unknown indication. The subject''s past medical history included stent placement. Concurrent medical conditions included malignant neoplasm of prostate. Concomitant products included enzalutamide. On an unknown date, the patient received Flu Seasonal QIV Dresden, COVID-19 VACCINE and Eligard at an unknown dose and frequency. On an unknown date, unknown after receiving Flu Seasonal QIV Dresden, the patient experienced unconscious (serious criteria GSK medically significant and other: Serious as per reporter). The subject was treated with ticagrelor (Brilinta) and acetylsalicylic acid (Aspirin). On an unknown date, the outcome of the unconscious was recovered/resolved. It was unknown if the reporter considered the unconscious to be related to Flu Seasonal QIV Dresden. Additional details were provided are as follows: The patient was enrolled in Astellas sponsored patient support program. The age at vaccination was not reported. The patient did not had known medical history and drug allergy. The patient received a dose of Influenza vaccine, a booster dose of Covid-19 vaccine and leuprorelin (Eligard) on the same day. It was reported that the patient was knocked out to where he could not function for almost 3 days. The patient was treated with Enzalutamide 160 mg once day for malignant neoplasm of prostate. The patient asked to pharmacist about taking Ticagrelor (Brilinta) and aspirin 325 mg together and the patient stated that he had stent put in the place and was started on ticagrelor twice daily and was taking once daily along with aspirin but read aspirin dose might be too high. The pharmacist advised per clinical pharmacist that usually ticagrelor was dosed twice daily (as prescribed) along with aspirin 81 mg and also discuss with MDP who prescribed ticagrelor about decreasing of aspirin dose. The action taken with Enzalutamide, leuprorelin, Covid-19 vaccine and influenza vaccine therapy in response to event was unknown. No lab test information were provided. The sender comment was mentioned as unconsciousness was assessed as serious due to medical significant. It was unknown if the reporter considered the unconscious to be related to leuprorelin and Covid-19 vaccine. Note: Enzalutamide was captured as concomitant as it seems patient was taking it for cancer.


VAERS ID: 2039556 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2021-11-02
Onset: 2021-12-03
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ741AC / 1 - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Aortic aneurysm, Surgery
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: AAA (abdominal aortic aneurysm) without rupture. Hospital admission, procedure. This visit is within 6 weeks of receiving the COVID Vaccine.


VAERS ID: 2709865 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Male  
Location: Unknown  
Vaccinated: 2023-10-26
Onset: 2023-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9300*SE-VFC / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS A2L45*SE-VFC / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: No adverse event, Product administered to patient of inappropriate age, Product administration error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: No adverse event. Vaccine administration error: Comirnaty administered to a 7 year old. (the patient''s weight is above the WHO growth chart''s 50th percentile for 12 year olds.)


VAERS ID: 2726794 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-19
Onset: 2022-03-03
   Days after vaccination: 135
Submitted: 0000-00-00
Entered: 2023-12-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9339N / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, COVID-19, Exposure during pregnancy, Vaginal haemorrhage, White blood cell count increased
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Adderall 20 mg daily, Maxalt 10 mg PRN
Current Illness: Migraine headaches, ADHD
Preexisting Conditions: Migraine headaches, ADHD
Allergies: Meperidine
Diagnostic Lab Data: White blood cell count 18,300 3/3/22
CDC Split Type:

Write-up: Presented to emergency department (ED) with 16week 2 day pregnancy, increased vaginal bleeding with clots and lower abdominal cramping. Started with vaginal spotting and bleeding at 14 weeks. LMP 11/9/2021. Had COVID-19 infection during first trimester. In ED BP 152/80, HR 96, afebrile. White blood cell count was elevated - 18,300. Pelvic examination revealed blood in the vault and fetal tissue at the cervical os consistent with a spontaneous abortion. Final diagnosis was spontaneous second trimester abortion.


VAERS ID: 2746769 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2023-10-16
Onset: 2023-10-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / -
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: unknown- pt didn''t answer


VAERS ID: 1942144 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-12-08
Onset: 2021-12-09
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Induration, Peripheral swelling, Skin warm, Tenderness
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: My upper left arm has a large, hard, swollen, hot red patch about 5 inches by 5 inches. It is a bit tender to the touch and very swollen.


VAERS ID: 2531890 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Unknown  
Vaccinated: 2021-10-04
Onset: 2021-12-20
   Days after vaccination: 77
Submitted: 0000-00-00
Entered: 2022-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3590 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100355859 / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Burning sensation, COVID-19, Cough, Dyspnoea, Fatigue, Headache, Hyperhidrosis, Myalgia, Oropharyngeal pain, Pharyngeal erythema, Pyrexia, Rhinorrhoea, SARS-CoV-2 test positive, Wheezing
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 12/20/2021@13:26 COVID-19 DIAG DETECTED 08/03/2021@00:11:02 COVID-19 NOTDETECTED 02/05/2021@15:00 COVID-19 SCR NotDetected 07/27/2020@01:42 COVID-19 NotDetected 06/07/2020@17:40 COVID-19 NotDetected
CDC Split Type:

Write-up: Narrative: COVID infection after COVID vaccine series 02/23 COVID vaccine dose #1 03/16 COVID vaccine dose #3 12/20 pt present w/ c/o cough, fatigue, rhinorrhea, sore throat, red throat; COVID POSITIVE 12/21 pt with continued SOB, reports burning up and sweating like crazy, c/o cough, fever, headache, myalgia, rhinorrhea, dyspnea, wheezing; seen in ED; treated with dexamethasone 6mg IV x 1, duoneb; r/o PE, discharged from ED


VAERS ID: 1642909 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated: 2020-11-01
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-08-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Dyspnoea, Pulmonary oedema
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USGLAXOSMITHKLINEUS2021AM

Write-up: lungs filled up with fluid; trouble breathing; This case was reported by a consumer via interactive digital media and described the occurrence of pulmonary edema in a patient who received Flu Seasonal QIV Dresden (Influenza vaccine Quadrivalent 2020-2021 season) for prophylaxis. Co-suspect products included COVID-19 VACCINE for prophylaxis. In November 2020, the patient received Influenza vaccine Quadrivalent 2020-2021 season. On an unknown date, the patient received COVID-19 VACCINE. On an unknown date, less than a year after receiving Influenza vaccine Quadrivalent 2020-2021 season, the patient experienced pulmonary edema (serious criteria hospitalization and GSK medically significant) and difficulty breathing. On an unknown date, the outcome of the pulmonary edema and difficulty breathing were unknown. It was unknown if the reporter considered the pulmonary edema and difficulty breathing to be related to Influenza vaccine Quadrivalent 2020-2021 season. Additional details were provided as follows: The case was reported by the patient for herself/himself. The age at vaccination was not reported. The patient reported that, he/she got the flu shot and have had trouble breathing ever since then. The patient''s lungs filled up with fluid and he/she had to go to the hospital. Till the time of reporting, the patient still seeing a lung doctor. The patient said that, no more poison for him/her. The patient reported that, they were no longer giving vaccines, but experimental drugs with MRA in them that destroy your immune system, wake up people. It was unknown if the reporter considered the pulmonary edema and difficulty breathing to be related to Covid vaccine. The follow-up would not possible as no contact details were available. Note: It was unknown if the patient had received Covid vaccine or not, as it was mentioned in source document under product field, hence conservatively captured as suspect. The clarification has been raised for the same.


VAERS ID: 1906490 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: Alaska  
Vaccinated: 2021-11-10
Onset: 2021-11-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3T4DH / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue, Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: When preparing the vial, 1.6mL of diluent (sodium chloride) mixed instead of 1.3mL. The vaccine given slightly weaker due to too much diluent mixed.


VAERS ID: 2506696 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Female  
Location: Alaska  
Vaccinated: 2021-09-20
Onset: 2021-09-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 203A21A / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abdominal pain, Autonomic nervous system imbalance, Balance disorder, Barium swallow, Blood test, Cardiac stress test, Computerised tomogram, Diplopia, Dizziness, Dysphagia, Dysphonia, Dyspnoea, Echocardiogram, Electrocardiogram ambulatory, Endoscopy, Fatigue, Gait disturbance, Gastric emptying study, Hypoaesthesia, Impaired gastric emptying, Magnetic resonance imaging, Migraine, Muscular weakness, Nausea, Orthostatic hypotension, Pain, Paraesthesia, Presyncope, Pyrexia, Sleep disorder, Swallow study, Syncope, Tachycardia, Tilt table test, Tinnitus, Tremor, Vision blurred, Visual impairment, Vocal cord dysfunction, Vomiting, Weight decreased
SMQs:, Torsade de pointes/QT prolongation (broad), Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Retroperitoneal fibrosis (broad), Parkinson-like events (broad), Gastrointestinal obstruction (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific dysfunction (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Optic nerve disorders (broad), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Hearing impairment (narrow), Vestibular disorders (broad), Ocular motility disorders (broad), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad), Immune-mediated/autoimmune disorders (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Synthroid, multivitamin, Super C, Topamax
Current Illness: None
Preexisting Conditions: Hypothyroidism, infrequent migraines
Allergies: At time of vaccination: Strawberries and shellfish
Diagnostic Lab Data: Blood test, CT scan, MRI?s, tilt table test, swallow study, modified barium swallow study, gastric emptying study, endoscopy, echo, stress test, halter monitor
CDC Split Type:

Write-up: Symptoms started on the evening of the injection. First reaction was fever of 105.8 degrees (f), over the next few weeks developed tachycardia, shortness of breath, fatigue, and dizziness. This progressed to near syncope and syncope, nausea, vomiting, migraines and increased fatigue . Over the next few months developed/ was diagnosed with: vasovagal syndrome, dysautonomic orthostatic hypotension syndrome, gastroparesis, weight loss, Dysphagia, swallowing difficulties, change in voice, tinnitus, vocal cord dysfunction syndrome, dysautonomia, paresthesia to hands and feet, pain, numbness and tingling to hands and feet, abdominal pain, balance disturbance, gait instability, weakness to extremities, vision disturbances, blurred vision and double vision, difficulties with visual tracking, motility issues , sleep disturbance and internal tremors


VAERS ID: 2043689 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Alaska  
Vaccinated: 2021-11-04
Onset: 2022-01-11
   Days after vaccination: 68
Submitted: 0000-00-00
Entered: 2022-01-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test negative, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Doterra: Terrazyme, probiotic FullWell: prental vitamin
Current Illness: n/a
Preexisting Conditions: PCOS
Allergies: dairy sensitivity, adverse reaction to codeine
Diagnostic Lab Data: Covid testing: 1/11 - negative; 1/13 - positive (PCR for both)
CDC Split Type:

Write-up: covid positive result. Symptoms: scratchy throat, fatigue, congestion


VAERS ID: 1906470 (history)  
Form: Version 2.0  
Age: 6.0  
Sex: Female  
Location: Alaska  
Vaccinated: 2021-11-10
Onset: 2021-11-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3T4DH / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue, Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: When preparing the vial, the 1.6mLs of diluent (Sodium Chloride)was mixed instead of 1.3mLs. The vaccine given was slightly weaker due to too much diluent mixed.


VAERS ID: 2718122 (history)  
Form: Version 2.0  
Age: 4.0  
Sex: Male  
Location: Alaska  
Vaccinated: 2023-11-07
Onset: 2023-11-21
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2023-11-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5551B / 4 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 99R27 / 6 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Bronchiolitis, C-reactive protein, Dyspnoea, Metabolic function test normal, Platelet count increased, Post-tussive vomiting, Prohormone brain natriuretic peptide, Pyrexia, Red blood cell sedimentation rate increased, Respiratory symptom, Troponin, Urticaria, Viral infection, Viral test negative, White blood cell count increased
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: None
Preexisting Conditions: Growth hormone deficiency
Allergies: NKA
Diagnostic Lab Data: 11/20/23 labs performed were WBC 14.4, Platelets 517, CMP wnl, ESR 28, CRP 8.5, troponin 5, pro-BNP 70, and negative viral panel.
CDC Split Type:

Write-up: One week after vaccine administration patient developed upper respiratory infection symptoms. One week after that (two weeks after vaccine administration) patient developed high fever, hive like rash to back that seemed to spread, and pain in his right knee. He then began to have post tussive vomiting and increased work of breathing which led him to our office to rule out strep. Patient began Benadryl , Zyrtec, steroids, and antibiotics for a possible pneumonia. Patient was then seen at the ER for continued increased work of breathing despite steroids and antibiotics where he was admitted for observation. His admission diagnoses were viral bronchiolitis, diffuse urticarial rash, and polyarticular arthralgias.


VAERS ID: 2697903 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Male  
Location: Alaska  
Vaccinated: 2023-10-17
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2023-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3032086 / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8038 / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Dizziness, Dysgeusia, Feeling abnormal
SMQs:, Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Dementia (broad), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: amitriptylline, gabapentin, meloxicam, cyclobenzapine, multivitamins
Current Illness:
Preexisting Conditions: rhinitis, TBI
Allergies: penicillin, codeine, peanuts, apples, lurasidone
Diagnostic Lab Data: none known.
CDC Split Type:

Write-up: Within 1 minute of injection, patient stated he had funny taste in mouth like sweet antifreeze, also felt funny, lightheaded and strange feeling. BP was taken 155/99, AP-69, O2 Sat. 98%. Gave pt. some water and a cracker since he stated earlier he did not like needles. Patient stated he has never felt like this after vaccine injection. After 5-10 minutes, symptoms began to improve. Pt. stayed with writer 15-20 minutes and then stated he felt okay to leave, he had another appt. at clinic today. Final BP 133/87, AP-68, O2 Sat. 98% before released.


VAERS ID: 2703955 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Female  
Location: Alaska  
Vaccinated: 2023-10-25
Onset: 2023-10-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5551B / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5452E / 2 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin D drops
Current Illness: None known
Preexisting Conditions: Slow weight gain
Allergies: NKA
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient received 0.5ml of the 6m-11yr Moderna Monovalent vaccine instead of 0.25ml.


VAERS ID: 1944683 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Female  
Location: Alaska  
Vaccinated: 2021-10-17
Onset: 2021-11-17
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2021-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK1127 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / N/A LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 0.2 mL Pediatric formulation Pfizer dose erroneously administered to 12-year-old who should have received 0.3 mL of Adult/Adolescent formulation Pfizer.


VAERS ID: 1847755 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Alaska  
Vaccinated: 2021-11-05
Onset: 2021-11-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025D21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ702AB / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site swelling
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: losartan, fluoxetine
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: swelling at injection site


VAERS ID: 2720385 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Male  
Location: Alaska  
Vaccinated: 2023-11-21
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 8058581 / UNK RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS A45NH / UNK RL / IM

Administered by: Public       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Spikvax 2023-2024 0.25mL given. Moderna 2023-2024 0.25mL is recommended due to <12yo.


VAERS ID: 1968450 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: Alaska  
Vaccinated: 2021-12-21
Onset: 2021-12-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH KF5618 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Blindness unilateral, Deafness, Visual impairment, Vomiting
SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Hearing impairment (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: moderate persistent asthma, environmental allergies (pets in home), urticaria, headaches, exphoria
Allergies: NKDA
Diagnostic Lab Data: none
CDC Split Type:

Write-up: a few minutes after vaccine administration patient informed her mother that she felt like she couldn''t hear and had some visual disturbance as she couldn''t see out of her left eye. Patient then vomited once. She was evaluated by staff RN and MD and a full set of vitals were taken. She was observed for an extra 15 minutes and was told to rest for the remainder of the day and mom was instructed to call our office with any questions.


VAERS ID: 1999363 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2021-12-04
Onset: 2021-12-05
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 045J21A / 3 AR / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Cough, Dysgeusia, Exposure to SARS-CoV-2, Fatigue, Feeding disorder, Headache, Influenza virus test negative, Insomnia, Pyrexia, SARS-CoV-2 test negative, Streptococcus test negative
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Cold
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: 12/8/2021 Covid, Strep, and Flu, all negative. 12/21/2021 Covid, negative. 12/27/2021 Covid, negative.
CDC Split Type: vsafe

Write-up: I woke up the night after I got the shot and I had a fever, chills, headache, and trouble falling back asleep. It continued into that day. The first day and second day were the same. I had a metallic taste in my mouth. I did not want to eat anything. The third day I started feeling a little bit better but I was very tired. I had a cough. The day after that I started feeling better but the cough, headache and exhaustion stayed around. On 12/8/2021 I went to a local medical Clinic to make sure I did not have Covid and it was negative. They also tested me for Strep and Flu, which were negative too. They told me to keep taking Tylenol and Dayquil. I was feeling better by the weekend. I did not have a fever anymore. I still had a bad cough and I was exhausted. That continued for a couple of weeks. The cough has mostly stopped by now. On 12/21/2021 I was exposed to Covid and tested negative. A couple of days after that I started feeling worse again. On 12/24 my cough got worse. On 12/25 I was feeling very tired, I had a headache and cough. On 12/27/2021 I went to the pharmacy and they tested me for Covid again and it was negative. They could not find anything wrong with me so they thought it was from the vaccine. They gave me an antibiotic and cough medicine. The cough has gotten better since 2 days ago. I am not as tired as I was before. Yesterday was the first day that I have not had to take Tylenol or Dayquil to feel better.


VAERS ID: 2575898 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Male  
Location: Alabama  
Vaccinated: 2023-01-31
Onset: 2023-01-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7136 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 41425P / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient was vaccinated with the COVID 19 PFIZER Monovalent vaccine instead of the COVID 19 PFIZER Bivalent vaccine.


VAERS ID: 1804287 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2021-10-20
Onset: 2021-10-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7384JA / N/A RA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. T039466 / 1 LA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U6767AA / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Inappropriate schedule of product administration, Myoclonus, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Medication errors (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: NONE
Allergies: NONE
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received 4 vaccines in this order: Pfizer BioNtech and fluzone quad in the right deltoid, then Adacel followed by Gardarsil-9 in the left deltoid. Within one minute of final vaccine administration patient had a syncopal episode while seated that involved myoclonus (aproximately 10 seconds). Patient regained consciousness and remained seated. Patient was dizzy for approximately 5 minutes. An ice pack was applied to the back of the neck while they drank a refrigerated fruit smoothie beverage. Patient recovered fully by the end of the15 minute post vaccine observation period. No other side effects or injuries were noted.


VAERS ID: 1964666 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2021-12-18
Onset: 2021-12-19
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 069H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7377JA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood donor, Chest pain, Headache, Injection site erythema, Injection site swelling
SMQs:, Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: percocet, flexeril
Current Illness: na
Preexisting Conditions: Chronic cervicalgia of occipito-axial region.
Allergies: sulfa, sulfasalazine, cephalosporins
Diagnostic Lab Data: na
CDC Split Type:

Write-up: Patient came to pharmacy stating she had an injection site reaction to both the flu shot and moderna booster. Patient received both shots on 12/18/21 in separate arms and started having swelling and erythema at both sites after 24 hours. She gave blood on 12/19/21 before injection site reactions started. She started having chest pains and a headache on 12/19/21 but was not sure if it was from the vaccines or from giving blood. She went to the ER to make sure everything was alright and they said she was experiencing side effects from the covid vaccine. I recommended she take benadryl and ibuprofen/tylenol and to apply a cold compress to the injection site. I recommended she follow up with her md about the chest pains and also if the injection site reaction continued to expand.


VAERS ID: 2716856 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2023-10-13
Onset: 2023-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS - / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site erythema, Injection site pain, Injection site rash, Injection site swelling, Pain, Pain in extremity, Sleep disorder
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Irbesartan 150 mg nightly, vegetarian Vit D3, Vit K2, B12, Biotin, Magnesium, Melanton 2.5, AllerTec
Current Illness: none
Preexisting Conditions: Alpha Gal Syndrome from Lone Star Tick bite in May of 2021
Allergies: Alpha Gal Syndrome allergy to all mammalian products including all red meat, gelatin, caragenaan, porcine gel caps
Diagnostic Lab Data: None - reported to pharmacist and was told to be sure to note my reaction whenever receiving vaccines in the future.
CDC Split Type:

Write-up: Awoke in the middle of the night with my left upper arm swollen more than double in size at site of RSV vaccine injection, reddened with a rash, sore at the injection site and painful to move left arm. Researched facility website for adverse reaction to RSV and followed instructions by taking antihistamine (extra dose of Allertec) & generic Pepcid and applying cold compress. Continued to do so for 3 days.


VAERS ID: 2042136 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2021-12-20
Onset: 2022-01-16
   Days after vaccination: 27
Submitted: 0000-00-00
Entered: 2022-01-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Rash and lymph node swelling with 2nd Moderna covid vaccine
Other Medications: Oral birth control
Current Illness: None
Preexisting Conditions: None
Allergies: Duck eggs
Diagnostic Lab Data: Positive binax self test
CDC Split Type:

Write-up: Covid positive


VAERS ID: 1894598 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: Alabama  
Vaccinated: 2021-11-15
Onset: 2021-11-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7384JA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthma, Oropharyngeal pain
SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patients mom stated son had asthma attack and sore throat after pfizer pediatric vaccine and flu shot


VAERS ID: 2691248 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2023-09-26
Onset: 2023-09-28
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH7595 / 6 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8104DA / 1 LA / IM
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS M4E4A / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Pain in extremity, Pyrexia, Tinnitus
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hearing impairment (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Mirtazapine Multivitamin Calcium +D3 D3 Magnesium Beef organ supplement
Current Illness:
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Sore arm, redness, low grade fever which resolved after 4-5 days Significant Tinnitus noticed 2 days after vaccinations and is ongoing. No treatment yet


VAERS ID: 2687132 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2023-09-27
Onset: 2023-09-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-09-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 202F23A / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8043BA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Condition aggravated, Seizure
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unkown
Current Illness: N/A
Preexisting Conditions: Hypothyroidism, hypertension, heart failure, seizures
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient reported having a seizure about 15 minutes after receiving vaccines.


VAERS ID: 2744565 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2024-02-05
Onset: 2024-02-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 208F23-3A / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8129KA / UNK RA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. 1965044 / 1 LA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR V1B901M / 3 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR U7903AD / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Head injury, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Patient denied taking any medications.
Current Illness: Mother:
Preexisting Conditions: Patient denied long standing health conditions
Allergies: Patient denied Allergies.
Diagnostic Lab Data: No records from hospital at this time.
CDC Split Type:

Write-up: At approximately 2:43pm patient received the following vaccines while on exam table: Polio, HPV and Meningococcal in left deltoid and Moderna (Spikevax) and Flu (Fluzone Quad) vaccine in right deltoid. Patient moved from exam table to chair and was talking to her mother, when she fainted at approximately 2:46pm. She fell forward and hit her head. I jumped in front of patient to prevent her falling to the floor. Yelled for immediate assistance. Nurse supervisor and other staff nurses came to assist. After approximately one minute patient regained consciousness. Assisted patient to exam table and BP checked: BP 120/68 @ 2:50pm. Pt began feeling better. BP at 3:10pm 104/69. No bleeding, bruises or abrasions noted to patient?s head. Encouraged patient?s mother to take patient to the hospital for eval due to patient hitting head. Nursing supervisor offered to call an ambulance for patient, but the mother desired to drive patient in private vehicle. Referral given for ER. Patient taken to mother?s private vehicle via wheelchair at 3:17pm. Pt remained alert and oriented for the remainder of visit after syncopal episode. Interpreter (Privacy) for immunization visit lab tech, assisted after syncopal episode.


VAERS ID: 2701920 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Male  
Location: Alabama  
Vaccinated: 2023-10-24
Onset: 2023-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 27BN7 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient was inadvertently administered the 10mcg Pfizer Covid 19 vaccine instead of the 30mcg COMIRNATY that is recommended for his age. No adverse events post vaccination reported. Parent is aware of error and Pfizer Medical consulted for advice. Advised that administration of age appropriate vaccine (30mcg COMIRNATY) is recommended per CDC and Pfizer guidelines.


VAERS ID: 2742006 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Alabama  
Vaccinated: 2023-09-28
Onset: 2023-11-16
   Days after vaccination: 49
Submitted: 0000-00-00
Entered: 2024-01-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Anal incontinence, Blood test, Breath sounds abnormal, Cardiac flutter, Catheterisation cardiac, Chest pain, Computerised tomogram, Computerised tomogram thorax abnormal, Dyspnoea, Exercise tolerance decreased, Fall, Heart rate abnormal, Hyperhidrosis, Injection site pruritus, Intensive care, Mobility decreased, Musculoskeletal disorder, Nausea, Oxygen saturation abnormal, Pulmonary thrombosis, Thrombosis, Ultrasound Doppler abnormal, Wheezing
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Parkinson-like events (broad), Thrombophlebitis (broad), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Tachyarrhythmia terms, nonspecific (narrow), Hypersensitivity (broad), Noninfectious diarrhoea (broad), Respiratory failure (narrow), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Infective pneumonia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None.
Current Illness: None.
Preexisting Conditions: None.
Allergies: None.
Diagnostic Lab Data: US, CAT scans, blood work.
CDC Split Type:

Write-up: She got her vaccine, initially the site itched for 2 weeks. The morning of 11/16/23 she got up to take her dog out, and she could not breathe, her chest hurt, had sweat dripping off of her. She fell onto the couch because she could not move, could not move her arms, could not move her legs. Her husband came in and asked what was wrong and she told him that she was dying. He called 9-1-1, tried to vomit, could not vomit and had stool all over her from trying to vomit. She possibly passed out, but then remembers the ambulance picking her up and putting her on the stretcher. She was taken to Hospital. The weekend before she took a 3 hour trip which is nothing for her. She normally walks 2 miles a day. They stopped several times in that 3 hour trip. They felt that the trip was probably not the reason for her blood clots. She noticed on the trip the weekend before she had some shortness of breath but did not think much of it. She spent 2 nights in another state on that trip, and went back home on Saturday. She was having some issues when she got home, her heart rate was not normal, fluttering a lot, and she could hear herself wheezing like 2 days before. Her daughter had hip surgery and had to take her to the doctor for her follow up. She got in the car and could hear a noise trying to figure out what it was, took a breath and realized that it was her. The ambulance then took her to the hospital, they did the usual lab work and they did a CT of her chest, and she had multiple clots in her chest. Then they did an US on her legs and she had clots in both legs. She went to the cath lab and they did a heart cath and they TPA''d her chest. She woke up Friday evening in ICU. They gave her medications that lasted 6 hours to break up the clots and then it was discontinued after that. She was in the hospital for 3 days. She was sent her home on Pradaxa as a blood thinner. She is still on Pradaxa until at least May or possibly forever. She still can feel the blood clots in her legs. She is feeling better, and they said that it would take about 3 months before she would get her oxygen back to hopefully normal. She does walk her 2 miles a day but it takes her longer.


VAERS ID: 2741486 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Alabama  
Vaccinated: 2024-01-27
Onset: 2024-01-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HM7006 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 99R27 / 1 RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS FH79Y / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Hyperhidrosis, Pallor, Tinnitus, Tunnel vision
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Optic nerve disorders (broad), Retinal disorders (narrow), Hearing impairment (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: no known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received all three of his shots and was waiting for his family to receive their vaccines. After the other 3 family members were finished about 10 minutes later, he looked pale and looked out of it. Patient stated he felt light headed, had tunnel vision, and his ears were ringing. Not more than a couple minutes later he started sweating as well. Emergency was called when he started sweating and they advised us through the event. Blood pressure was attempted before the paramedics arrived, but it was unable to be taken. The paramedics took over and was able to help the patient and he was fine after waiting it out.


VAERS ID: 1094197 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Male  
Location: Alabama  
Vaccinated: 2021-02-26
Onset: 2021-03-11
   Days after vaccination: 13
Submitted: 0000-00-00
Entered: 2021-03-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 014M20A / 2 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 010M20A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ500AB / 1 LA / IM
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. T033663 / 1 LA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS ZJ432 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Death, Feeling abnormal
SMQs:, Dementia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-03-11
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ELIQUIS, LASIX, PROTONIX,ALTACE, TRADJENTA, LUMIGAN, AMIODARONE, METOPROLOL
Current Illness: UNKNOWN
Preexisting Conditions: HBP, DIABETES, MAY BE OTHERS
Allergies: UNKNOWN
Diagnostic Lab Data: UNKNOWN - CONTACT PHYSICIAN OR HOSPITAL I AM NOT AWARE IF HE WAS TAKEN TO HOSPITAL OR DR''S OFFICE YESTERDAY OR NOT.
CDC Split Type:

Write-up: DEATH - PT''S WIFE CALLED 3-11 TO TELL US PATIENT WAS FEELING BAD, AND TO ASK WHAT TO DO. WE SENT A PULSEOXIMETER, AND ADVISED TO CONTACT DR. - ON MORNING OF 3-12, PT''S WIFE CALLED TO TELL US HE HAD PASSED AWAY DURING THE NIGHT.


VAERS ID: 1981031 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-12-20
Onset: 2021-12-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft 100 mg daily, levothyroxine 75 mcg daily, vitamin d
Current Illness: Common cold
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pain, redness, swelling, itching, calor at injection site of Moderna COVID-19 vaccine booster dose. (First two doses were Pfizer) Affected area is about 2 to 2.5 inches around the injection site. Pain was worst at one day after vaccination and all symptoms are still ongoing at day 5 post-vaccination


VAERS ID: 2753213 (history)  
Form: Version 2.0  
Age: 2.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2024-03-08
Onset: 2024-03-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
DTPPVHBHPB: DTAP+IPV+HIB+HEPB (VAXELIS) / MSP VACCINE COMPANY - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
HEPA: HEP A (VAQTA) / MERCK & CO. INC. - / UNK - / -
HIBV: HIB (PEDVAXHIB) / MERCK & CO. INC. - / UNK - / -
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / UNK - / -
PNC15: PNEUMO (VAXNEUVANCE) / MERCK & CO. INC. - / UNK - / -
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Inadvertently administered additional Hib vaccines in addition to combo Vaxelis.


VAERS ID: 2723189 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2023-12-07
Onset: 2023-12-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5553B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8091MA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Unknown
Preexisting Conditions: Unknown
Allergies: Unknown
Diagnostic Lab Data:
CDC Split Type:

Write-up: The Pediatric Moderna COVID-19 Vaccine 2023-2024 Formula was administered pass the beyond-use-date (30 days from thaw date per manufacturer). Vaccine was received and thawed on 10/19/23 and the BUD was 11/20/2023. Vaccine was administered on 12/07/2023. No adverse events besides determining whether vaccine was/is efficacious.


VAERS ID: 2724089 (history)  
Form: Version 2.0  
Age: 1.42  
Sex: Male  
Location: Arkansas  
Vaccinated: 2023-12-05
Onset: 2023-12-12
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2023-12-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HJ7224 / N/A RL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4E25J / N/A LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 17 month old child received dose of COVID vaccine for age 12+. This was discovered via chart audit. Patient''s parent notified. Upon speaking with parent, no signs and symptoms have been noticed. Child scheduled for follow up exam on 12/14/23 at 1:20 PM


VAERS ID: 2483044 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2022-10-17
Onset: 2022-10-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7138 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 346342 / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Aspirin, Carafate, Cholestyramine Light, Clotrimazole cream, Crestor, Eliquis, famotidine, Flonase, Lasix, and glipizide
Current Illness: Shortness of breath, hypertension, 1st Degree AV block, prolonged QT wave, elevated BNP, hematuria
Preexisting Conditions: Diabetes type 2, hypertension, restless leg syndrome, urinary incontinence, chronic pain, GERD, hyperlipidemia, A Fib, gait instability, hemiparesis
Allergies: Sulfa, Codeine, and NSAID''s
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient needed the bivalent dose of Pfizer, but received regular Pfizer, no adverse event or occurrences needed/noted.


VAERS ID: 1865448 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-11-09
Onset: 2021-11-11
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 058F21A / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Parotitis
SMQs:, Oropharyngeal infections (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: parotitis, acute, age 53, vaccination date 04/04/2021, Moderna Covid-19
Other Medications: Gabapentin, Levothyroxine, Trazodone, Omeprazole, vitamin D, Zyrtec, Intrathecal morphine
Current Illness: None
Preexisting Conditions: Hypothyroidism, Neuropathy, GERD, osteoarthritis, osteoporosis
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: parotitis, acute. Also occurred after 2nd injection in April 2021, but I didn?t report it. After both injections seems like a pattern. Both times lasting several days.


VAERS ID: 1829547 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-10-29
Onset: 2021-10-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 071F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ715AB / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Feeling hot, Loss of consciousness, Presyncope
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: patient had been given a moderma booster 0.25 ml IM into right arm. I turned and was getting left arm ready and was giving Fluzone Hd into LA when patient suddenly said that she was hot and something was wrong.. Patient started fanning herself. I got a cold compress to apply to forehead. Her husband came in to see what was going on. She started to go in and out of consciousness. Paramedics were called during this time. An eppi pen administered. Pearamedics arrived within 10 minutes. The accessed her . She continued to lose consciousness while being moniter and finally came back. Her husband transported her to hiopital ER for follow up. When I talked to the husband later in day she was home and recovered. Drs told husband they thought she a vegal response.


VAERS ID: 2481158 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2022-10-13
Onset: 2022-10-14
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-10-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH 9693 / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7752JA / 1 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Condition aggravated, Fatigue, Injection site induration, Injection site nodule, Injection site pain, Injection site swelling, Injection site warmth, Pain, Pain in extremity, Pruritus
SMQs:, Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Prolonged periods after 1 & 2nd covid shots (Phizer) Jan & Feb 2021; SIRVA issues after last year''s flu shot (Fluzone) on August
Other Medications: Humalog U-200 insulin Valsartan 320 mg Eye drops for glaucoma
Current Illness: Shoulder impingement syndrome Osteoarthritis
Preexisting Conditions: Diabetes High-blood pressure Glaucoma
Allergies: Cipro antibiotic
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Woke up next morning, October 14, 2022, with pain, swelling, hard knot, and hot (heat-wise) each thigh. Felt worse in right thigh. Hurt to walk or lift myself from seated position. Took Tylenol. Pain started subsiding today, October 17, 2022. Chronic pain in hands and right shoulder worsened. On October 17, extreme itching in legs and feet. Put antihistamine cream on the. Tiredness since vaccines


VAERS ID: 2692460 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2023-10-07
Onset: 2023-10-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8041BA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Circumstance or information capable of leading to medication error, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: I made an online appointment at this pharmacy for my son to receive the COVID19 vaccine. Upon arrival we told the clerk that we had a vaccine appointment. The clerk informed us that he could not find the appointment and so he was going to create one manually. He handed me the vaccine consent form and told me that I just needed to answer the exclusion criteria questions and then sign and date it on behalf of my son. He placed the vaccine prescription label on the form as I was walking away to the waiting area. The pharmacist did not confirm which vaccine was being given to my son, just cleaned his arm and injected. When asked for the lot info to put on the vaccine card, the pharmacist replied with, "Oh we don''t usually do that for flu vaccines. Was this supposed to be Covid? Upfront told me it was flu!" They then proceeded to draw up the covid vaccine and give that to my son. They only provided info on the covid vaccine and not on the flu vaccine. I had to return to the pharmacy to ask for the influenza vaccine information and also got the consent form that I signed which shows that I did not check any box for which vaccine was indicated. The clerk just assumed that it was influenza, and the pharmacist did not confirm before administration.


VAERS ID: 1902187 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-11-18
Onset: 2021-11-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 330268D / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 712CA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Syncope, Unresponsive to stimuli
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: hypothyroidism
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient became light-headed and unresponsive; fainted. The nurse administering the vaccines lowered her from a chair onto the floor and made sure she was still breathing. I called 911 to get an ambulance sent to our location.


VAERS ID: 2487459 (history)  
Form: Version 2.0  
Age: 86.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2022-10-24
Onset: 2022-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 052B22A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ925AB / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: nitroglycerin, atorvastatin, metformin, meloxicam, clopidogrel
Current Illness: hyperlipidemia, coronary artery disease, diabetes, osteoarthritis, GERD
Preexisting Conditions: hyperlipidemia, coronary artery disease, diabetes, osteoarthritis, GERD
Allergies: NKDA
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: None reported. Patient will receive bivalent vaccine in 2 months.


VAERS ID: 2710305 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2023-10-30
Onset: 2023-10-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5KT7B / UNK LA / IM

Administered by: Public       Purchased by: ?
Symptoms: No adverse event, Product administered to patient of inappropriate age, Product administration error, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AR2324

Write-up: On October 30, 2023, a 64 y/o female came in for covid vaccine. RN pulled vial of 5-11 y/o Pfizer vaccine instead of the intended Spikevax 12+ vaccine. 0.5 mL of the 5-11 y/o Pfizer was administered to patient. Error was not caught until vaccine was already administered. Patient was notified of the error and was observed for 30 minutes in clinic. The patient voiced that she was feeling fine, and no adverse reactions were noted upon patient leaving. RN notified RN, CDNS and she notified PCM, Regional Director, and Immunization Program Nurse. Per Dr, Patient will need to be revaccinated 3 weeks from vaccination date (10/30/23) with age appropriate COVID vaccine of patient''s choice.


VAERS ID: 2541961 (history)  
Form: Version 2.0  
Age: 4.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2022-12-15
Onset: 2022-12-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-12-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 3 UN / SYR
DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 UN / SYR
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Breath odour, Fatigue, Nausea, Pyrexia, SARS-CoV-2 test negative, Streptococcal infection, Streptococcus test positive
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 2nd dose COVID-19 behavior changed
Other Medications: None
Current Illness: Diarrhea for 2-3 days a week earlier
Preexisting Conditions: Apraxia
Allergies: None
Diagnostic Lab Data: 23DEC2022 COVID-19 test negative
CDC Split Type: vsafe

Write-up: My son received his 3rd dose of Pfizer on 12/15/2022. His Strep symptoms started around 05:00PM on 12/16/2022. He had fever and normally he doesn''t sleep early but that day he went to bed early. This wasn''t normal for him. On 12/17/2022 he had a fever of 104, nausea, tiredness, his breath was smelling. I work at a hospital so I knew it was Strep. I started giving him TYLENOL and MOTRIN to reduce his fever. I realized that the TYLENOL wasn''t helping so I only gave him MOTRIN. On 12/22/2022 I took him to the clinic around 12:30PM. They tested him for COVID-19 which was negative but he was positive for Strep. They prescribed him amoxicillin for 10 days. Now he is more active and slowly recovering from Strep.


VAERS ID: 1854910 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2021-10-29
Onset: 2021-10-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5X7J5 / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Condition aggravated, Diarrhoea, Extra dose administered, Nausea, Vomiting
SMQs:, Acute pancreatitis (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 40, Nausea, 3/23/2021 Moderna COVID 2nd dose
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nausea, vomiting, diarrhea


VAERS ID: 2689909 (history)  
Form: Version 2.0  
Age: 85.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2023-09-27
Onset: 2023-09-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 204F23-2A / 5 LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8150AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Dizziness, Loss of consciousness, Pain in extremity, Tenderness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Vasovagal syncope to some flu vaccine, unknown date.
Other Medications: Xarelto
Current Illness: None
Preexisting Conditions: Something Cardiac related from a snake bite out of country years ago. Hx of vasovagal syncope following a vaccination at a young age.
Allergies: Red Food Coloring (has hx of anaphylaxis to bee stings also)
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Feeling faint. Passed out at home x2. Pain and tenderness in left arm. Feeling weak x4days.


VAERS ID: 2364091 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-12-03
Onset: 2022-05-31
   Days after vaccination: 179
Submitted: 0000-00-00
Entered: 2022-07-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 0314212 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 58160088752 / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Lung disorder, Malaise, Respiratory disorder, SARS-CoV-2 test
SMQs:, Acute central respiratory depression (broad), Respiratory failure (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metoprolol, vitamin D, Zyrtec, dicyclomine
Current Illness:
Preexisting Conditions: High blood pressure, IBS
Allergies: Iodine
Diagnostic Lab Data: Home and clinic Covid test
CDC Split Type:

Write-up: Contracted Covid, severe, 3 weeks sick with ongoing breathing lung issues


VAERS ID: 2483084 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2022-10-18
Onset: 2022-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7138 / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 346342 / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Tylenol, amlodipine, atorvastatin, calcitriol, cetirizine, donepezil, Novolog flex pen, omeprazole, and Plavix
Current Illness: None on this day
Preexisting Conditions: Syncope, CAD, Diabetes type 2, ESRD, Pericardial effusion, elevated troponin, liver lesion, brain mass, GERD, ulcerative colitis, hypertension, diabetic nephropathy, hyperlipidemia, hypomagnesemia, aneurysm of carotid artery, CVA, Eosinophilia, stenosis of bilateral carotid arteries, hypocalcemia, vitamin D deficiency, anemia, leg edema, peritoneal dialysis, stasis dermatitis of both legs, hypothyroidism, and dementia
Allergies: Wasp, metformin, and lisinopril
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient needed the bivalent dose of Pfizer, but received regular Pfizer, no adverse event or occurrences needed/noted.


VAERS ID: 1999329 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-09-28
Onset: 2021-11-13
   Days after vaccination: 46
Submitted: 0000-00-00
Entered: 2022-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cough, Oropharyngeal pain, Pyrexia, Respiratory disorder, Upper-airway cough syndrome
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Estrace Vaginal Cream
Current Illness: No
Preexisting Conditions: No
Allergies: Penicillin
Diagnostic Lab Data: No
CDC Split Type: vsafe

Write-up: 11/13/2021, post nasal drip, sore throat. My symptoms were getting worse, I had low grade fever, cough, I was taking over the counter medications: Claritin, Mucinex, Afrin & Tylenol. 11/19/2021, I went to my doctor, because I was not getting better. He said it was an Upper Respiratory. He prescribed steroid shot, and a prescription for Mucinex D and Antibiotics. I filled them 4 days later. And I slowly got better. I was completely over that on 11/26/2021. I have not had anything like this for over 20 years. I just wasn''t able to get over it. It finally felt better on 11/26/20201.


VAERS ID: 1768105 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-10-06
Onset: 2021-10-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5AJ3B / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: albuterol (PROVENTIL HFA) 90 mcg/actuation inhaler benzoyl peroxide 10 % cream busPIRone (BUSPAR) 10 MG tablet clotrimazole (LOTRIMIN) 1 % cream fluconazole (DIFLUCAN) 150 MG tablet fluticasone propionate (FLONASE) 50 mcg/actuation nasal sp
Current Illness: N/A
Preexisting Conditions: Benign essential hypertension Type 2 diabetes mellitus without complication, without long-term current use of insulin (HCC) Asthma Abnormal uterine bleeding Anxiety Conductive hearing loss, bilateral Obesity (BMI 35.0-39.9 without comorbidity) Sensorineural hearing loss (SNHL) of both ears
Allergies: Aspirin Miconazole Nitrate
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt was in clinic for a flu shot, nurse got flu shot out and laid shot on computer. after verifying name and DOB picked up a covid shot off of table where covid shots held and gave covid vaccine. nurse explained to pt that wrong shot was given. Flu shot given in opposite arm. Nurse asked pt if it has been six months since last covid shot , and she said yes. nurse asked for shot record. Pt stated she got her covid shots at a pharmacy and did not have card. nurse asked pt if she had Pfizer or moderna. she stated moderna. nurse filled out the vaccine card with lot number and told pt to keep both cards and let pharmacy know she has had a Pfizer booster. Pt verbalized that she understands.


VAERS ID: 2437483 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2022-09-09
Onset: 2022-09-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7137 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7716NA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: na
Current Illness: no
Preexisting Conditions: na
Allergies: no
Diagnostic Lab Data: na
CDC Split Type:

Write-up: pt given monovalent covid vaccine instead of bivalent booster.


VAERS ID: 2559640 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2022-10-06
Onset: 2022-12-07
   Days after vaccination: 62
Submitted: 0000-00-00
Entered: 2023-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ5342 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Blood pressure increased, Cardiomegaly, Chest X-ray abnormal, Cough, Electrocardiogram abnormal, Pneumonia, Wheezing
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Hypertension (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (narrow), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: OTC Tylenol;OTC Aleve;OTC Benadryl
Current Illness: None
Preexisting Conditions: Hypertension
Allergies: None
Diagnostic Lab Data: Chest x_ray ; ECG
CDC Split Type: vsafe

Write-up: During my wellness check up I had an ECG and Chest x-ray and it was discovered that I had Pneumonia and an enlarged heart. I had wheezing and coughing due to Pneumonia. I also have had elevated BP of 160/90. I have an upcoming Cardiologist appointment in March to address my enlarged heart.


VAERS ID: 2507132 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2022-10-29
Onset: 2022-11-09
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2022-11-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cardiac monitoring, Chills, Cough, Dyspnoea, Echocardiogram, Electrocardiogram abnormal, Influenza, Influenza A virus test positive, Influenza B virus test, Pain, Pericarditis, Pyrexia, SARS-CoV-2 test negative, Ultrasound scan
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Claritin; Multivitamin; Lisinopril
Current Illness: No
Preexisting Conditions: High Blood Pressure
Allergies: No
Diagnostic Lab Data: EKG; Sonogram; Ultrasound; Echocardiogram; Heart monitor
CDC Split Type: vsafe

Write-up: I went to the doctor on Thursday 11/10/2022 because I had fever, chills, shortness of breath, cough, body aches. I was tested for COVID-19, Influenza A and B. The test for COVID-19, Influenza B came back negative but the test for Influenza A came back positive. I was given a prescription for Tamiflu for and cough medication. By Saturday I could not breath and was gasping for air. I went to an Urgent Care thinking I was getting pneumonia. They ran an EKG that came back abnormal and sent me to the hospital and had me admitted, I have pericarditis.


VAERS ID: 2743857 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2023-12-22
Onset: 2024-01-13
   Days after vaccination: 22
Submitted: 0000-00-00
Entered: 2024-02-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4589 / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8137DA / N/A LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS G75S4 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Gait disturbance, Gait inability, Guillain-Barre syndrome, Hypoaesthesia
SMQs:, Peripheral neuropathy (narrow), Anticholinergic syndrome (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (narrow), Demyelination (narrow), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Lisinopril, Amlodipine, and Meloxicam
Current Illness: n/a
Preexisting Conditions: High Blood Pressue
Allergies: n/a
Diagnostic Lab Data: diagnosed with Guillain-Barre Syndrome
CDC Split Type:

Write-up: He began with numbness to his feet, then difficulty walking, and then cannot walk at all to this day. Symtoms started 1/13/2024.


VAERS ID: 1813986 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2021-10-23
Onset: 2021-10-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 017F21A / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7378LA / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Interchange of vaccine products, No adverse event
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: No adverse event occurred. The patient intended to get the Covid vaccine alone but a miscommunication led to a flu vaccine being administered.


VAERS ID: 2595504 (history)  
Form: Version 2.0  
Age: 18.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2023-03-08
Onset: 2023-03-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2587 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7TP53 / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Chills, Dizziness, Feeling cold, Hyperhidrosis, Loss of consciousness, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type: AR2304

Write-up: 3/8/2023 1635pm I called Patient and his girlfriend to the lab area to administer Covid vaccine and flu shots. After going over both the flu and covid forms and possible ASE I administered both the flu shot and Pfizer monovalent vaccine in his left deltoid at 1638. After administering his vaccines he stood up and allowed his girlfriend to sit in the chair and I then administered her flu shot. I explained that he needed to return to the lobby and wait 15 minutes to ascertain that he does not have a reaction. They both proceeded to the lobby to wait ambulatory with steady gait.


VAERS ID: 2327032 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Arkansas  
Vaccinated: 2021-12-16
Onset: 2022-06-03
   Days after vaccination: 169
Submitted: 0000-00-00
Entered: 2022-06-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH F48030 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / SYR

Administered by: Work       Purchased by: ?
Symptoms: COVID-19, Cough, Diarrhoea, Fatigue, Headache, Impaired work ability, Influenza A virus test negative, Influenza B virus test, Nasal congestion, Oropharyngeal pain, Pyrexia, Respiratory syncytial virus test negative, SARS-CoV-2 test positive, Sneezing
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin D
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: June 6 2022 - PCR COVID test - positive. June 6, 2022 - Flu A & B and then RSV - all negative.
CDC Split Type: vsafe

Write-up: Beginning Friday, June 3, I developed fatigue, mild headache, sore throat and nasal congestion. That worsened over Saturday and Sunday. Monday morning June 6, I called into work and had my lab tech swab me in the parking lot. The PCR test came back positive. I called the pharmacy who we work with and prescribed PAXLOVID. I prescribed that myself and took that for 5 days for the standard dose. During those 5 days, my symptoms included fatigue, cough, nasal congestion, sneezing, some diarrhea, fever of 101. By Thursday I started to feel better and by Friday I was almost normal again June 10. I then returned to work the following Monday, June 13, with wearing a mask. Now feeling fine.


VAERS ID: 2483091 (history)  
Form: Version 2.0  
Age: 86.0  
Sex: Male  
Location: Arkansas  
Vaccinated: 2022-10-18
Onset: 2022-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7138 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 346342 / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Albuterol HFA, Vitamin B12, Carbidopa-levodopa, esomeprazole magnesium, Flonase, levothyroxine sodium, lisinopril, primidone, propranolol, and zyrtec
Current Illness: rib pain
Preexisting Conditions: hypothyroidism, lung cancer, hypertension, essential tremor, GERD, history of lymphoma, bladder wall thickening, hearing loss, depression
Allergies: valium
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient needed the bivalent dose of Pfizer, but received regular Pfizer, no adverse event or occurrences needed/noted.


VAERS ID: 2472568 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Male  
Location: American Samoa  
Vaccinated: 2022-09-07
Onset: 2022-09-15
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2022-10-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9694 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH - / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arteriogram coronary abnormal, Chest pain, Coronary artery bypass, Laboratory test
SMQs:, Embolic and thrombotic events, arterial (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Other ischaemic heart disease (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 10 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: One a Day Vitamins; Meloxicam 15mg; Genvoya; Testosterone; Lis
Current Illness: None
Preexisting Conditions:
Allergies: Meperidine: Oranges: Lattex
Diagnostic Lab Data: I had literally 100''s of tests. It is impossible for me to put them all here.
CDC Split Type:

Write-up: I started having mid-sternal chest pain at 2 PM on the 15th. I went to the hospital at 2 am on the 16th where I was diagnosed with an MI in progress. I had angiography on the 17th, and a four vessel Coronary Artery Bypass Graft on the 21st.


VAERS ID: 2487024 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-22
Onset: 2022-10-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 061B22A / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9249L / 1 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: None stated.


VAERS ID: 1750363 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-09-24
Onset: 2021-09-27
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Chills, Extra dose administered, Injection site pain, Pain, Pyrexia, Wrong product administered
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: This is not a report of an adverse event, but instead an administration error. My patient is a medical doctor, colleague and employee. The patient arrived on the first morning boosters were recommended and the first day offering flu shots to employees. We were swamped and overwhelmed. She stated she received her influenza vaccination at another clinic in the right deltoid earlier in the week. I screened her, and had no concerns. I administered and documented a COVID-19 vaccine in the left deltoid IM on 9/24/21. The pt tolerated the injection well and waited the 15 minute post-vaccination time period without problem. HOWEVER, she returned after the wait period to ask if the covid syringe was glass. This was an odd question. She recalled seeing me grab a glass syringe from a white tray in the fridge and screw on a needle and adjust the bubble. This is NOT consistent with the covid vaccine, which is pre -drawn in plastic syringes with the needles already attached. The covid vaccines are in a basket in the fridge, but NOT in a white tray. The white trays hold flu vaccines. She wondered if she received a flu shot and not the COVID vaccine. All documentation was done on paper and not interactively on the computer. I could not recall that exact vaccination in my memory, as I had given shots for hours. We discussed at length and decided there was a potential administration error, with the pt receiving and additional dose of flu vaccine instead of covid vaccine. With shared clinical decision making and a discussion of the risks (reactogenicity, no boosted coverage for covid as a HCP) and benefits (ensured coverage as a HCP), we decided to administer covid vaccine IM in the right deltoid. We did discuss that the ACIP meeting did not initially vote to offer boosters for HCPS and likely the coverage remains high for severe covid disease. We also discussed increased potential for reactogencity and Nonetheless, she wanted to proceed with an additional vaccination and I agreed. I f/u on 9/27 and she had anticipated mild to moderate side effects, including aches/chills, fever of 101, and sore arm (right delt) over the weekend of 9/25-9/26. Her side effects were similar to her 2nd dose of Pfizer vaccine.


VAERS ID: 1909514 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-30
Onset: 2021-11-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939909 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100371943 / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Pt is 15 years old. Pt received the Moderna vaccine in error on 29 OCT 21. Guardian brought pt to clinic for regular visit with provider. Pt due the second COVID vaccine. RN talked to physician who recommended that guardian be given the choice of completing series with Moderna or waiting until 3 DEC 21 for Pfizer. Guardian chose to complete the series with Moderna. RN administered Moderna.


VAERS ID: 2483301 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-18
Onset: 2022-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7682MA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: No known illnesses
Preexisting Conditions: No known long-standing health conditions
Allergies: No known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: No adverse events reported by patient. Report filed because Pfizer Monovalent was given in error instead of Pfizer Bivalent.


VAERS ID: 2493301 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-01
Onset: 2022-10-25
   Days after vaccination: 24
Submitted: 0000-00-00
Entered: 2022-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7741KA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: On Oct. 12, stores received an internal Urgent Removal Notice regarding Pfizer COVID-19 Vaccine- Pediatric 5-11 Years Tris-sucrose, Lot #FL2757 with manufacturer?s expiration date of Sept. 30.


VAERS ID: 1832113 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-10-11
Onset: 2021-10-13
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Blood test, Joint swelling, Peripheral swelling, Rash, Ultrasound Doppler normal
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: lisinopril,
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: blood test 10/20/2021 ultrasound no evidence of DVT 10/27/2021
CDC Split Type:

Write-up: rotating rash legs/buttocks, rotating feet/ankle/hand/calf swelling


VAERS ID: 2721210 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2023-12-05
Onset: 2023-12-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031897 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8070BA / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: No known allergies
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient (7 years of age) was injected with a dose of COVID 19 Moderna Monovalent Vaccine, for 12 years of age and older (0.5 ml=50 mcg). Patient was alert and oriented to person, place and time. Patient was monitored for 30 minutes, at which time there was no bumps, or redness noted to the left arm. Patient appeared to be in no discomfort. Patient was accompanied by his parent.


VAERS ID: 1913309 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-11-05
Onset: 2021-11-26
   Days after vaccination: 21
Submitted: 0000-00-00
Entered: 2021-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 33030BD / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100369749 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None known.
Current Illness: None known.
Preexisting Conditions: None known.
Allergies: Gets rash with penicillin.
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: 17 year old male was given Pfizer vaccine booster shot. Waited 15 minutes in vehicle with mother. No untoward reactions noted. Left to go home after the required wait.


VAERS ID: 1832332 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-26
Onset: 2021-10-27
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS HZ2JR / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Mobility decreased, Neck pain, Pain, Pain in extremity
SMQs:, Parkinson-like events (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient started pain on right arm within 24 hours from receiving the shot. She did not notice any swelling, redness or warmth around the injection site on her right arm. Patient was not able to raise her right arm, pain on the right upper arm was radiating to the neck and down the arm and into the torso. Patient tried taking Tylenol Extra strength with not much relieve. Patient came in on 10/31/21 to report to us. Patient will continue with Tylenol or Motrin and schedule an appointment with her PCP ASAP. We will follow-up with patient in the next few days.


VAERS ID: 2721064 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-11-30
Onset: 2023-12-01
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031632 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2F54G / 5 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Mass, Pain, Rash, Sensitive skin, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: NO KNOWN ALLERGIES
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was seen today for the following reason she received COVID and Influenza vaccine on 11/30/23 the next day she woke up with the following symptoms VERY SENSITIVE SKIN, PAIN, SWOLLEN, BUMP 4Centimeter AND RASH 7 Centimeter in her Left Arm.


VAERS ID: 2264964 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-05-05
Onset: 2022-05-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-05-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8094 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS L3HK9 / N/A RA / IM

Administered by: Public       Purchased by: ?
Symptoms: No adverse event, Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nurse administered undiluted dose of Pfizer for ages 5-11, dose #1 to patient. Guardian informed of error post vaccination via phone call. Guardian states all patients were feeling "fine" at time of phone call. Guardian advised to monitor injection sites for adverse reaction, and call clinic back if any adverse effects occur. Nurse addressed all questions and concerns. Dr. and supervisors aware.


VAERS ID: 2756855 (history)  
Form: Version 2.0  
Age: 1.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2024-03-25
Onset: 2024-03-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-03-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 2 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS BB222 / 3 LL / -
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS G79C4 / 1 LL / IM
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. X021754 / 1 RL / SC

Administered by: Private       Purchased by: ?
Symptoms: Product preparation error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Non
Current Illness: NONE
Preexisting Conditions: NONE
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given undiluted Pfizer 6m-4year vaccine.


VAERS ID: 1291367 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-05-05
Onset: 2021-05-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-05-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004C21A / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ552AB / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Inappropriate schedule of product administration
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nothing yet, unable to reach patient 2 hours after vaccination.


VAERS ID: 2209536 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-09-24
Onset: 2021-12-18
   Days after vaccination: 85
Submitted: 0000-00-00
Entered: 2022-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301308A / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / N/A LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Balance disorder, Biopsy lymph gland, Biopsy skin, Blood test, Computerised tomogram, Electroencephalogram, Fatigue, Granuloma annulare, Headache, Lymphoma, Malaise, Pain in extremity, Sensory disturbance, Skin lesion, Visual impairment, Weight decreased
SMQs:, Peripheral neuropathy (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Malignant lymphomas (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Trazadone 50mg; Estradiol 1mg; Levocetirizine; Fish Oil; Allergy Injections every two weeks Calcium Magnesium Citrate Supplement; Multivitamin; Probiotics; Biotin; Potassium
Current Illness: None
Preexisting Conditions:
Allergies: Demerol; Codeine; Surgical Tapes
Diagnostic Lab Data: Biopsy of hands 01/21/2022. Biopsy of lung lymph nodes 03/24/2022. CT scans (about 10) 02/2022 & 03/2022. Blood work 01/17/2022, 03/15/2022, 03/24/2022. EEG, upcoming on 04/07/2022.
CDC Split Type: vsafe

Write-up: I started getting sick in December 2021. I lost like 30 pounds in 10-12 week. The more wait I lost the more tired I felt. I also had these weird and painful lesions on the palms of my hands that have now been diagnosed as granuloma annulare. I am treating them with a steroid cream. I also started getting these weird lights in my eyes and saw a neurologist. I was diagnosed with ocular headaches without pain. My balance was affected as well. All of these symptoms started at the same time so I thought they were all connected but everything seems to separate. I ended up in the hospital on 03/15/2022 and I have a provisional diagnosis of lymphoma. I am waiting for results from the doctor. It is not confirmed yet. I have blood work done frequently as well.


VAERS ID: 2211424 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-10-21
Onset: 2022-01-03
   Days after vaccination: 74
Submitted: 0000-00-00
Entered: 2022-04-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Ear pain, Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prescriptions: Rosuvastatin, Steglatro, Omeprazole, Tamsulosin, Solifenacin, Sildenafil, Albuterol, Fluticasone Supplements: Multi-Vitamins, Multi-Minerals, Garlique, Neuriva, Qunol Ultra ,
Current Illness: Diabetes, High Blood Pressure, Asthma
Preexisting Conditions: Same as Item 11
Allergies: medication: Percocet
Diagnostic Lab Data: 4/29/2022
CDC Split Type:

Write-up: Constant ringing in ear, sporadic pain,


VAERS ID: 1929506 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-12-07
Onset: 2021-12-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3594 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / N/A RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U7190AA / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none listed
Current Illness: none
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Minor patient brought in by mother for second dose of Pfizer Covid Vaccine. Mother said she couldn''t find his card. Only ONE dose was recorded previously in our EHR, on 8/18/21. Vaccine was administered. Mother found patient''s card after dose administered, showing a previous "first" dose on 7/21/21. Both doses, July & Aug were given at Rec Center. Patient monitored for 15-20 min. with no immediate adverse reactions.


VAERS ID: 2218983 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-04-05
Onset: 2022-04-06
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8095 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS DB93X / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Acute pancreatitis
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient did not show any adverse events from the incorrect Covid-19 vaccine as of 0800 on 4/6/22


VAERS ID: 2218986 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-04-05
Onset: 2022-04-06
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8095 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS DB93X / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient received an undiluted dose of pediatric Pfizer Covid-19 on 4/5/22. Patient did not experience any adverse events as of 0800 on 4/6/22


VAERS ID: 2221228 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-04-05
Onset: 2022-04-06
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8095 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100363800 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Clotrimazole 1% topical cream
Current Illness: Tinea faciei
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient received an undiluted dose of the pediatric Pfizer Covid-19 vaccine in the ER pharmacy. The grandmother was notified approximately 2 hours later regarding the event since the mother was unavailable at the time. Despite multiple attempts to reach out, we have been unable to reach the mother to verify the status of the two children at this time.


VAERS ID: 2747165 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2024-02-15
Onset: 2024-02-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030337 / N/A LA / IM
DTAP: DTAP (DAPTACEL) / SANOFI PASTEUR 433NE / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8129LA / N/A LA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS 55M72 / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Patient had a sheet of 15 different vaccines she was to receive for immigration purposes. Four of them were circled. MA misunderstood patient and thought the four that were circled were the ones she wanted to get. The four that were circled were the four vaccines she received 12 days ago. CDC and manufacturers of each vaccine were called to assess risks/harms to look out for. Increase pain or swelling at the injection sites were the only things told to look out for. Patient left the office before we could assess for this. Patient did remain in the office approx 35-45 after administration. Patient was called two times and left messages to call the office back.


VAERS ID: 2248107 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-10-13
Onset: 2021-10-17
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2022-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 320308D / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 2122275-02056 / 1 RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS 2122278-02056 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Tinnitus
SMQs:, Guillain-Barre syndrome (broad), Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Tamsulosin (0.4mg) Vitamin D3 (5,000 IU)
Current Illness: NONE
Preexisting Conditions: Type II Diabetes (A1C normal - under control)
Allergies: NONE
Diagnostic Lab Data: None
CDC Split Type:

Write-up: PERSISTENT RINGING IN EARS, TINNITUS (debilitating, extremely loud)


VAERS ID: 1866875 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-09-01
Onset: 2021-09-22
   Days after vaccination: 21
Submitted: 0000-00-00
Entered: 2021-11-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Cough, Headache, Pain, Pyrexia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Smallpox, childhood, severe allergy.
Other Medications: Duloxetine, zoloft, Lasix, klor-con, metformin, venclexta, Gabapentin, apriso, Metoprolol, Bactrim DS, cyclobenzeprine, crestor, montelukast, Diltiazem, Allopurinol, Acyclovir, Tegretol, Armour thyroid , atrovent
Current Illness: None
Preexisting Conditions: CLL, DMII, Crohns, GERD, POTS syndrome, neuropathy, hypothyroidism, asthma
Allergies: Tagamet, codeine, fentanyl Nickel, wool, Tide detergent, adhesive tape
Diagnostic Lab Data: Self monitoring and temperature checks every 4 hrs.
CDC Split Type:

Write-up: Within 5 hrs. started with body aches, then chills. Within 8hrs earlier symptoms continued with additional symptoms of headache, dry cough, worsening of aching/pain, fever 103?. Symptoms lasted 4 days and stated to slowly resolve. Took motrin 800 MG and alternated with Tylenol 1000 MG, cool compresses, Benadryl 50 MG throughout course of symptoms.


VAERS ID: 2264957 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-05-05
Onset: 2022-05-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-05-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8094 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS L3HK9 / N/A RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product preparation error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nurse administered undiluted dose of Pfizer for ages 5-11, dose #1 to patient. Guardian informed of error post vaccination via phone call. Guardian states all patients were feeling "fine" at time of phone call. Guardian advised to monitor injection sites for adverse reaction, and call clinic back if any adverse effects occur. Nurse addressed all questions and concerns. Dr. and supervisors aware.


VAERS ID: 2264961 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-05-05
Onset: 2022-05-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-05-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8094 / 1 LA / ID
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS L3HK9 / UNK RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nurse administered undiluted dose of Pfizer for ages 5-11, dose #1 to patient. Guardian informed of error post vaccination via phone call. Guardian stated all patients felt "fine" at time of phone call. Guardian advised to monitor injection sites for adverse reaction, and call clinic back if any adverse effects occur. Nurse addressed all questions and concerns.


VAERS ID: 1744760 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-01-28
Onset: 2021-09-25
   Days after vaccination: 240
Submitted: 0000-00-00
Entered: 2021-09-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1283 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS JL5C3 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Bell's palsy, Facial pain, Facial paralysis, Head discomfort, Headache, Neck pain
SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Glaucoma (broad), Hearing impairment (broad), Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: N/a
Current Illness: Vascular malformation Breastfeeding
Preexisting Conditions: Vascular malformation
Allergies: N/a
Diagnostic Lab Data: 2 doctors office visits to rule out stroke one on Monday 9/27 and Tuesday 9/28.. Head pressure, neck pain facial pain and headache. If not better by Friday will go to ER
CDC Split Type:

Write-up: Facial droop-bells palsy


VAERS ID: 2745725 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2024-02-09
Onset: 2024-02-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Diarrhoea, Nausea, Vomiting
SMQs:, Acute pancreatitis (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Testosterone, Losartan, Monolukast, many supplements
Current Illness: COVID-19 in early February
Preexisting Conditions: Hand and wrist weakness and pain
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Nausea, vomiting, diarrhea, significant pain in the shoulder of injection


VAERS ID: 1943909 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-13
Onset: 2021-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 312831 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: ADMINISTRATION ERROR : Pt. was administered Influenza High-Dose 10/13/2021 (65+) being 64 at the time of administration.


VAERS ID: 2310288 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-26
Onset: 2022-02-07
   Days after vaccination: 73
Submitted: 0000-00-00
Entered: 2022-06-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 UN / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 UN / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Cardiac disorder, Chest X-ray, Cough, Dyspnoea, Malaise, Oropharyngeal pain, Oxygen saturation decreased, Pain, SARS-CoV-2 test positive, Vaccine breakthrough infection
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Respiratory failure (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: CITRACAL with D3; CULTURAL; omega; LECLAIR; black elderberry; multivitamins; B12; propranolol; omeprazole
Current Illness: None
Preexisting Conditions: High blood pressure
Allergies: Sulfa
Diagnostic Lab Data: Chest x-ray, COVID home test.
CDC Split Type: vsafe

Write-up: COVID breakthrough case. I received my 1 booster shot on 11/26/2021 and My COVID symptoms started on 02/07/2022 sore throat, body aches different than any other. Cough, blood oxygen level was down. 2 weeks it lasted. 03/25/2022 went to cardiologist because the breathing treatments were helping me. I tested positive for COVID on 02/08/2022. 03/04/2022 I went to see my PCP because I couldn''t breathe. My doctor gave me antibiotics and inhaler told me if I had pneumonia to take it since I didn''t have, I did not take it. I have problems with my heart since of the vaccine. I never had problem with my heart before now I will have to take medication for rest of my heart. 03/20/2022 I had to go to urgent care because I couldn''t breath and the cough won''t stop.


VAERS ID: 1962381 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-12-19
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041J21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ694AB / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna booster was given to patient under 18. Patient didn''t appear to have any symptoms or reactions. Patient''s dad was told to monitor for any side effects


VAERS ID: 2731237 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2024-01-07
Onset: 2024-01-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030372 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8040KA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Loss of consciousness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: SAME. PASSING OUT
Other Medications: Methocarbamol
Current Illness: Unknown
Preexisting Conditions: Unknown
Allergies: None
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: ABOUT 5 SECONDS AFTER THE SECOND SHOT (fLU) WAS GIVEN, THE PT SLUMPED FORWARD AND PASSED OUT. HE CAME TO IN 3 - 4 SECONDS. THEN 2 MINUTES LATER HE PASSED OUT AGAIN FOR 3 - 4 SECONDS. WE CALLED 911 FOR AN AMBULANCE BUT THE PATIENT REFUSED TREATMEANT SO THE OPERATOR CANCELLED THE EMTs. PATIENTED STATED THAT THIS HAS HAPPENED IN THE PAST AND NOT JUST WITH VACCINES. WE GAVE HIM A BOTTLE OF WATER AND HAD HIM SIT IN THE WAITING ROOM FOR 20 MINUTES. HE SAID HE WAS FEELING FINE


VAERS ID: 2728395 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-12-28
Onset: 2023-12-28
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Angina pectoris, Chest pain, Dyspnoea
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Other ischaemic heart disease (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pain in left side of chest, sharp pain in heart when inhaling, shortness of breath. Lasting 1 hour. Starting 20 minutes after vaccine shot.


VAERS ID: 2699692 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2023-10-20
Onset: 2023-10-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atemoxetine 25mg
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: I woke up this morning after my vaccinations to what sounds like a car blasting a loud bass outside. As I walked around the house, the sound didn?t change in volume whatsoever, and I realized that it was localized in my right ear. It?s a fairly loud, deep rumbling sound. I can hear over it, but it?s a constant thrumming that I have never had before until today.


VAERS ID: 1963616 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-10-11
Onset: 2021-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 UN / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site pain, Malaise, Mobility decreased, Nausea
SMQs:, Acute pancreatitis (broad), Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: imitrex, metoprolol
Current Illness: none
Preexisting Conditions: high blood pressure
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Severe site soreness within hours, Severe general malaise and nausea within hours that lasted for 5 days. Bed ridden the evening of the inoculation and for the next 2 days.


VAERS ID: 1844071 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-23
Onset: 2021-10-24
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 291DZ1A / 2 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Antibody test, Arthritis, Arthropathy, Fatigue, Headache, Hypoaesthesia, Muscle disorder, Musculoskeletal discomfort, Paraesthesia
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Systemic lupus erythematosus (broad), Guillain-Barre syndrome (broad), Arthritis (narrow), Immune-mediated/autoimmune disorders (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No prescriptions. Vitamins C, D3, zinc
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Had an antibody test and I am at a 2.0
CDC Split Type:

Write-up: Headache (I rarely get) and then all my muscles, joints, arthritis flared up, bad. I have been to the chiropractor 5 times now, gotten a massage and have tingling in my fingers and my arm is numb. My neck is totally messed up from the trauma, couldn''t sleep, and just totally exhausted from it for almost 2 weeks now.


VAERS ID: 1727344 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-09-16
Onset: 2021-09-01
Submitted: 0000-00-00
Entered: 2021-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 046C21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ742AA / N/A LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Asthenia, Diarrhoea, Feeding disorder, Inappropriate schedule of product administration, Mobility decreased, Neck pain, Urinary tract infection
SMQs:, Pseudomembranous colitis (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: Alzheimer''s Disease
Preexisting Conditions: unknown
Allergies: no known allergies
Diagnostic Lab Data: Pt treated at ER, per family report, records request pending. Family reports he was treated with antibiotics for a UTI.
CDC Split Type:

Write-up: Patient is new to hospice (admitted today). Per family report, he had COVID and Flu vaccine 1 week ago, and had a sharp a rapid decline since. Patient has been taken to the ER twice with severe neck pain, diarrhea and extreme weakness. Patient is now spitting out food and refusing all fluids. Patient was ambulatory a week ago, but he is now bedbound.


VAERS ID: 1870892 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-03
Onset: 2021-11-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 077C21B / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100347552 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, No adverse event, Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lexapro
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: Patient presented for COVID-19 booster and influenza vaccine. LPN checked for previous influenza vaccine status but did not review previous COVID-19 history, however patient presented COVID-19 vaccination record card with two documented Moderna vaccines on 12/22/2020 and 01/19/2021. She proceeded to administer the Moderna booster vaccine 0.25mL and influenza vaccine. When documenting the vaccines, the LPN realized she had not checked for prior COVID-19 vaccination status. There displayed were three COVID-19 doses as follows: 12/22/2020-Moderna, 01/19/2021-Moderna and 08/25/2021-Pfizer. When questioned about the third dose, she denied having a third dose. She attributed it to a documentation error, however, the following day she reported in fact she received a third dose but does not recall details due to going through a difficult time during that period and high stress levels. Patient''s significant other reminded her of receiving third dose. Patient denied having any adverse reactions and reported feeling fine. However, she reported left arm soreness for approximately 3 days after vaccine administration. Patient took ibuprofen once-soreness resolved. Patient instructed she does not need any additional COVID-19 vaccines at this time. Patient verbalized understanding.


VAERS ID: 2476609 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-09-01
Onset: 2022-10-01
   Days after vaccination: 30
Submitted: 0000-00-00
Entered: 2022-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 5 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Catheterisation cardiac abnormal, Electrocardiogram abnormal, Pericarditis
SMQs:, Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Wellbutrin, lamotrigine, trazodone, lisinopril, atorvastatin, metformin
Current Illness: Cancer survivor as of 9/2022
Preexisting Conditions: Asthma
Allergies: Tramadol
Diagnostic Lab Data: EKG, cardiac catheterization
CDC Split Type:

Write-up: Pericarditis


VAERS ID: 1840271 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-01
Onset: 2021-11-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: toporol protonix wellbutrin multiple vitamin Calcium and D3
Current Illness: 0
Preexisting Conditions: 0
Allergies: Penicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: feverish achiness tiredness


VAERS ID: 1805965 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-18
Onset: 2021-10-19
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7316MA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lymph node pain, Pain in extremity, Rash, Rash erythematous
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: erythematous truncal rash - 1-2mm papules without itching, pain, nor drainage. No significant spread or progression in severity after initial presentation. Preceded by tender left axillary lymphadenopathy (ipsilateral to covid vaccine; no right-sided LAD) and arm soreness - both of these sx were within expected severity for covid vaccine.


VAERS ID: 1888339 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-20
Onset: 2021-11-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 UN / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A UN / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Rash erythematous, Rash papular
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatiin 20mg, Losartan 100mg
Current Illness: none
Preexisting Conditions: HTN, hyperlipidemia
Allergies: SULFA
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient started with erythematous papular dry rash to face, neck and chest about 12 hours after receiving COVID pfizer booster and HD Flu vaccine. Rash has persisted x 15 days


VAERS ID: 2603883 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-11
Onset: 2021-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 6015226-0110 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 6015227-0110 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Back pain, Chills, Eye irritation, Fatigue, Headache, Pain, Pain in extremity, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Corneal disorders (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Symptoms started 7:30pm 10/11/2021 (fatigue,fever over 100 degrees, body chills, and mild headache). Symptoms worsened around 1:30am 10/12/2021 with (Fever 102.2 degrees, severe pounding headache and burning eye sensation, whole body aches especially low back pain and leg aches) All symptoms were treated with Ibuprofen 800mg every 4-6hours and alternating Tylenol 500mg every 4-6 hours. Cold compress was placed on my forehead and room temperature was turned down to a cooler degree. Later result: Fever and bodyaches decreased by 11:00am 10/12/2021. Mild headache stayed persistent through the whole 24hours of 10/12/2021. I''m still fatigued with mild headaches as of today.


VAERS ID: 2095704 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-01-27
Onset: 2022-01-31
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2022-02-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1614 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN TYPE & / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Cough, Fatigue, Headache, Malaise, Oropharyngeal pain, Respiratory tract congestion, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Claritin; Vitamin D; Iron
Current Illness: none
Preexisting Conditions: none
Allergies: Cephalaxin
Diagnostic Lab Data: Positive COVID test on 2/2/22 and 2/6/22
CDC Split Type:

Write-up: I started feeling ill on Monday, 1/31. Mostly a little tired and sore throat. It got worse on Tuesday and included a headache and congestion. I took a COVID test on Wednesday and started coughing; I got a positive COVID result the next day. I did not see a doctor, but I talked to a Telemed doctor who prescribed some cough medicine. I felt better by Saturday. I realize this might not be an adverse reaction to the COVID vaccine, but when I researched whether getting the COVID vax along with the flu could cause flu-like symptoms with a positive COVID test and it said there was no significant data to suggest any issues with taking both vaccines at same time. So I felt it was important for me to report my case so that it can be considered among the rest of the data.


VAERS ID: 2595286 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-12-28
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR5618 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7383NA / 4 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, Product storage error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Vaccine was expired. Had been drawn up 30 hours prior to being given.


VAERS ID: 2592496 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / N/A - / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / N/A LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: OZEMPIC, METFORMIN
Current Illness:
Preexisting Conditions: DM2
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592492 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / N/A RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: HYPERTENSION, HYPERTHYROIDISM
Allergies: POLLEN
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592489 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592479 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: IMITREX, OZEMPIC, ALBUTEROL MDI, IRON
Current Illness:
Preexisting Conditions: ASTHMA, DM2, HYPERTENSION
Allergies: EMPAGLOFOZIN, ERYTHROMYCIN
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592475 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ASPART INSULIN, JARDIANCE, LIPITOR, ASA, VIT. D, MAG OXIDE, LISINOPRIL, AMLODIPINE
Current Illness:
Preexisting Conditions: DM2, HYPERLIDIEMIA, HYPERTENSION,
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2038084 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-31
Onset: 2021-12-30
   Days after vaccination: 60
Submitted: 0000-00-00
Entered: 2022-01-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037K20A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 043L20A / 2 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Angiogram, Magnetic resonance imaging head, Scan with contrast, Ultrasound scan, Vasculitis
SMQs:, Vasculitis (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisinopril 20mg once daily, zyrtec 10mg daily, daily dietary collagen Alaya powder supplement 1 scope, infrequently 2 capsules of the vitamin supplement Performance Lab Nutrigenisis multi for women
Current Illness: none
Preexisting Conditions: none
Allergies: no
Diagnostic Lab Data: US neck, CTA Neck with contrast, MRA brain, MRI brain wo and with contrast
CDC Split Type:

Write-up: RT Common Carotid vasculitis


VAERS ID: 2592468 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FARXIGA, LANTUS, ACTOS, ASA, LORATIDINE, LOSARTAN
Current Illness:
Preexisting Conditions: DM2, CHRONIC ALLGERIES, ASTHMA CKD
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592459 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: HCTZ, JANUVIA, GLIPIZIDE, LISINOPRIL
Current Illness:
Preexisting Conditions: DM2, HYPERLIPIDEMIA
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 1807951 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-20
Onset: 2021-10-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Work       Purchased by: ?
Symptoms: Ear swelling, Erythema, Feeling hot, Pyrexia, Rash
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Developed a fever and body rash. Swelling in left ear at 5:00 pm on 10/21/2021 and then swelling in right ear on 10/22 at 6:00 am. Ears became red and hot and swelled. Still swollen now, at 9:00 am.


VAERS ID: 2592456 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592452 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 2R4504B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2592449 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 RA / SYR

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2590348 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-02-24
Onset: 2023-02-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 2 LA / IM
DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS 9HP9Z / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS J9PM3 / 4 RA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. W002614 / 1 RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENVEO) / NOVARTIS VACCINES AND DIAGNOSTICS AMVA750A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NA
Current Illness: NA
Preexisting Conditions: NA
Allergies: NA
Diagnostic Lab Data: NA
CDC Split Type:

Write-up: Patient received a DTaP vaccine. No adverse symptoms. Child is doing well.


VAERS ID: 1813587 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-23
Onset: 2021-10-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 77AJ9 / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Pruritus
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: LevoThyroxine Losartan Sertraline
Current Illness: None
Preexisting Conditions: None
Allergies: Demerol Penicillin Strawberries Melons
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Severe itching in feet including toes


VAERS ID: 2567770 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-01-24
Onset: 2023-01-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7723MA / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: NKA
Diagnostic Lab Data: none
CDC Split Type:

Write-up: I gave the monovalent not the bivalent vaccine.


VAERS ID: 2691720 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-03
Onset: 2023-10-04
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031283 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8130EA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Back pain, Chills, Nausea, Pain
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Covid 19- Moderna
Other Medications: Regular daily vitamins
Current Illness: none
Preexisting Conditions: acid reflux
Allergies: Penicillan
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Severe body aches, chills, low back ache, nausea


VAERS ID: 2699699 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-09
Onset: 2023-10-16
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2023-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4633 / 5 AR / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test, Electrocardiogram, Musculoskeletal stiffness, Seizure, Urine analysis, X-ray normal
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Arthritis (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: asthma
Allergies: None
Diagnostic Lab Data: EKG, urine test, blood test, x-ray done on 10/16/2023 with normal results
CDC Split Type:

Write-up: 45-60 second seizure - stiffening of entire body at approximately 1:00 pm on 10/16/2023


VAERS ID: 2698883 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-18
Onset: 2023-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 204F23A / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8135BA / UNK LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS A77L7 / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Dyspnoea, Erythema, Feeling abnormal, Hypersomnia, Loss of consciousness, Peripheral swelling, Pruritus, Rash, Urinary incontinence
SMQs:, Torsade de pointes/QT prolongation (broad), Cardiac failure (broad), Anaphylactic reaction (narrow), Angioedema (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Depression (excl suicide and self injury) (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: COPD
Allergies: Medication allergies: clindaymycin, codeine, penicillins, sulfa antibiotics
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient contacted pharmacy the following day to inform us of a reaction. Patient stated that she started to feel off (itching hands and feet) when she was driving home. States around 10am was having some difficulty breathing. Patient states difficulty breathing continued and around 12pm felt like she was blacking out but was able to use her albuterol inhaler at home (estimates 4 to 6 inhalations). Patient reported she lost consciousness and had urinary incontinence. Patient slept a lot the remaining of the day. Patient states has recovered. Reports right arm is currently red, swollen, and appears bumpy.


VAERS ID: 2697921 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-16
Onset: 2023-10-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4664 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8135AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Eye swelling, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: High cholesterol, Hypertension, and Diabetes
Allergies: NKA
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: She got the vaccine on Monday and woke up Tuesday morning with some swelling, the worst of which was her eyes. It did resolve itself as the day went on, and was back to normal when I talked to her on Wednesday.


VAERS ID: 2697594 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-06
Onset: 2023-10-08
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-10-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031047 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8091KA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Bumpy rash on arms and chest


VAERS ID: 2697589 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-16
Onset: 2023-10-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HD9835 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS A45NH / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Diarrhoea, Dizziness, Nausea, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Noninfectious diarrhoea (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fainting, diarrhea, nausea, light headedness, dizziness


VAERS ID: 2696174 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2023-10-01
Onset: 2023-10-08
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2023-10-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Condition aggravated, Headache, Malaise, Myalgia, Ventricular extrasystoles
SMQs:, Rhabdomyolysis/myopathy (broad), Ventricular tachyarrhythmias (narrow), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypokalaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: shingrix
Other Medications: Zoloft, Benicar, Crestor, vitamins (B12, D3), potassium/magnesium, low dose aspirin
Current Illness: none
Preexisting Conditions: COPD, PVCs, hyperlipidemia, hypertension
Allergies: penicillin
Diagnostic Lab Data: none
CDC Split Type:

Write-up: MALAISE, HEADACHE, JOINT AND MUSCLE ACHE, PVC FLARE-UP


VAERS ID: 2695868 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-11
Onset: 2023-10-13
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH - / UNK RA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS - / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Covid booster and Prevnar 20 were both given in the right arm, where the reaction was noted. RSV and the flu vaccine were given in the same day in the left arm. I take atorvastatin 10 mg PO daily and acyclovir 200 mg BID daily
Current Illness: none
Preexisting Conditions: high cholesterol ( treated with medication), hx of colon cancer in 2012 and anal cancer in 2022, osteoarthritis
Allergies: cipro IV contrast bee venom
Diagnostic Lab Data: topical benadryl cream, ice, benadryl
CDC Split Type:

Write-up: hives in the upper arms area


VAERS ID: 2050497 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-01-16
Onset: 2022-01-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Injection site erythema, Injection site pain
SMQs:, Extravasation events (injections, infusions and implants) (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: I have covid arm on the injection area on my left arm. Redness and soreness on arm even though it?s been 4 days.I?m also feeling fatigued.


VAERS ID: 1788740 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-12
Onset: 2021-10-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Chills, Pyrexia, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Gabapentin, Pramipexole Dihydrochloride ER, Fluoxetine Hcl, Glyburide, Metformin ER, atorvastatin, 81 mg aspirin, invokana, hydrochlorothiazide, trulicity, omeprazole,
Current Illness: surgery on ruptured patella tendon in right knee on Sept 13, 2021
Preexisting Conditions: diabetes type 2, high blood pressure, high cholesterol, restless legs, anxiety
Allergies: Sulfa, Tequin, Levequin, Cipro, Humira
Diagnostic Lab Data: none
CDC Split Type:

Write-up: severe chills and shaking which started suddenly about 11pm and lasted about 3 hours. slight fever of 99.3 to 100.2. i don''t know the exact name of the flu shot i got. it just said Senior-dose flu shot. i guessed on the exact type


VAERS ID: 2592483 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-10-03
Onset: 2022-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR4504B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AS2878B / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: JARDIANCE
Current Illness:
Preexisting Conditions: DM2
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Moderna Monovalent Adult Booster given instead of Moderna Adult BiValent Booster


VAERS ID: 2691706 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2023-10-05
Onset: 2023-10-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8138AA / 1 LA / IM
RSV: RSV (ABRYSVO) / PFIZER/WYETH HF5019 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ketoconazole 2% shampoo escitalopram 5mg 1qd carbidopa-levodopa 25-100 1 six times a day atorvastatin 20 1qd duloxetine 20 1qd
Current Illness:
Preexisting Conditions:
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: patient received the 5-11 dose of pfizer covid 19 instead of the 12+ dose


VAERS ID: 1780121 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-09-25
Onset: 2021-10-03
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 UN / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A UN / IM

Administered by: Private       Purchased by: ?
Symptoms: Angiogram normal, Asthenia, Body temperature increased, Computerised tomogram abdomen, Computerised tomogram head normal, Confusional state, Dyspnoea, Fatigue, Full blood count, Hepatobiliary scan, Hyperhidrosis, Laboratory test, Lethargy, Magnetic resonance imaging head normal, Metabolic function test, Mobility decreased, Nausea, Rash, Scan normal, Somnolence, Ultrasound abdomen normal, Vomiting, West Nile virus test
SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: PLAVIX 75 MG DAILY LISINOPRL 20 MG DAILY TAMSULOSIN 0.4 MG DAILY FINASTERIDE 5 MG DAILY SERTRALINE 100 MG DAILY
Current Illness: NONE
Preexisting Conditions: HYPERTENSION BPH HX OF STROKE 2012, NO LASTING SEQUELAE
Allergies: NONE
Diagnostic Lab Data: HOSPITALIZED 10/6/21 - ? STILL IN HOSPITAL. FOLLOWING WERE DONE IN HOSPITAL LAB WORK - BMP, CBC, OTHER LABS, WEST NILE VIRUS-RESULTS NOT AVAILABLE YET CT BRAIN - NEG MRI BRAIN - NEG CTA CHEST & Abdomen - NEG US - ABDOMEN - NEG HIDA SCAN - NEG
CDC Split Type:

Write-up: RASH BACK OF SHOULDERS, EXTREME FATIGUE, NAUSEA / VOMITING AT HOME X 3 DAYS. ADMITTED TO HOSPITAL 10/6/21 WHEN DEVELOPED SEVERE WEAKNESS, UNABLE TO GET UP, SHORTNESS OF BREATH, DIAPHORESIS, TEMP 99.7. ARRIVAL IN HOSPITAL - HAD TEMP $g 101. ADMITTED TO HOSPITAL. WORKUP DONE AS BELOW. POSSIBLE ENCEPHALITIS WITH ENCEPHALOPATHY - IN ADDITION TO ABOVE SYMPTOMS - SOME CONFUSION, VERY LETHARGIC, VERY DROWSY


VAERS ID: 1893865 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-21
Onset: 2021-11-22
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Chills, Eye pain, Eye swelling, Headache, Injection site pain, Ophthalmological examination, Pain
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Extravasation events (injections, infusions and implants) (broad), Glaucoma (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Asthma (mild); borderline obesity
Allergies: None
Diagnostic Lab Data: Eye pressure...normal. vision ...normal
CDC Split Type:

Write-up: Sharp shooting pain in left eye where I have a scleral buckle from a previous retinal detachment. It started in the middle of the night while I was sleeping and lasted about 6 hours where it was accute anytime I was on my left side. It felt like something was stuck in my eye or like I had a very bad scratch. After the first 6 hours the pain lessened but my eye still was swollen causing headache for the next 24 hours or so. I went to the eye doctor to have them check it on Monday afternoon about 14 hours after the pain began. They did not find that I had a scratch or anything in my eye. I think my eye was just swollen and pressing on my scleral buckle in a funny way. I also had the other normal joint aches in my whole body and chills whish lasted about 18 hours and a very sore left arm at the site of the injection


VAERS ID: 2691174 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-10-04
Onset: 2023-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4632 / 7+ RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Pyrexia, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multiple vitamins, Tums Ultra 1000, etodolac 200mg
Current Illness: None
Preexisting Conditions: Pinched nerve at L3 ans L4
Allergies: Shellfish, latex (rash), narcotic pain meds (severe nausea/vomiting)
Diagnostic Lab Data: None
CDC Split Type:

Write-up: 13 hours after the injections, developed Fever, chills, shaking that lasted several hours (overnight)


VAERS ID: 2700583 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Unknown  
Location: Arizona  
Vaccinated: 2023-10-21
Onset: 2023-10-22
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030340 / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8138CA / N/A LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS 3030340 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Body temperature increased, Erythema, Pain, Pain in extremity, Pruritus, Rash
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Hypertension, history of blood clots,
Allergies: Codeine, macrolides, penicillins
Diagnostic Lab Data:
CDC Split Type:

Write-up: Got the three vaccines in left arm and that night had pain and redness and had temperature of 102F. Woke up with pain in arm and rash going down to elbow. Rash has continued down arm and felt itching up until today.


VAERS ID: 2687325 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-09-27
Onset: 2023-09-01
Submitted: 0000-00-00
Entered: 2023-09-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030335 / UNK LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8044AA / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Patient states not taking any medications
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: When I arrived to the pharmacy there was a backlog of immunizations needing to be administered. So I started to process the immunizations that were pending. Because of the patients age they should of received FluQuad and not the FluzoneHD. The issue was not caught until the insurance billing information became available.


VAERS ID: 2684603 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-09-18
Onset: 2023-09-19
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 00069-2362-10 / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 49281-0123-65 / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Diarrhoea, Headache
SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Telmisartan, clopidogrel, HCTZ, Metformin, multivitamin, Calcium citrate-magnesium-zinc OTC, fish oil capsule
Current Illness: None
Preexisting Conditions: Low level diabetic controlled by meds
Allergies: ASA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Headache the next morning after injection, lasted 24hrs. Took Tylenol orally. Diarrhea the next morning aafter injection and has continued from Tuesday morning through mid-day Thursday and still continues . Took PeptoBismol tablets and Loperamide HCL anti-diarrheal tablets orally but has not seemed to lessen diarrhea.


VAERS ID: 2633552 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-04-28
Onset: 2023-04-28
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-05-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 215K22A / 2 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7682KA / 2 RL / IM
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS 9PG49 / 4 RL / IM

Administered by: Public       Purchased by: ?
Symptoms: No adverse event, Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: none
CDC Split Type:

Write-up: No adverse event; incorrect Moderna covid19 strength vaccine given. Reported to Nurse Practitioner. Directed to re-vaccinate with correct Moderna covid19 vaccine dose. Trying to contact parent, phone number listed is out of service. Mailed a letter to parent to have them call our office to have them come in to re-vaccinate.


VAERS ID: 2550792 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-12-09
Onset: 2022-12-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2587 / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100477700 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: adjustment disorder
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient''s 4th COVID vaccination was supposed to be the Bivalent Pfizer vaccine. However, the patient accidentally received the Pfizer monovalent vaccine.


VAERS ID: 1877375 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-11-17
Onset: 2021-11-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 95Z42 / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Administration error, Patient was supposed to receive pfizer covid vaccine but received fluarix. She had already received a flu vaccine for this season. Covid vaccine was administered in opposite arm.


VAERS ID: 2715446 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2023-11-07
Onset: 2023-11-14
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2023-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Chills, Decreased appetite, Headache, Pyrexia, Rash, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Losartan potassium, losartan potassium
Current Illness: None
Preexisting Conditions: Cholesterol,blood pressure
Allergies: Just seafood
Diagnostic Lab Data: No treatment , still have rash ... everything else went away after 3 days
CDC Split Type: None

Write-up: Savere headache,savere fever, chills, Avery joint hurt,no appetite, and broke out into hives/rash. Almost a week later started with headaches.


VAERS ID: 1906071 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2021-11-29
Onset: 2021-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 067F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 977EN / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest pain
SMQs:, Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: none
Preexisting Conditions: none
Allergies: None listed
Diagnostic Lab Data:
CDC Split Type:

Write-up: called at 1:25 pm stating that a couple hours after receiving the vaccine he had sharp pains on the left side of his chest. He states he had about 4 episodes where he had 2-3 sharp pains each. At 2:15 pm when I spoke to him he hadn''t had any further episodes but stated if he needed to he would go to urgent care or seek medical treatment as I had advised since this is not an expected side effect.


VAERS ID: 2006619 (history)  
Form: Version 2.0  
Age: 13.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-01-05
Onset: 2022-01-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 33130BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7Z3Y9 / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: The vaccination was administered inappropriately based on current CDC guidelines. Adult booster dose of the Pfizer COVID-19 vaccine was given to the patient, aged 13, at the time of injection. I spoke to the patient''s mother around 5:00pm and she states that the patient feels fine. She will monitor him closely for any adverse events. Mother was notified to call pharmacy with any questions or concerns.


VAERS ID: 2510716 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-08-17
Onset: 2022-10-30
   Days after vaccination: 74
Submitted: 0000-00-00
Entered: 2022-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7137 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Anosmia, COVID-19, Chest X-ray, Chills, Cough, Electrocardiogram, Fatigue, Headache, Hypoxia, Myalgia, Nausea, Pyrexia, SARS-CoV-2 test positive
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Respiratory failure (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Vitamin D tablets; rosuvastatin; fish oil; latanoprost eye drops; fluticasone.
Current Illness: None
Preexisting Conditions: Hyperlipidemia
Allergies: Lisinopril; seasonal allergies
Diagnostic Lab Data: COVID-19 10/30/2022 positive; chest x-ray; EKG.
CDC Split Type: vsafe

Write-up: COVID-19 symptoms; headache; coughing; fever; chills; lost sense of smell, nausea; muscle aches; fatigue. Also my oxygen levels was 80 I was admitted for Hypoxia and was given infusions of remdesivir and erythromycin.


VAERS ID: 2541969 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-09-18
Onset: 2022-09-19
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-12-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ5342 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest X-ray, Computerised tomogram abnormal, Lymphadenopathy, Neoplasm malignant, Ultrasound scan abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Doxycline; Birth Control
Current Illness: None
Preexisting Conditions: Back Pain
Allergies: Penicillin
Diagnostic Lab Data: CT Scans; Chest X-rays
CDC Split Type: vsafe

Write-up: The day after receiving the vaccine I had enlarged lymph nodes on the same side as I received the vaccine. I went to see my PCP, he told me they should go away two weeks later they were still there, he did an ultrasound and found that the swelling was still there. He sent me to see an ENT. He looked at the lump by using a camera through my nose down my throat he told me it was nothing to come back in three weeks. I was not happy with this answer, I went back to my PCP who referred me to another doctor who told me I should have come to see him sooner. The mass has gotten larger and continues to grow, I ended up in the emergency room I have been told I have stage four cancer.


VAERS ID: 2519013 (history)  
Form: Version 2.0  
Age: 93.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2022-10-17
Onset: 2022-10-18
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GS6665 / 5 LA / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood magnesium decreased, Blood potassium decreased, Blood test, Chest X-ray abnormal, Death, Dyspnoea, Fatigue, Feeling abnormal, Platelet count decreased, Pulmonary oedema, X-ray
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (broad), Haematopoietic thrombocytopenia (narrow), Systemic lupus erythematosus (broad), Dementia (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Hypokalaemia (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2022-10-31
   Days after onset: 13
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Eliquis, Lovastatin, Lovastatin, Amlodipine, Diltiazem, Montelukast, Albuterol sulfate, Arnuity, Alendronate, Oxybutynin
Current Illness: Mild COPD due to previous lung cancer in 2001 and removal of lobe, plus radiation.
Preexisting Conditions: None, just the COPD since 2001
Allergies: none
Diagnostic Lab Data: They drew blood and did X-rays. Perhaps a CT scan. You will have to check with the Hospital to get the complete records.
CDC Split Type:

Write-up: Patient was extremely tired the day after getting the shots. She kept expecting to get better but by the following Saturday, we took her to the Emergency room. She was very low on magnesium, potassium, and platelets. They admitted her to the hospital, and she had one good morning but most of the time she thought she was going to die. (She is not like that normally) I believe it was Saturday 10/29 that she woke up having a horrible time breathing. They gave her breathing treatments but nothing helped. They took an X-ray and her lungs were very full of fluids. They said that they could drain her lungs, but the fluid would probably come back. The other option was to put her on Comfort Care, which we did. Sunday afternoon around 2:30 she passed away.


VAERS ID: 2551966 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-12-09
Onset: 2022-12-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2587 / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100477700 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: phenytoin 100 mg ER cap levetiracetam 500mg tablet topirimate 100 mg tablet
Current Illness:
Preexisting Conditions: stroke of uncertain pathology epilepsy deaf mutism diverticulitis alcohol dependece
Allergies: ibuprofen - rash
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was supposed to receive the bivalent Pfizer booster shot. By error, the patient received the monovalent Pfizer vaccine shot.


VAERS ID: 1754506 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-09-29
Onset: 2021-09-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. - / 1 RA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR - / 1 RA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / 1 LA / SC
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR - / 1 LA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR - / 1 RA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / 1 RA / SC

Administered by: Other       Purchased by: ?
Symptoms: Skin warm, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Youth presented with Hives on both arms on the vaccinated area with warmth to touch.


VAERS ID: 2515352 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Male  
Location: Arizona  
Vaccinated: 2022-11-01
Onset: 2022-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Nausea
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Flovent BID Albuterol as needed
Current Illness: none
Preexisting Conditions: Asthma Myopia
Allergies: none to food or meds _ seasonal allergies
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received the COVID and Flu vaccien on the same day (mom thinks around November 1st,2022. He had nausea the next day and has had intermittent nausea since then no other symptoms


VAERS ID: 2713066 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2023-11-10
Onset: 2023-11-11
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 4 RA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 7+ RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site rash, Injection site swelling, Injection site warmth
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Trelegy, Basaglar/insulin, Metformin, Simvastatin, Citalopram, Losartan, magnesium, vitamin C, melatonin, zinc, super vitamin B complex, vitamin D3, Omega 3, digestive probiotics, multivitamin
Current Illness: Seasonal allergies
Preexisting Conditions: COPD, Diabetes type 2, heart disease, anxiety & depression
Allergies: Penicillin
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Left arm - 11/11/23 had a 2 inch area around injection site swollen with warm rash . Took Benadryl that evening. 11/12/23 woke up with the slightly improved condition due to the Benadryl the night before. Throughout the day the rash, swelling and heat increased. Now have a 3 inch swollen rash going down the arm from the injection site, toward the hand. I am taking Benadryl again tonight.


VAERS ID: 1762482 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Arizona  
Vaccinated: 2021-10-01
Onset: 2021-10-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2597 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN FLU SHO / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Headache, Myalgia, Pyrexia, SARS-CoV-2 test negative, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Penicillin at age 5; vomiting and fever
Other Medications: Metformin; Benicar; Levemir; Singular; Zetia; Celebrix; sertraline
Current Illness: None
Preexisting Conditions: Diabetes
Allergies: Penicillin
Diagnostic Lab Data: COVID-19 test with negative result
CDC Split Type:

Write-up: Extreme fatigue; fever of 101.8 degrees; overall muscle aches; headache; vomiting


VAERS ID: 1906215 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-30
Onset: 2021-11-01
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 32030BD / 3 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Blood test normal, Gait disturbance, Neck pain, Pain
SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec Methimazole
Current Illness: None
Preexisting Conditions: Environmental Allergies Grave''s Disease
Allergies: Bee Pollen
Diagnostic Lab Data: Blood work done and found to be normal (11/5, 11/18)
CDC Split Type: vsafe

Write-up: Extreme pain in joints, shoulders, hips, and neck, mainly. No swelling. Could barely walk. Blood work was done (normal) Doctor prescribed prednisone and advised continuing OTC pain regimen. Ongoing issue with pain.


VAERS ID: 1942863 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-07
Onset: 2021-12-09
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 0830341 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 0830742 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Extra dose administered, Pruritus, Skin warm, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: Diabetes type 2 HBP High cholesterol Seizure disorder
Allergies: Darvon
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pfizer booster reaction Severe itching, redness, heat, lump (golfball size) at deltoid insertion. Approximately 3 inches from injection site.


VAERS ID: 1917752 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: California  
Vaccinated: 2021-02-16
Onset: 2021-03-24
   Days after vaccination: 36
Submitted: 0000-00-00
Entered: 2021-12-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9262 / 1 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6201 / UNK - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 2593 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Cough, Hypopnoea, SARS-CoV-2 test negative, Upper-airway cough syndrome, Wheezing
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Acute central respiratory depression (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Respiratory failure (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: atvorstan10, asprin 81mg, fluticasone, glimepride2,
Current Illness: none
Preexisting Conditions: type 2 diabeties
Allergies: none
Diagnostic Lab Data: NO positive covid tests. I had three tests.
CDC Split Type:

Write-up: Worst ast, wheezing and coughing and increased post nasail drip in my life. worse when trying to go to bed. Wheezing cough, shallow breaths. went on for almost 3 months. I have noticed other people coughing quite a lot. Used rescue inhailer Ibuterol, nebulized with Ibuterol, Pumacort inhaile, Triligy, inhailer and Delsun cough syrup. On worst nights I had to take all above TWICE in a seriesover a 1.5-2 hour period to finally subdue the wheezing and coughing. Novenber 20th seems quite a bit better and have not been using the nebulized.


VAERS ID: 1941046 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-06
Onset: 2021-12-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 330308D / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Fatigue, Headache, Injection site pain, Lymph node pain, Lymphadenopathy
SMQs:, Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: 25mg Losartin daily, 5mg Tadalafil daily, B-6 daily
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Went to the local urgent care to have my under arm looked at b/c I was worried.
CDC Split Type:

Write-up: Chills, headache, fatigue for going on day three. Huge swollen area under left armpit (apparently swollen lymph node), about the size of an egg. Very painful as well. I doubt this had anything to do with my reaction but the tech was rushed, way behind schedule, and the shots hurt worse than I have ever experienced before. Usually I do not even feel them.


VAERS ID: 1936571 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-06
Onset: 2021-11-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 048F2IK / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Angina pectoris, Blood pressure increased, Chest discomfort, Chest pain, Dizziness, Dyspnoea, Echocardiogram, Electrocardiogram abnormal, Ultrasound scan normal
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hypertension (narrow), Cardiomyopathy (broad), Other ischaemic heart disease (narrow), Vestibular disorders (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: 80 mg Fluoxetine
Current Illness: N/A
Preexisting Conditions: Previously had Anorexia Nervosa 2014-2015 with Left Anterior Fascicular Blockage. Made a full-recovery from eating disorder & heart condition.
Allergies: No allergies to medications/foods/products
Diagnostic Lab Data: EKG''s were performed at Urgent Care Sunday 11/7/21. Received abnormal EKG results, instructed to go to Emergency Room. Admitted myself to the ER at apx. 11 AM, was seen by various nurses/dr.''s who confirmed abnormal EKG''s, noted that I had elevated blood pressure. I was admitted to the hospital from the ER Monday 11/8/21 at apx 5 AM. (the hospital was heavily impacted with COVID-19 patients) for observation and further testing. Ultrasound taken of heart muscle, no abnormalities. Discharged Tuesday 11/9/21 after EKG''s returned back to normal and blood pressure went back down to normal.
CDC Split Type:

Write-up: I had received Moderna Booster 11/6/21 and woke up the following morning 11/7/21 feeling chest pain & tightness where my heart is. It felt like my heart muscle was clenching very tightly with pain radiating up my left arm. I have recognized this feeling before as I previously had a heart condition some years back. The pain in my chest would tighten with achiness, then release, then tighten again. I began experiencing shortness of breath, dizziness. I admitted myself to Urgent Care at 10:00 AM, explained my symptoms to the medical provider, explained that I had received Moderna Booster, Flu vaccination in my left arm the day prior w/ Tetanus shot Friday 10/29/21.


VAERS ID: 2068851 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-27
Onset: 2022-01-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK9729 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3P3TY / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Chest discomfort, Dizziness, Electrocardiogram, Musculoskeletal stiffness, Nausea
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Anticholinergic syndrome (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: Hypertrophy of Tonsil and Adenoid
Allergies: unknown
Diagnostic Lab Data: EKG
CDC Split Type:

Write-up: 09:20 Patient walked up to observation station with monitor at side stating she felt lightheaded. Patient received Pfizer vaccine at 09:09 and felt symptoms around 09:12. Patient walked to gurney and placed in trendeleburg position. During RN assessment patient reports symptoms began with moderate chest tightness radiating to left shoulder, nausea followed by lightheaded. States she''s had chest tightness with anxiety in the past. Patient alert oriented x4 talking in full sentences with no respiratory distress, wheezing, stridor, lungs clear to auscultation. She denies intraoral swelling, itching and no visible rash. Vitals: BP 96/61, Pulse 86, RR 20 99% on room air, Temp 96.6. 09:22 Patient states mild chest tightness with no lightheadedness. Sat up on gurney. Vitals: BP106/53, Pulse 71, 100% on room air. 09:30 Patient reports chest tightness/lightheadedness/nausea resolved. 09:37 Dr. consulted and advised can order EKG if patient is worried. Patient agrees to EKG today when she leaves vaccine clinic. Advised to call 911 or go to Ed if necessary for reoccurring chest tightness/lightheadedness or worse symptoms or follow up with primary MD. 09:40 Patient states she feels fine and states ready to go. Her friend sitting at side and will take her to get EKG. 09:56 Vaccine adverse reaction form given and walked out with RN at side. Patient passed the walk test.


VAERS ID: 1866209 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-12
Onset: 2021-11-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8028 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4L97X / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Immediate post-injection reaction, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient fainted after immediately getting both vaccines. Had patient sit in chair for 1 hour and monitored. Gave patient food and water.


VAERS ID: 2075279 (history)  
Form: Version 2.0  
Age: 13.0  
Sex: Male  
Location: California  
Vaccinated: 2022-01-11
Onset: 2022-01-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ6369 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100360866 / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cold sweat, Dizziness, Dyspnoea, Hypoaesthesia, Pallor, Visual impairment
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Glaucoma (broad), Optic nerve disorders (broad), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Asthma
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Approx. 10 minutes after vaccination patient was pale, clammy, dizzy and said he was having trouble catching his breath. His breath, he said he had trouble seeing and that his arm felt numb. His mother requested Paramedics be called. While waiting for Paramedics, Pt''s Blood Pressure was taken (94/63, 98) Pt was let to drink some water and color came back to his face. Paramedics came approx. 10-15 minutes after and reported normal vitals signs & O2 saturation. Pt left to home.


VAERS ID: 1892737 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-13
Onset: 2021-11-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 017F21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7356MA / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Grip strength decreased, Injection site erythema, Lip swelling, Lymphadenopathy, Neuralgia
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Peripheral neuropathy (narrow), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: Latex
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient came to the pharmacy today 11/22/21. She informed pharmacist that after she was done waiting post covid & Flu immunization (on 11/13/21), on her way to her car she felt a swelling sensation in her lips which went away after 15 minutes and did not have any problems with her breathing. On 11/19/21 she developed redness on the injection site (left arm) where covid vaccine was administered. Her armpit also became swollen. She states that now she has gotten a lot better, and redness and swelling is gone for the most part. But she still feels a little bit of weakness and nerve problems in her left arm. She states that she cannot grab onto things well. Patient never made a trip to visit the doctor for this issue, but she will be seeing her provider on her upcoming appointment where she will address her concern.


VAERS ID: 2074608 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Male  
Location: California  
Vaccinated: 2022-01-28
Onset: 2022-01-28
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025L218 / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7415MA / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data:
CDC Split Type:

Write-up: The pharmacist at the local Clinic incorrectly injected a Covid-19 Booster Shot instead of a Flu Shot that I requested, which lead to me taking a total of (2) Covid-19 Moderna shots and 2 Moderna Booster Shot (4 Shots in total). I am not Immunocompromised; the first booster shot that I have taken previously was on 12/12/2021. I experienced slight fever, tiredness, headache and pain in my arms following the injection.


VAERS ID: 1891219 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-22
Onset: 2021-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939909 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ730AB / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Asthma
Allergies: Amoxicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient came to pharmacy only for moderna booster vaccination. Patient received flu vaccination intended for another patient. Patient confirmed their name multiple times before entering and after entering immunization booth. Patient was well informed in the booth prior to receiving vaccination that two vaccinations were prepared, flu and moderna booster, and confirmed with patient if they wanted both shots in one arm or one shot in each arm. Pt confirmed to have both shots in one arm. When patient was presented with their immunization card, they stated that that was not their name. Patient received an apology. The patient then stated they were sorry, that they were OK and did not appear to be upset. The patient only wanted their COVID vaccination card and left upon receipt of their card. Patient was not charged cost of flu HD vaccination


VAERS ID: 1999417 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-05
Onset: 2021-11-06
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 93Z32 / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Chills, Diarrhoea, Dyspnoea, Electrocardiogram, Electrocardiogram ambulatory, Headache, Myalgia, Palpitations
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Pseudomembranous colitis (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Emgality injection monthly; Losartan 100mg daily, Rosuvastatin 10mg daily, Protonix 40mg PRN; Astelin nose spray PRN; Flonase nose spray PRN; Albuterol PRN; Motrin 600mg PRN HA; Zofran PRN; Maxalt PRN, Venlafaxine 150mg daily
Current Illness:
Preexisting Conditions: HTN, elevated cholesterol, chronic allergies
Allergies: Ajovy injection; peanuts; tree nuts; olive tree; grass; dust, miscellaneous environmental allergies; cat and dog dander
Diagnostic Lab Data: Holter monitor; EKG.
CDC Split Type:

Write-up: Severe muscle and joint pain; chills, headache, SOB, diarrhea and palpitations. Treated muscle/joint pain with OTC NSAIDs. Seen in ER for palpitations; had Holter monitor.


VAERS ID: 1876094 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-07
Onset: 2021-09-28
   Days after vaccination: 21
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Balance disorder, Blood test, Computerised tomogram, Extra dose administered, Fall, Fear, Gait disturbance, Hypoaesthesia, Inappropriate schedule of product administration, Magnetic resonance imaging
SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Accidents and injuries (narrow), Vestibular disorders (broad), Medication errors (narrow), Hypoglycaemia (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisenipril, atrovatstatin, paxil, gabapentin, multi vitamin, magnesium, omerperzole, remicade infusion.
Current Illness: Psoriatic arthritis, high blood pressure, lumbar spinal stenosis, cervical spinal stenosis, degenerative disk disease, diverticulitis,
Preexisting Conditions: Same as above
Allergies: None known
Diagnostic Lab Data: I went to the ER and they did blood tests and a CT scan
CDC Split Type:

Write-up: I had the moderna booster shot and the flu shot at the same time one in each arm and 21 days later I had an infusion of Remicade. I believe all of these meds together caused my current situation. I am off balance and have fallen 3 separate times since receiving them, I can hardly walk and both my hands are numb. I feel very unstable on my feet, my gait is almost as if I have cerebral palsy or something. I fell again today trying to get into my chiropractors office. I''m scared, I go for an MRI on Nov. 23rd. I thought I should say something as I had none of these symptoms prior to getting all of these shots/infusions.


VAERS ID: 1890570 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-22
Onset: 2021-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 211D21A / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Disorientation, Dizziness, Extra dose administered, Paraesthesia
SMQs:, Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (broad), Medication errors (narrow), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Client stated, "I was sitting in my chair for 2 minutes and then I began to feel a rush to my head. It felt like a wave of tingling all over my body and I started to feel disoriented for like 10 seconds. I then felt fine but I said to myself I need to get up and let the nurse know." Secondary RN helped transfer client into anti-gravity chair at 12:05 PM. First set of vitals were then taken at that time by Observation RN prior to Co Lead PHN responding to observation room: BP 115/75, pulse 60, O2 SAT 100%, 16 respirations per minute. At 12:08 PM Co Lead PHN advised client to take face mask off and for client to take deep breaths. Client was offered water and snacks but client declined snacks and already had a water bottle. Client stated, "I am not surprised I felt like this after the shot because back when I received my first Janssen shot the next day I felt slight chest tightness while driving. It only lasted for 15 seconds then I felt fine. I am not sure if it was due to the covid-19 vaccine so I didn''t feel the need to let my doctor know." Co Lead PHN clarified whether she was short of breath during that experience while driving to which client said "no." Client stated, "I felt like I was gasping for air and not so much choking. It only lasted for 15 seconds while I was driving and I then felt fine." Client then disclosed to Co Lead PHN, "I''ve had similar experiences with blood draws where I feel like I''m going to faint." Client does not have any medical conditions nor is taking any medications. Client has no history of allergies. Client did state, "I am sensitive to soaps, lotions, and I always take half the dose of any medication." Co Lead PHN observed client to be A&Ox4 throughout entire conversation. Co lead PHN recommended for client to follow up with PCP regarding post vaccination symptoms and to enroll in V-SAFE. Client stated, "I have an appointment with my PCP on Tuesday, I will let them know." At 12:16 PM secondary RN educated the client on when to call 911 or go to urgent care for adverse symptoms of covid-19 vaccination. Client verbalized understanding. Co Lead PHN recommended for client to call a family member to assist the client in driving home to which client declined because she only lives 1 mile away from vaccination site. Co Lead PHN recommended for one last set of vitals after another 10 minutes of monitoring. at 12:27 PM Secondary RN took last set of vitals: BP LA 115/70, pulse 64, O2 SAT 100%. Client expressed she was ready to go home. At 12:31 PM Co Lead PHN walked with client as standby assist towards the exit of vaccination site. Client walked with steady gait and thanked us for assisting her.


VAERS ID: 2085628 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: California  
Vaccinated: 2022-02-03
Onset: 2022-02-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ5683 / 4 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Extra dose administered, Interchange of vaccine products
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: None, patient was physically fine and expressed no pain or discomfort after vaccination. Patient was accidentally given a second Pfizer booster when it should have been a Flu vaccine. Patient was informed of the misdose and then still consented and received the Flu vaccine in the same arm, per request, after the Pfizer dose.


VAERS ID: 1876062 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-15
Onset: 2021-11-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3590 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ769AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site bruising
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: none known
Preexisting Conditions: not known.
Allergies: none mentioned
Diagnostic Lab Data: none
CDC Split Type:

Write-up: patient came back today concerned about the 1.5 inch bruise surrounding the bandaid from his flu shot, it was not uncomfortable and he says he was on no blood thinner or asprin like product. The Pfizer vaccine on the left arm had no discomfort or brusing at all


VAERS ID: 2131434 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-03
Onset: 2021-11-10
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025D21A / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK AR / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Arthritis, Condition aggravated, Imaging procedure abnormal, Mobility decreased, Sleep disorder
SMQs:, Systemic lupus erythematosus (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Parkinson-like events (broad), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Moderna 2nd dose: progression of arthritis in right arm to severe.
Other Medications: Ibuprofen; multivitamin
Current Illness: None
Preexisting Conditions: Severe arthritis (in the right shoulder)
Allergies: White wheat
Diagnostic Lab Data: Imaging of the left shoulder: progression of arthritis from mild to severe
CDC Split Type: vsafe

Write-up: About a week after receiving my booster dose, the pain in my right shoulder had markedly improved and instead now my left shoulder was extremely painful, hard to move/lift and hard to lay on. I saw a PA for an orthopedic surgeon who ordered imaging of my left shoulder and it indicated a progression of mild arthritis to severe arthritis in my left shoulder. They ordered a complete shoulder replacement of the left shoulder but it has been delayed due to other health issues.


VAERS ID: 1997273 (history)  
Form: Version 2.0  
Age: 18.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-21
Onset: 2021-12-23
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-01-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1620 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3477H / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abnormal faeces, Alanine aminotransferase increased, Aspartate aminotransferase increased, Blood fibrinogen increased, Blood lactate dehydrogenase increased, Brain natriuretic peptide normal, C-reactive protein increased, Cardiac imaging procedure normal, Chest X-ray normal, Colonoscopy, Cytomegalovirus test positive, Echocardiogram normal, Electrocardiogram T wave abnormal, Epstein-Barr virus antibody positive, Epstein-Barr virus infection, Fibrin D dimer increased, Gastrointestinal haemorrhage, Haemoglobin decreased, Hypotension, Inflammation, Inflammatory marker test, Intensive care, International normalised ratio decreased, Oesophagogastroduodenoscopy, Parvovirus B19 test positive, Prothrombin time prolonged, Pyrexia, Tachycardia, Transfusion, Troponin increased, Vomiting
SMQs:, Liver related investigations, signs and symptoms (narrow), Liver-related coagulation and bleeding disturbances (narrow), Anaphylactic reaction (broad), Acute pancreatitis (broad), Haematopoietic erythropenia (broad), Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhage laboratory terms (broad), Neuroleptic malignant syndrome (broad), Myocardial infarction (narrow), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal haemorrhage (narrow), Biliary system related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Other ischaemic heart disease (broad), Noninfectious diarrhoea (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad), Hypokalaemia (broad), Opportunistic infections (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Flovent 44 mcg, 2 puffs twice daily, vitamin C, Vitamin D
Current Illness: subjective sensation of dyspnea since COVID 10/15/21
Preexisting Conditions: History of COVID 10/15/21
Allergies: none
Diagnostic Lab Data: all 2021: Troponin-I: 12/26 .51 ug/ml, 12/26 .53, 12/27 .18, 12/27 .14, 12/29 .21, 12/30 .04 CRP: 12/26 176.8 mg/L, 12/27 121, 12/28 81.9, 12/29 38.8 BNP: 12/27 <5 pg/dl,12/28 9, 12/29 25, 12/30 24 Below from 12/26-12/30 left to right Hgb: 13.6 8.5 Low 8.2 Low 9.0 Low 9.0 Low 8.0 Low 8.6 Low 9.3 Low 8.8 AST: 23 14 17 38 High 71 High ALT: 23 14 17 38 High 71 High Fibrin D Dimers 902 * High 1,740 * High 1,936 * High 2,681 * High 1,830 * High Fibrinogen 566 High 431 High 386 449 High 458 High 393 397 PT/INR: (12/26-12/28) 15.0 High 15.7 High 15.6 High 14.0 14.4 1.2 1.3 High 1.3 High 1.1 1.2 VIRAL TESTS EBV IGM POS CMV igM Pos Parvo IgG pos Normal Echo Normal Cardiac MRI
CDC Split Type:

Write-up: The patient developed low grade fevers 24 hours after his flu vaccine and pfizer booster. Approx 48 hours after the vaccines, his fevers started spiking to tmax 103.7. He was treated at home until 12/26 with alternating ibuprofen and tylenol until 12/26 when, upon discussion with his primary care doc, me, he went to the ER. In ER noted to be hypotensive, tachycardic, and w fever. Also developed vomiting. Given fluids and ceftriaxone. Noted to have elevated troponin, crp, ldh. Normal chest xray. EKG with mild t wave abnormalities which resolved on second EKG. Normal bedside echo. Stabilized, sent to ICU for monitoring. Labs generally improved. Formal Echo normal. On 12/27 developed GI bleed w melanotic stool. sent for EGD and colonoscopy which showed possible mallory weiss tear/gastritis. Placed on protonix and received blood transfusion for drop of hemoglobin from 13 to 8. Advanced diet slowly. Meanwhile ebv serology came back igm positive, heterophile neg. CMV igm also positive. NO EBV DNA found. Patient stablized well with down trending troponins and inflammatory markers Hemoglobin stable able to eat and drink Discharged home on protonix and carafate on 12/30/21 Ultimately diagnosed with EBV and hyperinflammatory state. No Misc given self resolving fever and downtrending inflammation without treatement. No myocarditis given normal echo, ekgs, and normal cardiac MRI. It was felt that the elevated troponins were due to cross reactivity with EBV.


VAERS ID: 2629517 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Unknown  
Location: California  
Vaccinated: 2021-10-05
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / -
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / UNK RA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Rash, Rash erythematous, Rash papular
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multi-vitamin
Current Illness: non smoke, non alcohol
Preexisting Conditions:
Allergies: apparently to Product: FLULAVAL QUAD 2021-2022 (PF)
Diagnostic Lab Data:
CDC Split Type:

Write-up: red rash began on R thoracic region about three weeks after administration of FLULAVAL QUAD flu vaccine. The rash became very extensive over my lateral R thoracic area, and spread up to mid chest and lower abdomen, consisting of closely spaced numerous red, raised, fluid-exuding papules. The rash was present for over a month before resolving. The FLULAVAL QUAD vaccinated was administered on the same day as my third Pfizer Covid-19 vaccination, in the opposite deltoid. However, I had no adverse reactions to either of the first two Pfizer vaccinations. Administered on Oct 5, 2021 Manufacturer: ID Biomedical Product: FLULAVAL QUAD 2021-2022 (PF) Lot #: 3A9ZG NDC: 19515-818-41 Dose: 0.5 mL Route: Intramuscular Site: Right deltoid Location: INTERNAL MEDICINE


VAERS ID: 2043980 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-12
Onset: 2022-01-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 066H21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7Z3Y9 / UNK RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: UNKNOWN
Current Illness: UNKNOWN
Preexisting Conditions: UNKNOWN
Allergies: PENICILLIN, PER PT REPORT, NON ANAPHYLAXIS
Diagnostic Lab Data: UNKNOWN - UNABLE TO GET AHOLD OF PATIENT ON 1/18/2022 BY PHONE - VOICEMAIL BOX FULL
CDC Split Type:

Write-up: FLU AND COVID VACCIANTION EFFORT FROM PUBLIC HEALTH DEPARTMENT. LAST PATIENT OF DAY, RN REVIEWED PAPERWORK AND PREPARED MODERNA 0.25ML DOSE AND PRE-FILLED FLUARIX SYRINGE. RN MISTAKENLY NEVER DREW UP THE MODERNA VACCINE AND ACCIDENTALLY INJECTED 0.2ML OF AIR INTO THE PATIENT''S RIGHT DELTOID. RN NOTICED AFTER THE FACT AND EXPLAINED TO THE PATIENT WHAT HAPPENED AND THAT A REPORT WOULD BE FILED, ALSO APOLOGIZED. RN REVIEWED S/SX STROKE / OTHER REASONS TO SEEK EMERGENCY MEDICAL ATTENTION. ALSO GAVE CLIENT LOCAL URGENT CARE PHONE NUMBER AND RN''S DIRECT OFFICE LINE.


VAERS ID: 1925380 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-06
Onset: 2021-12-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8028 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ772AC / 2 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: n/a
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: high dose fluzone was given to the patient instead of requested pfizer covid booster shot. patient was called and patient came back into pharmacy and received pfizer covid booster


VAERS ID: 1997644 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-31
Onset: 2021-12-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1611 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR ? / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Angina pectoris, Chest pain, Chills, Fatigue, Headache, Heart rate increased, Injection site pain, Myalgia, Neck pain, Pain, Palpitations, Pollakiuria, Tremor
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Other ischaemic heart disease (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Daily Vitamin, Co-Q10, Calcium, Ginko biloba, Lutein
Current Illness: None
Preexisting Conditions: Varicose veins
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Chest pain over heart area, pounding, fast-beating heart, pulse 101, fever 100.3, headache, fatigue, shakes, teeth chattering, muscle aches, injection site pain radiating to left side of neck,urinating every 20 minutes.


VAERS ID: 1907163 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-27
Onset: 2021-11-28
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Headache, Nausea, Pain, Pyrexia, Skin warm, Thirst
SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Second covid shot 6 months prior gave me severe body aches and fatigue for 24 hours after shot.
Other Medications: Ortho tri cycles, simvastatin
Current Illness:
Preexisting Conditions:
Allergies: Penecillin, steroids
Diagnostic Lab Data:
CDC Split Type:

Write-up: 12 hours after I had chills and could not get warm. Then 3 hours after, I had a fever of 102 that did not subside for 24 hours. I also had intermittent body aches, headache, nausea and increased thirst.


VAERS ID: 1991128 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-06
Onset: 2021-12-08
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK RA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Angiogram, Arthralgia, Blood test, Computerised tomogram, Injection site hypoaesthesia, Injection site pain, Intervertebral disc protrusion, Magnetic resonance imaging abnormal, Muscle tightness, Myalgia, Neck pain, Nerve compression, Pain, Pain in extremity, Sleep disorder, Tearfulness, Ultrasound scan
SMQs:, Rhabdomyolysis/myopathy (broad), Dystonia (broad), Accidents and injuries (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Depression (excl suicide and self injury) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Occasionally deal with asthma, carpel tunnel and knee pain at times
Allergies: Sensitive to strong pain medicine like Vicodin, it makes me vomit
Diagnostic Lab Data: I had 2 CT scans, MRI, ultrasound, blood work and angiogram. MRI shows bulging disc in C5-C6 that is compressing a nerve. I don?t have history of this issue. I just woke up a day and a half after the vaccines with 10/10 pain. The right side is where I got my flu shot. I get it pretty often and have never had any issue.
CDC Split Type:

Write-up: Woke up 12/8 with severe pain in right upper arm, it got progressively worse with an hour of being awake that I was in tears. Felt like my muscle in my arm was twisting and burning and it would not stop. It?s been 3 weeks. I had Toradol injection, dilaudid injection, morphine and Valium in the ER and still felt pain. I had 2 CT scans, MRI, ultrasound, blood work and angiogram. I cannot lay down with intensifying pain so I have sleep sitting up since 12/8. Will get a cervical epidural steroid injection in my neck on 1/4. I tried a cortisone shot in shoulder with short term minor relief and I?m taking Neurontin and Flexiril 3 times daily. Prednisone once daily, started at high dose and gradually reduced every 4 days, this helped but with medicine reduced, pain returned to severe unmanageable feeling and I?m taking Percocet as needed. MRI shows bulging disc that is compressing a nerve. All my consistent pain comes from my arm where the stuff was given. It?s been numb for almost 3 weeks as well. I do have ache in my neck at times and shoulder pain a lot, pain even radiates to my forearm at times. My upper arm is the worst however and it feels like a tight band is around my bicep.


VAERS ID: 2199866 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: California  
Vaccinated: 2022-03-04
Onset: 2022-03-07
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2022-03-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK9894 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dysgeusia, Parosmia
SMQs:, Taste and smell disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: not known
Current Illness: not known
Preexisting Conditions: none
Allergies: no known allegies
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: THE DAY AFTER VACCINES ADMINISTRATION PT STARTED HAVING A BAD TASTE IN THE MOUTH AND A BAD SMELL IN HER NOSE WHICH ACCORDING TO HER IS SO DISTINCT. ALL THESE LASTED FOR 2 WEEKS. SHE STILL SMELLS IT UNTIL NOW BUT IT IS NOT AS STRONG


VAERS ID: 1928916 (history)  
Form: Version 2.0  
Age: 18.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-03
Onset: 2021-11-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK RA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Dysphagia, Dyspnoea, Laboratory test, Urticaria
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Psychiatric-depression, history of anxiety and self cutting
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data: ER-unknown what tests and lab results were obtained
CDC Split Type:

Write-up: Shortness of breath, hives, difficulty swallowing


VAERS ID: 1877419 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-17
Onset: 2021-11-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8208 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS Z6474 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood glucose, Dizziness, Electrocardiogram, Feeling hot, Loss of consciousness, Somatic symptom disorder, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: No known health conditions
Preexisting Conditions: No known health conditions
Allergies: No known allergies
Diagnostic Lab Data: Vital Signs (EKG, oxygen saturation, HR, blood pressure) and Blood Glucose levels were measured by the EMT at 4 minutes post-incident (but results were not disclosed to me or the pharmacy staff).
CDC Split Type:

Write-up: Patient received their COVID-19 Pfizer booster at 12:50PM and reported feeling fine. The Influenza (Fluarix) vaccine was administered at approxiametly 1:05 PM into the same arm. After 10-15 seconds, I noticed the patient''s head had tilted to their left and they had slumped in their chair (leading me to believe they had syncope). After receiving no verbal response for 3 seconds, I made sure the patient was stable in their chair and rushed to advise the pharmacist on staff of the incident (I called 911 while Dr. checked on the patient). The patient had regained consciousness and reported feeling dizzy, faint, and hot when he awoke about 30 seconds after initially losing consciousness. Police and EMT''s arrived within 4 minutes of the incident and confirmed vitals were stable before transporting the patient into their ambulance for transport to the ED.


VAERS ID: 2048186 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-28
Onset: 2022-01-07
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2022-01-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 067F21A / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100373391 / 1 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Pruritus, Rash, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Errin
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: Not yet.
CDC Split Type:

Write-up: Urticaria: Rash/hives 10 days after shot. Very itchy especially on palm of hands and scalp. Urgent care doctor put me on prednisone and Benadryl but the allergist changed it to Montelukast 10mg 1 tablet at night, fexofenadine 1180 mg 1 tablet a day, carbinoxamine 4mg 1 tablet at night, and famotidine 40mg 2 times a day.


VAERS ID: 1936495 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-09
Onset: 2021-12-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Dizziness, Hypoacusis
SMQs:, Anticholinergic syndrome (broad), Hearing impairment (narrow), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: latex
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: On Friday, 12/9/21, patient came to ECC Covid-19 Vaccination Site for her Pfizer Covid-19 booster vaccine and Flu shot. Client received her Pfizer Covid-19 booster dose (LOT #: FF8841) at 11:07 AM in her left deltoid and her Fluarix Quadravalent (LOT #: 7557A) in her right deltoid at 11:08 AM. During assessment questions, client stated her medical history included allergies to latex. Client was to be a 30 minute observation. At 11:33 AM, while waiting in Observation Area, client stated to EMT , she is feeling "10 out of 10 dizzy and hard for her to hear" while sitting in the observation chair. EMT had client sit in anti-gravity chair and vitals started. At 11:35 AM: BP: 138/88, O2 sat: 96%, HR: 80, RR: 16. Client was given a bottle of water that she drank and a granola bar. At 11:40 AM: BP: 132/80, O2 sat: 97%, HR: 70, RR: 16. Client stated to EMT she was feeling "5 out of 10 dizziness and was able to hear normally. Client denied any other symptoms including nausea, SOB, chest pain or stomach pain. Client stated in 2018 she experienced a similar sensation of dizziness and fainting after receiving a flu shot while pregnant and went to the emergency room. Client did eat breakfast this morning. At 11:55 AM: O2 sat: 97%, HR: 77, RR: 16. Client is drinking water and states she "feels better." At 12:05 PM: BP: 126/82, O2 sat: 97%, HR 65, RR 16 client stated her dizziness was a "1 out of 10" however when she tried to stand up she felt dizziness "8 out of 10" again. Client sat back down in anti-gravity chair and felt better immediately. At 12:10 PM, BP: 126/86, O2 sat: 98%, HR: 75, RR 16. EMT offered client Benedryl for moderate symptoms of allergic reaction and client denied. At 12:15 PM, BP: O2 sat: 97%, HR: 72, RR: 16. EMT offered to call 911 for client and client denied and stated her husband would drive her to hospital for further evaluation. Client stated she no longer felt any sensation of dizziness. No further interventions needed. Client was educated by EMTon signs and symptoms of adverse reactions and when to go to the ED/call MD. Client was also encouraged to sign-up on v-safe. At 12:20 PM, EMT used site''s wheelchair to wheel client down to her husband''s car. Client denied any dizziness upon standing up for the transfer.


VAERS ID: 1895365 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-17
Onset: 2021-11-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 32030BD / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 75FZ7 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Cough, Vomiting, Wheezing
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Asthma/bronchospasm (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: albuterol inhaler, azelastine 0.05% nasal spray, spiriva inhaler, wixela inhaler, montelukast, cetirizine
Current Illness:
Preexisting Conditions: asthma, allergic rhinitis
Allergies: none known
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Pt developed coughing , vomiting one time , abdominal pain and wheezing


VAERS ID: 1920653 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-03
Onset: 2021-12-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ767AB / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Pt. was given dose intended for 5-11 year olds not dose intended for 12 and over. No adverse sequelae


VAERS ID: 1877411 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-16
Onset: 2021-11-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 065FUA / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Chills, Condition aggravated, Diarrhoea, Headache, Hypoaesthesia, Injection site pain, Nausea
SMQs:, Acute pancreatitis (broad), Peripheral neuropathy (broad), Pseudomembranous colitis (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Possibly ate moldy tomato sauce one day prior, mild nausea and weakness but no vomiting or diarrhea
Preexisting Conditions:
Allergies: Ceclor
Diagnostic Lab Data:
CDC Split Type:

Write-up: Experienced moderate headache, pain at injection site, chills (chattering teeth), numbness in hands from 6:00pm to 10:30pm day of vaccination. Experienced diarrhea, weakness, and nausea the following day.


VAERS ID: 2052284 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-20
Onset: 2022-01-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL3209 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100369479 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient got the Pfizer booster along with a flu shot. After getting both shots, she sat down on the observation chair in front of the pharmacy. As soon as she noticed she couldn''t, she told her grandpa. A technician was there at the time and immediately called the pharmacist for assistance. The patient was taken back to the consultation room where she leaned on the technician for support and fainted on the chair. Her blood pressure was 88/44 and O2 saturation was 98%. We called 911 paramedics. By the time paramedics came, she was stable. Paramedics confirmed she was fine. The last BP reading was 112/68. She declined to be taken to the hospital.


VAERS ID: 1868209 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-13
Onset: 2021-11-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8030 / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7411LA / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Flushing, Hyperhidrosis, Syncope, Unresponsive to stimuli, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Systemic: Fainting/Unresponsive-Severe, Systemic: Flushed/Sweating-Severe, Systemic: Vomiting-Medium, Additional Details: Patient fainted after receiving COVID-19 vaccine and Fluzone Quadrivalent vaccine (batch/lot#UT7411LA) concurrently. Paramedics called. Patient vitals checked in the store. Patient left unassisted approximately 30 minutes after the incident.


VAERS ID: 2043590 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-07
Onset: 2021-12-30
   Days after vaccination: 84
Submitted: 0000-00-00
Entered: 2022-01-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30158BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ745AC / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Computerised tomogram abdomen, Diverticulitis, Laboratory test
SMQs:, Gastrointestinal nonspecific inflammation (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lansoprazole, Duloxetine, Rizatriptan, vitamins
Current Illness: None
Preexisting Conditions: Migraine headaches, GERD
Allergies: Sulfa, tape
Diagnostic Lab Data: Lab test 1/3/2021; abdominal CT with contrast 1/5/2021.
CDC Split Type:

Write-up: I developed diverticulitis on January 30, 2021.


VAERS ID: 2014322 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-07
Onset: 2022-01-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U7328BA / UNK - / -
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U6602AA / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Hydrocodone, promethazine, metoclopramide, wellbutrin, zoloft, flonase, clonidine
Current Illness: None
Preexisting Conditions: Other chronic pain, hyperlipidemia, depression
Allergies: NKDA
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: PATIENT WAS GIVEN PEDIATRIC 5-11 DOSE OF COVID BOOSTER INSTEAD OF THE ADULT PFIZER DOSE.


VAERS ID: 2147795 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-20
Onset: 2022-01-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 75FZ7 / UNK RA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR U1A452M / UNK RA / IM
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. U029148 / UNK LA / SC

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Inappropriate smaller amount of diluent was added leading to more concentrated dose of vaccine


VAERS ID: 1962392 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-17
Onset: 2021-12-18
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 066H21A / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site erythema, Injection site pain, Injection site pruritus, Injection site rash
SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prazosin, rexulti, vitamin d, cetirizine
Current Illness: None
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Arm soreness, itchy red and like a small rash at injection site


VAERS ID: 1904568 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-06
Onset: 2021-11-20
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2021-11-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Chest discomfort
SMQs:, Anaphylactic reaction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Loratadine
Current Illness: none
Preexisting Conditions: none
Allergies: cats, dust
Diagnostic Lab Data: none
CDC Split Type:

Write-up: On Saturday, November 27, 2021 client came for vaccination POD accompanied by his Mother for his second Covid-19 Pfizer pediatric dose. During assessment questions, Mom stated to RN, patient received his first dose Covid-19 Pfizer pediatric dose (LOT #: FK5127) on 11/6/21 in his right arm and and a flu shot on his left arm. Two weeks later, Mom stated patient experienced a "pinching sensation" on left side of chest. Mom stated patient would experience this sensation once or two times a day intermittently. The last time it happened was on 11/25/21, Thanksgiving day. Mom stated they spoke with his MD who recommended a 30 minute wait after second vaccination. Patient has no chronic medical conditions and takes Loratadine every day due to allergies to cats and dust. Lead Nurse elevated to Vaccine Operations Lead who was on site, who consulted with County MD. Per County MD, Pfizer pediatric dose was approved and advised client to receive his second dose of Pfizer Covid-19 vaccine with 30 minute observation. Client was vaccinated with Covid-19 Pfizer vaccine (LOT #: FK5618) in his left arm at 2:07 PM. Client and client''s Mother was educated by RN on signs and symptoms of adverse reactions and when to go to the ED/call MD. Client''s Mother was also encouraged to sign-up on v-safe. Client experienced no adverse reaction while waiting in Observation Area and left vaccination site with a steady gait at 2:45 pm.


VAERS ID: 1962402 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-14
Onset: 2021-12-19
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2021-12-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Chest discomfort, Chills, Dyspnoea, Headache, Hyperhidrosis, Malaise, Migraine, Muscular weakness, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Flu vaccine, various years w/in last five years. Largely swollen arm and flu-like symptoms requiring bedrest
Other Medications: Daily multi vit gummy, Omeprazole twice daily 1000mg acetaminophen for pain first two days after shots
Current Illness: Sinus issues, vaginal yeast overgrowth
Preexisting Conditions: Reynaud?s syndrome. Allergy-induced Asthma. Seasonal/food allergies. Sternal Rib dislocation RHS
Allergies: Methocarbomal, eggs, latex, many other food allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Still sick (headache became migraine all hours of wake, feverish no fever, sweating through clothes, chills, muscles weak and sore, joints MAJOR pain all joints, chest tight, hard to breathe


VAERS ID: 1913518 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-30
Onset: 2021-11-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8762 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ772ACPVT / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chest discomfort, Pain in extremity
SMQs:, Anaphylactic reaction (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: tamsulosin 0.4mg lovastatin 20mg potassium chloride ER 10mEq acetaminophen 300mg-codenine 30mg omeprazole 20mg Os-Cal 500 mg + D3 500mg losartan 50mg hydrochlorothiazide 12.5mg Mapap 500mg Ibuprofen 600mg Fosamax 70mg
Current Illness: Central retinal vein occlusion, right eye chronic sinusitis glaucoma hyperlipidemia HTN hypertensive retinopathy impaired glucose tolerance Insomnia mixed anxiety and depressive disorder senile osteoporosis tension headache
Preexisting Conditions: ABD pain, ER visit, Kidney stones
Allergies: Amoxicillin
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: 11/30/2021 Patient reported heat on her chest and pain in left hand 6/10 15 minutes post flu vaccine and Pfizer booster. Rapid Response team activated. Vital signs and reported symptoms monitored continuously for 1.5hrs in clinic. Symptoms resolved and patient was released to self care. Telehealth visit f/u complete by provider 12/1/2021. Per note full resolution of symptoms.


VAERS ID: 1873400 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-16
Onset: 2021-11-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 744T3 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Dry throat, Pharyngeal swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Hydrocortisone 2.5% topical ointment; Kenalog 0.1% topical ointment; Albuterol 90mcg inhaler as needed
Current Illness: None
Preexisting Conditions: Atopic Dermatitis; Food Allergies; Snoring
Allergies: Nuts, eggs, fish, milk, sunflower seeds
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: 0910: Patient brought into clinical observation area after reporting that his throat felt dry and swollen, shortly after receiving 1st dose Pfizer Vaccination and Flu shot. Patient accompanied by his mother who reports child has a history of anaphylaxis with nuts, eggs and milk. Patient assisted to gurney. Alert and oriented x 3, speaking in complete sentences. Able to swallow saliva and juice. No drooling noted. Patient denies feeling throat itchiness or difficulty breathing. 0915: VS: Temp: 98.2, BP 97/68, HR 88, RR 16, 02 sats 100% RA, no pain 0916- Call placed to ED physician on call, Dr, informed of patient symptoms above. Verbal order given for Cetirizine 2.5ml x 1 now. Continue to monitor patient for 30 minutes. Patient to go to ED if his symptoms worsen or if he develops any shortness of breath, rash or diarrhea. Verbal order read back and confirmed. 0925: Cetirizine 2.5ml given as ordered. Will continue to monitor. 0955: Patient states throat feels fine. Dry swollen feeling in throat has resolved and no new symptoms noted. VS: Temp: 98.8, BP: 95/54, HR 82, RR 18, 02 sats 100% RA. Discharge instructions given to mom to seek emergent care if patient symptoms return or if he reports shortness of breath or any worsening symptoms. Mom states she has Epi Pen on hand and knows how to use it if needed. Advised to call 911 if she uses Epi Pen. 0956: Patient discharged home in stable condition, accompanied by mom.


VAERS ID: 2024939 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-21
Onset: 2021-12-27
   Days after vaccination: 6
Submitted: 0000-00-00
Entered: 2022-01-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD7218 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Antinuclear antibody positive, Chest pain, Fatigue, Inflammation, Laboratory test, Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (narrow), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Just low-grade fevers for both 3/2021 and 4/2021 Pfizer COVID vaccines.
Other Medications: Rybelsus, metformin, glipizide, lisinopril
Current Illness: None
Preexisting Conditions: Diabetes 2, Bipolar II
Allergies: amoxicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: I had regular symptoms of exhaustion, body aches and low-grade fever (nothing over 100.9) for the first 6 days or so. The body aches got worse into the week of Dec 27th - to the point where I could not get out of bed. The body aches continued and so did the exhaustion. On new years eve, I started having chest pains and so I went to the Emergency room. They found that I did not have a heart attack so they sent me home. I followed up with a doctor at Facility (Dr.) and I briefly mentioned that I think this was related to the COVID booster. He told me that it is highly unlikely that it is the vaccine and that adverse reactions are minimal. To this day I am still easily exhausted and have to lie down often. Dr. ordered labwork and it showed some inflammation and tested positive for ANA. Saw rheumatologist today and again, I expressed my concerns that this is all related to the booster shot. He listened and told me there is a chance it could be, but that we are going to rule out everything else first.


VAERS ID: 1962440 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-15
Onset: 2021-12-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Dizziness, Hyperhidrosis
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Unknown
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: RN noted blood at the site of the Fluarix Quadrivalent vaccine, grabbed an additional cotton ball, cleaned around the site, and applied an additional piece of tape. Client reported feeling dizzy to RN. Lead responded with the anti-gravity chair. The client stood up unassisted and sat down in the anti-gravity chair. The anti-gravity chair was placed in a semi-fowler''s position. RN noted blood on the client''s right hand. The client reported a history of dizziness after seeing blood. RN cleaned off the client''s right hand with an alcohol wipe. RN noted the client''s face appeared diaphoretic. The client denied any blurry vision, shortness of breath, or nausea. Vitals obtained at 1:22PM were as follows: BP 107/68, HR 78, O2 98%. The client stated he last ate a burrito at 10:00AM. The client denied any history of loss of consciousness associated with seeing blood. The client stated his symptoms normally last 2-3 minutes. A cool pack was placed on the client''s chest. The client denied any history of dizziness associated with receiving vaccines. The client denied any chronic conditions, current medications, or known allergies. The client denied any dizziness after receiving previous doses of COVID vaccine Pfizer. The client stated his symptoms have resolved. The anti-gravity chair was adjusted to a high-fowler''s position. The client denied any current dizziness. The client stated he felt comfortable ambulating to the observation area. The client ambulated unassisted to the observation area and sat down in the anti-gravity chair. The client denied any dizziness. RN provided education regarding s/s of anaphylaxis and when to seek EMS. The client voiced understanding of this education. RN responded and evaluated the client''s vaccine administration site on the right arm. No blood was noted on the arm or the bandage. Vitals obtained by EMT at 1:43PM were as follows: O299%, HR 84, BP 110/74. The client denied any current symptoms and stated "I feel normal." The client reported a history of low blood pressure. The client ambulated unassisted with a steady gait out of the observation area at 1:52PM.


VAERS ID: 2006517 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-05
Onset: 2022-01-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1822809 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7Z3Y9 / N/A LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Injection site pain, Sensory disturbance, Underdose
SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Extravasation events (injections, infusions and implants) (broad), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Unknown
Preexisting Conditions: Unknown
Allergies: None noted on pre-screening vaccination paperwork for flu and COVID shots.
Diagnostic Lab Data: None at this time
CDC Split Type:

Write-up: Patient reported painful injection that felt like COVID vaccine hit her bone, reported right arm felt "full" after vaccination complete, as compared to Left arm with flu vaccine feeling normal. (1" needle used on 3mL syringe, 0.5mL dose of Janssen. Deltoid bunched up by RN vaccinator. Resistance felt by vaccinator. Not all vaccine went in, <0.1mL remained, per CDC no indication to revaccinate)


VAERS ID: 1910247 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Male  
Location: California  
Vaccinated: 2021-08-20
Onset: 2021-11-01
   Days after vaccination: 73
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / 2 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cough, Influenza, Influenza A virus test positive, Malaise, Respiratory tract congestion, SARS-CoV-2 test negative, Sneezing, Throat irritation
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Sickness from Hepatitis B
Other Medications: Biktarvy Atorvastatin Abilify Trintellix Xanax PreserVision Areds Vitamin D Vitamin C
Current Illness: None
Preexisting Conditions: HIV Positive
Allergies: None
Diagnostic Lab Data: 11/2/2021 - COVID-19 test - negative 11/2/2021 - Influenza A - positive 11/6/2021 - COVID-19 rapid test - negative 11/6/2021 - COVID-19 PCR test - negative 11/26/2021 - COVID-19 rapid test - negative
CDC Split Type: vsafe

Write-up: On Monday 11/1/2021, I woke up and a little stuffed up and congested. I was sneezing a few times that day. By Tuesday, I was not getting any better getting worse. Did not go to work on Tuesday. Late that afternoon, I went to the urgent clinic to get a COVID-19 test and I was negative and came back positive with Influenza A. I also got another test that Saturday 11/6 - I had more tests done for COVID-19, rapid and PCR - both negative. The doctor prescribed me with Tamiflu, and I took that and got better. Prior to vaccination I was instructed to avoid crowds of more than 25 people and I work at church. Had a farewell party and got sick 11/14/2021 after that. After that, I did home remedies for that sickness. On the 11/22/2021, I flew out of town, and everything was fine when I went. I started coughing and had an itchy throat when I got there. I had a mask on at the family table and sat apart from them. On 11/26, I went to urgent care ? COVID-19 test there was negative, and they gave me a Azithromycin. I''ve recovered from all three instances. May have been stress related.


VAERS ID: 2131353 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-12
Onset: 2022-01-14
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Feeling cold, Hypertension, Vision blurred
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Glaucoma (broad), Hypertension (narrow), Lens disorders (broad), Retinal disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: ibuprofen 800 mg oral tablet, losartan 50MG, Metformin 500 mg, Topamax 15 mg, Triamcinolone 0.1% topical cream
Current Illness: Diabetis, Hypertension, migraines
Preexisting Conditions: Diabetes, Hypertension
Allergies: Trazadone
Diagnostic Lab Data: Patient was referred for an MRI of the brain and orbit
CDC Split Type:

Write-up: Patient had blurry vision, excessive cold flashes, high blood pressure Patient was referred ASAP to ophthalmology and to neurologist. Patient is being treated by ophthalmologist and is pending for visit with neurologist


VAERS ID: 1869779 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: California  
Vaccinated: 2009-12-22
Onset: 2021-11-15
   Days after vaccination: 4346
Submitted: 0000-00-00
Entered: 2021-11-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 49LC5 / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Seizure like phenomena
SMQs:, Convulsions (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness:
Preexisting Conditions: unknown
Allergies: egg whites
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt received covid vaccine then flu vaccine (lot 49LC5) right after. Started having seizure like episode. MD stat and EMTs called. Pt went to local ED via ambulance.


VAERS ID: 2165562 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Female  
Location: California  
Vaccinated: 2022-03-07
Onset: 2022-03-08
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8095 / 2 LA / IM
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS 5N259 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS DB93X / 1 LA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS YG7YJ / 1 RA / IM
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. UO28178 / 1 RA / SC

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: NKA
Preexisting Conditions: NKA
Allergies: NKA
Diagnostic Lab Data: NKA
CDC Split Type:

Write-up: Patient reports fever. The adverse event was that Pfizer was not diluted and patient was administered non diluted Pfizer. Mother informed and follow up revealed a fever today, will treat, no other major adverse reactions.


VAERS ID: 2098707 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: California  
Vaccinated: 2022-02-02
Onset: 2022-02-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood glucose increased, Dermatitis allergic, Pain, Pruritus, Rash, Rash erythematous
SMQs:, Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: albuterol 90 mcg/inh aerosol inhaler, 2 puffs, Inhale, every 4 hrs, PRN benazepril-hydrochlorothiazide 20 mg-12.5 mg oral tablet, 1 tab, Oral, Daily cetirizine 10 mg oral capsule, 10 mg= 1 cap, Oral, Daily, PRN Lipitor 40 mg oral tablet, 40
Current Illness: Diabetes High Cholesterol Hypertension
Preexisting Conditions:
Allergies: no known allergies
Diagnostic Lab Data: 2/8/22 Glucose poc: 389
CDC Split Type: 12541

Write-up: HPI: 50 Years old Female with history of diabetes and hypertension who presented to the emergency department for rash to her neck and ears. Patient states that she received her shingles vaccine, COVID vaccine and her flu shot on February 2, 2022. She states since after receiving the vaccines she began having red bumps and rash to her neck and ears TX: Motrin 600 mg Percocet 10 Benadryl 50 upon reevaluation patient itching improved as well as pain Medical Decision Making: After consideration of a broad differential, patient appears to be having a non-specific mild allergic skin reaction that does not have ongoing systemic symptoms. Patient has no evidence of other emergent process such as, but not limited to, anaphylaxis, sepsis, vasculitis etc. Patient will be discharged with strict return precautions and follow up with primary MD within 24-48 hours for further evaluation. Patient understands that they may require reevaluation if their symptoms recur or worsen.


VAERS ID: 2021788 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-16
Onset: 2021-11-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abdominal distension, Fatigue, Influenza, Intermenstrual bleeding, Muscle spasms
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Infective pneumonia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: I have had no medical tests by this date.
CDC Split Type:

Write-up: I''m not sure of the Flu shot so I just checked the top one. I had both shots the same day. By the next morning I felt like I had the flu and was extremely tired. I also started experiencing menstrual cycle symptoms. I had bloating, cramps, headache and spotting for 5 days. Almost exactly a month later it came back and I had spotting for 8 days. My doctor was contacted (not my primary but my Nurse Practitioner) and she suggested I let her know if it continues. After the second month they made an appointment to do another PAP. I have not had a period in 15 years. This happened the next day after my 3rd shot which is too coincidental.


VAERS ID: 2019267 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-29
Onset: 2022-01-03
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-01-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dizziness, Fatigue, Headache, Vertigo
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Fatigue following second dose of Pfizer Covid 19 vaccine in May 2021 that lasted for one day.
Other Medications: 50mg Zoloft, 50mg lamictal, 100mg trazodone, magnesium, ginko biloba, iron, multivitamins, melatonin, l-theanine, inositol, fish oil, cbd/cbn/thc gummies.
Current Illness: None
Preexisting Conditions: OCPD, depression, anxiety
Allergies: None
Diagnostic Lab Data: None. Discussed with primary care physician on 1/6/2022
CDC Split Type:

Write-up: Vertigo / dizziness, fatigue, headache


VAERS ID: 2014616 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-01
Onset: 2021-11-09
   Days after vaccination: 39
Submitted: 0000-00-00
Entered: 2022-01-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Ageusia, Anosmia, Asthenia, Headache, Productive cough, Pyrexia, Rhinorrhoea, SARS-CoV-2 test negative
SMQs:, Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Niacin Valsarten Vitamin C Vitamin D Magnesium Zinc
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Rapid Test 11/14/21 Negative PCR Lab Test 11/18/21 Negative Rapid Test 11/20/21 Negative
CDC Split Type:

Write-up: Mucous in throat Cough Runny nose Headache Fever 101.8 No energy, weak Loss of taste and smell


VAERS ID: 1884944 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-19
Onset: 2021-11-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 499ZC / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. U007665 / 1 RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U7191AB / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Dizziness, Headache
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none known
Current Illness: none known
Preexisting Conditions: Asthma, hypermetropia, astigmatism, anisometropia, obesity, hyperlipidemia, hx of COVID infection, allergic rhinitis
Allergies: NKA
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Dizziness, headache about 15 mins after vaccine administration. Had pt lay down, gave some apple juice. Pt reported having not eaten yet this morning. Vitals: BP 94/63, P 109, R 20, SPO2 97% RA. Pt assessed by Doctor. Pt started to feel better about 10 mins after lying down and given apple juice.


VAERS ID: 1904020 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-26
Onset: 2021-11-27
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012H21B / UNK RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Exposure via breast milk, Extra dose administered, Hypersensitivity
SMQs:, Angioedema (broad), Neonatal exposures via breast milk (narrow), Hypersensitivity (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft, Wellbutrin, Prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: Coconut and coconut oil
Diagnostic Lab Data:
CDC Split Type:

Write-up: Currently breastfeeding. Toddler (2.5 years) had marks/allergic reaction to vaccine the morning after booster shot. Reaction was small compared to the reaction after the 1st dose of pfizer (ew0162 4/16/21). 1st dose the next morning face was covered with red spots. Benadryl helped until the second day when it was needed again. By day 3 better. 2nd dose, no reason. Booster similar reaction as the first. But nursing much less and the red spots were less.


VAERS ID: 2014916 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-27
Onset: 2021-12-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8762 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: fainted within 5 minutes of injections; drank water; recovered within 15 minutes; no other side effects


VAERS ID: 1923984 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-05
Onset: 2021-12-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ694AB / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Cerebrovascular disorder, Electrocardiogram abnormal, Fall, Sinus bradycardia, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Disorders of sinus node function (narrow), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/a
Current Illness: None
Preexisting Conditions: Low Heart rate. Client stated that his heart rate is normally low.
Allergies: None
Diagnostic Lab Data: 12 lead EKG performed to client @ 12:20 pm, with Sinus Bradycardia result and Heart rate of 42. Last vital signs of Blood pressure: 131/91, HR- 65, and Oxygen saturation of 99% on room air.
CDC Split Type:

Write-up: -@12:04pm, Client fainted while he''s getting up from sitting position from a chair. Fell on the floor, felt unconscious for less than a minute. Assisted back to chair, offered gatorade and water, Doctor and EMS onsite assisted with further assessment monitoring. -Client had his Pfizer vaccine booster dose @ 11:47 am and Influenza Vaccine 2-3 minutes before he fainted. -Client stated that he only had a light breakfast and cup of coffee, and normally does high stress activities. He claims that he has history of vasovagal with blood draws, and anxiety of needles. He stated that having low heart rate is normal for him.


VAERS ID: 1898007 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-19
Onset: 2021-11-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0173 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ775AA / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Anxiety, Nausea, Pallor, Throat tightness
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: booster given and pt also received flu vaccine . During observation, pt complained to RN of nausea and "throat was feeling tight. Patient looked pale and anxious. Pt was evaluated by provider. Pr received EpiPen 0.3 mg x1. 911 was called for pt. paramedics provide pt Benadryl 50mg IV.


VAERS ID: 1952210 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-15
Onset: 2021-12-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE 3594 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4L97X / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Inappropriate schedule of product administration, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient got first covid 19 pfizer adult vaccine on 11/5/21 and got another covid 19 adult pfizer vaccine and an influenze vaccine on 12/15/21, Patient didn''t report any adverse events at time of administration


VAERS ID: 1952649 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-15
Onset: 2021-12-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3594 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4L97X / UNK LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Blood glucose normal, Chest pain, Dyspnoea
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: insulin, rheumatoid arthritis meds, antidepressants (unsure of which)
Current Illness: diabetes claimed to have heart disease but not sure what it is
Preexisting Conditions: heart condition (unsure of what) diabetes rheumatoid arthritis
Allergies: patient said no
Diagnostic Lab Data: Paramedics did assessment of BP, HR and Blood sugar
CDC Split Type:

Write-up: Patient complained of chest pain within 15 minutes of vaccination, pain level 3/10. Heavy breathing. Called mgr/charge nurse. Advised to call paramedics. Pt did not appear to be in distress. Paramedics arrived within 10 minutes. Were not able to get BP because pt reportedly has low BP and difficult to measure. HR=97 Bloodsugar=163 Paramedics took over. Pt refused transport to ER. (Pt is not alone, has 2 people living with her)


VAERS ID: 1902852 (history)  
Form: Version 2.0  
Age: 18.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-26
Onset: 2021-11-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1611 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7383NA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dizziness, Haemoglobin normal, Nausea, Pallor, Syncope, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: history of vasovagal syncope
Allergies: none
Diagnostic Lab Data: hemoglobin 11/26 13.9
CDC Split Type:

Write-up: About 5 minutes (425pm) after both vaccines and routine hemoglobin finger poke (POC) pt was seated on the table, turned pale and fainted. She was out for 10 minutes, and after waking was dizzy and light-headed, although some of her pallor had improved. We gave her water and had her continue to rest. When sitting up, she felt nauseated and had one episode of emesis. After that, parent brought her a snack and she felt better. It was then I learned she had slept in late and hadn''t eaten or drank much before her appointment with me that day. She was released with her parents, and walked out of the office by herself.


VAERS ID: 1980952 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-21
Onset: 2021-12-24
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-12-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Seizure
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Proventil, Keppra
Current Illness: None
Preexisting Conditions: Asthma
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Seizure


VAERS ID: 2091859 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-08
Onset: 2021-11-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Pallor, Somnolence, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Unknown
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Client reported feeling nauseous to RN after receiving the Fluarix Quadrivalent vaccine. RNs responded. RN noted the client appeared pale and was holding an emesis bag provided by RN. The client stood up and transferred to the anti-gravity chair without assistance. The anti-gravity chair was placed in a semi-fowler''s position. RN noted trembling of the client''s legs bilaterally. RN offered the client water or juice and the client declined. RN provided the client with a cotton swab with peppermint oil on it and the client began smelling the peppermint oil. The client then agreed to take a small sip of juice. The client stated she did not like the juice. The client''s mother reported the client ate an egg sandwich this morning. The client and her mother denied any chronic conditions, medications, or known allergies. The client''s mother reported that the client has a history of feeling nervous when receiving vaccines and "other situations." Vitals obtained with the pulse oximeter at 12:31PM were as follows: HR 80 and O2 97%. The client stated that she was feeling better, denied any current nausea, and reported persistent trembling. Vitals obtained at 12:35PM were as follows: BP 110/79, HR 76, O2 99%. The client ambulated unassisted with a steady gait to the observation area at 12:38 PM. The client sat in the anti-gravity chair in the observation area. The client began drinking water. Vitals obtained at 12:45 PM were as follows: BP 122/77, HR 96, O2 97%. Vitals obtained at 12:51 PM were as follows: BP 146/79, HR 78, O2 99%. Repeat blood pressure taken at 12:54PM was 108/70. The reported feeling "sleepy" but denied any other symptoms. RN provided education regarding s/s of anaphylaxis and when to seek EMS. The client and her mother voiced understanding of this education. The client ambulated with a steady gait out of the vaccination site at 12:55PM.


VAERS ID: 1955957 (history)  
Form: Version 2.0  
Age: 88.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-16
Onset: 2021-12-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 069H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Dizziness, Extra dose administered, Headache, Hypertension, Inappropriate schedule of product administration, Neck pain
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypertension (narrow), Vestibular disorders (broad), Arthritis (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: None
Preexisting Conditions: Hx of breastcancer
Allergies: NKDA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Client received the Moderna COVID vaccine booster dose (lot 069H21A, expiration 01/07/2021) to her left arm and Fluarix Quadrivalent (Lot 7557A, Expiration 6/30/2022) to her right arm at approximately 1320. Patient reported to EMT at 1345 that she was experiencing mild dizziness. EMT notified Co-Lead RN. RN assisted client to anti-gravity chair. At this time, client stated that dizziness started approximately 15 minutes after receiving both vaccinations. Vital signs at 1346 were as follows: O2 98%, pulse 75, blood pressure 172/82, respirations 17. Client also reported a mild headache in back of her head and neck. Upon assessment, client is alert and oriented to person and place. Client could not recall year, month or president. The client''s husband agrees that client''s orientation is typical for her and that client " has been having recent issues with her memory". Clients skin is appropriate for ethnicity, dry and warm to touch. Pupils are equal and reactive. Client denies shortness of breath, chest pain, itchiness, palpitations, swelling of throat or tongue and any other symptoms of concern. Medical conditions include: history of breast cancer. Client''s husband reports she does not have a history of high blood pressure, but reports her systolic blood pressure has been reported in the 150-160s during her last few visits at her doctor''s office and reports that the client normally complains of a tension headache in her neck and back of her head. Client denies allergies and reports that she last ate a cookie and cup of coffee at 0800. Vital signs at 1355 are as follows: O2 99%, pulse 82, blood pressure 160/82, respirations 18. Client reports that dizziness and headache have improved, but reports symptoms are still present. At 1410 vital signs at are as follows: O2 99%, pulse 83, blood pressure 172/80, respirations 18. Client offered EMS due to continued symptoms of dizziness and high blood pressure. Client and husband declined EMS. Co-Lead RN advised client and husband to follow up with physician immediately. Lead RN educated client and husband on ER precautions. Client and husband verbalized understanding. Client''s husband stated he would drive client home and reported " I will call her doctor right away". At 1430, Co-lead RN and Lead monitored client while she ambulated to her car with a steady gait. No further nursing interventions required at this time.


VAERS ID: 2032441 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Female  
Location: California  
Vaccinated: 2022-01-13
Onset: 2022-01-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 330368D / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7347JA / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received an additional influenza vaccine (administered 1/13/22) in the same flu season. Previous influenza vaccine was administered on 11/2/2021. The error was discovered about 4 hours after the vaccine was administered.


VAERS ID: 2093169 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: California  
Vaccinated: 2022-02-06
Onset: 2022-02-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939906 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lip swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Synthroid
Current Illness: none
Preexisting Conditions: hypothyroid - stable for 25yrs.
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: The top right side of my lip is extremely swollen like I got a lip implant or something - its extremely swollen. I never had a side effect from the other three Moderna shots so it may be the flu shot (that I didn''t want but was convinced to get).


VAERS ID: 2039363 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-24
Onset: 2021-12-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL8095 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100369747 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ATORVASTATIN, LEFLUNOMIDE, TAMSULOSIN, FERROUS SULFATE, NITROFURANTOIN, FLUCONAZOLE
Current Illness:
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: PATIENT RECEIVED PEDIATRIC DOSE OF VACCINE WHEN THEY WERE ALREADY 12 YEARS OLD. THERE IS EVIDENCE THAT THIS IS OKAY AS LONG AS PATIENT RECEIVES THE ADULT DOSAGE ON THE ON THEIR SECOND SHOT. WAS CAUGHT WHEN PATIENT CAME IN FOR SECOND SHOT AND PATIENT WILL BE INFORMED


VAERS ID: 1999639 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-01
Onset: 2021-12-29
   Days after vaccination: 28
Submitted: 0000-00-00
Entered: 2022-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD7218 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 744T3 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 19 year old, 1996, yellow fever
Other Medications: None
Current Illness: None
Preexisting Conditions: Asthma
Allergies: Sulpha
Diagnostic Lab Data:
CDC Split Type:

Write-up: Muscle and joint pain with mild fever (99 to 100 degrees) lasting approximately 24 hours


VAERS ID: 2001182 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-30
Onset: 2021-12-31
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 066H21A / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Chills, Pain
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Received the flu shot at the same time as the Moderna booster on a weekly course of flucanazole
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: none
CDC Split Type:

Write-up: woke up with chills, body aches, no fever. Lasted until the early afternoon


VAERS ID: 1888118 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-20
Onset: 2021-11-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0191 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5NF7J / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Dizziness, Erythema, Loss of consciousness, Orthostatic hypotension
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: patient reported this after both vaccines had been administered that this has happened to him 5-6 times prior
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: no
Diagnostic Lab Data: 911 was called and he was transported to the hospital
CDC Split Type:

Write-up: Patient presented today requesting COVID-19 booster dose. The immunization screening questions were reviewed. Booster dose given in accordance with Health Officer guidance at 8:28am. Patient requested flu vaccine. Administered at 8:27am. Shortly after at about 8:29am patient stood up still in nurse vaccine station and stated he felt dizzy, and he needed to lie down. PHN gently helped guide patient to the floor, into the supine position. Patient went unconscious immediately and PHN began to hear a gurgling noise, PHN took off his face mask, checked his airway nothing was found, rolled him onto his right side, PHN helped and lifted his legs. Patient was out for about 15 seconds. PHN then placed him back onto his back and he began to talk. He then went out again and made the gurgling noise, his face turned red. PHN assessed airway, nothing found rolled patient onto his right side. PHN continued to hold his legs up, he was out for approximately 15 seconds again. Patient returned to conscious level and was placed back onto his back, he began talking to the nurses and stated he has a history of vasovagal episodes, patient was encouraged to take a few deep breaths. PHN asked if he had eaten before coming in today, he stated he had not. He was given a cookie and a juice, he had two sips of the juice. The ambulance was called at 8:30am by site lead. PHN notified patient that the ambulance was on the way, vital signs were taken B/P 120/70, P86, O2 Sat 99% RA, he remained lying on the floor until the ambulance arrived at 8:50m. He continued to have trouble with orthostatic hypotension, the ambulance crew took him to the hospital.


VAERS ID: 1959325 (history)  
Form: Version 2.0  
Age: 21.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-17
Onset: 2021-12-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 069H21A / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7557A / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Dizziness, Interchange of vaccine products
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Not taking any medications.
Current Illness:
Preexisting Conditions:
Allergies: No known allergies.
Diagnostic Lab Data:
CDC Split Type:

Write-up: Client received her first dose of COVID vaccine (Janssen on 04/09/21 lot: 1808980). Client requested to receive a Moderna COVID Vaccine Booster and a FLU shot. RN spoke with client about mixing of vaccines, and client did report that she did not have any adverse reaction with her Janssen COVID vaccine. RN administered Moderna Booster COVID vaccine Lot: 069H21A first and then the Fluarix Lot: 7557A to client. At 11:35 AM client complained of dizziness after the Fluarix was administered. RN then called both EMTs to bring the gravity chair to her station. Both EMTs stood near client to ensure client does not fall upon transfer to gravity chair and RN followed. Client reported that she ate this morning and did not have any reaction with a previous FLU shot nor with her Janssen COVID vaccine, client does not take any medications, no pertinent medical history and has no known allergies. 11:39 AM Vital Signs obtained: Oxygen Saturation: 98% on room air, Heart Rate: 58, Respiration Rate: 16 and Blood Pressure: 105/76. Skin is warm and dry and reported that she''s feeling better. 11:45 AM Vital Signs obtained: Oxygen Saturation: 99% on room air, Heart Rate: 65, Respiration Rate: 18 and Blood Pressure: 105/73. Client did state, "I''m feeling better and the dizziness only lasted for a minute." Client was able to stand unassisted from gravity chair and no dizziness reported after client stood up. RN advised for client to stay another 15 minutes at observation area, so we can continue to monitor her; however client declined. RN and EMT then escorted client to the car where her father was waiting for her. Client was able to ambulate unassisted to their car. Client left facility at 11:50 AM.


VAERS ID: 1960119 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-17
Onset: 2021-12-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD0809 / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100386142 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: none reported
Preexisting Conditions: none reported
Allergies: No known allergies
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Patient had an appointment for Pfizer Covid vaccine booster dose, pt was processed for the correct vaccine and filled out correct form, however at time of vaccination pharmacy technician gave a flu shot of afluria inadvertently to the patient, Pt was informed she received the flu shot and was given the correct Pfizer covid vaccine. So patient received both the flu shot and the covid vaccine although she did not originally make an appt for a flu shot after consultation with the pharmacist she was informed that the flu vaccine and covid vaccine can be administered together per the CDC. Pt was then processed for the flu vaccine so records can reflect that she did also receive the flu shot. Pt was asked to wait 30 minutes after receiving both shots and did not report any adverse events. pt was informed of the expected side effects: sore arm, tiredness, drowsiness, etc .


VAERS ID: 1905511 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-05
Onset: 2021-11-09
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 033F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367893 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Pain in extremity
SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metformin 750mg Glipizide 2.5mg Aspirin 81mg Lisinopril 5mg Simvastatin 20mg
Current Illness: None
Preexisting Conditions: Diabetes T2 Asthma Hypertension
Allergies: None
Diagnostic Lab Data: None yet.
CDC Split Type:

Write-up: About 3 days after vaccines I experienced pain in right hand between thumb and forefinger. Fourth day after vaccine started experiencing joint pain in left hip and left knee. 23 days later, Nov 29, I still have both in both areas.


VAERS ID: 1914226 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-01
Onset: 2021-12-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS ZG474 / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient collapsed about a couple of minutes after vaccines. Eyes were open and still conscious. Mother was by her side and caught her. She rested on the floor for a few minutes to regain focus, then placed in a seat to rest. Duration was a matter of minutes. Per mom, she has fainted before: once when she saw a syringe/needle, and another when watching someone have a seizure on a video. But has never collapsed/fainted with any other vaccines. Per mom, has not had more than 1 vaccine administered at a time before, at least not recently. Walked outside with family for 20 minutes to get fresh air. After 20 minutes, they checked in and she was fine, just tired.


VAERS ID: 2119359 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-13
Onset: 2021-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL3925 / 3 AR / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain upper, Anal incontinence, Asthenia, Decreased appetite, Discomfort, Feeling hot, Headache, Injection site irritation, Pain, Pyrexia, Sleep disorder, Urinary incontinence, Vomiting projectile
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 1/30/2021 Pfizer vaccine 1st dose EL9265, Age 68 2/20/2021 Pfizer vaccine 2nd dose EL9266, Age 68
Other Medications: Thyroid medication; compounded estriol cream; amino acids; calcium; l-theanine; potassium citrate; adrenal support supplement; 5-HTP; huperzine A; phosphatidylcholines; fish oil; probiotics; quercetin; beta carotene; brain support supplemen
Current Illness: N/A
Preexisting Conditions: Blindness; Brain injury 2005 rehabilitated
Allergies: Penicillin; azithromycin; aspirin; viomycin; CIPRO; wheat; gluten; dairy; corn; lentils; garbanzo beans; pinto beans; walnuts; brazil nuts; mildew; pet fur dandruff
Diagnostic Lab Data: N/a
CDC Split Type: vsafe

Write-up: On the day of my 3rd vaccine, I was also given the flu vaccine, Starting with headaches and I had a fever around 101, I had terrible stomach cramping, projectile vomiting, urinary inconsonance, fecal inconsonance, injection site irritation. I was extremely weak and had no appetite. I had to take homeopathic medicine for my stomach cramps, body aches. The Fever stopped after 3 days, and slowly day by day I started to feel the symptoms were going away. My lymph nodes under my ear and armpits were extremely hot and discomforting after the booster. These symptoms affected my sleep extremely. On the first and second vaccinations I had severe injection site sensitivity, body aches were constant and very painful. Stomach pain was generally there as well. Fatigue was severe as well, however no stomach cramping that was severe. Less extreme for the symptoms and my stomach was really bothering me as well. I was given new probiotics to help my stomach as well and no real fever. I would strongly recommend not getting a vaccination with a flu shot at the same time.


VAERS ID: 2005989 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-21
Onset: 2021-12-22
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029A21A / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Bronchitis, Cough, Injected limb mobility decreased, Peripheral swelling, SARS-CoV-2 test negative, Sinus disorder
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisinopril 10mg, Promethazine PM
Current Illness: No
Preexisting Conditions: Blood Pressure
Allergies: Penicillin, Codeine and Sulfa
Diagnostic Lab Data: Dr. told patient that she developed bronchitis, then gave a Covid test and it came back negative. Dr. prescribed promethazine and Doxycycline.
CDC Split Type: vsafe

Write-up: Experienced the left side of arm swollen and could barely raise arm. Stated having sinus allergies, and started coughing violently and went to the Urgent Care. Can''t lay down without coughing and have to sleep sitting up.


VAERS ID: 2699168 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-19
Onset: 2023-10-20
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4677 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8131AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abnormal dreams, Nightmare, Sleep disorder
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatin, Eliquis, Estradiol vaginal cream, Humalog, Lantus, levothyroxine, methotrexate
Current Illness: UTI, now chronically treated.
Preexisting Conditions: Diabetes and RA
Allergies: n/a
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Pt reports having vivid nightmares, which had disrupted her sleep. This is not a normal occurance.


VAERS ID: 2689674 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-02
Onset: 2023-10-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HD9876 / 1 LA / SC
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8138CA / 1 RA / SC

Administered by: Pharmacy       Purchased by: ?
Symptoms: Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: swelling on her right arm


VAERS ID: 2689675 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Male  
Location: California  
Vaccinated: 2023-09-22
Onset: 2023-09-25
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / N/A AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Malaise, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Calcium channel blockers and ibuprofen
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient wife reported that patient suffered an episode of syncope that resulted in an emergency hospital visit and subsequent hospital stay of about 7 days and patient is still not feeling well.


VAERS ID: 2689878 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-02
Onset: 2023-10-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HD9876 / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AU1057A / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received a second Afluria for the year instead of the requested Comirnaty shot. Patient states they do not currently feel any side effects from either shot and is feeling fine.


VAERS ID: 2690699 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: California  
Vaccinated: 2023-09-30
Onset: 2023-10-01
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4628 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Condition aggravated, Seizure
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levetiracetam 500 mg tablet twice daily
Current Illness: none
Preexisting Conditions: cognitive disability; seizure disorder, well-controlled with medication
Allergies: hives in response to cefaclor for ear infections as a toddler
Diagnostic Lab Data: None. Reported to neurologist, just as an FYI, who confirmed out decision not to double up on vaccinations in the future (no two on the same day).
CDC Split Type:

Write-up: Breakthrough seizure (normally well-controlled with medication. The last one before this one was February 2019). There were no seizures after vaccinations in the past (flu or COVID). The difference this time was that the two were administered on the same day.


VAERS ID: 1794343 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-17
Onset: 2021-10-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1822809 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Interchange of vaccine products
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: CL
CDC Split Type:

Write-up: Client received the 1st COVID vaccine Janssen (Lot #1822809 exp 03/07/2022) at 3:01PM and the Fluarix Quadrivalent vaccine (Lot # 3NA4M exp 06/3/2022) at 3:07PM. After receiving both vaccines, the client disclosed to RN that he had received a Moderna COVID vaccine about 2 weeks ago. The client stated he received the 1st dose of COVID vaccine Moderna "about two weeks ago." The client stated that he did not have any documentation of the Moderna COVID vaccine and was unsure what location he received the vaccine. Prior to receiving the COVID vaccine Janssen RN had asked the client if he had received any other COVID vaccines. The client denied having received any previous COVID vaccine. The client denied any s/s of anaphylaxis. RN recommended the client wait 30 minutes in the observation area. The client voiced understanding of this education. RN checked in with database representative, who stated no records appeared when they searched the client in database prior to receiving the COVID vaccine Janssen. Representative again searched the client in database and RN verified no records appeared. RN returned to the client. The client denied any current symptoms. The client stated that his 30 minutes had elapsed since he received the COVID vaccine Janssen. The client stood up unassisted and left the vaccination site at 3:20PM. After the client left the vaccination site, Representative noted a record matching client information received the 1st COVID vaccine Moderna (Lot#058E21A exp 01/10/2022).


VAERS ID: 2691425 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-02
Onset: 2023-10-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 5 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 7+ LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Headache, Injection site erythema, Injection site pruritus, Pain in extremity, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Crohn''s disease, Rheumatoid Arthritis, Sclerosing Cholangitis, Migraines
Allergies: Sulfa drug allergy Lactose intolerant
Diagnostic Lab Data:
CDC Split Type:

Write-up: 7~48 hours post vaccination: fever, chills, headache, sore arm that is red and itchy at injection site 7~80+ hours post vaccination: sore arm that is red and itchy at injection site continued


VAERS ID: 2692845 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-04
Onset: 2023-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4XY5D / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No available history at the time.
Current Illness: No available history at the time.
Preexisting Conditions: No available history at the time.
Allergies: None applicable per screening consent form.
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: The student received both his vaccines (covid-19 & influenza), and promptly fainted. His head relaxed backwards, yet he remained upright in the chair. He did not fall out of the chair, and remained seated upright the entire time. I noted no skin color change, but a loss of consciousness for 15 seconds. He regained consciousness and was verbal. I checked his pulse and felt a radial pulse, while he regained consciousness. He continued breathing and I noted his chest rising and falling. I had RN take vital signs and that is what was charted on this consent. He was verbal and sat to the side and drank some water. He was alert and verbal and oriented to himself and where he was and what was going on. We contacted the vice principal, who notified the parents and let them know what had happened, but that he was fine. He returned to class with no further incidents while we were on site.


VAERS ID: 1786199 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-11
Onset: 2021-10-12
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2579B / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Hypotension, Immunisation, Lymphocyte count decreased, Lymphocyte percentage decreased, Nausea, Neutrophil count decreased, Neutrophil percentage increased, Pyrexia, Tremor
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Agranulocytosis (broad), Haematopoietic leukopenia (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Flu vaccine 2018. Low blood pressure; possible fever. No hospitalization/ER required.
Other Medications: Sertraline 50mg; Buspirone 22mg; Trazodone 50mg; Multivitamin; Probiotic vitamin
Current Illness: Stopped skin treatment 9/3/2021 (Accutane)
Preexisting Conditions: Depression, anxiety, migraines, skin inflammation (unspecified)
Allergies: Clarithromycin; Miconazole; Neosporin; Adhesive; fruit preserves; lactose intolerance
Diagnostic Lab Data: Blood pressure: 90/60. Fever: 99. Absolute Lymphocytes: 0.6. Absolute Neutrophil/Ab Lymph. Ratio: 13.1. Neutrophils: 88.8. Lymphs: 6.6.
CDC Split Type:

Write-up: At 02:30 pm on 10/12/21 (20 hours after the injections), I began shaking uncontrollably. I developed nausea and sever light headedness. The paramedics called, and I was taken to the hospital and admitted for fever and low blood pressure.


VAERS ID: 2695973 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-09
Onset: 2023-10-10
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lymph node pain, Lymph nodes scan abnormal, Lymphadenopathy
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Lymph nodes; Result Unstructured Data: Test Result:pain of underarm lymphnodes on R side
CDC Split Type: USPFIZER INC202300323838

Write-up: Swelling/pain of underarm lymphnodes on R side (same side as COVID vaccine administration).; Swelling/pain of underarm lymphnodes on R side (same side as COVID vaccine administration).; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 38-year-old female patient (not pregnant) received bnt162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), on 09Oct2023 at 16:30 as dose 1, single (Batch/Lot number: unknown) at the age of 38 years, in right arm for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX QUADRIVALENT), on 09Oct2023 at 16:30 as dose 1, single (Batch/Lot number: unknown), in left arm for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Pfizer biontech (DOSE 2, SINGLE), administration date: Apr2021, when the patient was 36 years old, for Covid-19 immunization; Pfizer biontech (DOSE 1, SINGLE), administration date: Mar2021, when the patient was 36 years old, for Covid-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 10Oct2023, outcome "not recovered" and all described as "Swelling/pain of underarm lymphnodes on R side (same side as COVID vaccine administration). ". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of lymphadenopathy, lymph node pain. Additional information: The patient did not have covid prior to vaccination, and covid was not test post vaccination. The information on the batch/lot number for bnt162b2 omi xbb.1.5 has been requested and will be submitted if and when received.


VAERS ID: 2696171 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-14
Onset: 2023-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031894 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8055MA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hot flush
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None reported
Preexisting Conditions: None reported
Allergies: None reported
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt received Fluzone Quad and Moderna Spikevax around 3pm. Pt stepped out of the room and a hot flash started within 5 minutes. The hot flash resolved after a few minutes of deep breathing and sitting down. No other intervention was required


VAERS ID: 2698702 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-19
Onset: 2023-10-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3032086 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7KA3T / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Electrocardiogram, Paraesthesia oral, Rash, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Simvastatin Allopurinol Lisinopril/hydrochlorothiazide fluticasone aspirin omega-3-acid ethyl esters
Current Illness:
Preexisting Conditions:
Allergies: phenothiazines
Diagnostic Lab Data:
CDC Split Type:

Write-up: 66-year-old male patient came in for seasonal flu vaccine and covid-19 vaccine appointment on 10/19/2023 at 10:00am. Patient received both doses, covid (left deltoid) at 10:01am and flulaval (right deltoid) at 10:04am and returned to his car where he decided to wait 30 mins before leaving. At 10:30am patient returned to the flu clinic to report rashes on both arms and tingling in his mouth/tongue. Patient was assessed by RN, RN, and myself RN Rashes were visible on both arms, two distinct areas of hives on his left elbow and hand. He also had one area of hives on his right wrist. Due to the ?tingling on tongue? as reported by the patient, we collectively decided to administer 0.3 mg of epinephrine injection per policy for administering epinephrine for anaphylaxis; given by RN at 10:40am in patients right thigh, patient remained stable. RN called urgent care and spoke to charge nurse, who informed me to ?call 911 per protocol.? Per the RN?s in the flu clinic it was recommended to the patient that we call 911 due to protocol. Patient agreed, 911 was called by RN and the ambulance arrived around 11:00am to the flu clinic. Patient report and snapshot of his chart was given to the paramedics by RN. Patient was assessed by paramedics where vitals were taken as well as two EKG?s. One paramedic called their base to inform their Dr. of situation. Dr. requested to speak with patient over the phone. Paramedic spoke with the Dr. to double check that patient needs to be transported to the hospital because he was given epinephrine. Paramedic informed patient that he will need to go to the emergency room for further monitoring. Patient declined ambulance transportation and opted to have his wife pick him up and bring him to nearest emergency room. Paramedics had patient sign a liability waiver that he was declining transportation via ambulance. RN signed waiver as a witness. Patient was brought via wheelchair to main entrance of the clinic by RN and was safely transferred to his wife?s car.


VAERS ID: 1795217 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-14
Onset: 2021-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Anxiety, Asthenia, Chills, Diarrhoea, Dysgeusia, Extra dose administered, Insomnia, Maternal exposure during breast feeding, Migraine, Nervousness, Pain, Photopsia, Pyrexia, Tremor, Vaccine positive rechallenge, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Retinal disorders (narrow), Neonatal exposures via breast milk (narrow), Noninfectious diarrhoea (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: same symptoms, but less intense and faster recovery after 2nd Pfizer COVID-19
Other Medications: post-natal vitamins, Omega 3 supplement
Current Illness: Had COVID-19 - positive test on 08/06/2021;
Preexisting Conditions: None
Allergies: NKDA; bee sting venom
Diagnostic Lab Data: No work up done. Stayed at home to convalesce. Pt is mostly recovered, by some symptoms persist - see above.
CDC Split Type:

Write-up: 10/14/21 at 10:30pm: body aches, unable to sleep, by 1am violent body chills and shakes (subjective fever), teeth chattering, feeling anxious and shaky; by 2:30am vomiting, diarrhea, migraine HA (when closed eyes, saw flashing), metal taste when not vomiting, felt very weak. Vomiting resolved by 5-6 am on 10/15/21, but the rest of the symptoms persisted throughout the weekend. As of today, still feels shaky and week, anxious, with periods of body chills/shakes. Patient was breast feeding during the time she received the third dose and with both of the prior Pfizer vaccine doses. The child had no symptoms after the first one, sick (fussy, crying, fever, decreased appetite) after second dose, and no symptoms after third dose.


VAERS ID: 1783065 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-01
Onset: 2021-10-04
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30145819 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Herpes zoster
SMQs:, Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatin, losartan, felodipine, citirizine HCl, aspirin, AREDS 2 preservision, calcium citrate, vitamin B complex, vitamin D
Current Illness: None
Preexisting Conditions: Coronary artery disease, diverticulosis, high blood pressure, osteopenia, migraine
Allergies: Penicillin, sulfa drugs
Diagnostic Lab Data:
CDC Split Type:

Write-up: Shingles outbreak, right shoulder, mild 3-4 lesions Outbreak started 3 days after immunization. Started Valacyclovir and continued 7 day treatment course.


VAERS ID: 1782724 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-08
Onset: 2021-10-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0185 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dysphagia, Flushing, Throat irritation
SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hypersensitivity (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 2033-Employee c/o an itchy throat, difficulty swallowing, feeling flushed. Rapid Response called to vaccine clinic. 2035-BP 178/112, HR 86, RR 16, Temp 97.7, O2 98% 2038-BP 178/114, HR 82, RR 16, O2 98% 2043-BP 182/119, HR 83, RR 16, O2 98% 2044-Rapid Response took employee to ER for further evaluation/monitoring. When the rapid response team reported back to the charge nurse of the vaccine clinic, he stated the employee did well once he was in the ED and was discharged approximately 15 minutes after arriving in the ED.


VAERS ID: 2699742 (history)  
Form: Version 2.0  
Age: 3.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-21
Onset: 2023-10-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5555B / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3X379 / N/A LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Interchange of vaccine products, Product administered to patient of inappropriate age, Vaccination error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: I am reporting vaccine administration error that occurred on 10/21/2023 patient was given the pediatric dose of the XBB Moderna vaccine today but patient previously received Pfizer vaccine series. since patient is under 5 years old no mix and match is allowed for this age group. parents were informed that PCP will be contacted .


VAERS ID: 1780454 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-04
Onset: 2021-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 308472 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dyspnoea, Extra dose administered, Wrong product administered
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Covid vaccine dose #4 given in error (pt was suppose to get flu shot + 1 covid 3rd dose), pt instead received 2 covid 19 vaccine and once rph realized error, pt received flu shot. Error occurred due to distraction and talking to patient. Rph followed up with patient next day and husband stated pt had some shortness of breath earlier but no problems (24 h later)


VAERS ID: 1779280 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-29
Onset: 2021-09-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Appendicectomy, Appendicitis perforated, Blood test, Computerised tomogram abdomen, Pyrexia, SARS-CoV-2 test negative
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Gastrointestinal perforation (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Nora-be (contraceptive) Iron Probiotic Zinc Vitamin-D Claritin
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: I had a COVID test (negative) and did blood work on 10/6. I had an abdominal CT scan on 10/7.
CDC Split Type:

Write-up: I started experiencing abdominal pain and fever on 10/1. I was told to take ibuprofen for the fever and Pepcid and Pepto Bismol for the abdominal pain. I was admitted to the hospital for an appendectomy on 10/8. The doctors found my appendix had completely ruptured.


VAERS ID: 2700383 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-23
Onset: 2023-10-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG2282 (NCAL HO / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8137AA (NCAL / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Dizziness, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Both vaccines administered at 2:02 pm, at approximately 2:05 pm patient said she is feeling dizzy and almost immediately experienced vasovagal syncope. Team Alert called and team monitored patient, vitals taken. Patient released after monitoring.


VAERS ID: 2702257 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-18
Onset: 2023-10-23
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4589 / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AU1064C / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lymphadenopathy
SMQs:, Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CholestOff, Fish Oil, Multivitamin, Acetaminophen, Ibuprofen
Current Illness: None
Preexisting Conditions: Exercise-induced asthma, benign microscopic hematuria
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Lymphadenopathy on left side of neck starting approximately 5 days after vaccination with both the Comirnaty (Pfizer 2023-2024 formula) COVID-19 vaccine and Afluria quadrivalent flu vaccine.


VAERS ID: 1777069 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-10
Onset: 2021-10-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2588 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT317KA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Paraesthesia
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Tingling of lower face area several hours post vaccination.


VAERS ID: 2705815 (history)  
Form: Version 2.0  
Age: 19.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-23
Onset: 2023-10-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU3912B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS NT2M9 / 1 LA / IM
SMALLMNK: SMALLPOX + MONKEYPOX (JYNNEOS) / BAVARIAN NORDIC FDP00013 / 2 RA / IM

Administered by: School       Purchased by: ?
Symptoms: Incorrect route of product administration, No adverse event
SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atropine Sulfate 1 % Ophthalmic SOLUTION
Current Illness: COLD SYMPTOMS, IMPROVING, AT TIME OF VACCINE
Preexisting Conditions: MYOPIA
Allergies: NKA
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: NO ADVERSE REACTION EXPERIENCED. PATIENT RECEIVED JYNNEOS #2 VIA THE INCORRECT ROUTE (WAS GIVEN IM INSTEAD OF SC). FOLLOWED UP WITH PATIENT 2 DAYS AFTER AND HE REPORTED NO INCREASED REACTION OR SIDE EFFECTS.


VAERS ID: 2707311 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-31
Onset: 2023-10-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4675 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8148KA / 1 LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS LL942 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Loss of consciousness, Nausea
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: TDAP - PT GOT THIS AT DR''S OFFICE A LONG TIME AGO. PT HAD VASOVAGAL SYNCOPE. BRAND NAME UNKNOWN. PT RECOVERED QUICKLY.
Other Medications: XANAX 0.25MG, KCL 10MEQ
Current Illness: NONE
Preexisting Conditions: ANXIETY
Allergies: NONE
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: PT PASSED OUT 1 MINUTE AFTER THE AREXVY. PT MENTIONED THAT HE WAS DIZZY AFTER THE TDAP SHOT MANY YEARS AGO, AND HAS A VASAL VAGAL RESPONSE. HE SAID HE STILL WANTED TO DO ALL 3 SHOTS AT THE SAME TIME - AREXVY, COMIRNATY, FLUZONE QUAD. I MADE SURE PT WASSTABLE - STABALIZED HIS HEAD AND NECK WHILE PT PASSED OUT FOR ABOUT 7 SECONDS IN THE CHAIR. PT CAME TO VERY QUICKLY AND SAT UP. WE GAVE PT BOTTLE WATER AND ICE PACK WRAPPED IN PAPER TOWEL TO HELP PT. PT SAID HE WAS NAUSEOUS ALSO, SO I LAID DOWN A SHEET ON THE FLOOR, WHERE HE LIED DOWN ON HIS BACK, THEN IN RECOVERY POSITION. PT SAID HE WAS OK, AND JUST NEEDED A WHILE TO LET THE NAUSEA AND DIZZINESS GO AWAY. PT SAID THIS HAS HAPPENED IN DR''S OFFICES BEFORE AFTER ANY PROCEDURE INVOLVING NEEDLES. WE MONITORED PT FOR 50 MINUTES - WE KEPT THE PT IN THE VACCINE ADMIN AREA FOR PRIVACY, AND I MONITORED THE PT. PT IS FEELING A LOT BETTER NOW. PT ALSO CALLED HIS WIFE, WHO IS A NURSE, WHO HAS A LOT OF EXPERIENCE WITH THE PT''S VASOVAGAL RESPONSE.


VAERS ID: 2707322 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-16
Onset: 2023-10-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH MRNA LNP-S / 6 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain upper, Atrial fibrillation, Brain fog, Cough, Diarrhoea, Dizziness, Dysgeusia, Dyspnoea, Flatulence, Headache, Hyperacusis, Oropharyngeal pain, Pain, Photophobia, Renal pain, Taste disorder, Weight decreased
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Supraventricular tachyarrhythmias (narrow), Pseudomembranous colitis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Cardiomyopathy (broad), Corneal disorders (broad), Retinal disorders (broad), Hearing impairment (narrow), Vestibular disorders (broad), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Ibandronate, Diltiazem, Pradaxa, Centrum vitamin, Calcium, Glu
Current Illness: none
Preexisting Conditions: AFIF, moderate kidney disease, prior breast cancer
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Headache, bodyache, sore throat, Severe AFIB, sensitive to light and sound, cough, stomach pains/gas, some diarrhea, kidneys hurt, dizziness, foggy head. Lost 8 pounds in four days. Everything I tried to eat was either too salty or too spicy, even though it would not normally be so. A couple days later, tried to shower, got dizzy and then was totally unable to get any breath in. That lasted for at lease 30 seconds.


VAERS ID: 1804474 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-15
Onset: 2021-10-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / N/A LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Fatigue, Feeding disorder, Inflammation, Pain, Pain in extremity, Pyrexia, Stomatitis
SMQs:, Severe cutaneous adverse reactions (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer dose 2 experienced fever, chills. body aches, nausea 03/13/2021
Other Medications: Propranolol 20 mg twice daily
Current Illness: None
Preexisting Conditions: Migraines
Allergies: Seasonal Allergies
Diagnostic Lab Data: None
CDC Split Type: vsafe

Write-up: I woke up the next morning with fever, body aches, sore arm, chills, and fatigue. Two day later, I developed painful sores along the roof of my mouth, and it became difficult to eat. I called my doctor and she believed it was an inflammatory response to the vaccine. She offered a medicine to reduce to reaction, but I declined. They finally went away after 4 days.


VAERS ID: 2564780 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Female  
Location: California  
Vaccinated: 2023-01-19
Onset: 2023-01-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS1417B / 2 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS CA52L / 2 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Febrile convulsion, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: vitamin D
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: High fever to 104 F. @ 5pm precipitating a simple febrile seizure of about 2 minutes.


VAERS ID: 1814906 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-03
Onset: 2021-10-13
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Angiogram cerebral normal, Anion gap decreased, Arteriogram carotid normal, Autoimmune disorder, C-reactive protein increased, CSF glucose increased, CSF protein increased, CSF red blood cell count, CSF white blood cell count, Computerised tomogram head normal, HIV test negative, Human herpes virus 6 serology negative, Lumbar puncture, Magnetic resonance imaging, Magnetic resonance imaging abnormal, Magnetic resonance imaging head abnormal, Meningitis, Mental status changes, Paraneoplastic syndrome, Perfusion brain scan normal, Pyrexia, Red blood cell sedimentation rate increased, Scan with contrast abnormal, Seizure, Toxic encephalopathy, Viral test negative, West Nile virus test negative
SMQs:, Torsade de pointes/QT prolongation (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Dementia (broad), Convulsions (narrow), Malignancy related conditions (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (narrow), Noninfectious meningitis (narrow), Cardiomyopathy (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: None
Allergies: NKDA
Diagnostic Lab Data: On admission: CT head, CTA Head and Neck, CT Perfusion, MRI w/o contrast shows no acute abnormalities. - MRI with contrast shows subtle FLAIR signal of cerebral cortex especially in region of temporal lobes, possibly inflammation - LP (10/14): CSF studies: 153 glucose, 105 protein, 6.9 AG, 0 RBC, 5 wbc''s - CRP and ESR elevated - Meningitis/encephalitis panel negative - Solu-medrol 1g daily; 5 doses completed on 10/20/21. - switch to PO Keppra 1500mg BID for seizures - Seizure precautions - HIV, HHV6, WNV PCR - negative. - Dr. (Stroke Neurology) consulted. Appreciate recommendations: - the patient can be discharged and will follow up with Dr. in 4 weeks.
CDC Split Type:

Write-up: Unknown Brand or lot numbers of Vaccines Patient had Covid booster shot (3rd injection) on October 5th along with getting Flu vaccine as well as Shingrex at an different facility, Admitted to Hospital on 10/13/21 with Diagnosis: Principal Problem: Acute metabolic encephalopathy Active Problems: Seizure (CMS/HCC) Altered mental status Fever Neurologic: Metabolic encephalopathy, secondary meningitis vs paraneoplastic vs autoimmune vs. Seizure vs post-vaccination


VAERS ID: 2566910 (history)  
Form: Version 2.0  
Age: 0.67  
Sex: Male  
Location: California  
Vaccinated: 2023-01-20
Onset: 2023-01-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS1417B / 2 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3K75S / 3 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: Ear infection Viral URI
Preexisting Conditions: none
Allergies: Amoxicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt was accidentally given a 3rd dose of Flu vaccine for this season. Parents notified Dr of the mistake the next day, medical assistants were unaware of the mistake the day it occurred. Dr counseled parents stating that the extra dose was safe for the patient and they may have a mild or normal vaccine response. Further investigation at beginning of the next week showed that miscommunication led to the extra dose being given. The manufacturer was contacted and parents were notified that the manufacturer had no other concerns to add. Mom stated that patient did not have any adverse reaction in the days following the vaccination.


VAERS ID: 1813879 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-21
Onset: 2021-10-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS N959G / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chills, Cough, Fatigue, Headache, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Both Covid Vaccine (Pfizer) Doses: 2/13/21 and 3/6/21 Age: 52 Symptoms: fever, chills. muscle pain, fatigue
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Symptoms: fever overnight, chills, fatigue, headache, muscle pain, some coughing Treatment: Tylenol


VAERS ID: 2580473 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: California  
Vaccinated: 2022-11-11
Onset: 2022-11-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 015H22A / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hypoaesthesia, Pain
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Omeprazole; Carvedilol; Multivitamin; Fish Oil; Eliquis; Slow FE; Aspirin; Vitamin D; Vitamin C; CoQ10; Turmeric; Atorvastatin
Current Illness: N/A
Preexisting Conditions: Heart Disease; Iron Count Low
Allergies: Penicillin; Codeine
Diagnostic Lab Data: N/A
CDC Split Type: vsafe

Write-up: After the vaccination, my right shoulder was feeling numb, and I had pain as well. I had motion in my arm it just didn?t feel good. It started to progress over to my shoulder and neck within a month. I went to the doctor, and she told me to go to physical therapy. I haven?t gone to many times to see progress.


VAERS ID: 2587281 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-16
Onset: 2022-11-21
   Days after vaccination: 340
Submitted: 0000-00-00
Entered: 2023-02-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 018F21A / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest pain, Dyspnoea, Dyspnoea exertional, Exercise tolerance decreased, Post-acute COVID-19 syndrome, Productive cough
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Infective pneumonia (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Lamotrigine; WELLBUTRIN; ZYRTEC; FLONASE; testosterone; magnesium; vitamin D; B complex
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Blood pressure medication; latex; ibuprofen
Diagnostic Lab Data: N/A
CDC Split Type: vsafe

Write-up: I had long COVID syndrome. I couldn''t breathe properly and couldn''t get enough air in my lungs. I was so winded from doing any activities in the house. I tried to exercise and I would get chest pain. When I tried to catch my breath or cough, I would cough up a watery substance. I went to the urgent care and they gave me an albuterol inhaler, cough syrup, and steroid pack.


VAERS ID: 2589964 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: California  
Vaccinated: 2023-01-27
Onset: 2023-01-28
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-03-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 046H22A / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2PC35 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cerebrovascular accident, Computerised tomogram head normal, Magnetic resonance imaging head abnormal
SMQs:, Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Vitamin C 1000 mg daily, Vitamin D3 125 mcg daily, aspiring 81 mg 3x per week, lions mane mushroom 500 mg daily, biotin 10k mcg daily, Vitamin B-complex 2x per week, lutein 40 mg daily, 600-1000 mg calcium daily, Vitamin B12 1250 mcg daily,
Current Illness: none
Preexisting Conditions: hypothyroidism
Allergies: penicillin, garlic
Diagnostic Lab Data: I had a CT Scan on Jan 28 that showed no stroke, however an MRI on Jan 31 showed a stroke in my left parietal lobe.
CDC Split Type:

Write-up: I had a combination COVID-19 and flu vaccination at 8 pm on Friday. At 2 pm on Saturday, I had a stroke.


VAERS ID: 1808758 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-22
Onset: 2021-10-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 2 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 - / IM

Administered by: Other       Purchased by: ?
Symptoms: Dizziness, Exposure during pregnancy, Headache
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Client takes zofran and prenatal vitamins
Current Illness: None reported
Preexisting Conditions: Anxiety, PTSD
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnant client. 22 weeks pregnant. Due date is 02/22/2022.10 minutes after vaccination, the client reports feeling light headed. Client''s vitals stable. She sat in an anti-gravity chair for over 30 minutes. Client reported feeling well to drive herself home, but that she did have a slight headache.


VAERS ID: 1808235 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-01
Onset: 2021-10-01
   Days after vaccination: 30
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Arthritis, Magnetic resonance imaging, Meniscus injury, X-ray
SMQs:, Systemic lupus erythematosus (broad), Accidents and injuries (narrow), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Topicals for knee pain in both knees
Current Illness: N/A
Preexisting Conditions: Knee pain since 1st vaccine dose
Allergies: Fosamax
Diagnostic Lab Data: MRI X-Ray after 2nd dose; Torn meniscus; Arthritis in knee Appointment with doctor next week
CDC Split Type: vsafe

Write-up: Throbbing joint pain in both knees


VAERS ID: 1805989 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-20
Onset: 2021-10-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Immunodeficiency
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: healthy
Allergies: aspirin, penicillin, amoxycillin,statin shellfish, peppers, latex
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Flu shot -hives started after 3 hours. by 1230am itchy and swollen; hives on my left arm-vaccination site


VAERS ID: 1804732 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-13
Onset: 2021-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301458QA / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 524R7 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Injection site bruising, Oedema peripheral, Swelling, Tenderness
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Claritin
Current Illness: none
Preexisting Conditions: none
Allergies: n/a
Diagnostic Lab Data:
CDC Split Type:

Write-up: Flu vaccine and COVID-19 booster received on the same day, same arm (left). The following day the left side of neck down to the armpit were swollen and tender to touch. There was also bruising on the site of flu injection.


VAERS ID: 2708518 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-31
Onset: 2023-11-01
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Chills, Fatigue, Nausea, Pain, Pyrexia
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: all COVID-19 vaccines
Other Medications: Hydroxyzine pamoate Montelukast
Current Illness: NA
Preexisting Conditions: Asthma
Allergies: Lactose intolerant
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fever - 11/01 morning and still ongoing Chills - 11/01 pm and ongoing Tiredness - 11/01 morning and ongoing Body aches - 11/01 morning and ongoing Nausea - 11/01 pm and ongoing


VAERS ID: 2598602 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: California  
Vaccinated: 2022-05-06
Onset: 2022-06-04
   Days after vaccination: 29
Submitted: 0000-00-00
Entered: 2023-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 056A22A / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acupuncture, Aphasia, Epidural injection, Hypoaesthesia, Magnetic resonance imaging spinal abnormal, Pain in extremity, Scan normal, Spinal X-ray abnormal, Spinal osteoarthritis, Transient ischaemic attack
SMQs:, Peripheral neuropathy (broad), Ischaemic central nervous system vascular conditions (narrow), Dementia (broad), Embolic and thrombotic events, arterial (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Amlodipine; losartan; famotidine; simvastatin; dorzolamide; latanoprost
Current Illness: N/A
Preexisting Conditions: High Blood Pressure; High Cholesterol; Glaucoma
Allergies: Penicillin
Diagnostic Lab Data: 13JAN2023 Spine X-ray, degeneration on the spine; 27JAN2023 MRI test, degeneration of the spine; 03FEB2023 Scan test normal.
CDC Split Type: vsafe

Write-up: I had a pain in my leg, like a pinch in my nerve, it got worst & worst. In October when it got worst, I went to the doctor. And I had therapy, acupuncture, X-ray, MRI. On Feb 2nd I had a TIA (mini stroke), transient ischemic attack, I had numbness in my leg and arm and difficult speaking. I went to the ER and had a lot of tests. I have been with a Cardiologist. I will get an epidural to deal with the pain on my leg.


VAERS ID: 2600265 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: California  
Vaccinated: 2022-09-17
Onset: 2023-02-07
   Days after vaccination: 143
Submitted: 0000-00-00
Entered: 2023-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9694 / 5 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS J2K2C / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Condition aggravated, Exposure to SARS-CoV-2, Fatigue, Headache, Lichen sclerosus, Nasopharyngitis, Oropharyngeal pain, Productive cough, Rhinorrhoea, SARS-CoV-2 test positive, Throat irritation
SMQs:, Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamin; WELLBUTRIN
Current Illness: N/A
Preexisting Conditions: Lichen Sclerosus
Allergies: N/A
Diagnostic Lab Data: 06FEB2023 COVID-19 test negative; 07FEB2023 COVID-19 test positive
CDC Split Type: vsafe

Write-up: I was exposed to COVID-19 on Sunday. I started feeling symptoms on Monday of scratchy throat, mild headache, and tiredness. I tested negative on Monday, but I retested on Tuesday and was positive. My sore throat was worse on Tuesday with a more intense headache, and runny nose. I contacted my doctor to try to get PAXLOVID, but they couldn''t prescribe it to me at the time. My headache and sore throat went away after a couple of days. I just had a severe runny nose and head cold symptoms. I also kept coughing up phlegm although I didn''t have chest pain. Although my symptoms went away, I was still extremely exhausted two weeks after that. I also had a pretty severe break out with my lichens sclerosis.


VAERS ID: 2603443 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-22
Onset: 2023-03-19
   Days after vaccination: 178
Submitted: 0000-00-00
Entered: 2023-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 4 AR / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / N/A AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Alcohol test, Analgesic drug level, Anxiety, Electrocardiogram, Full blood count, Hallucination, Iron deficiency anaemia, Liver function test, Metabolic function test, Smoke sensitivity, White blood cell count
SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Keppra; Dilantin; Ibuprofen: Vita fusion Multi Vitamins; Airborne; Vitamin C Gummy
Current Illness: Seizures
Preexisting Conditions: Seizures for two years
Allergies: N/A
Diagnostic Lab Data: Acetaminophen; Alcohol Test; Basic Metabolic panel (MET 10 ) CBC Diffractal; Liver Panel; Salicylate; EKG 12 leads
CDC Split Type: vsafe

Write-up: He was diagnosis on March 6, 2023 with anemia and they added vitamin D3 and iron to his medication. March 19, 2023, he was taking by ambulance to the hospital. They diagnosis him with hallucination and anxiety. They also said he should avoid smoke because it may be a trigger to the seizure.


VAERS ID: 2603461 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-01
Onset: 2022-01-01
   Days after vaccination: 61
Submitted: 0000-00-00
Entered: 2023-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8731 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 7R9NM / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acoustic stimulation tests abnormal, Deafness, Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: - sertraline (ZOLOFT) 100 mg tablet; Take 1.5 tablets by mouth Daily. Dispense: 180 tablet; Refill: 1 - atorvaSTATin (LIPITOR) 40 mg tablet; Take 1 tablet by mouth Daily. Dispense: 90 tablet; Refill: 1 - buPROPion (WELLBUTRIN
Current Illness: None
Preexisting Conditions: Fibromyalgia, asthma, fatty liver disease, spinal stenosis, insomnia, generalized anxiety disorder
Allergies: Penicillin and codeine
Diagnostic Lab Data: hearing test shows high frequency hearing loss
CDC Split Type:

Write-up: tinnitus both ears


VAERS ID: 2609529 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-03
Onset: 2023-02-19
   Days after vaccination: 139
Submitted: 0000-00-00
Entered: 2023-04-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ6665 / 4 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR N/A / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, COVID-19, Myalgia, SARS-CoV-2 test positive
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: Microvalve Prolapse
Allergies: N/A
Diagnostic Lab Data: 02/22/2023 - test COVID-19 Positive
CDC Split Type: vsafe

Write-up: I had my vaccination on 10/03/2022. I started to experience extreme muscle and joint aches and pains on 02/19/2023. I tested COVID-19 Positive on 02/22/2023. I contacted my physician on 02/24/2023 and was stated because my case was mild. I was not prescribed Paxlovid.


VAERS ID: 1801006 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-14
Onset: 2021-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / ID

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Extra dose administered, Headache, Lymphadenopathy, Malaise
SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: COVID Pfizer 2nd dose
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Sulfa Medications MSo4
Diagnostic Lab Data:
CDC Split Type:

Write-up: swollen lymph nodes, headache, sore joints, malaise


VAERS ID: 2620852 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-21
Onset: 2022-12-01
   Days after vaccination: 41
Submitted: 0000-00-00
Entered: 2023-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 060F22A / 5 - / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Blood test, CSF test, Fatigue, Hypoaesthesia, Laboratory test, Lumbar puncture, Magnetic resonance imaging, Nerve conduction studies, Pain, Pyrexia
SMQs:, Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Flu shot at same time as covid vaccine. omerprazole dr 40 probiotic
Current Illness: None
Preexisting Conditions: GERD
Allergies: amoxicillin, penecillin
Diagnostic Lab Data: I went to my Chiropractor, who sent me to my primary care Dr., Then to the Emergency room. MRI preformed. then referred to a Catalyst Neuromedial Center. Labs, blood tests, MRI''s, nerve testing & spinal tap and spinal fluid testing.
CDC Split Type:

Write-up: the day Moderna & Flu shot I was very sore tired and feverish. I had never had a reaction this sever with the 4 prior Moderna Covid 19 Vaccinations. After this my Left Leg started to go numb also my pinky fingers on both right and left hands. in December 2022 my entire saddle area went numb and my left foot on top of the already numb areas I had. No outcome. Just come back in 1 year unless symptoms worsted. No answers.


VAERS ID: 1798081 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-11
Onset: 2021-10-14
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest pain, Dyspnoea, Heart rate increased
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient reports getting both vaccines in same arm on 10/11/2021. Patient reports needing to go to the hospital on 10/14/2021 due to increased heart rate, chest pain, and difficulty breathing.


VAERS ID: 2687220 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: California  
Vaccinated: 2023-09-25
Onset: 2023-09-27
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-09-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 7+ RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: fatigue and arm pain. moderna covid vaccine.
Other Medications: Yes
Current Illness: No
Preexisting Conditions: Heart
Allergies: No
Diagnostic Lab Data: No
CDC Split Type:

Write-up: I threw up 2 days later. Fatigue.


VAERS ID: 1795776 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-14
Onset: 2021-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 007C214 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain upper, Chills, Fatigue, Myalgia, Pain, Pyrexia, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Eliquis, lamictal, lamotrogene, gabapentin, chlorozoxazone, b-12, iron, d-3
Current Illness: N/A
Preexisting Conditions: Lupus, Back, knee, and hip pain Prothrombin factor 2
Allergies: Reglan, bupronephine,
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Fever, chills, vomiting, stomach pain, general pain and muscle pain, fatigue


VAERS ID: 2743254 (history)  
Form: Version 2.0  
Age: 86.0  
Sex: Female  
Location: California  
Vaccinated: 2024-01-13
Onset: 2024-01-26
   Days after vaccination: 13
Submitted: 0000-00-00
Entered: 2024-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Gait disturbance, Vertigo
SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Vestibular disorders (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamins
Current Illness: None.
Preexisting Conditions: A-fib.
Allergies: None.
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: She got her vaccines, had no problems. Then about 10 days later in the evening after dinner she started to feel dizzy and it was like a merry go round without any flooring. She stayed put on the sofa but eventually she had to go to the bathroom. Then continued. She canceled her eye APT on the 30th, as she was not steady and did not want to fall. Yesterday evening she had dizziness, but most of the time it comes in the morning. She hasn''t had any dizziness in the morning today. Yesterday morning she still had some. She had contacted the doctor because she did not know if it was related to her BP, and he did not respond or call her back. She then got worried and a friend told her to write down what she had done day by day and then realized that possibly due to the vaccine. Then read the AE and believes it''s related to this.


VAERS ID: 2721376 (history)  
Form: Version 2.0  
Age: 0.67  
Sex: Male  
Location: California  
Vaccinated: 2023-11-29
Onset: 2023-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5551B / 1 RL / IM
DTPPVHBHPB: DTAP+IPV+HIB+HEPB (VAXELIS) / MSP VACCINE COMPANY U7296AA / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 99R27 / 1 LL / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH HA2258 / 3 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Cyanosis, Lethargy, Oedema peripheral, Pyrexia
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: IBUPROFEN
Current Illness: FEVER , VIRAL URI
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data: PARAMEDICS EVALUATION, IBUPROFEN
CDC Split Type:

Write-up: PERIPHERAL EXTREMITY EDEMA, CENTRAL ACROCYANOSIS, FEVER, LETHARGY


VAERS ID: 1736016 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: California  
Vaccinated: 2021-09-25
Onset: 2021-09-26
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-09-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Headache, Injection site pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Headache, fever, soreness at injection site, fatigue beginning at 0100. Managed with rest, fluids, and ibuprofen.


VAERS ID: 2726829 (history)  
Form: Version 2.0  
Age: 1.08  
Sex: Male  
Location: California  
Vaccinated: 2023-12-19
Onset: 2023-12-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 3 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8219JA / 2 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Unknown
Preexisting Conditions: Food allergy- eggs
Allergies: Eggs
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient was administered expired; vaccine expiration date sticker 12/18/2023, given 12/19/2023


VAERS ID: 1728836 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-20
Onset: 2021-09-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 049E21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ747AB / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Diarrhoea, Dizziness, Fatigue, Malaise, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: asthma, mild copd
Allergies: nkda
Diagnostic Lab Data:
CDC Split Type:

Write-up: That evening after getting both injections patient started feeling unwell. Patient was fatigued and dizzy the next day following immunizations. Mild fever for about 6 to 8 hours. Vomiting and diarrhea was also present. Patient went to emergency room on wednesday. Discharged with anti-nausea and anti-diarrhea medications.


VAERS ID: 1719569 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Male  
Location: California  
Vaccinated: 2021-09-14
Onset: 2021-09-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0191 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 49LC5 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Loss of consciousness, Tremor
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatin Bisoprolol Aspirin Folic Acid Niacin
Current Illness:
Preexisting Conditions: History of Myocarditis History of Heart Failure
Allergies: Nimesulide Ketoprofen
Diagnostic Lab Data: HR 60 Sat 99 BP 130/94. BP lowered to 118/64 after 15 minutes rest lying down.
CDC Split Type:

Write-up: Vaccine administering nurse observed 5-15 second loss of consciousness along with mild tremors all over body. Did not collapse on floor from chair; did not bite tongue or urinate.


VAERS ID: 1716926 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Male  
Location: California  
Vaccinated: 2021-09-20
Onset: 2021-09-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7316MA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Fall, Head injury, Loss of consciousness, Skin laceration
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hostility/aggression (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none known
Current Illness: none known
Preexisting Conditions: none known
Allergies: none known
Diagnostic Lab Data:
CDC Split Type:

Write-up: After receiving vaccines, patient was directed to sit in designated post-immunization observation area for 15 minutes. While seated, patient became light-headed and lost consciousness, causing him to fall from his chair to the floor. He regained consciousness within moments and experienced no additional symptoms. In course of falling from the chair, patient sustained a head injury, causing a minor scalp laceration. Paramedics were summoned. Patient declined transport to medical facility, and was urged to seek follow-up care for the injury to his head.


VAERS ID: 2728344 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-20
Onset: 2023-10-28
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2023-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031419 / 6 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8076LA / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Condition aggravated, Headache, SARS-CoV-2 test negative
SMQs:, COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: See discussion in block 18 and continuation
Other Medications: topamax
Current Illness: None
Preexisting Conditions: None, see block 18
Allergies: Shellfish
Diagnostic Lab Data: MRI, April 2022 negative
CDC Split Type:

Write-up: I have been experiencing headaches, since ~ January 2022 - this would have been shortly after my 3rd COVID shot (all 3 were Moderna). They seem to be a cough or extertional pressure headache, somewhat mitigated by Topamax. Since Dec of 2021, I have had 2 boosters of Pfizer, and then most recently a booster of Moderna. Eight days after this most recent booster, my head really seemed to "fill up", and the headaches got quite severe for a few days, then subsided to a more controlled level, where they remain. I am wondering if you have had this reported by anyone, and if there is any association with the vaccine (inflammatory response?). Further, in December of 2022, I started developing a cough. Right around Christmas of 2022, my husband developed COVID-19 (note, my most recent boosters prior to this #4: 4/12/22 and #5: 10/19/22, both Pfizer). I tested repeatedly for COVID, but never tested positive. Instead, I had this cough that became worse over time. It persisted into January and I couldn''t get rid of it. Finally, I went to the doctor and she told me I had asthma. I was shocked. I had never had asthma before. I was on a steroid inhaler (Alvesco) for months, and finally was back to normal in late spring. So, I am wondering ? could the asthma have been cause by an inflammatory response to the vaccine or a response to an exposure to the virus? I was fine until early August, when I went to a movie theatre where I think I may have been exposed to COVID. The asthma returned and I was back on an inhaler, but just for a month this time. Then, I got a booster vaccination in October (Moderna, discussed above), and the very strange thing happened with my head and my headaches. So, I am wondering: 1) Has anyone else ever reported any issues like this before? 2) Are the headaches and the asthma just a coincidence in timing with the vaccinations? 3) Do I continue to get COVID vaccinations and just try to manage the headaches and the asthma (whether they are related or not)? 4) Do I avoid further COVID vaccination due to potential severe effects (if I weren''t managing my headaches with the Topamax, I''m wondering what would have happened to my head due to the pressure ? of course, that assumes? the pressure was caused by an immune/inflammatory response to the vaccine)? As an interesting additional point, to my knowledge, I have never had COVID-19 (no doubt, thanks to my immunizations). Thank you for your thoughts.


VAERS ID: 1709679 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-14
Onset: 2021-09-15
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-09-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 048F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Feeling hot, Rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NO
Preexisting Conditions: NONE
Allergies: SULFA AND CODEINE
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: RED, WARMTH, RASH


VAERS ID: 2731660 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: California  
Vaccinated: 2024-01-11
Onset: 2024-01-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031895 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8144JA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: N/A
Preexisting Conditions: None
Allergies: No known allergies
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient had 1 vaccine for Spikevax on her left arm and then experienced syncope for approximately 5 seconds after her second vaccine (Fluzone Quad) on her right arm. She remained in her seat, didn''t injure herself and initially felt light headed. She also vomited and stated that previously had history of syncope due to menstrual cramps which she is currently on day 3 of. She recovered, had no further symptoms, and able to leave after 15 minutes.


VAERS ID: 2733111 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-11
Onset: 2023-10-16
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2024-01-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 7+ - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Bronchoscopy abnormal, Chemotherapy, Death, Endotracheal intubation, Imaging procedure abnormal, Lung cancer metastatic, Lung opacity, Metastases to central nervous system, Pneumonia, Pneumonitis, Respiratory failure, Tracheostomy
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Interstitial lung disease (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (narrow), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Non-haematological malignant tumours (narrow), Infective pneumonia (narrow), Hypokalaemia (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2023-11-23
   Days after onset: 38
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 38 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Lung cancer
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received his flu shot and 7th dose of COVID vaccine on 10/11/2023. He had underlying diagnosis of lung cancer. On 10/16/2023, he presented to the hospital with hypoxic respiratory failure with lung opacities on imaging consistent with diffuse pneumonitis. He was intubated and initial bronchoscopy result was negative for infection. Patient was given empiric antibiotics, steroids and a trial of chemo. He had prolonged intubation and eventually developed ventilator associated pneumonia and required tracheostomy placement. Patient''s cancer progressed and he developed brain metastasis. Given the overall poor prognosis with no good assurance of quality of life, family opted for comfort care and he passed away on 11/23, after 38 days in the hospital.


VAERS ID: 2741973 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Male  
Location: California  
Vaccinated: 2024-01-29
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2024-01-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 8057658 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS XA4K5 / 2 LA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS 9R5LC / 1 LA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X021284 / 1 LA / SC

Administered by: Public       Purchased by: ?
Symptoms: Incorrect dose administered, Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: Pollen - seasonal allergies
Diagnostic Lab Data: NA
CDC Split Type:

Write-up: Child was administered 0.5cc IM of Spikevax. Parents notified. Parents contacted again 17 hrs later - child in good health and constitution. Besides tender arm no other side effects reported. Parent to call if any concerns.


VAERS ID: 1745725 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Male  
Location: California  
Vaccinated: 2021-09-27
Onset: 2021-09-29
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-09-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FDO809 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ694AB / 1 - / IM

Administered by: Public       Purchased by: ?
Symptoms: Extra dose administered, Interchange of vaccine products, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: blood thinners, and unknown
Current Illness: none known
Preexisting Conditions: heart failure
Allergies: no known allergies
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received a third dose of the Covid vaccine. His first two vaccines were Moderna. On 9/27 he was given a Pfizer additional dose by mistake. He was called and he is having no side effects that are out of the ordinary.


VAERS ID: 1939158 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-03
Onset: 2021-09-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939902 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A92G / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Loss of consciousness, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: WITHIN 5 minutes of BoTh vaceinations , patient fainteD to flooR. RegaineD consciousness after a Few seconds (approx). patient states she Doesn''t think she hit any- thing on way Down DenieD amBulance , was proviDED wateR.


VAERS ID: 2744517 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-09
Onset: 2022-11-01
   Days after vaccination: 23
Submitted: 0000-00-00
Entered: 2024-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ3275 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ918AB / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Albumin globulin ratio normal, Alpha 1 globulin normal, Alpha 2 globulin normal, Amino acid level increased, Antineutrophil cytoplasmic antibody negative, Antinuclear antibody, Antinuclear antibody negative, Antinuclear antibody positive, Beta globulin normal, Biopsy skin normal, Blood albumin normal, Blood parathyroid hormone normal, Borrelia test negative, Burning sensation, C-reactive protein increased, Electrophoresis protein normal, Globulin, Heavy metal normal, Histology normal, Laboratory test normal, Magnetic resonance imaging head normal, Magnetic resonance imaging normal, Magnetic resonance imaging spinal normal, Pain, Red blood cell sedimentation rate normal, Rheumatoid factor negative, Skin burning sensation, Sleep disorder, Treponema test negative, Vitamin B1, Vitamin B12 increased, Vitamin B6
SMQs:, Peripheral neuropathy (broad), Systemic lupus erythematosus (narrow), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: synthroid, escitalopram, Vitamin D, E, C, Mg, Ca,
Current Illness: none
Preexisting Conditions: Hashimoto''s thyroiditis
Allergies: penicillin, sulfa
Diagnostic Lab Data: 12/29/22: ANA direct, neg, CRP 25 2/6/23: MRI of brain, cervical, thoracic and lumbar spine all negative 3/10/2023: SPEP T protein 6.7, Albumin 3.7, alpha 1 glob 0.2 alpha 2 glob 0.8, Beta glob 1.1, gamma glob 0.9 M spike not observed, glob T 3.0, A/G Ratio 1.2 sjogrens (-) Rheumatoid factor (-) heavy metals (-) methyl malonic acid 130 CRP < 1 ESR 2 6/8/23: ANCA profile (-) sjogrens AB, Anti-SS-A & SSB all (-) Lyme disease serum (-) Syphillis non-reactive 9/8/23: skin biopsies x 3 areas: all normal for phosphorylated alpha-synuclein, intraepidermal nerve fibers, amyloid deposition & skin histology 11/6/23: ANCA profile (-), ENA RNP antibodies < 0.2, smith antibodies < 0.2 B6 160.6, B1 118.8, B12 1,193, PTH 25
CDC Split Type:

Write-up: 1. In late October, early November 2022: Started experiencing acute bilateral stinging/burning sensation to scalp, face, arms, torso, legs 24 hours/day, worse in the evenings, disrupting sleep. 2. Referred by PCP to neurosurgeon due to history of nerve root decompression at C5-6 and C6-7. Started gabapentin 300 mg at HS, ordered MRI. 3. 2/21/23: Saw neurologist, who ordered labs 4. 3/16/23: Neurosurgery f/u: stated MRI results were negative, increased gabapentin to 600 mg at HS, referred to rheumatologist for possible autoimmune neuropathy 5. 6/8/23: Rheumatologist ordered prednisone 40 mg daily x 2 weeks, then taper x 1 week (taper completed 7/1/23). Symptoms ceased completely, then returned on 7/7/23. 7/11/23: Rheumatologist gave Kenalog 80 mg IM & started Plaquinil PO. 10/11/23: Plaquinil stopped due to lack of improvement & (+) side effects.


VAERS ID: 1658633 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated: 2021-08-31
Onset: 2021-08-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-08-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 017E21A / 1 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Burning sensation, Dyspnoea, Pruritus, Wheezing
SMQs:, Anaphylactic reaction (narrow), Angioedema (broad), Asthma/bronchospasm (broad), Peripheral neuropathy (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Claritin, albuterol
Current Illness: None
Preexisting Conditions: Asthma
Allergies: Pulmacort, Qvar, Advair, Beta Blockers, white fish, apples, bananas, latex, carrots
Diagnostic Lab Data:
CDC Split Type:

Write-up: Burning and itching down right arm, then up right side of neck, difficulty breathing, wheezing.


VAERS ID: 2748471 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-27
Onset: 2023-11-07
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2024-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Aortic dissection, Cardiac operation, Transfusion
SMQs:, Cardiomyopathy (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Levothyroxin, birth control, Adderall
Current Illness: None
Preexisting Conditions: Turner Syndrome
Allergies: Augmentin
Diagnostic Lab Data: Open-heart surgery (performed the morning of 11/08/2023), 18 blood transfusions, etc.
CDC Split Type:

Write-up: Class-A aortic dissection repaired through open heart surgery. I survived, but only because I got to the hospital in time. I had no symptoms before, and previous echocardiograms were normal.


VAERS ID: 2748519 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: California  
Vaccinated: 2024-02-21
Onset: 2024-02-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 8057658 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4XY5D / 1 RA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS G79C4 / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. X014788 / 1 LA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR W1C751M / 4 RA / SC
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. X007586 / 1 LA / SC
MNQ: MENINGOCOCCAL CONJUGATE (MENVEO) / NOVARTIS VACCINES AND DIAGNOSTICS BL3ES / 1 RA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X021284 / 1 - / SC

Administered by: Public       Purchased by: ?
Symptoms: Lip dry, Loss of personal independence in daily activities, Pallor, Posture abnormal, Retching, Skin discolouration, Vomiting
SMQs:, Acute pancreatitis (broad), Dementia (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Unknown.
Preexisting Conditions: Unknown
Allergies: Per vaccine screening form, not allergic to any vaccine products.
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: I was vaccinating a 15 year old female client with her father present in vaccine room. She received 8 vaccinations and within about 2 minutes after receiving them, started to appear pale and some green general coloration of her skin on her face. I immediately had her elevate her feet on a nearby stool and had her dad support her on her right side, with his arms. She stayed upright the entire time. Father stood next to her the entire time. I asked her if she was ok, and she said yes. I left the room to grab some apple juice for her to drink. She was having difficulty poking the straw through the hole of the juice box, and started to appear to close her eyes and drop her head slightly. I grabbed her juice box for her, poked the straw in and brought it to her lips to drink. Her lips looked dry, ashen and pale. She took a sip and immediately her face turned a light red as her circulation seemed to be improving. Then she made a gagging motion with her mouth and I brought a trash can close and she vomited twice. I gave her water next, and instructed her to take small slow sips. She vomited again and then stopped. She was conscious the entire time, no vitals were taken. She was responsive to all my verbal commands. She rested with me for another 10 minutes. All her color returned to her face. I explained the vaccine record to her father, gave him an Resource Guide and how to get resources and walked her and her father to the lobby. After I walked the client to the lobby and left her to hand-off with Registration staff. I advised she did not need to stay in the clinic any longer. I confirmed they had no more questions, father and daughter verbalized understanding and I walked away. Client appeared alert and verbal when I left.


VAERS ID: 2751303 (history)  
Form: Version 2.0  
Age: 4.0  
Sex: Female  
Location: California  
Vaccinated: 2024-02-20
Onset: 2024-03-02
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2024-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 - / IM
DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 3 - / IM
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. - / 2 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Febrile convulsion, Influenza virus test negative, Respiratory syncytial virus test negative, SARS-CoV-2 test negative
SMQs:, Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: not ill during vaccination
Preexisting Conditions: none
Allergies: none known
Diagnostic Lab Data: flu/covid/rsv negative
CDC Split Type:

Write-up: patient presented 12 days after 4 year well child check including MMRV, DTAP-IPV, flu vaccine and covid with simple febrile seizure


VAERS ID: 2752787 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: California  
Vaccinated: 2023-11-20
Onset: 2023-11-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8203EA / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age, Product storage error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt received Covid vaccine HH3252 - 3mcg/0.3mL 6mo-4yrs. Patient should have received 12+ dose.


VAERS ID: 1592320 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: California  
Vaccinated: 2021-08-16
Onset: 2021-08-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-08-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 045B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ685AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lip swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: amlodipine-benazepril 5-20mg, vitamine d3 50000units, ventolin HFA
Current Illness: no
Preexisting Conditions: no
Allergies: nka
Diagnostic Lab Data:
CDC Split Type:

Write-up: lip swollen


VAERS ID: 2753206 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Male  
Location: California  
Vaccinated: 2023-12-07
Onset: 2023-12-11
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2024-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030948 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8138DA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2023-12-11
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: No
Preexisting Conditions: no
Allergies: No
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient daughter states patient recieved Spikevax(Covid) vaccine and Fluzone HD(Flu shot) and 4 days later her father died


VAERS ID: 2753386 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: California  
Vaccinated: 2024-03-08
Onset: 2024-03-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU3918E / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8200AA / UNK LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. 1957404 / UNK LA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. W028734 / UNK LA / SC

Administered by: Private       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Bactrim
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given Spikevax instead of Moderna 6m-11yr formulation


VAERS ID: 2753738 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: California  
Vaccinated: 2024-03-07
Onset: 2024-03-08
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2024-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 210E23A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AU1060C / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Bacterial test positive, Cold sweat, Contusion, Cyanosis, Dizziness, Fall, Full blood count normal, Hypotension, Loss of consciousness, Metabolic function test normal, Mutism, Pallor, Red blood cells urine positive, Syncope, Urine analysis abnormal, White blood cells urine positive, X-ray limb normal
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Psychosis and psychotic disorders (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Chronic kidney disease (broad), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (broad), Hypokalaemia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Acetaminophen, Benzoyl Peroxide, Calcium Carbonate, Docusate Sodium, Magnesium Hydroxide, Naltrexone, Pramipexole, Risperidone.
Current Illness: Suspected UTI and dehydration.
Preexisting Conditions: Unknown
Allergies: no known allergies
Diagnostic Lab Data: 3/8/2024- CBC and CMP- unremarkable, urinalysis- elevated WBC, RBC, bacteria. XR-shoulder no acute osseous abnormality.
CDC Split Type:

Write-up: Patient was seen leaning on the wall by the nurse''s station and started to fall on the floor. She was observed very pale and mute, with circumoral cyanosis. Initial VS: BP 98/61 P 67/min RR 22/min O2 Sat 98% Temp 97%. Patient is oriented to time, place, person, situation. Glasgow coma scale 15. MD evaluated patient who started to become dizzy again, skin cold and clammy, looks very pale, VS at 0528 64/40, O2 Sat 98%. Patient is transferred to QVMC for further evaluation of loss of consciousness, hypotension. Discharge from hospital QVMC diagnosis: Syncope, Vasovagal; Contusion of Left Upper Extremity.


VAERS ID: 2716494 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Male  
Location: California  
Vaccinated: 2023-11-17
Onset: 2023-11-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031416 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8144LA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, Inappropriate schedule of product administration
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: Chest pain, unspecified, snoring, hypertension, obesity.
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient received two flu vaccines in a flu season.


VAERS ID: 2708797 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Male  
Location: California  
Vaccinated: 2023-11-01
Onset: 2023-11-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030949 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8130EA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Influenza like illness, Myalgia, Tremor
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: OMEPRAZOLE 40MG
Current Illness: K219 - ICD 10 Diagnosis Code - Gastro-esophageal reflux disease without esophagitis
Preexisting Conditions: K219 - ICD 10 Diagnosis Code - Gastro-esophageal reflux disease without esophagitis
Allergies: NONE
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: PT CALLED US AND REPORTED HAVING AE TO VACCINES. STARTING MIDNIGHT 12AM-3AM 11/2/23 - EXPERIENCED SHAKES FOR 30-45 MINUTES (LIKE SHAKES ASSOCIATED WITH FLU); ALSO EXP MUSCLE ACHES FOR 3 HOURS. DID NOT TAKE ANY MEDS FOR THE SX. - THIS MORNING, FEELING ALOT BETTER, ATE BREAKFAST - I ASKED IF THERE WAS ANYTHING WE CAN DO, AND HE SAID HE WAS FEELING BETTER, SO OK. HE JUST WANTED THIS TO BE RECORDED AND SENT TO VAERS


VAERS ID: 1770008 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-06
Onset: 2021-10-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0185 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / N/A RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Axillary pain, Chills, Lymphadenopathy, Tenderness
SMQs:, Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Intermittent chills, left axillary pain, tenderness and lymphadenopathy


VAERS ID: 1768411 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-29
Onset: 2021-09-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Chills, Extra dose administered, Headache, Injection site induration, Injection site mass, Injection site pain, Injection site pruritus, Injection site swelling
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: hx of Cellulitis of LE
Preexisting Conditions: unknown
Allergies: unknown
Diagnostic Lab Data: None
CDC Split Type:

Write-up: sx onset 9/30/21. Sx started with headache, chills, pain at injection site, warmth at injection site, burns, itching. Hard lump noted at injection site which progressed to swelling. Swelling spread to 4 inches above elbow.


VAERS ID: 1768190 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-04
Onset: 2021-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Myalgia, Pain, Pain in extremity
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Arm pain( muscle pain) and body ache.


VAERS ID: 2710609 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Female  
Location: California  
Vaccinated: 2023-11-06
Onset: 2023-11-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HD9876 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8192BA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Disorientation, Hypotonia, Loss of consciousness, Pallor, Unresponsive to stimuli
SMQs:, Torsade de pointes/QT prolongation (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (narrow), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: concerta
Current Illness: no
Preexisting Conditions: no
Allergies: none
Diagnostic Lab Data: Blood pressure 98/94 11/6/23
CDC Split Type:

Write-up: Patient loss conscientiousness after administration of second vaccine. Patient went limp in chair and was non response for 2 minutes. Then patient woke up and was pale and disoriented. After several minutes patient could respond to questions and was breathing normally. Color returned to patients face.


VAERS ID: 2710938 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-06
Onset: 2023-10-08
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Burning sensation, Ear pain, Facial pain, Hypersensitivity, Influenza like illness, Malaise, Pain, Paraesthesia
SMQs:, Angioedema (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Glaucoma (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 3rd COVID shot felt super sick, then went away in 3 days and was fine.
Other Medications: Zyzol, Singulair, Vitamin D, fish oil, Dyabred, Spironolactone; Famotadine, Ambien, Melatonin.
Current Illness: None.
Preexisting Conditions: Asthma, foot surgery 8/31/2023.
Allergies: Shell fish, NSAID''s, tree nuts, #red 40, yellow, cats, dogs, Pollen
Diagnostic Lab Data: None yet.
CDC Split Type:

Write-up: She got her vaccines, and she did not have a lot of reaction, just soreness as well as the day after just sore. Then she felt like she was getting the flu, had the sick feeling like something was coming on. It was not as bad as the other COVID shots. The next day is when her head was on fire, the base of her back by her ears hurt when she moved her eyebrows on the left side. She also had tingling down her arm. She feels it radiated to the right side but it goes all the way down to her left leg. It is just a tingling sensation. She does not know what it is. When she is in the shower the water hits her head and feel slike it is burning. When she rubs her hands across her thighs sometimes it is such a prickly sensation. Behind her left ear is sore. Within the next few days her armpit lymph node was huge on the left side. It just got so big, and then suddenly that went away. Eventually the pain in her arm and soreness went away. The tingling is still present and will not go away. Sometimes it felt like it was moving, didn''t feel like it was always only in the center of her head, sometimes if felt like it was a little more halfway down, but has stayed in the middle of her head. At the neck as well as behind her ear, it goes behind her jaw as well. It goes down her shoulders, top half of her arm, and then downward. She had a bunionplasty and ankle surgery on 8/31/23 and it was getting better and suddenly when the bunionplasty is is very super sensitive again and she does not know if this is the surgery itself, or maybe starting to go into other areas. She has contacted her doctor yesterday as she was on a virtual appointment with another doctor and he told her that it could be the COVID shot, and had no clue until she internet searched it and has an appointment to see her tomorrow.


VAERS ID: 2711506 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated: 2023-11-07
Onset: 2023-11-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031419 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8192BA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Deafness, Malaise, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hearing impairment (narrow), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Provider gave this patient two vaccines, Fluzone Quad and Spikevax. After getting the vaccines the patient reported feeling not well. Provider came to get me to tell me he patient wasn''t feeling well. I spoke to the patient and tried to calm her by taking deep breaths while sitting in the vaccine chair. She said she couldn''t hear me, I put both hands on her shoulder to keep her in the chair. She fainted in the chair and provider and I carefully moved her to the floor. As we were moving her to the floor she woke and quickly oriented herself. I had her still lay down ground and raised her legs.


VAERS ID: 2712775 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: California  
Vaccinated: 2023-11-11
Onset: 2023-11-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8097AA / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: PATIENT STARTED SHAKING 5 MINUTES AFTER BOTH VACCINES WERE GIVEN. PATIENT WAS GIVEN WATER AND RESTED IN VACCINE CHAIR AND WAS FINE


VAERS ID: 1761761 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-01
Onset: 2021-10-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0185 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Hypersomnia, Pyrexia, Rash
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: naltrexone, vitamin d, iron, zyrtec
Current Illness: MS, iron deficiency
Preexisting Conditions: MS
Allergies: bee venom, cipro, septra,
Diagnostic Lab Data:
CDC Split Type:

Write-up: Around 8:15/8:30p on 10/1/21 first 3 bumps seen on arm 6a 3 on leg and just kept coming, 10/2/21 3 bumps on stomach and upper back, around noon had fever 100.9, slept for 20 hours between noon and Sunday evening, 10/3/21 found 3 more on lower back and 3 on face, 10/4/21 7 new ones just on hands, 10/5/21 6a found 3 on face 1 on neck, 1 on right upper arm.


VAERS ID: 2715262 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-06
Onset: 2023-10-17
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2023-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4680 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AU 1060D / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Computerised tomogram thorax abnormal, Fibrin D dimer increased, Haemoptysis, Pleural effusion, Pleuritic pain, Pulmonary embolism, Pulmonary infarction, Scan with contrast abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhage laboratory terms (broad), Systemic lupus erythematosus (broad), Embolic and thrombotic events, venous (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: atorvastatin, tadalafil, Centrum Silver
Current Illness:
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data: As above.
CDC Split Type:

Write-up: Pleuritic chest pain started 11 days following vaccinations and hemoptysis 13 days following vaccinations, with markedly elevated D-dimer. Right lower lobe segmental and sub-segmental pulmonary emboli and pulmonary infarction with pleural effusion diagnosed by contrast CT. Enoxaparin 1 mg/kg SQ q12 X 2 dosed followed by standard dose apixaban loading doses and therapy. Full symptomatic recovery after 1-2 weeks.


VAERS ID: 1759496 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-04
Onset: 2021-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ742AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest discomfort, Hypoaesthesia
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Unknown
Preexisting Conditions: None listed
Allergies: Dye (IVP) per pt
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient stated chest tightness and her arm felt numb. started about 10 minutes after patient had vaccine.


VAERS ID: 1861834 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-02
Onset: 2021-11-03
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC 3183 / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS NK45F / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Chills, Headache, Hyperhidrosis, Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: WELLBUTRIN,BUSPAR,BYSTOLIC,CRESTOR,LOTREL,VALTREX,TAMSULOSIN
Current Illness: NONE
Preexisting Conditions: HIGH BP, ENLARGED PROSTATE,, DEPRESSION/ANXIETY
Allergies: PENICILLIN
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: FEVER 100.1-101.9, CHILLS, SWEATING, BODY ACHES, SLIGHT HEADACHE, LASTING 12-15 HOURS, BED REST. I TAKE ADVIL AND TRAMODOL FOR OTHER MEDICAL ISSUES. I DID NOT TAKE ADDITIONAL MEDICATION. FULL RECOVERY.


VAERS ID: 2716843 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-03
Onset: 2023-10-05
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030535 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UTB148KA / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Injection site pain, Pain, Pain in extremity, Sleep disorder, Weight bearing difficulty
SMQs:, Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metformin Cozaar Wellbutrin Famatodin
Current Illness:
Preexisting Conditions: PCOC Depression
Allergies:
Diagnostic Lab Data: Physiotherapist evaluation
CDC Split Type:

Write-up: Continued pain in my right arm and shoulder when I perform lateral motion, especially with some weight in my hand, like lifting a jug of milk or opening a heavy door. The pain is so strong that it wakes me up at night.


VAERS ID: 2718079 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-30
Onset: 2023-10-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 8057658 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5KT7B / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: NO ADVERSE REACTIONS OCCURRED.


VAERS ID: 2718083 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: California  
Vaccinated: 2023-10-30
Onset: 2023-10-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 8057658 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5KT7B / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: NO ADVERSE REACTIONS OCCURRED


VAERS ID: 1756828 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-30
Onset: 2021-10-02
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7H994 / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Computerised tomogram head, Facial paralysis, Hypoaesthesia
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Mirena IUD Hydro-chlorothiazide ibuprofen Cyclobenzaprine
Current Illness: unknown
Preexisting Conditions: HYPERTHYROIDISM HTN (HYPERTENSION) GRAVES DISEASE
Allergies: NKDA
Diagnostic Lab Data: CT head 10/2/2020
CDC Split Type:

Write-up: left sided facial numbness and droop


VAERS ID: 2719057 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: California  
Vaccinated: 2023-09-29
Onset: 2023-09-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4633 / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8148MA / N/A RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS TF3A9 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Condition aggravated, Magnetic resonance imaging ear, Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer-BioTech Covid-19 Bivalent booster on 11/7/2022 (lot # GJ6738). Age: 63. But the decibel level was so low that I really di
Other Medications: Rosuvastatin 10mg /day Metformin HCL 500mg/day Multi Vitamins Vitamin D3 - 10,000 iu Omega 3 - 2150mg Omega 3 - Krill oil - 240mg
Current Illness: None
Preexisting Conditions: Pre-Diabetic
Allergies: Penicillin
Diagnostic Lab Data: Going to do an MRI internal auditory canal and posterio fossa (wo contrast) on 12/4/2023
CDC Split Type:

Write-up: Ringing was probably started after the Pfizer BioNTech Covid-19 vaccine Bivalent booster on 11/07/2022 (Lot # GJ6738). But really didn''t even take notice of it until after the last booster (lot # HG4633) which was on 9/29/23. Ringing seems more to be in the left ear but really hard to distinguish left from right ear and basically it is a low ringing sound in my head. The ringing is 24/7.


VAERS ID: 2719089 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: California  
Vaccinated: 2023-09-29
Onset: 2023-10-04
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2023-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4629 / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Allergy test, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Allergy Tests
CDC Split Type:

Write-up: Random hives breakouts only on neck


VAERS ID: 2720278 (history)  
Form: Version 2.0  
Age: 2.0  
Sex: Female  
Location: California  
Vaccinated: 2023-12-01
Onset: 2023-12-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 4 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8202CA / UNK RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: None
Preexisting Conditions: None
Allergies: No Known Allergies
Diagnostic Lab Data: none
CDC Split Type:

Write-up: The pfizer 6months - 4 yeard old 2023-2024 formulation was administered 1 day past expiration date. Vaccine expired on 11/30/2023 and was administered on 12/1/2023


VAERS ID: 2720281 (history)  
Form: Version 2.0  
Age: 4.0  
Sex: Female  
Location: California  
Vaccinated: 2023-12-01
Onset: 2023-12-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8202CA / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: none
Allergies: No Known Allergies
Diagnostic Lab Data: none
CDC Split Type:

Write-up: The pfizer 6months - 4 yeard old 2023-2024 formulation was administered 1 day past expiration date. Vaccine expired on 11/30/2023 and was administered on 12/1/2023


VAERS ID: 1750027 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Male  
Location: California  
Vaccinated: 2021-09-27
Onset: 2021-09-28
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301308A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7316MA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Costochondritis, Electrocardiogram normal
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: FIBROMYALGIA
Allergies: NONE
Diagnostic Lab Data: EKG NORMAL ON 9/30/2021
CDC Split Type:

Write-up: Costochondritis (MID TO LEFT UPPER LEFT SECTION)


VAERS ID: 2720437 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: California  
Vaccinated: 2023-10-02
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2023-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Heart rate increased, Palpitations
SMQs:, Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Rapid heart rate palpitations


VAERS ID: 2485276 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-13
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT768MA / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Monovalent Covid vs Bivalent


VAERS ID: 2482621 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-18
Onset: 2022-10-01
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft, Buspar, Singular
Current Illness: None
Preexisting Conditions: Chronic Fatigue
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Broke out in hives on right hand


VAERS ID: 2482925 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: California  
Vaccinated: 2022-10-11
Onset: 2022-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 4 OT / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7733CA / UNK OT / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given Pfizer monovalent vaccine dose.


VAERS ID: 2303416 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-19
Onset: 2022-05-17
   Days after vaccination: 179
Submitted: 0000-00-00
Entered: 2022-05-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027H21B / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / SYR

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Chills, Cough, Feeling hot, Headache, Pain, Paranasal sinus discomfort, SARS-CoV-2 test positive, Sinus congestion, Upper-airway cough syndrome
SMQs:, Anaphylactic reaction (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamin
Current Illness: None
Preexisting Conditions: Medullary Sponge Kidney; Depression
Allergies: Penicillin
Diagnostic Lab Data: 05/17/2022 - At-Home COVID Test - Positive; 05/28/2022 - At-Home COVID Test - Positive; 05/31/2022 - At-Home COVID Test - Negative
CDC Split Type: vsafe

Write-up: Symptoms I experienced were head and body aches, alternating chills and overheating, sinus congestion and pressure, postnasal drip, and coughing. I did not have a fever at any point. I was prescribed by the doctor Paxlovid antiviral medication. That was a 5 day course and I started it on Thursday, May 19 through May 24. Unsure of the effects with or without the medication. I did experience a side effect from the medication, strong chalk or metallic taste in my mouth while taking the medication. I had symptoms for about two weeks. I still have some lingering symptoms today. Really at this point, lingering cough and congestion. The other symptoms have improved. I did retest using a home test this morning and it came back negative. Symptoms have improved, in recovery, but not 100% fully recovered.


VAERS ID: 2289926 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-01
Onset: 2021-09-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 LA / IM
DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Pemphigus
SMQs:, Severe cutaneous adverse reactions (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisinopril
Current Illness: none
Preexisting Conditions: hypertension
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pemphigus vulgaris


VAERS ID: 2482930 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Male  
Location: California  
Vaccinated: 2022-10-11
Onset: 2022-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 3 OT / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7PE77 / UNK OT / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given Pfizer monovalent vaccine dose.


VAERS ID: 1851337 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-08
Onset: 2021-10-13
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3590 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / N/A RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Asthenia, Biopsy lymph gland, Blood culture negative, Blood electrolytes normal, Chest X-ray normal, Decreased appetite, Differential white blood cell count normal, Discomfort, Dizziness, Fatigue, Full blood count normal, Hyperhidrosis, Lymphadenopathy, Myalgia, Nausea, Pyrexia, Thyroid function test normal, Visual impairment, White blood cell count normal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Eosinophilic pneumonia (broad), Retinal disorders (broad), Vestibular disorders (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Concerta, weaning off of Klonopin, Celexa, BCP, iron, B supplement, vitamin C, vitamin D, Biotin, Magnesium Citrate.
Current Illness: Hashimoto''s, asthma, swollen lymph gland being watched.
Preexisting Conditions: Hashimoto''s, asthma, chronic depression from PTSD.
Allergies: Codine makes me sick, do not eat gluten because I have Hashimoto''s.
Diagnostic Lab Data: CBC, blood culture for bacteria and fungus, chest x-ray, thyroid panel, white blood cell differential, electrolytes. All labs normal.
CDC Split Type:

Write-up: I had the booster vaccine on October 8th. I then had a lymph node biopsy on October 13th. Within a day or two, I had extreme fatigue, excessive sweating, random fevers, muscle aches, dizziness, seeing spots, nausea, loss of appetite, weakness, general discomfort, swollen glands all over my body, especially the left side where the biopsy was. It was described to me as an "autoimmune storm". No further testing has been done. I was prescribed Meloxicam. I needed to take two to feel close to "normal". A follow up phone visit with a different doctor suggested that I try to take just one tablet, but all the symptoms returned. I did that on 11/5/2021, but had to return to taking two. I am still recovering from that on 11/8/2021. I have been to work four non-consecutive days in the past month.


VAERS ID: 2277938 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-26
Onset: 2021-11-26
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2022-05-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 UN / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test abnormal, Type 1 diabetes mellitus
SMQs:, Hyperglycaemia/new onset diabetes mellitus (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: I now have type 1 diabetes. I started having symptoms about 1 month after my vaccination.
Allergies: Penicillin
Diagnostic Lab Data: Blood work completed 12/22/21 and in January to confirm it was type 1.
CDC Split Type:

Write-up: I don?t remember what kind of flu shot I had. I developed type 1 diabetes after having my 3rd Covid shot. I showed symptoms of diabetes about a month after vaccination and I was diagnosed in December 2021.


VAERS ID: 2482935 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-11
Onset: 2022-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 4 OT / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT7733CA / UNK OT / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given Pfizer monovalent vaccine dose.


VAERS ID: 1833382 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-01
Onset: 2021-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH F00809 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 499ZC / 5 RA / IM
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS F22EZ / 3 RA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS 2K57N / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. U007652 / 1 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U7190AA / 1 RA / IM
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS XK524 / 1 LA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. U015684 / 1 LA / SC

Administered by: Public       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient was only eleven years old and received Pfizer vaccine approved for ages 12 and older.


VAERS ID: 2307620 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-19
Onset: 2021-11-19
   Days after vaccination: 61
Submitted: 0000-00-00
Entered: 2022-06-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Chest X-ray, Computerised tomogram, Cranial nerve paralysis, Eye movement disorder, Headache, Laboratory test, Lumbar puncture, Magnetic resonance imaging head abnormal, Pupil fixed
SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Ocular motility disorders (narrow), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Metoprolol, Centrum Silver
Current Illness: None
Preexisting Conditions: Asthma
Allergies: Iodinated Diagnostic Agents, Cephalosporins, Singulair
Diagnostic Lab Data: MRI, CT, Labs, LP, EKF, CXR
CDC Split Type:

Write-up: Extreme headache, 3rd cranial nerve palsy with enhancement to 3rd cranial nerve seen on MRI causing right eye to closed, eye ball to turn outward and down, pupil fixed and dilated


VAERS ID: 2485278 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-13
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7682MA / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Monovalent Covid vs. Bivalent


VAERS ID: 2485790 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-27
Onset: 2021-11-01
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / IM

Administered by: Military       Purchased by: ?
Symptoms: Arthralgia, Drug hypersensitivity, Insomnia, Laboratory test normal, Pain, Rheumatoid factor negative
SMQs:, Angioedema (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Mericaprine, Ascol, Tumeric, Multi Vitamin, Biotin, Probiotic, Vitamin D, Fish Oil, HCI, prednisone,
Current Illness: None.
Preexisting Conditions: I have UC and take maintenance medicines for my condition.
Allergies: At the time of vaccination nothing. Now, penicillin products.
Diagnostic Lab Data: I had full lab work to check for gout and RA but the results came back negative. Anti uninflammatory drugs did not help much. Physical therapy has not help.
CDC Split Type:

Write-up: A couple of days after the Pizer Booster, my left hand and finger joints were EXTREMELY painful to move. 24/7 my left hand had zero relief from just day to day activities. On December 22 the same pain from my hand and finger joints moved to my right hand and finger joints. I had a hard time even sleeping, throbbing''s pain went through my hands. One year later I am better, but still have hand pain in both left and right. That is why I am contacting you today.


VAERS ID: 1851584 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-08
Onset: 2021-11-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3527 / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367896 / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient came in for flu shot. Technician went to administer shot.Technician states verbally verified Covid shot with pt. Covid shot was given. Upon review with patient error was discovered. Patient was upset but no adverse effects were noted. Patient was consulted and asked if still wanted flu shot. Patient did and flu shot was given also.


VAERS ID: 2271110 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-09
Onset: 2022-05-08
   Days after vaccination: 180
Submitted: 0000-00-00
Entered: 2022-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 034FZ1A / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Anosmia, COVID-19, Cough, Fatigue, Malaise, Nasal congestion, Oropharyngeal pain, SARS-CoV-2 test positive, Sneezing, Throat irritation
SMQs:, Anaphylactic reaction (broad), Taste and smell disorders (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad), Infective pneumonia (broad), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin B complex; vitamin D; fluvoxamine
Current Illness: None
Preexisting Conditions: Lower back pain
Allergies: None
Diagnostic Lab Data: Covid 05/10/22 positive.
CDC Split Type: vsafe

Write-up: Covid symptoms started on 05/08/22; tested positive on 05/10/22. First symptoms were sore throat and I would say maybe fatigue. The sore throat sort of started fading and was replaced by stuffy nose, sneezing, a little coughing from scratch in throat, and fatigue. Then today, I had stuffy nose, loss of smell, sneezing, and the sore throat is gone. First 2 doses were Pfizer.


VAERS ID: 2489994 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-26
Onset: 2022-10-19
   Days after vaccination: 23
Submitted: 0000-00-00
Entered: 2022-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ3277 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ918AA / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Body temperature increased, COVID-19, Cough, Fatigue, Nasal congestion, Rhinorrhoea, SARS-CoV-2 test negative, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prescriptions: Wixela inhalor, Linsinopril, Propranolol, Metformin, Glipiside, rosuvastatin, 81 mg aspirin, insulin N and R Over the counter: sudafed, ibuprofen vitamins: magnesium, multivitamin, D, B complex, C, E, Folic Acid, Omega 3-6-9
Current Illness:
Preexisting Conditions: diabetis
Allergies: none
Diagnostic Lab Data: Home covid test: 2--10/20/22, 1--10/21/22; all 3 positive Home covid test: 2-- 10/24/22, 1-- 10/25/22; all 3 negative
CDC Split Type:

Write-up: symptoms: nazel congestion, running nose, temp elevated by 1 degree, cough, tired, 3Positive covid tests over 2 days. Treatment: bedrest, fluids, Isolated from family outcomes: on day 5 felt better, 3 negitive covid test, will isolate till day 10.


VAERS ID: 1852049 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-08
Onset: 2021-11-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011D21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3P3TY / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, Interchange of vaccine products
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given Moderna Booster Vaccine instead of Flulaval vaccine, but patient wanted to get both at the end. Moderna was given by mistake but patient was due for a booster vaccine, had previously received Pfizer 2 doses, last dose in 04/2021.


VAERS ID: 2499547 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Female  
Location: California  
Vaccinated: 2022-11-01
Onset: 2022-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR9236B / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7751KA / 2 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: nkda
Diagnostic Lab Data:
CDC Split Type:

Write-up: No reactions to vaccines. Moderna vaccine was expired by 3 days.


VAERS ID: 2499947 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-25
Onset: 2022-10-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U7684DB / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received the monovalent Pfizer COVID-19 vaccine for their third dose instead of the bivalent vaccine.


VAERS ID: 2499966 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Male  
Location: California  
Vaccinated: 2022-10-25
Onset: 2022-10-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U7684DB / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given a monovalent Pfizer COVID-19 vaccine for their third dose instead of the bivalent Pfizer vaccine.


VAERS ID: 2427936 (history)  
Form: Version 2.0  
Age: 85.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-01
Onset: 2022-09-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011B22A / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ901AA / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatin, Amlodipine
Current Illness: Essential hypertension, Hyperlipidemia
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: On 9/01/2022 patient received expired Moderna with beyond use date of 8/26/2022.


VAERS ID: 2455706 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-16
Onset: 2022-09-19
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2022-09-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2C77G / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Rash, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Started with Rash on both feet 9/19/22 Diffuse urticaria w/o Respiratory Involvement.


VAERS ID: 2451486 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: California  
Vaccinated: 2022-09-15
Onset: 2022-09-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-09-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Balance disorder, Dizziness, Impaired driving ability, Loss of personal independence in daily activities, Nausea, Vertigo
SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: No
Preexisting Conditions: None
Allergies: Penicillin
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: Dose #1: 02/2021 Dose #2: 03/2021 Dose #3: 10/2021 Dose#4: 09/15/2022. After receiving Dose #4, I woke up the next day with considerable dizziness. As soon as I lifted my head off of the pillow, I felt the room spinning and extremely dizzy (almost nauseating). I rested my head back down immediately and closed my eyes until it passed (less than a minute). Slowly, I sat back up felt dizzy again so I closed my eyes and waited until it passed (still sitting up). I then stood up and nearly lost my balance, dizzy again. After a few minutes, I tried to get up again and slowly, I was able to do so, however, I kept feeling small bout of dizziness that were shorter in duration. I decided to stay home that day as I was afraid I would lose my balance and fall, much less, be able to drive. The next day, I woke up dizzy again and it lasted throughout the day-but much shorter in duration from onset to recovery (happens only after moving my head up from a rested position). As time progresses, I still feel dizzy but am able to drive and carry out my daily routine-albeit with short episodes of dizziness. With each day, I feel it is slowly resolving, very slowly. I am otherwise healthy, 5''3"; 144lbs and a mother of 3. No medications and live an active lifestyle; no major health related surgeries or physical trauma.


VAERS ID: 1843821 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated: 2021-05-28
Onset: 2021-10-29
   Days after vaccination: 154
Submitted: 0000-00-00
Entered: 2021-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 002C21A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 033C21A / 2 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 803523 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Chills, Cough, Malaise, Oropharyngeal pain, Pain, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: Covid rapid test on 11/4/2021
CDC Split Type:

Write-up: Sore throat, chills, aches, cough - all 4 days following flu vaccine. Went to urgent care on the 6th day after symptoms began and tested positive for covid-19.


VAERS ID: 1846714 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-03
Onset: 2021-11-04
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH PFIZER FE3592- / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK AR / SYR
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK AR / -

Administered by: Other       Purchased by: ?
Symptoms: Arthralgia, Diarrhoea, Headache, Inappropriate schedule of product administration, Insomnia, Nasopharyngitis, Pain, Pyrexia, Tremor, Vision blurred
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Aspirin, Vitamin D, Omega 3, Tramadol, Tylenol. Novolin, Atorvastatin,, ibuprofen, , oxybubutyn, proglitazone,prednisolone, ozempic, oxubutynin, pioglitazone,acemaminophen, vitamin c, Tylenol ,tumaric.
Current Illness: Back pain, numbness at r foot, light headache, low blood sugar.
Preexisting Conditions: Diabetic , cholesterol, high blood pressure
Allergies: No
Diagnostic Lab Data: N/A . Off work, sleep a lot to recover. Eat in small amounts of food to avoid nausea and vomiting and diarrhea. Drink a lot of water.
CDC Split Type:

Write-up: Fever, cold, can not sleep, diarrhea, shaking trembling , light headache, body ache, sharp pain in left shoulder, blurry vision on 2nd day. Take Tylenol, aspirin. Stop all other medicine. Blurry vision, on 2nd day.


VAERS ID: 1846993 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-26
Onset: 2021-10-27
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7330LA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Alanine aminotransferase normal, Albumin globulin ratio normal, Aspartate aminotransferase normal, Basophil count normal, Basophil percentage decreased, Blood albumin decreased, Blood alkaline phosphatase normal, Blood bilirubin normal, Blood calcium decreased, Blood chloride decreased, Blood glucose normal, Blood potassium normal, Blood sodium decreased, Blood urea nitrogen/creatinine ratio increased, Blood urea normal, Carbon dioxide normal, Eosinophil count normal, Eosinophil percentage decreased, Eye swelling, Globulin, Glomerular filtration rate normal, Haematocrit normal, Haemoglobin normal, Immunisation, Lymphocyte count decreased, Lymphocyte percentage, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume normal, Monocyte count decreased, Monocyte percentage, Neutrophil count, Neutrophil percentage, Platelet count normal, Protein total decreased, Pruritus, Rash, Rash maculo-papular, Red blood cell count normal, Red cell distribution width normal, Skin reaction, Urine analysis normal, Urticaria, White blood cell count decreased
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Anaphylactic reaction (broad), Angioedema (narrow), Haematopoietic leukopenia (narrow), Systemic lupus erythematosus (broad), Hyponatraemia/SIADH (narrow), Chronic kidney disease (broad), Hypersensitivity (narrow), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Levetiracetam 2000 mg tab Vimpat(Lacosamide) 150mg tabs Polyethylene Glycol (Miralax)3350 Calcium Citrate 250 mg tab Omeprazole 40 mg capsule KRILL OIL 500 mg PO Milk of Magnesia-400mg/5ml Senna Tablet 8.6mg (Senokot) Pregabalin (Lyrica
Current Illness: UTI - Urinary Tract Infection treated with Augmentin for 7 days (10/21/2021-10/27/2021)
Preexisting Conditions: Profound Intellectual Disability, Hypothyroidism, Epilepsy partial-complex,s/p VNS Implant, Osteopenia, GERD, Dysphagia, Left hydronephrosis due to renal cyst, Congenital Rubella, chronic constipation, Fibrocystic breast disease. Kidney stone s/p lithotripsy on 8/10/2021
Allergies: No known allergies: Side effects include: Alendronate sodium (Fosamax) (Gastritis, Food Refusal) Clobazam (Onfi) (Agitation, Compulsive eating, screaming) Valproic Acid (Edema, Lethargy, Weight Gain, screaming)
Diagnostic Lab Data: CBC Urinalysis complete metabolic panel 10/29/2021, WHITE BLOOD CELL COUNT 3.3 L 3.8-10.8 (Thousand/uL), RED BLOOD CELL COUNT 4.81 3.80-5.10 (Million/uL), HEMOGLOBIN 15.4 11.7-15.5 (g/dL), HEMATOCRIT 44.8 35.0-45.0 (%), MCV 93.1 80.0-100.0 (fL), MCH 32.0 27.0-33.0 (pg), MCHC 34.4 32.0-36.0 (g/dL), RDW 12.1 11.0-15.0 (%), PLATELET COUNT 140 140-400 (Thousand/uL), MPV 11.4 7.5-12.5 (fL), ABSOLUTE NEUTROPHILS 2264 1500-7800 (cells/uL), ABSOLUTE LYMPHOCYTES 828 L 850-3900 (cells/uL), ABSOLUTE MONOCYTES 188 L 200-950 (cells/uL), ABSOLUTE EOSINOPHILS 20 15-500 (cells/uL), ABSOLUTE BASOPHILS 0 0-200 (cells/uL), NEUTROPHILS 68.6 (%), LYMPHOCYTES 25.1 (%), MONOCYTES 5.7 (%), EOSINOPHILS 0.6 (%), BASOPHILS 0.0 (%), Complete Metabolic Panel GLUCOSE 137 65-139 (mg/dL), Non-fasting reference interval F UREA NITROGEN (BUN) 12 7-25 (mg/dL), CREATININE 0.36 L 0.50-1.05 (mg/dL), For patients $g49 years of age, the reference limit - for Creatinine is approximately 13% higher for people - identified as. F eGFR 119 $g OR = 60 (mL/min/1.73m2, eGFR 138 $g OR = 60 (mL/min/1.73m2), BUN/CREATININE RATIO 33 H 6-22 ((calc)), SODIUM 134 L 135-146 (mmol/L), POTASSIUM 3.7 3.5-5.3 (mmol/L), CHLORIDE 95 L 98-110 (mmol/L) F CARBON DIOXIDE 29 20-32 (mmol/L) F CALCIUM 8.4 L 8.6-10.4 (mg/dL) F PROTEIN, TOTAL 5.9 L 6.1-8.1 (g/dL) F ALBUMIN 3.5 L 3.6-5.1 (g/dL) F GLOBULIN 2.4 1.9-3.7 (g/dL (calc),F ALBUMIN/GLOBULIN RATIO 1.5 1.0-2.5 ((calc)), BILIRUBIN, TOTAL 0.4 0.2-1.2 (mg/dL), ALKALINE PHOSPHATASE 60 37-153 (U/L), AST 26 10-35 (U/L), ALT 9 6-29 (U/L) Urinalysis - No UTI
CDC Split Type:

Write-up: The patient had her Covid booster vaccine and Flu vaccine on 10/26/21. She was doing well not until 10/27/21 evening started to scratch her upper back shoulder. Around 10 pm noticed to have hives around the belly, upper and lower extremities. Her doctor was notified and ordered to start giving Benadryl 25 mg po every 6 hrs. until hives are gone and Tylenol po too. Recently she was treated for UTI with Augmentin from 10/20/21 ? 10/27/21. On 10/28/2021 morning, the rash did not get any better. Her vital sign was stable, no fever, O2 sat stable, not in any respiratory distress. Gave Claritin PRN orders with Tylenol at 9AM . RN was called and informed about the patient''s condition and to relay message to her doctor. 12:20pm the rash become more worst and spread more to the face and eyes were slightly swollen. Called RN that we will bring the patient to emergency department at the Hospital for further management and to avoid anaphylactic response. Arrived at the hospital around 1:20 pm. The ED was fully packed and they were very busy during that time. Some of the patients have to wait outside. Luckily, we were able to get in on time at the waiting area. We waited for a long time to be seen by MD not until almost 5 pm. She was treated with Decadon 6 mg IM and was also given Vistaril 25 mg PO. The patient was discharged at 7:25 pm and arrived home at 7:40Ppm. Her doctor was called and informed about the patient''s condition status. She was diagnosed to have Maculopapular rash, generalized and adverse reaction to COVID 19 vaccine. With new discharge order from the hospital to give Atarax mg po every 6 hrs. PRN for itching.


VAERS ID: 2431043 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-07
Onset: 2022-09-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FM7553 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7682MA / N/A LA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U7534AA / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: CEREBAL PALSEY
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: body pain / fever 101.9


VAERS ID: 1843284 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: California  
Vaccinated: 2021-09-25
Onset: 2021-09-26
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain upper, Arthralgia, Influenza like illness
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Edarbyclor 40/12.5mg od-am Carvedilol 25mg td-am+pm Amlodipine Besylate 5mg od-pm Rosuvastatin Calcium 10mg od-pm Metformin HCL ER 500mg td-am & pm Finasteride 5mg od-am Allopurinol 300mg od-am Spectravite multivitamin od-am Aller-Tec 10
Current Illness: none
Preexisting Conditions: Diabetes Gout High Blood Pressure
Allergies: codeine
Diagnostic Lab Data:
CDC Split Type:

Write-up: Flu-like symptoms for two days. Bad stomach cramps. All joints ached.


VAERS ID: 2463146 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-16
Onset: 2022-09-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 054A22A / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ901AA / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: METROCREAM
Current Illness: n/a
Preexisting Conditions: Dyslipidemia Benign prostatic hyperplasia
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient was given the Original Moderna vaccine booster vs the Moderna Bivalent booster on accident. No treatment and no adverse reaction to the additional original moderna booster.


VAERS ID: 1840992 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-31
Onset: 2021-11-02
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, Injection site erythema, Injection site swelling, Pain in extremity
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Got both the Seasonal Flu vaccine and COVID-19 booster shot on the same day (10/31/2021) in the right and left arms respectively. Right arm was sore for a couple of hours and then got better. Left arm (COVID injection site) started feeling sore a few hours after, there was slight redness and swelling about 1/2 inch in diameter around the site the day after (11/1/2021). On 11/2/2021 swelling had increased to the size of an egg and stayed like that until 11/3/2021 until about 9:40 AM. At around 10:15AM that same day, the swelling and redness spread to the entire arm from the top of the shoulder to the elbow and has remained as such until now at 5:03PM on 11/3/2021.


VAERS ID: 2486420 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Male  
Location: California  
Vaccinated: 2021-12-10
Onset: 2021-12-24
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2022-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 033H21A / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Deafness, Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Centrum Multivitamin, Fish Oil, and Curcumin
Current Illness:
Preexisting Conditions:
Allergies: None Known
Diagnostic Lab Data: ENT and Audiologist tested and confirmed slight hearing loss and tinnitus on 10/15/2022.
CDC Split Type:

Write-up: I developed tinnitus ~2 weeks after receiving my influenza and Covid19 (Moderna) vaccination. Constant high-pitched ringing.


VAERS ID: 2463456 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: California  
Vaccinated: 2022-09-13
Onset: 2022-09-14
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS7144B / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 346338 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Condition aggravated, Myalgia, Polymyalgia rheumatica
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Vasculitis (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Polymyalgia Rheumatica
Allergies: None
Diagnostic Lab Data: None, just contacted my rheumatologist and started back on prednisone, 5mgs. It?s somewhat managing the symptoms although I have days of joint and muscle pain.
CDC Split Type:

Write-up: I was in remission with Polymyalgia rheumatica and off prednisone for 3 months. Getting both vaccines at the same time cause my immune system revved up and cause a relapse of the condition. Really regret getting both shots at the same time. The information on the news was getting both at the same time is fine and it isn?t. They really should be spaced out.


VAERS ID: 1848995 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-06
Onset: 2021-11-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK1527 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Fall, Loss of consciousness, Pallor, Skin warm
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Client received the Pfizer COVID vaccine (lot#FK1527) in the L deltoid and the Fluarix Quadrivalent Influenza Vaccine (Lot#3NA4M) in the R deltoid at approximately 1050 from vaccinator RN. After the client received both vaccines, he stood up to wait next to his mother who was receiving her COVID vaccine from the same vaccinator. Due to a limited supply of chairs at the mobile event there was not an available chair to allow the client to sit down while waiting with his mother. At approximately 1055, as the client was standing next to his mother, he began to slouch over the vaccination table and vaccinator RN''s assisted client to the ground. Client lost consciousness for approximately 2 seconds. RN assessed non obstructed airway, no respiratory distress, and raised the client''s legs while he was laying on the floor. RN assessed client who presented with mild pallor of the face, no diaphoresis, and pupils equal and reactive. RN took client vitals at 1103 with BP 100/60 in the L arm laying down, 70 HR, and 16 RR. Lead RN assessed client at 1103 presented A&O x4 and talking in full sentences, grip strong and equal, cap refill < 3 seconds, and skin pink and warm to touch. Client''s mother reported that the client ate breakfast at 0830 and had a muffin. Client denied dizziness, SOB, headache, numbness, or tingling. Client was assisted to zero-gravity chair and Lead RN advised that the client be observed for 30 minutes. Client''s father reported that he has a history of fainting but reported that the client has never fainted in the past. Lead RN provided client with water, juice, and graham crackers. Client took sips of the water and juice and ate his snacks. Client reported to Lead RN that he was "feeling good now" and denied any dizziness, SOB, headache, numbness, or tingling. RN reviewed when to f/u with PCP. At 1140 the client left the vaccine site with his parents. Client walked out of the vaccine site with a steady and symmetrical gait.


VAERS ID: 1849025 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-04
Onset: 2021-11-06
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039F21A / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ747AA / 2 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abdominal pain, Night sweats, Weight decreased
SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FLECAINIDE 50MG; MECLIZINE 50MG; PRAVASTATIN 40MG; DONEPEZIL 5MG; TAMSULOSIN 0.4MG; VIRAMIN D 1.25MG; AZELASTINE 137mcg; KETOCONAZOLE 1%; CYCLOSPORINE 0.05% Ophth; ASPIRIN 81MG; CANNABIS
Current Illness: NO
Preexisting Conditions: COLONIC POLYPS; ATRIAL FIBRILLATION
Allergies: NIGHT SWEATS FOR THE PREVIOUS 4 NIGHTS.
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: PT report having night sweats for the 4 previous night after vaccine, lost weight with in the last 2 weeks. Pt was evaluated by PA and pt left and was seen at the urgent care for abdominal pain.


VAERS ID: 1839253 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-30
Onset: 2021-11-01
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939902 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2579B / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Vertigo
SMQs:, Vestibular disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine (50mg), sertraline (150mg), albuterol (PRN), Flovent (PRN), Benadryl (PRN), Claritin (PRN), Flonase (daily)
Current Illness: None
Preexisting Conditions: Hypothyroidism, depression, anxiety
Allergies: Allergies to grasses & dander. No known food products.
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fatigue initially, subsided after 24 hours. Approximately 48 hours after the vaccinations vertigo began and is not consistent. Vertigo happens when laying down, getting up too quickly, or excessive movement.


VAERS ID: 1838639 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: California  
Vaccinated: 2021-10-25
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal distension, Chills, Decreased appetite, Headache, Hyperhidrosis, Lacrimation increased, Nausea, Pyrexia, Rhinorrhoea
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Lacrimal disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Heart disease, unspecified; Immunodeficiency
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USGLAXOSMITHKLINEUS2021AM

Write-up: Severe headache; runny nose; watery eyes; severe fever; severe chills; nausea; reduced apetite; bloating; sweats; This case was reported by a consumer and described the occurrence of headache in a patient who received Flu Seasonal QIV Dresden (Fluarix Quadrivalent 2021-2022 season) for prophylaxis. Co-suspect products included flu seasonal qiv dresden pre-filled syringe device (Fluarix Tetra Pre-Filled Syringe Device) injection syringe for prophylaxis and TOZINAMERAN (COVID 19 VACCINE PFIZER) for prophylaxis. Concurrent medical conditions included heart disease, unspecified and immunodeficiency. On 25th October 2021, the patient received Fluarix Quadrivalent 2021-2022 season, Fluarix Tetra Pre-Filled Syringe Device and the 3rd dose of COVID 19 VACCINE PFIZER. In October 2021, 4 hrs after receiving Fluarix Quadrivalent 2021-2022 season and Fluarix Tetra Pre-Filled Syringe Device, the patient experienced headache, runny nose, watering eyes, fever, chills, nausea, decreased appetite, bloating and sweating. On an unknown date, the outcome of the headache, runny nose, watering eyes, fever, chills, nausea, decreased appetite, bloating and sweating were recovered/resolved. It was unknown if the reporter considered the headache, runny nose, watering eyes, fever, chills, nausea, decreased appetite, bloating and sweating to be related to Fluarix Quadrivalent 2021-2022 season and Fluarix Tetra Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional details were reported as follows: The case was reported by the patient. The age at vaccination was not reported. The patient received the 3rd Covid vaccine from (Pfizer) along with the Flu vaccine on Monday. Four hours after the injections of Covid vaccine and Flu vaccine, the patient started with a severe headache, runny nose and watery eyes. Then, every two to three hours (less than a day after vaccination), the patient developed severe symptoms of fever and chills, nausea but no vomit, reduced appetite, bloating and sweats. This all ended in a 12 hour period. The patient was extremely cautious there, wearing masks and taking our exposure seriously and had not been exposed to anyone with any Flu like symptoms. The patient had reported this to his/her Immunologist and in the last 24 hours, his/her sense of normal had return. The patient would not get a Covid vaccine and a Flu vaccine at the same time if at all in the future. It was unknown if the reporter considered the headache, runny nose, watering eyes, fever, chills, nausea, decreased appetite, bloating and sweating to be related to Covid vaccine.


VAERS ID: 1849515 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-12
Onset: 2021-10-13
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT2593 / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Myalgia, Pain, Pain in extremity, Pyrexia, Tenderness
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Flu vaccine was given at the same time.
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: For approximately 5 days after I received the first shot of the Pfizer vaccine I had muscle pain up and down both arms and both legs. It hurt to sit, stand, and walk. Certain areas on my arms and legs were sensitive to touch. I also had a low-grade fever during that entire period. I had to see a doctor about the symptoms and I was diagnosed with myalgia.


VAERS ID: 2482057 (history)  
Form: Version 2.0  
Age: 4.0  
Sex: Male  
Location: California  
Vaccinated: 2022-10-15
Onset: 2022-10-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS K77B2 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: hydrocortisone 1%
Current Illness: N/A
Preexisting Conditions: Polydactyly
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Pt. did not have any adverse events that occured during the time of vaccination. PCP has been in contact and on call MD recommend that pt. return in 8 weeks to complete vaccine series with either moderna or pfizer


VAERS ID: 2315597 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated: 2021-12-09
Onset: 2022-04-03
   Days after vaccination: 115
Submitted: 0000-00-00
Entered: 2022-06-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 0679208 / 3 AR / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test positive, Throat irritation
SMQs:, Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: Codeine.
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: Developed an itchy throat. Tested positive on 4/3.


VAERS ID: 1861588 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-01
Onset: 2021-11-03
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA FH8020 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3NA4M / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Deep vein thrombosis, Fibrin D dimer, Pain in extremity, Peripheral swelling, Ultrasound Doppler abnormal
SMQs:, Cardiac failure (broad), Angioedema (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: D-dimer and ultrasound were preformed to evaluated whether it was a clot (Sat. morning, Nov. 6). Tests indicated that is was.
CDC Split Type:

Write-up: Pain in my right foot began on Wed. morning. Pain and swelling spread from foot to lower right leg. Intense pain Friday night. Symptoms were similar to blood clot, and a blood clot was suspected so I went to the ER Saturday (11-6). DVT was confirmed (11-6).


VAERS ID: 2512972 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: California  
Vaccinated: 2022-11-15
Onset: 2022-11-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The BIVALENT covid vaccine was ordered and meant to be administered. However the regular covid vaccine was administered in error.


VAERS ID: 2238180 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: California  
Vaccinated: 2022-01-31
Onset: 2022-02-07
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2022-04-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 066H21A / 3 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / IM

Administered by: Work       Purchased by: ?
Symptoms: Anxiety, Arthralgia, Cognitive disorder, Disturbance in attention, Exercise tolerance decreased, Fatigue, Feeling abnormal, Pain in extremity
SMQs:, Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Depression (excl suicide and self injury) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer 2nd dose, 06/04/2021; symptoms began approximately 2 weeks after: GI issues, joint pain, fatigue, itchiness, brain fog an
Other Medications: Vitamin D, Fish oil
Current Illness:
Preexisting Conditions: IBS/GERD following 2nd dose (6/04/2021)
Allergies: None
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: No reaction immediately following vaccine other than sore arm. Approximately a week later: Joint pain, and pretty bad brain fog. Joint pain subsided after 3 weeks. Brain fog still present, worse when attempting to workout. I''ll workout and a few hours later I''m hit with a big wave of brain fog, difficulty concentrating, diminished cognitive ability and fatigue. I''ve also notice coffee no longer provides me with clarity (doesn''t wake me up as it used to). Anxiety has definitely increased.


VAERS ID: 2514387 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: California  
Vaccinated: 2022-11-22
Onset: 2022-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GL2042 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS PN5PL / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Contusion, Disorientation, Dry skin, Fall, Feeling cold, Head injury, Headache, Loss of consciousness, Nausea, Pallor, Tinnitus
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hearing impairment (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: not available
Current Illness: unknown
Preexisting Conditions: Anemia
Allergies: Amoxicillin
Diagnostic Lab Data: None per DO at scene
CDC Split Type:

Write-up: Pt received Pfizer 0.3ml Bivalent booster in the left arm at 1429 with a flu vaccine in the right arm. While standing up and waiting for her brother to be vaccinated, patient was observed to fall backwards to the ground, hitting the back of her head. Pt had a momentary loss of consciousness and RN observer was at the scene promptly. Team alert was called in and hospital staff arrived on scene. Dr. DO arrived on scene at 1440 with MA and MA. The patient was placed in a wheelchair to the triage tent. Sitting BP was initially taken at 1438 79/39, HR 56. 100% O2 on room air. at 1440, BP was 100/65, HR 69, 99% o2 on room air. while on stretcher at 1447, BP was 114/77, HR 89, 100% O2 on room air. At 1455, patients standing BP was 112/90, HR 81, 100% O2 on room air. During assessment, the pt experienced difficulty answering basic orientation questions. Pt was complained of right side of head Headache (4-5/10 on pain scale) and ringing in her left ear. After examination of the back of pts head, she had a small, bruised area. Pt also complained of feeling nauseous and appeared pale, cold, and dry. Mother reports pt has no history of syncope. Mother was present at the scene. Pt was examined by DO present at the scene and was cleared to return home at 1456. Pt declined to go to the ER, however, was instructed to call 911 or go to nearest emergency room if symptoms worsen. Pt walked out of vaccine tent with steady gait with mother at her side.


VAERS ID: 1858135 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: California  
Vaccinated: 2021-11-08
Onset: 2021-11-10
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 80777-0273-98 / 1 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 58160-0887-52 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lymph node pain, Nausea, Swelling, Underdose
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Melatonin
Current Illness:
Preexisting Conditions: "long Covid" symptoms (parosmia, fatigue)
Allergies: None
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Quantity flu shot: .5, Quantity Moderna Covid-19 vaccine shot: .25 Noticed slight nausea today (11/10/2021) and slight painful lymph node reaction with small lump on right side of neck.


VAERS ID: 2501403 (history)  
Form: Version 2.0  
Age: 0.83  
Sex: Female  
Location: California  
Vaccinated: 2022-10-14
Onset: 2022-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 3 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UT7682MA / N/A LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Inappropriate schedule of product administration, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: 3rd dose of initial Pfizer Covid-19 vaccine was given 6.5 weeks after 2nd dose instead of 8 weeks. No adverse events occurred with the early administration of this 3rd dose.


VAERS ID: 2524366 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: California  
Vaccinated: 2022-12-03
Onset: 2022-12-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9703 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Malaise, Nausea, Pain, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lantus, Novolog, Metoprolol, Felodipine, Hydrochlorothizide, Spironolactone, Atorvastatin, Levothyroxiner, Azathioprine, Sulfasalazine, Gabapentin, Diclofenac Sodium Topical Gel, Lidocaine Patch, Boniva
Current Illness:
Preexisting Conditions: Diabetes, Hypertension, Osteoarthritis, Osteoporosis
Allergies: Penicillin, Lisinopril, Diovan
Diagnostic Lab Data:
CDC Split Type:

Write-up: Chills, Nausea, Vomiting, Feeling unwell, overall Body Aches


VAERS ID: 1859434 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Male  
Location: California  
Vaccinated: 2021-11-07
Onset: 2021-11-09
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Condition aggravated, Extra dose administered, Fatigue, Headache, Herpes simplex, Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad), Medication errors (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer, 34 , mild fatigue arm pain
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Penicillin
Diagnostic Lab Data: Dermatology photographic review, telemedicine
CDC Split Type:

Write-up: Hepetic whitlow present on finger 2 days after injection General fatigue for less than 24 hrs, minor headache, moderate arm pain for 24 hrs mainly on covid vaccine arm


VAERS ID: 1819535 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-26
Onset: 2021-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 320308D / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ767AB / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: na
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: pt came in for a flu shot but was accidently given a third covid vaccine . he is almost due for a booster. he got his first covid moderna vaccine on 04/05/21 , second one on 05/05/21 and got a pfeizer vaccine today 10/26/21. pt felt fine and was happy that he got his third dose, he also said that he still wants the flu shot so we gave him a flu shot as well. when asked if we should report this to his primary, he said he did not have a primary doctor.


VAERS ID: 2528473 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: California  
Vaccinated: 2022-12-07
Onset: 2022-12-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 12/2021
Other Medications:
Current Illness: Diagnosis of influenza A on 11/24/2022
Preexisting Conditions: Adult onset asthma.
Allergies: Codien, pennisillin, blue cheese, dust, squash/melon, pineapple.
Diagnostic Lab Data:
CDC Split Type:

Write-up: Ringing in ears. Started about an hour after I got my shots. Slightly increased/worse today. I can still hear fine but it?s significant tinnitus. I?ve not reported to my doctor yet. Will if it doesn?t go away within 10 days.


VAERS ID: 1821243 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-24
Onset: 2021-10-22
   Days after vaccination: 28
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301305A / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site pruritus, Scratch
SMQs:, Accidents and injuries (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer Dose 2, filled out a VAERS report
Other Medications: Multiple Vitamin Vitamin D Calcium Magnesium Vitamin B-12
Current Illness: No
Preexisting Conditions: No
Allergies: Kiwi Fruit Macrobid
Diagnostic Lab Data: No
CDC Split Type: vsafe

Write-up: On 10/13/2021 I had a colonoscopy. I had pain for up to a week after the colonoscopy. I have had colonoscopies in the past and I have not had any pain before. There was no treatment. I called my doctor, they recommended to take a medication, that I never took. About a week after my vaccination, 09/24/2021, my left arm, at the site of the injection, has been significantly itching for the past 3 weeks, and even now 10/27/2021. I find myself unconsciously scratching. There is not any visible bump or anything. I have put cortisone cream to calm down the itching and it helps. I have not seen a doctor for it. I keep thinking it will go away. The pain after the colonoscopy has gone away, but the itching in my arm has not.


VAERS ID: 2204352 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: California  
Vaccinated: 2021-09-27
Onset: 2022-01-11
   Days after vaccination: 106
Submitted: 0000-00-00
Entered: 2022-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abscess, Abscess drainage, C-reactive protein abnormal, Condition aggravated, Incisional drainage, Inflammation, Tenderness
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 1st: Pfizer vaccine: EL3248 Date: 02/13/2021 No initial reaction after vaccine was administered. July 19th 2021, Abscess formed
Other Medications: Nortriptyline
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Allergies to a number of antibiotics; Sulfa drugs; Penicillin; Quinolones antibiotics
Diagnostic Lab Data: Infectious Disease Doctor called for blood tests: High level of inflammation from C-Reactive protein test. Everything else was in normal range.
CDC Split Type: vsafe

Write-up: 4 months after my Booster shot, on 1/11/2022 I noticed a large abscess formed above my elbow on my right arm and a second on my lower back above the waist, palpating it when noticing it when it was marble shaped. It continued to grow and became painful to the touch and I could feel it when I wasn''t touching it as well. On Feb. 15th one on my back opened up and had to be drained. Feb. 25th the right arm abscess and back abscess had an IND performed. They are still in the process of healing and have not completely healed since. I was not given any prescriptions as well.


VAERS ID: 1818513 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Male  
Location: California  
Vaccinated: 2021-10-24
Onset: 2021-10-26
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 076C21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site rash, Vaccine positive rechallenge
SMQs:, Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Similar rash after second dose of Moderna on 4/9/21
Other Medications: Tirosint, rosuvastatin, compounded T3, multivitamin (Nutrient 950 with K), TMG, fish oil, magnesium
Current Illness: None
Preexisting Conditions: Hypothyroid, familial hypercholesterolemia
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Large red rash around the site of the Moderna Booster injection on the right arm. The patient had a similar rash after the 2nd Moderna dose.


VAERS ID: 2530151 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-27
Onset: 2022-11-27
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2022-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013H22A / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ932AD / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Chills, Cough, Epistaxis, Fatigue, Hyperhidrosis, Influenza like illness, Lower respiratory tract infection, Nasopharyngitis, Pyrexia, SARS-CoV-2 test positive, Sinus congestion, Sinus pain, Tremor
SMQs:, Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: "COVID-Arm" Moderna Vax #5, Lot 013H22A
Other Medications: Febuxostat, Famotimide, Centrum Silver Women, Probiotics+Prebiotic Fiber. I had a flu shot simultaneously with the COVID vaccine. (Got "COVID-Arm"
Current Illness: None
Preexisting Conditions: Gout, GERD
Allergies: Amitriptyline HCl, Allopurinol
Diagnostic Lab Data: none
CDC Split Type:

Write-up: 11/26/22 Sudden severe fatigue, sinus pain 11/27/22 Positive at-home COVID test, Fever 101.7 worse sinus pain/congestion, fatigue, chills and hard tremors 11/28/22 fever 100.9, started medication Paxlovid100 mg pack 5 days; continued flu and cold symptoms 11/29/22 fever broke, sweats, chest cold started 11/30-31 no fever, head and chest cold symptoms 12/2/22 positive COVID test; continuing cold symptoms 12/3/22 Dark red coagulated blood from nose, large pieces, dry cought 12/8/22 Positive COVID test, chills/sweats, continued cold symptoms, dry cough 12/13/22 Positive COVID test, mild head cold, dry cough


VAERS ID: 2537391 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: California  
Vaccinated: 2022-11-28
Onset: 2022-12-02
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2022-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Back pain, Muscle disorder, Spinal disorder
SMQs:, Rhabdomyolysis/myopathy (broad), Retroperitoneal fibrosis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Finasteride, atenolol, lisinopril, atorvastatin, aspirin, tamsulisin
Current Illness: None
Preexisting Conditions:
Allergies: Cipro
Diagnostic Lab Data:
CDC Split Type:

Write-up: I started developing a lower back pain that does not go away and I cannot associate it with anything else. Thinking it could be renal pain, I consulted with an urologist while in vacation, but my kidneys are okay. They suggested there is something to do with my muscles /spine in my lower back. The doctor prescribed me a temporary anti-inflammatories, muscle relaxant and pain medication and is helping . I cannot asure it is due to the COVID vaccine, but I can. It associate this lower back pain with anything else. I just wanted to reported


VAERS ID: 2538176 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: California  
Vaccinated: 2022-09-19
Onset: 2022-12-12
   Days after vaccination: 84
Submitted: 0000-00-00
Entered: 2022-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9702 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Cough, Nasal congestion, Rhinorrhoea, SARS-CoV-2 test positive, Sinus congestion
SMQs:, Anaphylactic reaction (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metformin; Pepcid; Aspirin; Gaviscon
Current Illness: N/A
Preexisting Conditions: Diabetes; Obese; Acid Reflux; Hay Fever
Allergies: N/A
Diagnostic Lab Data: COVID-19 Test, Positive, 12/12/2022
CDC Split Type: vsafe

Write-up: I had a running nose, nasal congestion, cough, and sinus congestion. I tested positive for COVID-19 at home. I talked to my doctor through e-visit, and he prescribed me Paxlovid. I started to feel better after 2 or 3 days later.


VAERS ID: 1815922 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-22
Onset: 2021-10-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301558A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P1003655587 / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Dizziness, Feeling abnormal, Feeling hot, Hyperhidrosis, Hypotension, Injection site haemorrhage, Injection site swelling, Malaise
SMQs:, Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Vestibular disorders (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: no illnesses
Preexisting Conditions: no health condition
Allergies: no allergy
Diagnostic Lab Data:
CDC Split Type:

Write-up: pt got covid vaccine may be 1 min ago ,gave her flu shot ,even before putting the flu syringe back in shart container ,injection site swoll up right away ,bled little bit ,stop bleeding,pt started filling weak ,like she was gonna pass out ,sweating and feeling hot ,after paramedics came ,bp was low ,pt was not filling well ,paramedics wanted to take patient to hospital ,pt did not go,patient husband is a doctor ,was on speacker phone with patient ,told to take benadryl ,pt took 4 teaspoon of benadryl ,waited for husband who is a doctor almost 40 -45 min ,paramedics was still with patient ,patient went home wiht husband ,called patien twice ,got holf of her on 10/25/21 around 3.30 - 4 pm ,pt was doing ok ,still not feeling 100 % normal


VAERS ID: 1815693 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-11
Onset: 2021-10-12
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 UN / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 95Z42 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Antibody test, Biopsy brain, Cerebral disorder, Electroencephalogram abnormal, Imaging procedure, Immunoglobulin therapy, Laboratory test, Lumbar puncture normal, Magnetic resonance imaging head abnormal, Mental status changes, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 14 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: albuterol 108 (90 Base) MCG/ACT inhaler, Inhale 2 puffs by mouth every 6 hours as needed for Shortness of Breath., Disp: 1 each, Rfl: 3 ? aspirin 325 MG tablet, Take 1 tablet (325 mg) by mouth daily., Disp: 100 tablet, Rfl: 0 ? Atorvastat
Current Illness: Interstitial lung disease with exacerbation of shortness of breath 2 weeks prior covid vaccination 1st dose moderna - 2 weeks prior
Preexisting Conditions: Scleroderma/ systemic sclerosis focal epilepsy with complex partial seizures Raynaud''s disease without gangrene Hypothyroidism GERD secondary to scleroderma Iron deficiency anemia secondary to poor absoprtion Anemia of chronic disease mixed stress and urinary urge incontinence and urinary retention history of NSTEMI history of CVA of R middle cerebral artery with residual cognitive defect - secondary to scleroderma age relate macular degeneration superficial punctate keratitis
Allergies: Reglan [Metoclopramide Hcl] Shortness of Breath ? Tomato Other
Diagnostic Lab Data: Extensive hospitalization that is ongoing with numerous procedures and lab results. Brain biopsy 10/25/21 - results pending LP x2 10/18 and 10/21 - bland CSF Ongoing prolonged EEG - most recent results recorded from 10/24/21: Impression: This is a mildly abnormal study secondary to: 1. Theta frequency background slowing with overlying focal delta activity over the left hemisphere. 23 imaging studies during hospitalization and numerous serial labs - too numerous to include without timing out the reporting.
CDC Split Type:

Write-up: Patient presented to ED with fever and alerted mental status 10/12/21. Initially concerned for stroke with negative imaging and then infectious etiology and possible encephalitis, but workup also negative with benign LP x2. Prolonged EEG without perceptible seizures. Given empiric IVIG. L sided unilateral hemispheric gyral thickening/leptomeningeal enhancement found on repeat brain MRI, not present previously, and brain biopsy completed 10/25/21. Results from biopsy as well as auto immune encephalitis and MOG antibodies pending. Patient clinically slightly improved but MRI worse. Remains hospitalized and workup is ongoing.


VAERS ID: 2556290 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: California  
Vaccinated: 2022-09-23
Onset: 2022-10-17
   Days after vaccination: 24
Submitted: 0000-00-00
Entered: 2023-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS7163B / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ875AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Cough, Rhinorrhoea, SARS-CoV-2 test positive, Sneezing
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Calcium; Vitamin D3
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: 17OCT2022 - COVID-19 at home test - positive
CDC Split Type: vsafe

Write-up: Rather sudden onset of sneezing, runny nose, and coughing. Temperature was 99.9 degrees. Pulse was 111. Oxygen level fluctuated between 84% and 94%. I took Tylenol.


VAERS ID: 2501822 (history)  
Form: Version 2.0  
Age: 0.5  
Sex: Male  
Location: California  
Vaccinated: 2022-11-01
Onset: 2022-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR9236B / 1 LL / IM
DTPPVHBHPB: DTAP+IPV+HIB+HEPB (VAXELIS) / MSP VACCINE COMPANY U7125AA / 2 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7751KA / 1 LL / IM
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH FX0078 / 3 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: NO REACTION. MODERNA VACCINE EXPIRED 10-29-2022. VACCINE WAS GIVEN ON 11-01-2022.


VAERS ID: 2503650 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: California  
Vaccinated: 2022-10-17
Onset: 2022-10-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ878AB / N/A RA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. U028825 / 1 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR U7218AA / 1 RA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U7534AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: N/A - Reporting incorrect vaccine given - COVID booster


VAERS ID: 2503646 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: California  
Vaccinated: 2022-10-17
Onset: 2022-10-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ878AB / N/A RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: N/A - Reporting incorrect vaccine administered


VAERS ID: 2263413 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: California  
Vaccinated: 2021-10-18
Onset: 2021-11-01
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2022-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH8020 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Allergy to chemicals, Blood cholesterol increased, Blood test, Cardiac monitoring, Computerised tomogram normal, Dizziness, Dysmenorrhoea, Echocardiogram normal, Fatigue, Feeling abnormal, Hangover, Head discomfort, Heart rate increased, Hypersensitivity, Hypertension, Menstruation irregular, Migraine, Ocular discomfort, Palpitations, Presyncope, Treatment noncompliance, Vision blurred, Vitamin D decreased
SMQs:, Angioedema (broad), Dyslipidaemia (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Glaucoma (broad), Hypertension (narrow), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Lipodystrophy (broad), Fertility disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: CT Scan-normal Heart ultrasound-normal Blood panel
CDC Split Type: vsafe

Write-up: I had my last booster and flu shot on same date. Since then I have had to call the emergency number 3 times due to my heart beating super fast. It was worse than heart palpitations. The last time I called was last week. I think that it was a change in my blood pressure. I was light headed and felt I would pass out and my vision was blurry. I also had pressure in the top of my head. The medics came over and checked my blood pressure. They determined it was high but it was ok. I still asked to be taken to the ER. They kept me there for 4 or 5 hours and gave me a prescription for migraine. The symptoms returned shortly after they gave me the medicine. I was sent to have a CT scan performed. The results were normal. I scheduled an appointment with my doctor after that. He referred me to an ophthalmologist. The ER prescribed 2 medications for migraines but I have not taken them. In November I had a heart ultrasound done and was placed on a heart monitor for 1 week. I went to see a cardiologist. He advised the heart ultrasound was normal. I called the ER because my heart was beating like crazy for more than a minute. I had no stress factors that contributed. I have also been experiencing extreme fatigue so I had a full panel blood test and determined that my Vitamin D was low and that cholesterol was slightly high. I do still the pressure in my head and my eyes. It feels like my eyes have changed and it comes and goes. I have also experienced brain fog and extreme fatigue. I had a change in my periods. They are extremely painful and they are showing up a week earlier. When I drink wine, it seems that I am having an allergic reaction. After having half a glass of wine, I started having the palpitations and feeling like I am having a hangover.


VAERS ID: 2503653 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: California  
Vaccinated: 2022-10-18
Onset: 2022-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ878AB / N/A RA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. U028825 / 1 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR U7218AA / 1 RA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U7534AA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: N/A - Reporting incorrect vaccine given - COVID booster


VAERS ID: 2246213 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Male  
Location: California  
Vaccinated: 2022-04-19
Onset: 2022-04-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-04-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025L21B / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5NF7J / UNK RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: On 4/19/2022, at 9:02 am, flu vaccine administered to patient, despite having received one October 2021. He was monitored for 15 minutes after receiving both the flu and Moderna vaccines. No signs of distress observed or reported. He was provided with education on what to expect, adverse effects, and when to seek care (both verbal and written) on both the flu and COVID-19 vaccine. Reviewed dates of flu season with all staff, and how to better view the records in the system. It was found most staff were using the wrong page, which doesn''t reveal as easily which vaccines are due versus completed. Provided instructions to contracted staff to double check.


VAERS ID: 2507560 (history)  
Form: Version 2.0  
Age: 90.0  
Sex: Male  
Location: California  
Vaccinated: 2022-11-14
Onset: 2022-11-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ3275 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ895AC / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: General physical condition abnormal, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: NKDA
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient received the Pfizer COVID booster and then the high dose senior flu shot. After getting the flu vaccine, the patient looked off but insisted that he was fine. After taking a few steps out the vaccination room, he collapsed. Patient was offered water and EMS was contacted. EMS offered to take him to the ER but patient refused. Pharmacy staffed called and left message at 1500 to check on the status of the patient.


VAERS ID: 2246207 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: California  
Vaccinated: 2022-04-19
Onset: 2022-04-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-04-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025L21B / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5NF7J / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: On 4/19/22 at 9:02 AM, a flu vaccine was administered to the pt, despite the pt having received one in September 2021. Per staff report, the September dose in database was not observed due to the most recent administration being at the bottom of the record. Pt was monitored for 15 minutes after receiving both the flu and Moderna vaccines. No signs of distress were observed or reported. Pt was provided with education on what to expect, adverse effects, and when to seek care ? both verbal and written ? on both the Flu and COVID-19 vaccine.


VAERS ID: 2503379 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: California  
Vaccinated: 2022-11-08
Onset: 2022-11-09
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 5 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / -
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal discomfort, Arthralgia, Chills, Diarrhoea, Headache, Insomnia, Malaise, Pain, Pain in extremity, Tremor, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer Covid vaccine: chills fever bodyaches hives from the knees down that took three weeks to get rid of
Other Medications:
Current Illness:
Preexisting Conditions: Had melanoma 17 years ago, surgery
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Received shingles vaccine along with Covid and flu shot. Extremely sick beginning about 2 AM throwing up diarrhea chills so bad my whole body shakes. Fierce headache unable to sleep, Whole body aches although I do have arthritis. Pain in the calves and the joints. Stomach feels like I?ve been punched. Do I really have to get the second shingles vaccine? one study showsit?s just as effective just getting one vaccine. I am an extremely active yoga teacher who swims laps every day of the week and bikes three days of the week.


VAERS ID: 2719028 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-11-29
Onset: 2023-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS FC22G / 2 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FLINTSTONES
Current Illness: INFESTATION BY SARCOPTES SCABIEI VAR HOMINIS, THROMBOCYTOSIS, VITAMIN D DEFIENCY
Preexisting Conditions: THROMBOCYTOSIS, VITAMIN D DEFIENCY
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: FATHER OF CHILD REQUESTED SECOND DOSE OF FLU VACCINE. CHILD WAS VACCINATED WITH ADDITIONAL PFIZER COVID VACCINE AROUND 9AM ON 11/28/23 IN ERROR. PATIENT HAD RECEIVED THE COVID VACCINE PREVIOUSLY ON 10/25/23. FOC RETURNED TO PHARMACY AFTER BEING NOTIFIED OF ERROR. CHILD WAS THEN ADMINISTERED FLULAVAL. THERE WERE NO SIGNS OF ADVERSE REACTION.


VAERS ID: 1906743 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-11-27
Onset: 2021-11-29
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 058H21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Interchange of vaccine products, Pruritus, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Oral Allergy Syndrome (OAS) triggered by dry/soaked kidney beans. Canned is okay.
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Moderna booster received same day/time as seasonal flu shot. Have received flu shots in the past without any adverse reactions. Prior to Moderna booster, received Pfizer SARS-COV2 vaccine dose 1 on 4/17/2021 and Pfizer SARS-COV2 vaccine dose 2 on 5/8/2021 without any adverse side effects. This leads me to believe Moderna is the issue. Hives on mid-section of body, extending from hips to chest, front and back. Not overly itchy or red. Hives are small and do not touch (relatively spaced out). Took Benadryl.


VAERS ID: 1908673 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-07
Onset: 2021-11-18
   Days after vaccination: 42
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Body temperature, Decreased appetite, Extra dose administered, Fatigue, Pyrexia, Wrong product administered
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20211119; Test Name: body temperature; Test Result: 100.3 {DF}; Result Unstructured Data: 100.3
CDC Split Type: USSA2021SA392822

Write-up: The patient was vaccinated with FLUZONE HIGH DOSE QUADRIVALENT instead of COVID-19 VACCINE; The patient was vaccinated with FLUZONE HIGH DOSE QUADRIVALENT twice instead of COVID-19 VACCINE; Initial information regarding an unsolicited valid non-serious case was received from a other health care professional via Regulatory Authority (RA) (Reference number- 00868442) and transmitted on 22-Nov-2021. This case involves a 66-year-old female patient who had no appetite (decreased appetite), fever of 100.3 (pyrexia) and fatigue after receiving INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] instead of Coronavirus disease (COVID-19) VACCINE (wrong product administered and extra dose administered) The patient''s medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE lot number not reported via unknown route in unknown administration site for prophylactic vaccination. On 18-Nov-2021, the patient received 0.7 ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ7760C, expiry date: 30-Jun-2022) via intramuscular route in the right deltoid for prophylactic vaccination instead of booster dose of COVID-19 VACCINE. It was a case of an actual medication error due to extra dose administered and Wrong vaccine administered (latency same day) On 19-Nov-2021 the patient developed a non-serious no appetite (decreased appetite), fever of 100.3 (pyrexia) and fatigue 1 month 12 days following first dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE and 1 day following last dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. It was reported "The caller stated that a patient came into the office to receive a COVID Booster vaccine on 18 NOV 2021, however the patient was given the FLUZONE HIGH DOSE QUADRIVALENT injection in error. The caller stated that the patient has now received 2 doses of the flu shot, as she received a prior flu shot on 07 OCT 2021. The patient reported fatigue, fever of 100.3 and no appetite on 19 NOV 2021. The caller wants to know how to care for the patient. consumer who received two Fluzone HD. She asks for appropriate follow-up" No other relevant test was provided. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome of clinical events was unknown This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in the Directive 2001/83/EC and Module. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.


VAERS ID: 2271017 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-11-22
Onset: 2021-11-24
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test normal, Chest pain, Electrocardiogram normal
SMQs:, Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: EKG- Normal Blood test: Unknown - Normal
CDC Split Type: vsafe

Write-up: I was having chest pain. I went to an urgent care and an EKG was performed. My results were normal. I went to my primary care and had an exam. My results were normal. I am still experiencing chest pain and under doctor''s care.


VAERS ID: 2756215 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-11-29
Onset: 2023-11-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2024-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030592 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8091KA / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Nodule, Pain
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient suffered from knot in muscle for about 3 months. Now they are having pin-point ache with weight barring movements.


VAERS ID: 2754030 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2024-03-12
Onset: 2024-03-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-03-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 8058856 / 2 LA / SC
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7Z423 / 1 LA / IM
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. W036194 / 1 RA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. X000178 / 1 RA / SC

Administered by: Public       Purchased by: ?
Symptoms: Incorrect route of product administration, No adverse event
SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: COVID-19 vaccine administered subcutaneous instead of intramuscular. No symptoms or signs at time of vaccination. Interim clinical considerations consulted. Pt advised of administration error, that dose does not need to be repeated, repeated education on local and systemic side effects.


VAERS ID: 2742822 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2024-01-30
Onset: 2023-12-01
Submitted: 0000-00-00
Entered: 2024-02-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU3916D / 1 - / IM
DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS 9R2D7 / 1 - / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100600181 / UNK - / IM
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS 92M5G / 1 - / IM
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. X021129 / 1 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient is 7 years old but was given 0.5ml dose of Moderna COVID19 vaccine that is meant for people aged 12 and up. Error was noticed after giving vaccine. No adverse reactions in 30 mins after patient was given vaccine. Attempted to contact patient 2/1/24 to check for concerns or adverse reactions. Patient/family unable to be reached at this time.


VAERS ID: 2719025 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-11-29
Onset: 2023-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS FC22G / 2 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FLINTSTONES, RIFAMPIN, IBUPROFEN, ACETAMINOPHEN
Current Illness: ANEMIA, ACTIVE AND INACTIVE TUBERCULOSIS, INFESTATION BY SARCOPTES SCABIEI VAR HOMINIS, SERUM THYROID STIMULATING HORMONE LEVEL OUTSIDE REFERENCE RANGE, VITAMIN D DEFICIENCY
Preexisting Conditions: ANEMIA, ACTIVE AND INACTIVE TUBERCULOSIS, INFESTATION BY SARCOPTES SCABIEI VAR HOMINIS, SERUM THYROID STIMULATING HORMONE LEVEL OUTSIDE REFERENCE RANGE, VITAMIN D DEFICIENCY
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: FATHER OF CHILD REQUESTED SECOND DOSE OF FLU VACCINE. CHILD WAS VACCINATED WITH ADDITIONAL PFIZER COVID VACCINE AROUND 9AM ON 11/28/23 IN ERROR. PATIENT HAD RECEIVED THE COVID VACCINE PREVIOUSLY ON 10/25/23. FOC RETURNED TO PHARMACY AFTER BEING NOTIFIED OF ERROR. CHILD WAS THEN ADMINISTERED FLULAVAL. THERE WERE NO SIGNS OF ADVERSE REACTION.


VAERS ID: 1992747 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-09-28
Onset: 2021-12-17
   Days after vaccination: 80
Submitted: 0000-00-00
Entered: 2021-12-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 024M20A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 036A21A / 2 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 035C21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS N959G / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, Cough, Oropharyngeal pain, Pyrexia, Rash, Respiratory tract congestion, Rhinorrhoea, SARS-CoV-2 test positive, Vaccine breakthrough infection
SMQs:, Anaphylactic reaction (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Warfarin Effexor Zyrtec Prozac Topamax Wellbutrin Trazadone
Current Illness: n/a
Preexisting Conditions: DVT depression/anxiety
Allergies: none that I am aware of
Diagnostic Lab Data: Positive COVID results December 21
CDC Split Type:

Write-up: Breakthrough COVID - sore throat started December 17, fever of 100.4 on December 19, rash, congestion, runny nose, cough, positive COVID test results December 21


VAERS ID: 1924003 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-12-05
Onset: 2021-12-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 330308D / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7356MA / 1 RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The patient received flu shot first, then Covid 19 shot. Patient fainted/slumped in chair after covid shot. Patient recovered quickly.


VAERS ID: 2736923 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2024-01-05
Onset: 2024-01-01
Submitted: 0000-00-00
Entered: 2024-01-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest X-ray normal, Cough, Electrocardiogram normal, Fatigue, Head discomfort, Headache, Nasopharyngitis, Oral herpes, Palpitations, Paraesthesia, Pyrexia, Rhinorrhoea, Tinnitus, Toothache
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Oropharyngeal infections (narrow), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hearing impairment (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: I take vitamins every day including: Vitamin D, Magnesium, Alpha Lipoid, adrenal supplement, Vitamin B complex, probiotic, milk thistle
Current Illness: I had a slight sore throat a week prior to the vaccine, but not when I got it.
Preexisting Conditions: I am obese and have some arthritis that I control with PT exercise and activity.
Allergies: Penicillin allergy, I always have allergies in general (cough in the morning and a runny nose after eating - I have had this my whole life).
Diagnostic Lab Data: They did an EKG and chest X-ray. They checked my blood pressure, which was about 129/80. My oxygen was normal - I dont'' remember what it was.
CDC Split Type:

Write-up: I am confused about this vaccine name and type. The tech said it was Pfizer. The document she gave me says: Medication: COMIRNATY 12+ (COVID) 23-24 NF, Quantity 0.3, Brand Names: Comirnaty: Moderna Covid-19 Vac 6m-11u; Pfizer COVID-19 Vac-Tris 5-11y/ Pfizer COVID- 19 Vac -Tris 6m-4y; Spikevax. It also says: Generic Ingredient COSVI-19 Vaccine (mRNA) (KO vid nine teen van SEEN m RNA. The day after I got the shot, I was very very tired. When I woke up the next morning, my fingers and toes were slightly tingly. 3 days later, I had a runny nose. 4 days later I had a low grade fever of 100.4 that lasted a day and a half. I started a cough then as well that was a dry hacking cough that felt like I couldn''t clear my throat. I also had a head ache and my teeth hurt. My ears were also ringing and I had a pressure in my ears. It felt like a bad head cold. About 10-11 days later, I still had a runny nose, so much that I got a cold sore on my lip and inside my nose from blowing it with tissues. My headache and fever went away after about 7 days, but my cough stayed and got worse. On about the 10-11 day mark, I started having hard chest palpitations that would cause me to cough even though it was still a dry cough that just felt like I couldn''t clear my throat. I got scared about my heart palpitations and made a doctor appointment on Jan. 18th. I originally had one scheduled on the 19th, but moved it up because aI was afraid I would have a heart attack. My EKG and chest X-rays all came out normal. The heart palpitations were lasting less than a minute, and seem to be getting less and less. I don''t think I will ever get a covid vaccine again. I don''t know if it was the flu shot or the covid shot. My brother got Guillan Barre from a flue shot once, so this has me very nervous.


VAERS ID: 1847625 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-10-01
Onset: 2021-10-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1685 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Asthenia, Burning sensation, Fatigue, Pain
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Tramadol, robaxin, buspar, cymbalta, rosuvastatin, meloxicam, prot
Current Illness: None
Preexisting Conditions: Chronic back pain, HLP, muscle spasms, PTSD, depression and anxiety
Allergies: Lipitor and zocor? muscle pains
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Burning pains around whole body with weakness and fatigue- still a month later, I am having burning in legs with out exertion. I could be standing and my legs will start burning.


VAERS ID: 2724706 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-12-15
Onset: 2023-12-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA NDC:80777-0102- / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR NDC:49281-0423- / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Body temperature decreased, Chills, Pain in extremity, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Hives, arm pain with Moderna covid
Other Medications: Rosuvastatin, propranolol
Current Illness: None
Preexisting Conditions: High Cholesterol, anxiety, migraines
Allergies: Penicillin
Diagnostic Lab Data: None
CDC Split Type:

Write-up: 7pm 12/15 moderate arm pain, chills, decreased temperature 11am hives on chest, stomach, thighs


VAERS ID: 1912774 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-08
Onset: 2021-10-22
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2021-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Bell's palsy, Dry eye, Eye pruritus
SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Corneal disorders (broad), Hearing impairment (broad), Conjunctival disorders (narrow), Lacrimal disorders (narrow), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Glucosamine supplement, multivitamin, brain booster
Current Illness: None
Preexisting Conditions: None
Allergies: No allergies to meds or food. Allergic to cats, cottonwoods, roses.
Diagnostic Lab Data: None
CDC Split Type:

Write-up: On October 22 I began experiencing an extremely dry, scratchy right eye. By October 25 I had full-blown Bell''s Palsy on the right side of my face. I saw my eye doctor on October 26 and he recommended Refresh Mega-3 and Refresh PM eyedrops. I also saw my regular doctor, on November 16 and he prescribed Prednesone for a 6-day course.


VAERS ID: 2729991 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-11-22
Onset: 2023-11-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 8058876 / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Amnesia
SMQs:, Dementia (broad), Noninfectious encephalopathy/delirium (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received the vaccine at 11:30 am 11/23/23. The patient states he went to work, picked up his badge and radio, and was working. He does not remember how he got home that day. He was home with his work supplies but has no recollection of driving home that night. He went to the emergency room at 8pm that night upon realizing what had happened.


VAERS ID: 2749826 (history)  
Form: Version 2.0  
Age: 18.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2024-02-20
Onset: 2024-02-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2024-02-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HM7006 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8096AA / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Lip swelling, Swelling face, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Pre-diabetes, microcytic anemia, Vitamin D insufficiency, obesity
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient had total body urticaria, face and lip swelling that started the day after receiving vaccines on 2/21/24. Came to the clinic on 2/27/24 with persistent symptoms.


VAERS ID: 2728240 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Colorado  
Vaccinated: 1959-07-07
Onset: 2023-12-22
   Days after vaccination: 23544
Submitted: 0000-00-00
Entered: 2023-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9835 / N/A RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3P993 / N/A LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Product expiration date issue
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Proair, Duloxetine, Simvastatin, and Anoro Ellipta.
Current Illness: None
Preexisting Conditions: Cardiac And Vasculature Bradycardia Mixed hyperlipidemia Endocrine And Metabolic Weight loss Pre-diabetes Ent Tinnitus of both ears Vertigo Gastrointestinal And Abdominal GERD (gastroesophageal reflux disease) Elevated AST (SGOT) Epigastric pain Acute biliary pancreatitis Cholelithiasis with choledocholithiasis Health Encounters Health care maintenance Hematology And Neoplasia Elevated WBC count Mental Health Alcohol dependence in sustained full remission Severe episode of recurrent major depressive disorder, without psychotic features Neuro Leg numbness Pulmonary And Pneumonias Asthma Shortness of breath Obstructive lung disease (generalized) COPD exacerbation Centrilobular emphysema Symptoms And Signs Fatigue Hot flashes Tobacco Tobacco dependence
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Covid vaccine box had 2 expiration dates and wrong date used.


VAERS ID: 1855077 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-11-09
Onset: 2021-11-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 0077C21B / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367901 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, Heart rate decreased, Hypotension, Inappropriate schedule of product administration, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Medication errors (narrow), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: MESALAMINE
Current Illness: Chrohn''s disease
Preexisting Conditions: Chrohn''s disease
Allergies: None
Diagnostic Lab Data: Blood pressure 101/58, heart rate 47; blood pressure after 15 minutes and water 115/81, heart rate 57.
CDC Split Type:

Write-up: Patient fainted and had low blood pressure/heart rate (45) about 5 minutes after receiving flu and covid booster vaccine. Blood pressure readings are as follows, 1100am after incident 101/58, 47 heart rate; 103/58, 51 heart rate; 103/67, 52 heart rate. Patient was given full glass of water and a small fruit bar. The patient raise his legs while waiting in lobby area. Rechecked blood pressure at 11:15am where it was 115/81, heart rate 57. Patient declined for us to call 911. Urged him to go home, have a meal, take it easy, and keep an eye on heart rate. Patient denies previous infection, reaction to vaccines, or history of seizures. wife will stay with him rest of day. Informed him to avoid driving and alcohol today as well. The patient left at 11:23. The patient called his doctor and he was not concerned. The patient has an appointment with doctor in a few months.


VAERS ID: 2732549 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2024-01-12
Onset: 2024-01-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HM7006 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8200BA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Pallor, Visual impairment
SMQs:, Anticholinergic syndrome (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Patient states history of fainting, unknown vaccines
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient stated prior to giving shots that he has past medical history of fainting with vaccine administration. Gave patient both shots in right deltoid normally, patient''s mother stated that he was looking paler than normal. After a few minutes of sitting, patient noted that he was having trouble seeing, at which point I had the patient lay down on the floor and elevated his feet. Patient continued to talk and had consistent pulse during this time. After ~5 minutes, patient regained vision and he stayed laying down for another 10 minutes before moving to a chair, and after 10 minutes he was ok to walk around the store.


VAERS ID: 2728239 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-12-22
Onset: 2023-12-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9300 / N/A RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5452E / N/A LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, Product label confusion
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Omeprazole , Sertaline, and Trazadone.
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Covid vaccine box had 2 expiration dates, and the wrong date used.


VAERS ID: 2728238 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-12-22
Onset: 2023-12-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9300 / N/A RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5452E / N/A LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Covid vaccine box had 2 expiration dates , and wrong date used.


VAERS ID: 1917799 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-11-24
Onset: 2021-11-27
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-12-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Electrocardiogram normal, Palpitations
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None.
Current Illness: None.
Preexisting Conditions: None.
Allergies: Sulfa.
Diagnostic Lab Data: 12/2/21 - EKG - Normal.
CDC Split Type:

Write-up: Heart palpitations lasting 5-10 minutes. Presented when exercises but continued when at a standstill. They had not occurred previously or since.


VAERS ID: 1962344 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-12-19
Onset: 2021-12-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 060H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7384MA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest discomfort, Chills, Dizziness, Feeling hot, Malaise, Nausea, Paraesthesia, Vision blurred, Visual impairment
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None reported
Current Illness: No chronic diseases reported
Preexisting Conditions: none reported
Allergies: None reported
Diagnostic Lab Data: none reported
CDC Split Type:

Write-up: Patient reported not feeling well, including feeling nauseous on her way to the bathroom. Patient reported feeling like she would faint. She went to a chair to sit down and notified pharmacy staff. Patient reported feeling warm and having chills. Slight heaviness in the chest was reported. She also reported blurred vision and seeing white spots. Tingling in her fingers was also reported.


VAERS ID: 2727111 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-12-24
Onset: 2023-12-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5553B / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8202CA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fall, Fatigue, General physical condition abnormal, Loss of consciousness, Pallor, Somnolence
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: n/a
Diagnostic Lab Data:
CDC Split Type:

Write-up: 7-year-old patient received 2 vaccinations (fluzone and Moderna 6-11 covid vaccine) on 12/24/23. After receiving the vaccines, he was fine walking around waiting for his sister''s vaccination turn. About 5 minutes later he came back to the clinic booth, sat on the chair with mom, started to fall (on Mom''s hand patted against the table), losing consciousness for about 15 seconds, then got back up slowly. Code White was called. His pulse was at normal range. We gave him some orange juice and he got better. He got better for about 5 minutes and then started to look pale and droopy again. We tried to talk to him to keep him awake, and the patient said he was very tired and sleepy. Ambulance was called. When the ambulance arrived, the patient got better and became active again.


VAERS ID: 2747310 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-17
Onset: 2023-10-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Hypoaesthesia, Injection site hypoaesthesia, Injection site pain, Injection site paraesthesia, Paraesthesia
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline: 150 mg, Wellbutrin: 150 mg
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: A few hours post vaccination, a tingling, numbness, and painful sensation developed near where the vaccine was given. This spread through the left shoulder blade area, and has not changed since. Treatment has not been successful. I have tried heat, ice, ibuprofen, per doctor''s requests, and none of it has helped. This has been a constant numbness with frequent tingling and stabbing sensations that only cease at rest.


VAERS ID: 2210228 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-29
Onset: 2022-01-01
   Days after vaccination: 64
Submitted: 0000-00-00
Entered: 2022-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 058F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Feeling abnormal, Impaired work ability, Oropharyngeal pain, SARS-CoV-2 test negative, SARS-CoV-2 test positive, Streptococcal infection
SMQs:, Dementia (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: 01/01/2022 COVID test(positive); 01/13/2022 COVID test(negative)
CDC Split Type: vsafe

Write-up: 01/01/2022 Took a COVID test because I was around others on that possibly had COVID and felt off on the next day. 01/03/2022 Felt pretty bad and decided not to go to work and got the results back and found it positive. 01/04/2022 My sore throat was feeling really bad thinking I may have strep on top of my COVID issue. Sent a photo to my doc to confirm. Was prescribed a Z-pak and did not work. Therefore, I got penicillin and prednisone. That seemed to have done the trick for my throat. By 01/14/2021 was clear of both strep and COVID.


VAERS ID: 2724977 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-12-15
Onset: 2023-12-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9300 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS FC22G / UNK LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: form was marked as "none"
Preexisting Conditions: unknown
Allergies: form was marked as "none"
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Front desk staff member wrote the wrong age for child. Child received Pfizer covid vaccine for age 12+ and child is only 10 years 3 months. Error was noticed at the end of day.


VAERS ID: 2473144 (history)  
Form: Version 2.0  
Age: 1.5  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-10-06
Onset: 2022-10-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR9236B / 1 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS T9HA2 / 2 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Extra dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received second influenza vaccine this season. First dose: 10/3/2022. Second dose 10/6/2022. No adverse reaction after immunizations given. Parent advised to monitor for increased soreness, fever or other adverse reaction.


VAERS ID: 2724731 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-12-13
Onset: 2023-12-15
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-12-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HM7010 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8043CA / 1 LA / IM
RSV: RSV (ABRYSVO) / PFIZER/WYETH HA3217 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site erythema, Injection site warmth
SMQs:, Extravasation events (injections, infusions and implants) (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: called pt and left message to call back. on file warfarin, tramadol, allopurinol
Current Illness: a fib
Preexisting Conditions: a. fib
Allergies: nkda,
Diagnostic Lab Data: will go to medical doctor monday to check on it if still doing bad
CDC Split Type:

Write-up: red and hot around area vaccine was given


VAERS ID: 2749020 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2024-02-23
Onset: 2024-02-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. - / UNK - / -
MNQ: MENINGOCOCCAL CONJUGATE (MENVEO) / NOVARTIS VACCINES AND DIAGNOSTICS - / UNK - / -
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Public       Purchased by: ?
Symptoms: Dizziness, Fall, Fatigue, Head injury, Headache, Paraesthesia, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: NA
Current Illness: None reported
Preexisting Conditions: None reported
Allergies: NKA
Diagnostic Lab Data: Unknown
CDC Split Type:

Write-up: The above vaccines administered without incident. Nurse walked with patient and MOC to checkout without incident. At the checkout, patient fainted, the fall resulting in him hitting the back of his head. Patient woke within seconds, responded appropriately verbally, VS assessed. BB 96/78, Pulse 69. Pupils equal and reactive, no blurry vision reported. Patient assisted to a sitting position, ice pack place on back of head/neck and juice given. After approximately 20 minutes, patient continued to pain of headache and dizziness and fatigue and a "tingly" right arm. 911 called. After EMS assessed patient, recommendation made to take child to ER. MOC chose to transport him to ER via personal vehicle. EMS to help patient to personal vehicle.


VAERS ID: 2722378 (history)  
Form: Version 2.0  
Age: 0.5  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-12-07
Onset: 2023-12-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS B94B3 / 1 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin D3 drops
Current Illness: none
Preexisting Conditions: none
Allergies: nka
Diagnostic Lab Data: none
CDC Split Type:

Write-up: in addition to above vaccines pt received adult RSV vaccine Abyrsvo, NDC # 0069-0207-01, LOT # HF5016, intramuscular, Right Thigh, dose 1 in series


VAERS ID: 1835805 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-14
Onset: 2021-10-23
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8439 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blister, Herpes zoster
SMQs:, Severe cutaneous adverse reactions (broad), Hypersensitivity (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Estradiol, mirena IUD, red rice yeast, magnesium
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin and sulfa
Diagnostic Lab Data: I was seen in urgent care on 10/25 and started on valcyclovir, I was seen on 10/26 by an optometrist who determined there was no ocular involvement despite vesicles on my lower eyelid. No lab tests were done but the vesicles and symptoms have continued to improve with Valtrex but not fully resolved.
CDC Split Type:

Write-up: On 10/23/21, nine days after the Pfizer COVID booster and flu shot on (10/14/21) I had an outbreak of shingles on my right face. I was seen in urgent care on 10/25 and started on valcyclovir, I was seen on 10/26 by an optometrist who determined there was no ocular involvement despite vesicles on my lower eyelid.


VAERS ID: 2155536 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-09-30
Onset: 2021-10-15
   Days after vaccination: 15
Submitted: 0000-00-00
Entered: 2022-03-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Balance disorder, Erythema, Gait disturbance, Limb discomfort, Muscular weakness, Myalgia, Pain, Pain in extremity
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Premarin 0.625 mg, Aspirin, Levothyroxine 25 mg, Kriill Fish Oil Omega 3, Multiple Vitamin, Calcium, Zinc, Hydrochlorothiazide (pee pill) 25 mg., as needed, Vitamin D3
Current Illness: None
Preexisting Conditions: Bulging Disc
Allergies: Prednisone, Erythromycin, Sulfa Drugs
Diagnostic Lab Data: Provider did hands-on muscle test on legs January 5, 2022. Test indicated muscle weakness.
CDC Split Type:

Write-up: Approx. 2 weeks after 3rd shot (Booster), my legs became heavy and weak. I could not walk normally and experienced loss of balance. THIS IS ONGOING. I am also experiencing stabbing pains at the top and bottoms of my feet and in my calfs, along with reddish toes. Both thigh muscles pain to the touch. Stabbing pain occurs randomly. No fever at any time. As stated, condition has not gotten better even though I use a stationary bike daily to strengthen muscles.


VAERS ID: 2608517 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2022-10-02
Onset: 2023-01-24
   Days after vaccination: 114
Submitted: 0000-00-00
Entered: 2023-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ6665 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Oropharyngeal pain, Pyrexia, SARS-CoV-2 test positive, Subdural abscess
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 20 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Multi-vitamins; Vitamin D-3; Iron; Timolol; Amlodipine; Endostatin; Trazodone
Current Illness: None
Preexisting Conditions: Controlled Hypertension
Allergies: None
Diagnostic Lab Data: 04APR2022 - COVID-19 Rapid Test - Tested positive
CDC Split Type: vsafe

Write-up: I tested positive for COVID-19 and was put on Paxlovid by the infectious diseases doctor at the hospital while I was being treated for a Subdural Abscess which did not have anything to do with the COVID-19 vaccine. I am experiencing painful sore throat, slight fever of 99 degrees off and on (sometimes it is 98 - 99 degrees). I am currently on Day 2 of COVID-19.


VAERS ID: 2611224 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-10-19
Onset: 2023-04-01
   Days after vaccination: 164
Submitted: 0000-00-00
Entered: 2023-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ6665 / 4 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Cough, Headache, Nasal congestion, Pyrexia, SARS-CoV-2 test positive, Throat irritation
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamin; Glucosamine Chondroitin; Vitamin C; Vitamin D; Fish Oil; Vitamin Multi B-Complex
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: 02APR2023 - COVID-19 At Home Test - Positive
CDC Split Type: vsafe

Write-up: It started as a scratchy throat. That night became nasal congestion, cough, and a headache. The next day I called the doctor to try and get on Paxlovid. I probably had a slight fever but didn''t take my temperature. I was able to do a Telehealth visit and was prescribed Paxlovid.


VAERS ID: 1900013 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-08-25
Onset: 2021-09-06
   Days after vaccination: 12
Submitted: 0000-00-00
Entered: 2021-11-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Blood potassium decreased, Blood test, Electrocardiogram normal, Feeling hot, Gait disturbance, Hepatitis, Peripheral coldness, Peripheral swelling, Skin exfoliation, Ultrasound scan normal
SMQs:, Cardiac failure (broad), Hepatitis, non-infectious (narrow), Severe cutaneous adverse reactions (broad), Angioedema (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Hypokalaemia (narrow), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Symbacort
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillan
Diagnostic Lab Data: Blood work done 4 times and an Ultrasound performed. EKG also done. Nothing showed any problems so we were told.
CDC Split Type:

Write-up: Radiating heat from chest to stomach. Extreme swelling of feet and legs. Skin broken open and peeling. Feet go from hot to cold. Blood work done 3 times at physicians office and once at the ER. Recommended Podiatrist. She recommended to see a Nuerologist. Referral was done and was scheduled for December 2. Now we are told she doesn''t have an appointment there. A different referral was given to another Nuerologist but she can''t be seen until December 14. Meanwhile no Dr at the ER nor at her primary care office will give any reason why she is having continued problems. They did say the blood work showed Liver inflamation but basically gave no reason why. ER said low in Potassium. Extremely painful to walk. She was given hormone therapy and muscle relaxor. Also Gabapatenin. Nothing given to help with pain.


VAERS ID: 1776851 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-05
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR YT377LA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: None stated.


VAERS ID: 2702234 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-24
Onset: 2023-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 5 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Peanuts, tree nuts
Diagnostic Lab Data:
CDC Split Type:

Write-up: Currently 24 weeks pregnant. Due 2/12/2024


VAERS ID: 2617535 (history)  
Form: Version 2.0  
Age: 5.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-04-10
Onset: 2023-04-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-04-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FY3680 / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ899AB / 1 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Incorrect vaccine given for this age of patient. Received 6mo-4yr covid monovalent dose instead of 5-11yrs covid monovalent dose. No adverse reaction.


VAERS ID: 2701474 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-24
Onset: 2023-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG5967 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8069LA / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. W026977 / 1 RA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. W033287 / 1 LA / SC
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X010534 / 1 RA / SC

Administered by: School       Purchased by: ?
Symptoms: Blood pressure decreased, Cold sweat, Dizziness, Fatigue, Feeling cold, Pallor
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Unknown information regarding previous vaccines or if other vaccines were also prescribed at that time.
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was updating vaccines since moving to the country. After vaccines were administered, she felt dizzy, clammy, cold and tired. Her BP was checked and was 68/40 at that time. Water offered and watched patient and rechecked BP after about 10 minutes and was 92/58. After another 10 minutes BP was 107/71. Patient was pale in color and clammy and cold, but all symptoms resolved within about 20-30 minutes after vaccines. Patient stated after that this BP drop has happened with each covid vaccine, but she didn''t report prior to administration. Oxygen and Heart rate were stable throughout. Patient didn''t faint.


VAERS ID: 1873844 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-11-16
Onset: 2021-11-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 071F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 42M9S / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Disorientation, Loss of consciousness, Pallor, Seizure, Tremor
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Convulsions (narrow), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: hx of syncope after a vaccine a few years ago.
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: NONE. hx of syncope with vaccines. hasnt happened in years.
Allergies: NONE
Diagnostic Lab Data: N/A. Paramedics called to transfer patient to hospital to get checked out.
CDC Split Type:

Write-up: patient passed out less than 5 minutes after receiving the moderna booster vaccine (0.25mL) and the influenza vaccine (flulaval quadrivalent). He had received the first two moderna shots in the past and had no issues. They were both administered in the left deltoid muscle. After I administered both vaccines a couple minutes later, the patient lost all color in face and began to seize (no history of seizures in the past). His arms began to shake, he made a loud moan, and starting moving his head around. Patient was sitting in a chair at the time and so I lowered him slowly and safely to the floor and laid him on his left side supporting his head. He lost consciousness for about 30 seconds (thats how long the seizure lasted) and afterwards regained consciousness. Was alert and able to answer questions correctly, but expressed that he didnt know what had occurred but that he felt disoriented. Two to three minutes went by and he began to seize again for the next 30 seconds. paramedics were called. no injury to the patient. trasnferred to the hospital to get checked out. documented accordingly in VAERS report and in patients chart. Patient should not receive another moderna vaccine or another flulaval vaccine in the future.


VAERS ID: 2621558 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-10-21
Onset: 2023-03-20
   Days after vaccination: 150
Submitted: 0000-00-00
Entered: 2023-04-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ3277 / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chronic lymphocytic leukaemia, Full blood count abnormal, Lymphocyte count increased
SMQs:, Haematopoietic leukopenia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Crestor
Current Illness: None
Preexisting Conditions: High Cholesterol
Allergies: Penicillin; Cephalosporin
Diagnostic Lab Data: CBC elevated lymphocytes.
CDC Split Type: vsafe

Write-up: On 20MAR2023 my Doctor diagnosed the following information; CBC shows elevated lymphocytes consistent with CLL. There are may treatments for CLL but I have no indication for treatment.


VAERS ID: 2706538 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-30
Onset: 2023-10-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 30320899 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8200BA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood pressure decreased, Cold sweat, Feeling of body temperature change, Hyperhidrosis, Loss of consciousness, Pallor, Paraesthesia, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: n/a
Diagnostic Lab Data: BP DROPPED TO 49/30 O2 SAT WAS NORMAL PULSE 47
CDC Split Type:

Write-up: VAGAL SYNCOPE WITH DROP OF THE BLOOD PRESSURE (BP READING 49/30), LOSS OF CONSCIOUSNESS FOR LESS THAN 10 SECONDS. TINGLINESS IN THE FINGERS. PALOR. FEELING WARM THEN COLD. CLAMY. SWEAT. RESOLVED IN NEXT 30MINUTES WITH LEGS ELEVATED .


VAERS ID: 2699772 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-19
Onset: 2023-10-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031912 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8131AA / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dysgeusia, Hypoaesthesia oral, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Taste and smell disorders (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: FLU LIKE SYMPTOMS FROM PAST MODERNA SHOTS
Other Medications: Xanax
Current Illness: na
Preexisting Conditions: na
Allergies: penicillin, sulfa, shellfish
Diagnostic Lab Data:
CDC Split Type:

Write-up: NUMB LIPS AND TONGUE, WELT ON ARM SIZE OF BASEBALL, TRAVELING UP NECK TO TOP OF HEAD, METALLIC TASTE


VAERS ID: 1799136 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-10-07
Onset: 2021-10-10
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / 1 RA / IM

Administered by: Military       Purchased by: ?
Symptoms: Laboratory test, Rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Cetirizine, metoprolol, aspirin 81mg
Current Illness: Bronchitis
Preexisting Conditions: Major depression disorder, high blood pressure
Allergies: No known allergies.
Diagnostic Lab Data: Fasting labs are being conducted on 20 OCT 21/ Referral was given to allergy specialist from a dermatologist.
CDC Split Type:

Write-up: Rash/bumps with redness on chest, abdomen, upper arm(biceps). Sights do not have ?itchy? sensation however does feel good when scratched. No course of action being taken via facility


VAERS ID: 2685976 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-09-24
Onset: 2023-09-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-09-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4629 / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 371624 / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Chills, Listless, Musculoskeletal stiffness, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 69 Covid Pfizer September 2021
Other Medications: Losartan Statin Prozac
Current Illness: none
Preexisting Conditions: High Blood Pressure
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Severe chills and shaking for 1 hour the night of 9/24/23. Day of 9/25/23 extreme stiffness and joints were achy. Chills returned in the late morning. Listlessness.


VAERS ID: 2694825 (history)  
Form: Version 2.0  
Age: 1.17  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-10
Onset: 2023-10-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5509B / 2 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8069LA / 1 RL / IM
HIBV: HIB (PEDVAXHIB) / MERCK & CO. INC. W032687 / 4 LL / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. W033285 / 1 RL / SC
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X007372 / 1 LL / SC

Administered by: Public       Purchased by: ?
Symptoms: No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: No reaction. Pt was supposed to get Pfizer vaccine due to age and new 23-24 requirements.


VAERS ID: 2693436 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-06
Onset: 2023-10-07
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 80777-0102-96 / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR 49281-0123-65 / N/A LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS 58160-0848-11 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Asthenia, Fatigue, Gait disturbance, Injection site pain, Mobility decreased, Myalgia, Pain, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Estradiol, Atorvastatin, Omeprazole, Fish Oil, Melatonin Vit.D3, Zyrtec
Current Illness: Bronchitis, sinusitis
Preexisting Conditions: None
Allergies: Sulfa
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Within twelve hours of getting three vaccines, I experienced soreness and tenderness at the injection sites. Then, fever (101.2); muscle, joint and body aches; extreme fatigue; weakness; joint pain; difficulty walking. Today - day 4 - left arm tenderness minimal, but unable to use right arm because of pain and tenderness of whole deltoid area; joint pain and fatigue and difficulty walking persists.


VAERS ID: 2495149 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2022-11-01
Onset: 2022-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 083BB22A / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR IJ879AB / N/A LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Unknown
Preexisting Conditions: unknown
Allergies: Amoxicillin allergy - hives
Diagnostic Lab Data: This nurse called the legal guardian (Grandmother) of client on 11/1/2022. Client''s grandmother was understanding of the situation that took place. Ensured that this incorrect dose was not harmful and provided education on what to expect after vaccination. Notified client''s grandmother that the client could still receive his COVID-19 Bivalent Booster, 2 months from today.
CDC Split Type:

Write-up: Client presented to Clinic on 11/1/2022 for COVID-19 Moderna 12+ Bivalent Booster (0.5mL dose). Client inadvertently received COVID-19 Moderna 12+ Monovalent (0.5mL dose). Following CDC guidance, the recommendation is that providers may administer 1 bivalent booster dose as a repeat dose based on clinical judgement and patient preference. If a repeat dose is given it must be adminstered at least 2 months after the dose given in error.


VAERS ID: 2065987 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2022-01-23
Onset: 2022-01-24
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1619 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fluid retention, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Sulfa
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Pt. states that after receiving the 1st dose of Influenza 01/23/2022, started experiencing symptoms 01/24/2022 of swelling at the lower back region with fluid build-up (Quarter-Sized Pocket located at the base of the spine). No noted Primary visit/communications.


VAERS ID: 1795358 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-15
Onset: 2021-10-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 035C21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Anxiety, Condition aggravated, Disturbance in attention, Feeling abnormal, Impaired driving ability, Impaired work ability, Panic attack
SMQs:, Dementia (broad), Noninfectious encephalopathy/delirium (broad), Depression (excl suicide and self injury) (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: TDAP/ Feb 2019/ swelling and welt at injection site
Other Medications: Augmentin
Current Illness: Sinus Infection
Preexisting Conditions: Anxiety. Cancer Survivor
Allergies: Vincristine, Adriamycin, Estrogens, Morphine
Diagnostic Lab Data:
CDC Split Type:

Write-up: I woke up feeling like I was in a Fog around 0530. I felt drugged and sedated. I work in an inpatient Pharmacy, that morning I worked in the sterile IV room. I reported to work at 0630. I told me coworkers how I felt. They asked me if I should be working, I told them I was fine. As the morning progressed my mind grew more frenzied, more sporadic. I spiraled, I couldn''t maintain thought patterns, I couldn''t think straight. As 0800 came, I knew that there was a strong possibility that I could make some mistakes and took a break and sat down in the hospital library. It didn''t help. I grew more frantic and foggy. Around 1100 I left work, my coworkers asked me if I was ok to drive. I told her I was fine, it was only two and a half miles to home. I shouldn''t have driven. I drove frantic that I was going to crash and sure that someone was in my blind spot as i switched lanes. I got home safely, kicked off my shoes, took a Xanax that I have prescribed for Panic attacks ( Since i had been fighting one off for about 4 hours at that point) and fell into bed, where i stayed in the same position for 5 hours, by 2000 that night I was still feeling foggy, but the anxiety was still there, though not as severe. It is now Monday after the test and I still feel elevated anxiety levels, though less of the fog. If I had not had the xanax at home I would have admitted myself to the ER.


VAERS ID: 2074925 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-12-12
Onset: 2021-12-21
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2022-01-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / N/A RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test normal, Mechanical urticaria, Pruritus, Rash, Urticaria, Urticaria chronic
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Vienva (oral contraceptive)
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin
Diagnostic Lab Data: Blood tests for multiple auto immune diseases (lupus, rheumatoid arthritis, etc.) and all tests have come back negative. I will be undergoing allergy testing on 1/30/2021.
CDC Split Type:

Write-up: Chronic urticaria and dermatographia. Persistent Hives, painful rashes, wheals, itching all over head, face, neck, torso, limbs, hands, and feet since 12/20/21.


VAERS ID: 1765111 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-09-30
Onset: 2021-10-02
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3592 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100350381 / 1 RA / SYR

Administered by: Work       Purchased by: ?
Symptoms: Extra dose administered, Injection site erythema, Injection site swelling, Lymphadenopathy
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 01/09/21 COVID Vaccine Phizer
Other Medications: Pepcid (40) MG and BComplex Oral
Current Illness: No
Preexisting Conditions: No
Allergies: Codeine and Sulfa
Diagnostic Lab Data: Put on steroids for 12 days for injection site infection and swollen left lymph node
CDC Split Type:

Write-up: Left lymph node swelled up to size of orange under left arm. Swelling (3 to 4 inches) round red area round injection site going down arm.


VAERS ID: 2573918 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-02-01
Onset: 2023-02-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 022H22A / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ943AB / N/A RA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U762AA / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Hyperhidrosis, Loss of consciousness, Pallor, Tinnitus
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hearing impairment (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none known
Current Illness: none known
Preexisting Conditions: none known
Allergies: none known
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received 3 vaccines. Immediately after, while still seated, he felt faint and passed out for less than 30 seconds. When he awoke on his own, he had ringing in his ears, was sweaty and pale in color. Patient was provided a cold wet towel for his forehead and some water. He sat for 20 minutes or so until he was ready to leave.


VAERS ID: 2713789 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-26
Onset: 2023-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Immediate post-injection reaction, Injected limb mobility decreased, Injection site pain, Pain in extremity, Product administered at inappropriate site
SMQs:, Drug abuse and dependence (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lexapro, wellbutrin, focalin
Current Illness: None
Preexisting Conditions: Depression, ADHD
Allergies: None
Diagnostic Lab Data: MRI - planned; ortho referral pending
CDC Split Type:

Write-up: Vaccines were adminstered high in left shoulder. The second injection caused immediate significant pain. Pain in arm continued with minimal improvement for ~ 10 days with difficulty fully moving shoulder despite regular ibuprofen use. Discussed with pediatrician around day 5 who recommended continuing ibuprofen. When pain continued we discussed again with pediatrician who prescribed decadron x 5 days. Pain improved by day 4. One ~ day 3 following decadron course, pain in left shoulder returned and worsened over next 3 days with limitation in movement. Seen by PCP office on 11/14 and shoulder MRI, ortho referral and repeat course of decadron for pain management were recommended. Vaccines were covid spikevax moderna and fluzone quad - I don''t know which was administered 2nd - both were in a similar location.


VAERS ID: 2577045 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-01-31
Onset: 2023-01-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FX5095 / 1 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7682MA / 1 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Unevaluable event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vit D
Current Illness: none
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: None


VAERS ID: 2001873 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-01-03
Onset: 2022-01-04
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Feeling hot, Headache, Myalgia, Nausea, Pain, Pain in extremity, Pyrexia, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: I had no symptoms with my other two covid-19 shots so I was expecting the same for my booster. When I got home my arm was getting more sore throughout the night but I just kept trying to stretch it before I went to bed. I woke up around 4 AM and I had a headache, muscular pain & body aches, and I felt rather warm. I took my temperature and it was 99.7 and I took some medicine and made myself some tea. Before I could drink it I threw up everything and that happened around 5:45 AM. I have had the same symptoms all day until time of reporting this (1:50 PM) including nausea, body aches & muscular pain, headaches, fever, chills.


VAERS ID: 2591932 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-10-01
Onset: 2023-02-22
   Days after vaccination: 144
Submitted: 0000-00-00
Entered: 2023-03-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cough, Headache, Influenza A virus test negative, Influenza virus test negative, Oropharyngeal pain, Pyrexia, SARS-CoV-2 test negative, Throat irritation
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Daily vitamin
Current Illness: No
Preexisting Conditions: Low white cell blood count
Allergies: Ceftin; Cobalt; Nickel
Diagnostic Lab Data: Home COVID-19 test - negative; PCR COVID-19 - negative; Influenza A and B - negative
CDC Split Type: vsafe

Write-up: I had returned from a trip, I noticed I started scratchy throat and headache on Wednesday. I took a several home COVID-19 test that came back negative. I still felt feverish, was coughing, my throat was hurting and scratchy, so I went to the local Urgent Care and did the drive-up test for COVID-19 and flu A and B. All tests came back negative. I was advised to get plenty of rest and stay hydrated.


VAERS ID: 2713181 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2023-10-28
Onset: 2023-11-01
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2023-11-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Crying, Dysmenorrhoea, Heavy menstrual bleeding, Menstruation irregular, Mobility decreased, Muscle spasms
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Parkinson-like events (broad), Depression (excl suicide and self injury) (broad), Fertility disorders (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: same terrible cramps and heavy period has occurred after every COVID vaccine I''ve received. Usually it lasts for 2 cycles. As a
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: When my monthly period arrived (slightly earlier than usual), my cramps were incredibly painful and my period was unusually heavy. This has happened for a cycle or two after every COVID vaccine I have received. The cramps are so bad that I stay in bed and cry, heat compresses don''t help, pain relievers don''t help. They last for 2 full days.


VAERS ID: 2006293 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-12-20
Onset: 2021-12-28
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2022-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH - / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Cough, SARS-CoV-2 test negative, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Triamterene losartan phenytoin b-12, fish oil, turmeric, magnesium, cranberry, condjointran, glucosimen,
Current Illness: None
Preexisting Conditions: None
Allergies: penicillin
Diagnostic Lab Data: Dr. prescribed steroid, and cough medication. Completed the prescriptions, tested negative for covid 01/03/2022. Test Name 2019 RNA Virus
CDC Split Type:

Write-up: Developed a cough, and went to Dr. on 28, December 2021. Tested positive for covid


VAERS ID: 1881185 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-26
Onset: 2021-11-01
   Days after vaccination: 6
Submitted: 0000-00-00
Entered: 2021-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1822811 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Gait inability, Magnetic resonance imaging, X-ray
SMQs:, Anticholinergic syndrome (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Progesterone, Armour Thyroid, Esomeprasole-Magnesium, DIM, Probiotics, Cucumin, Collagen, MCT Oil powder, Benefiber
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: X-Ray MRI
CDC Split Type:

Write-up: Sudden, significant pain in right knee. Resulted in inabilty to walk.


VAERS ID: 2710611 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-11-01
Onset: 2023-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG6396 / N/A LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG6396 / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8103CA / N/A LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8103CA / N/A LA / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Extra dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Antidepressants. Vitamin D
Current Illness: Dementia, unspecified. Benign neoplasm. PTSD. RLS.
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Resident received Influenza Fluzone High-Dose and Covid 19 vaccinations at approximately 9:00am and then received both vaccines again at approximately 12:30pm. Resident had no immediate adverse reactions, vital signs were taken and within normal range. He was monitored for 30 minutes and after no signs or symptoms of an adverse reaction, Pt was okay to leave the clinic.


VAERS ID: 1808538 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-10-22
Onset: 2021-10-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 035C21 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ694AA / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Intended to give Influenza and Moderna Booster. Gave two doses of Influenza vaccine instead. Discussed with patient and provider and booster Moderna dose administered. Patient observed with no reaction.


VAERS ID: 2455243 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-09-22
Onset: 2022-09-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ7150 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5CY7T / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Paraesthesia oral, Throat tightness, Tongue dry
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Orsynthia 0.1mg-20mcg
Current Illness: None
Preexisting Conditions: None
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received first Pfizer Covid shot (along with Fluarix lot # 5cy4t exp 6/30/2023; patient has annual flu shots and has not had an adverse reaction to these before). After 15 minute waiting period, her tongue was dry and tingly. We requested she remain seated here for an additional 10-15 minutes to make sure she wasn''t getting worse and had a staff member remain present with her. Few moments later, the staff informs me the patient says her throat feels tight. Proceeded to call EMS who arrived within 2 minutes of phone call. Patient was alert and oriented, did not fall or faint, and remained that way with EMS as they left for further evaluation.


VAERS ID: 2526831 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2022-12-08
Onset: 2022-12-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GD1857 / 1 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7752KA / 1 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: guanfacine, clonidine, elderberry, zyrtec
Current Illness: none
Preexisting Conditions: autism
Allergies: penicillin- steven johnson syndrome
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt received covid vaccine at 3pm, then flu shot 5 minutes later, then 5 minutes after that had hives on face, chest, and neck. hives began improving 15 minutes later on face, but still has hives on chest and neck.


VAERS ID: 1758994 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2021-10-02
Onset: 2021-10-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Fatigue, Nausea, Thirst, Vomiting
SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Nausea, fatigue, thirst
Other Medications: Metoprolol, Benazepril, simvastatin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Nausea, vomiting, severe fatigue, severe thirst, cold chills


VAERS ID: 2709834 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Male  
Location: Colorado  
Vaccinated: 2023-10-11
Onset: 2023-10-20
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2023-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / -
RSV: RSV (ABRYSVO) / PFIZER/WYETH - / UNK RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Brain scan normal, Chest X-ray normal, Chest pain, Computerised tomogram abdomen normal, Fall, Feeling abnormal, Hepatitis acute, Hypertension, Liver disorder, Liver function test abnormal, Mobility decreased, Pyrexia
SMQs:, Liver related investigations, signs and symptoms (narrow), Hepatitis, non-infectious (narrow), Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hypertension (narrow), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: benazepril, 10 mg atorvastatin, 40 mg
Current Illness: none
Preexisting Conditions: arterosclerosis (stent installed 12 years ago)
Allergies: none
Diagnostic Lab Data: Blood tests were performed on 10/24/2023, 10/25/2023, and again on 10/27/2023 More are scheduled 11/6/2023. CT scans of the abdomen were performed on 10/24/2023
CDC Split Type:

Write-up: 1. 10/20/2023 9:18 pm -- Checked into ER with chest pain and spiking high blood pressure (180/75). Blood tests showed that there were no heard or kidney issues. Chest x-ray was normal. Was released from ER after blood pressure subsided some and chest pain lessened. The following day, I noticed a mild f3ever that broke in the evening as which my blood pressure returned to normal (130 / 60 ) and I felt much better. 2. 10/24/2023 -- I awoke early and felt very dopy. I fell and was unable to get myself up after which my wife managed to get me up and into the ER again. Blood tests indicated liver issues and a number of other blood results that were out of normal range. I was diagnosed with acute hepatitis. Scans of the abdomen and head were normal.


VAERS ID: 2476633 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2022-10-12
Onset: 2022-10-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7741LA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vaccine was pulled from our fridge with a BUD date of 10/31 and administered. Later that day we received a notice from our corporate that the lot used was short-dated by the manufacturer and expired on 9/30 regardless of when it was placed in our fridge.


VAERS ID: 1825685 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Colorado  
Vaccinated: 2021-10-28
Onset: 2021-10-28
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939903 / 4 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ773AC / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Technician was providing immunization. There were 2 people with the same name getting vaccinations at the time. The incorrect patient came in to the room and when asked if she was receiving the Moderna booster dose today, she confirmed it. However, this was incorrect as she was signed up for a flu shot. The patient reports "being in a haze" when the question was asked and "not hearing what was said" while she responded in the affirmative. Patient had already received a Moderna booster dose 1 week previously so we will monitor her for any adverse events.


VAERS ID: 2511958 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-11-18
Onset: 2022-11-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 057F22A / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: No known illnesses
Preexisting Conditions: No known health conditions
Allergies: No known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Syncope after receiving COVID 19 vaccine, patient recovered within a few minutes after lying down. Provided patient with water and food.


VAERS ID: 2453651 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-09-21
Onset: 2022-09-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7137 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3393T / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. W010663 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event, Product administration error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: no
Preexisting Conditions: carnitine deficiency
Allergies: no
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nurse gave patient PFizer covid shot, NOT the BILVALENT that was ordered by provider. So patient received a 3rd dose of the original covid vaccine and was not able to get his bivalent booster today because of the error. Patient had no adverse effects in the office.


VAERS ID: 1936504 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-11-16
Onset: 2021-11-25
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2021-12-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA U58F21A / 3 AR / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 518160008752 / 1 AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Metamorphopsia
SMQs:, Retinal disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: advair, incruse ellipta, aspirin 81mg, simvastatin, amlodipine, all those everyday; albuterol, valtrex, as needed
Current Illness: none except chronic conditions
Preexisting Conditions: copd, high blood pressure, high cholesterol, 1 prior tia 5 years ago
Allergies: sulfa drugs
Diagnostic Lab Data: Seeing opthomologist on Dec 10.
CDC Split Type:

Write-up: warped vision - lasted a few seconds each time - think it was both eyes - not sure; also not sure if related to either vaccine. Nov 25, Nov 30, Dec 2


VAERS ID: 2109142 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Connecticut  
Vaccinated: 2022-01-12
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-02-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / OT
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Crying, Drug ineffective, Dry skin, Haemorrhage, Poor quality sleep, Pruritus
SMQs:, Anaphylactic reaction (broad), Lack of efficacy/effect (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Depression (excl suicide and self injury) (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: MULTIVITAMIN [VITAMINS NOS]; CLOBETASOL PROPIONATE
Current Illness: Allergy to gold; Contact dermatitis; Dermatitis; Eczema; Insomnia; Latex allergy; Malignant neoplasm NOS
Preexisting Conditions: Comments: ALLERGIES:GOLD AU 198,LATEX,UNSP CONT DERMATITIS UNSP CAUSE,CONTACT DERMATITIS&OTHER ECZEMA DUE UNSPEC CAUSE,malignant neoplasm,Unspecified Insomnia
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSA2022SA028709

Write-up: bleeding; DISTURBS SLEEP; CRACKED AND DRY EVERYDAY; weeping; SKIN IS ITCHY; NOT SEEN ANY CHANGES YET; Initial information received on 24-Jan-2022 regarding an unsolicited valid serious case received from a consumer/non-hcp (non healthcare professional ). This case involves a 43 years old female patient who reported bleeding, disturbs sleep, cracked and dry everyday, weeping, skin is itchy and not seen any changes yet while receiving vaccine Influenza Quadrival A-B Vaccine [Fluzone Quadrivalent] and while treated with Dupilumab [Dupixent] via prefilled syringe and Covid-19 Vaccine. The patient''s past medical treatment(s), vaccination(s) and family history were not provided. At the time of the event, the patient had ongoing Contact dermatitis, Dermatitis, Eczema, Malignant neoplasm NOS(not otherwise pecified), Insomnia, Allergy to metals and Rubber sensitivity. Concomitant medications included Vitamins NOS(not otherwise specified) (Multivitamin); and Clobetasol Propionate. On 12-Jan-2022, the patient started taking Dupilumab at a dose of 300 mg QOW(every other week) via subcutaneous route, strength-300 mg/2mL (with an unknown batch number,formulation) for Dermatitis atopic. On an unknown date, the patient started taking Covid-19 Vaccine (with an unknown batch number,formulation,strength,frequency, route, administration site) for Immunisation. On an unknown date, the patient received a dose of suspect Influenza Quadrival A-B Vaccine lot number not reported via unknown route in unknown administration site for immunization. On an unknown date the patient developed a serious event bleeding (haemorrhage) (unknown latency) and non-serious event disturbs sleep (poor quality sleep),cracked and dry everyday (dry skin),weeping (crying),skin is itchy (pruritus) and not seen any changes yet (drug ineffective)(unknown latency) following the first dose intake of Dupilumab,Influenza Quadrival A-B Vaccine and of Covid-19 Vaccine. Patient reported that she has not seen any changes yet. patient says over the last week, skin is itchy, disturbs sleep, bleeding, weeping, cracked and dry everyday. Action taken : Not applicable for drug ineffective and unknown for other events with Dupilumab, Quadrivalent influenza vaccine and Covid-19 Vaccine was not applicable. Corrective treatment : No corrective treatment reported for the events. Event outcome : Unknown for all the events. Seriousness criteria : This event(haemorrhage) was assessed as medically significant.; Sender''s Comments: Sanofi company comment dated 02-Feb-2022. This case involves a 43 years old female patient who reported bleeding, disturbs sleep, cracked and dry everyday, weeping, skin is itchy and not seen any changes yet while receiving vaccine Influenza Quadrival A-B Vaccine [Fluzone Quadrivalent] and while treated with Dupilumab [Dupixent] via prefilled syringe and Covid-19 Vaccine. Based on the limited information provided regarding this case, causal role of the company suspect product cannot be excluded. Case will be re-evaluated post further update on the patient''s underlying disease conditions, past medical and drug history, concurrent illnesses, and concomitant medications. The role of the vaccine cannot be assessed this.


VAERS ID: 2612255 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-05-27
Onset: 2022-06-01
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2023-04-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS7140C / 4 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / N/A RA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Glycosylated haemoglobin normal, Hypoaesthesia, Musculoskeletal stiffness, Pain
SMQs:, Peripheral neuropathy (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Arthritis (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin D; Vitamin C; magnesium
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Tested A1C and had a physical as well and everything came back. A1C was borderline at 5.9
CDC Split Type: vsafe

Write-up: Numbness of arms and feet. Sometimes it hurts but mostly feels like I am walking on bubble wrap. Going to see neurologist soon about it since podiatrist tested me for diabetes and that came back negative. I wake up and my legs and arms are stiff. My left side seems worse then my right side. Feels like a circulation problem. I still function normal but it is a problem that was not there before the vaccine.


VAERS ID: 1019921 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2021-02-08
Onset: 2021-02-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042L20A / 1 - / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100276665 / UNK - / IM

Administered by: Military       Purchased by: ?
Symptoms: Chills, Fatigue, Headache, Inappropriate schedule of product administration, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: unknown
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient arrived to clinic to receive a flu vaccine for the 2020-2021 season. Upon arrival to clinic, patient completed flu questionnaire. Patient was then vaccinated with Moderna Covid-19 vaccine by error. Upon realization of incorrect vaccine being administered, staff then vaccinated with correct vaccine (afluria) in opposite arm. Upon speaking with the patient the next day, he reported feeling chills, fever, fatigue continuing throughout the day. States did have a headache on 2/9/2021 that then subsided. Was taking tylenol and theraflu for side effects


VAERS ID: 2709157 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2023-10-23
Onset: 2023-10-26
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030592 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8162CA / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 3 days after receiving the vaccine the pt came in with the bandaids still on the skin. There was redness around the bandaids and below towards the elbow. patient states it wasn''t irriated at all, he just noticed the redness in the mirror.


VAERS ID: 2441015 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2022-09-12
Onset: 2022-09-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2G7K9 / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Product preparation error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: cetirizine hcl 1mg/ml, 5ml PO once a day
Current Illness: none
Preexisting Conditions: none
Allergies: nkda
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received 0.2 ml of undiluted Pfizer Covid vaccine 5-11yrs. No symptoms reported to date


VAERS ID: 2456151 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-09-22
Onset: 2022-09-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7689KA / 5 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR U7447AC / 1 LA / IM
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS 2ZF9N / 5 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Children''s Chewable Multivitamin
Current Illness: None Known
Preexisting Conditions: ADHD
Allergies: None Known
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Covid vaccine found to have not been diluted prior to administration.


VAERS ID: 2441011 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2022-09-12
Onset: 2022-09-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2G7K9 / UNK RA / IM
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS CM294 / UNK LA / IM
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS CN3G5 / UNK LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. U0311051 / UNK RA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR V1A024M / UNK RA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. W009104 / UNK LA / SC
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS 2ZF9N / UNK LA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. W005206 / UNK RA / SC

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Undiluted Covid19 pfizer 5-11 vaccine administration. 0.2ml
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: 0.2ml of undiluted covid19 pfizer 5-11 administered, no symptoms/signs to date.


VAERS ID: 2441010 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2022-09-12
Onset: 2022-09-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2G7K9 / N/A LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. U031051 / 1 RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR U7373AA / 1 RA / IM
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS 2ZF9N / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event, Product preparation error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Proventil HFA inh
Current Illness: none
Preexisting Conditions: asthma
Allergies: nkda
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Patient received 0.2 ml of undiluted Pfizer Covid vaccine 5-11yrs. No symptoms reported to date


VAERS ID: 2456159 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-09-22
Onset: 2022-09-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7689KA / 7+ RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None Known
Preexisting Conditions: Facial Scar Worries
Allergies: None Known
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Covid vaccine found to not have been diluted prior to administration


VAERS ID: 2559516 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-10-13
Onset: 2023-01-09
   Days after vaccination: 88
Submitted: 0000-00-00
Entered: 2023-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ6665 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UT7716MA / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Cough, Fatigue, Headache, Myalgia, Restlessness, Rhinorrhoea, SARS-CoV-2 test positive
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Dementia (broad), Akathisia (broad), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Albuterol Sulfate; Fluticasone; Robitussin; Mucinex
Current Illness: N/A
Preexisting Conditions: Underdeveloped Lungs
Allergies: N/A
Diagnostic Lab Data: COVID-19 Test
CDC Split Type: vsafe

Write-up: On Monday I started having runny nose and a cough not really tired just restless. I also had sore muscles and I tested the next day in which I was positive for COVID-19. I started having a headache Aleve and it did eliminate the pain. I called the doctor, and they did prescribe Paxlovid, and I haven''t taken because everything is kind of going away on their own. Its really strange how I got it I have been wiping everything down and staying away from people.


VAERS ID: 2476351 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-10-07
Onset: 2021-12-01
   Days after vaccination: 55
Submitted: 0000-00-00
Entered: 2022-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2588 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acne, Blood test, Epistaxis, Magnetic resonance imaging, Scab, Scan, Staphylococcal infection, Thrombosis
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Infective pneumonia (broad), Opportunistic infections (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: LYRICA; donepezil; biotin; probiotic 10; XTAMPZA; duloxetine; zolpidem; levothyroxine; ADDERALL; nystatin
Current Illness: None
Preexisting Conditions: Fibromyalgia; Arthritis
Allergies: None
Diagnostic Lab Data: Blood work; MRI; multiple scans
CDC Split Type: vsafe

Write-up: About two months after receiving my third dose of the Pfizer vaccine, I started to experience a nosebleed. I was trying to pinch my nose, but it kept flowing. I was using a paper towel to try and cover my nose, but I was bleeding so much that it was dripping like a faucet. After a little while, the dripping blood started to clot, and it was they were the size of quarters. I was able to call 9-1-1 and the EMT''s came also. While in the back of the ambulance, the blood was still clotting, but a clot the size of the palm of my hand, came out of my nose. I went to the emergency room, and they were not able to find anything wrong with me after all of the scans and tests that were performed. The bleeding finally stopped and I went home. A few days later, I was driving and my nose started to bleed again. The blood was dripping down my face and I went to back to the emergency room. While there, they performed more tests, but they still were not able to find anything wrong. A few months later, I noticed that I was starting to have scabs on my arms. I went to my PCP and he wasn''t able to tell me what it was. Eventually, I was told that it was Staph infection. They looked like shingle spots to me, but they had whiteheads on them. I am still fighting this infection and it has been almost a year.


VAERS ID: 2724685 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2023-12-12
Onset: 2023-12-15
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-12-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / N/A LA / SYR
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH - / N/A LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test, Burning sensation, Chest discomfort, Erythema, Headache, Heart rate irregular, Pain, Pain in extremity, Peripheral swelling, Pruritus, Skin warm, Vascular access site bruising, Vascular access site discolouration
SMQs:, Cardiac failure (broad), Anaphylactic reaction (narrow), Angioedema (broad), Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiac arrhythmia terms, nonspecific (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lots of prescription maintenance meds
Current Illness:
Preexisting Conditions: COPD, Heart Failure, Diabetes, Non-Hodgkin''s Lymphoma
Allergies: Penicillin, Aspirin, Vancomycin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Only Moderna COVID shot in the right arm, other shots in left arm. 1. Headaches from initial shot date 12/12 and ongoing. 2. Right arm swollen, hot, itching, burning, painful, large area of redness, 5" in diameter. Started 12/15 and ongoing. 3. On same arm, blood draw spot on lower arm had a bruise, bruise is now accentuated and dark purple. 4. Body Aches. 5. Unusual heartbeat and chest tightness. 6. Took Benadryl and Tylonol to help with pain (headaches and arm) and itchiness in arm. 7. Redness and pain in arm seems to be continuing unabated. 8. This is the first Moderna shot. Previously all COVID shots were Pfizer.


VAERS ID: 2486866 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2022-10-22
Onset: 2022-10-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GK1657 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 79ED9 / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FLUOXETINE, MIRALAX, EPIPEN, ALBUTEROL
Current Illness: NONE KNOWN
Preexisting Conditions: AUTISM, ANXIETY, INTERMITTENT ASTHMA, AND CONSTIPATION
Allergies: PEANUTS
Diagnostic Lab Data: NONE REQUIRED
CDC Split Type:

Write-up: PATIENT RECEIVED 5-11 BIVALENT BOOSTER INSTEAD OF 12+ BIVALENT BOOSTER


VAERS ID: 2708799 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2023-10-18
Onset: 2023-10-20
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9275 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8072AA / 1 RA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH GT0538 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Anion gap, Blood chloride increased, Blood creatinine increased, Blood glucose normal, Blood potassium normal, Blood sodium normal, Blood urea decreased, C-reactive protein, Carbon dioxide normal, Creatinine urine, Full blood count normal, Glomerular filtration rate decreased, Glycosylated haemoglobin normal, Haematocrit normal, Haemoglobin normal, Inflammation, Oral mucosal eruption, Platelet count normal, Protein urine, Rash, Rash erythematous, Rash macular, Rash pruritic, Red blood cell count normal, Red blood cell sedimentation rate increased, Urine analysis normal, Urine protein/creatinine ratio, White blood cell count normal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Anaphylactic reaction (broad), Retroperitoneal fibrosis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Chronic kidney disease (broad), Hypersensitivity (narrow), Tumour lysis syndrome (broad), Proteinuria (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Acetaminophin 500mg 2 every 8 hrs, Diclofenac top gel, Amlodipine 10mg daily, Atorvastatin 20mg daily, lidocaine oint, Lisinopril 20mg daily, Sildenafil 100mg PRN, Allopurinol 100mg BID
Current Illness: none
Preexisting Conditions: Chronic Hep C, HTN, Steatosis of Liver, OSA, Gout, Low Back Pain, toenail fungus, acute sinusitis
Allergies: no known allergies
Diagnostic Lab Data: CRP inflammation 4.5, Na 144, K+ 4.1, CHL 107, CO2 27, BUN 9, Creatinine 1.30, Egfr 60, Glucose 91, anion gap 10, ESR 32, WBC 6.9. RBC 4.9, Hgb 14.7, HCT 43.9, plt 199, all other CBC results normal, A1c 5.0, Urinalysis neg, Urine Protein 14.1, Creatinine spot urine 273.9, Prot/Creat ratio spot urine 51
CDC Split Type:

Write-up: He developed a full body rash, red like bumps and blotchy. Very itchy. Bumps were in his mouth and everywhere. He was put on Steroids and Benadryl Rash is still resolving. He hasn''t needed Benadryl in 2 days and is almost done with the steroids No respiratory issues


VAERS ID: 2148513 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-12-16
Onset: 2022-02-22
   Days after vaccination: 68
Submitted: 0000-00-00
Entered: 2022-02-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Otitis media, Physical examination, Rhinitis allergic, SARS-CoV-2 test negative
SMQs:, Hypersensitivity (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: metoprolol, rosuvastatin, Glucophage, zinc, vitamin C, glucosamine/chondroitin/MSM, aspirin, CoQ10, multivitamin, magnesium, vitamin B12, probiotic
Current Illness: none
Preexisting Conditions: Effects from heart attack 12 years ago, borderline diabetic, high cholesterol
Allergies: Plavix
Diagnostic Lab Data: Covid-19 test and was negative. Physical exam.
CDC Split Type:

Write-up: Otitis media, Allergic Rhinitis.


VAERS ID: 2705321 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2023-10-25
Onset: 2023-10-27
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: valsartan HCTZ; aspirin 81 mg; omeprazole 20 mg
Current Illness: None
Preexisting Conditions: Hypertension
Allergies: unknown antihypertensive - angioedema
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Swelling of right hand and joint pain in right hand. Symptoms persisted into the next day but lessened after 1 tablet Aleve 220 mg


VAERS ID: 2703672 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2023-10-20
Onset: 2023-10-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030536 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U884BA / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Nervous system disorder, Unresponsive to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: PATIENT GOT 2 VACCINES, A FEW MINULTES LATER , SHE WAS UNRESPONSIVE AND CNS SIDE EFFECTS


VAERS ID: 2701620 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2023-10-25
Onset: 2023-10-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HE2391 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5EK43 / 1 LA / IM
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS 32M5G / 1 LA / IM
HEPA: HEP A (VAQTA) / MERCK & CO. INC. X010374 / 1 LA / IM
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. 1965044 / 1 LA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR W1B511M / 1 RA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. W029539 / 1 RA / SC
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS 54G74 / 1 RA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X017489 / 1 LA / SC

Administered by: Private       Purchased by: ?
Symptoms: Pruritus, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: none reported
Current Illness: none reported
Preexisting Conditions: unknown
Allergies: none reported
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient reported generalized pruritus that started within 30mins of vaccine administration. This was not reported to medical providers and patient left the office. Approximately 1hr and 30mis later patient was brought back to the clinic with generalized hives. Benadryl 25mg PO given, EMS services were called and patient was taken to the nearest Emergency Department for evaluation and treatment.


VAERS ID: 2700002 (history)  
Form: Version 2.0  
Age: 1.5  
Sex: Female  
Location: Connecticut  
Vaccinated: 2023-10-20
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 1 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4E25J / 1 RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event, Product preparation error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Vaccine was not diluted before 0.3mL was administered from MDV of 3 doses No known adverse reaction As of 10/21/23 ~5pm - No reported side effects per mother


VAERS ID: 2730270 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2023-12-22
Onset: 2023-12-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 032F / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. AU1060D / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood lactic acid, Chills, Culture urine, Differential white blood cell count, Erythema, Full blood count, Influenza A virus test, Influenza B virus test, Injection site cellulitis, Injection site pain, Nausea, Night sweats, Pain, Pain in extremity, Peripheral swelling, Pruritus, Pyrexia, SARS-CoV-2 test, Urine analysis, Vomiting
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Advair Diskus 250-50 MCG/DOSE diskus inhaler albuterol (PROVENTIL HFA; VENTOLIN HFA) 108 (90 Base) MCG/ACT inhaler Blood Glucose Monitoring Suppl (OneTouch Verio Reflect) w/Device Kit celeCOXIB (CeleBREX) 100 MG capsule diclofena
Current Illness: asthma, prediabetes, anemia, migraines
Preexisting Conditions: Chronic neck and shoulder pain, cervical spondylosis, frozen shoulder, partial rotator cuff tear, tear lumbar spine
Allergies: Fish, wheat, contrast dye with EpiPen prescription for allergic reactions as needed
Diagnostic Lab Data: On 1/4/24 the following tests: INFLUENZA A/B, RSV, SARS-COV-2 NAA MULTIPLEX LACTIC ACID, PLASMA URINALYSIS W/ REFLEX TO MICROSCOPIC AND CULTURE LACTIC ACID, PLASMA COMPLETE BLOOD COUNT, WITH DIFFERENTIAL
CDC Split Type:

Write-up: On 12/22/24 at 10:30am I received a flu shot and covid 19 booster shot in my left arm by a pharmacy tech at Pharmacy. The shots were very painful but I was told the pain would go away shortly. By that night my arm was bright red, swollen, extremely painful, and itchy. I had a fever, night sweats and chills and my body was achy all over. This continued with the pain getting worse and my arm becoming more swollen. I tried Benadryl and Tylenol and ice but there was no relief. I went to the Urgent Care on 12/24/23 at 4:28 pm and the doctor diagnosed me with cellulitis at both injection sites. She prescribed Keflex 500mg for 2x a day for 10 days. After 3 days I developed nausea, vomiting, and continued to have fevers. After finishing the antibiotics this continued and my primary Dr. asked me to come in. She referred me to the Emergency Room out of concern that the infection had become septic. I underwent several tests at Emergency Department on 1/4/24. They said infection had not spread but to follow up with my primary regarding the continued nausea, vomiting and fevers. Presently I am still battling I continue to deal with nausea, vomiting, fevers, and have extreme pain in my left arm.


VAERS ID: 2131460 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-11-18
Onset: 2021-12-28
   Days after vaccination: 40
Submitted: 0000-00-00
Entered: 2022-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 023M20A / 3 RA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: SARS-CoV-2 test
SMQs:, COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Spiriva, pantoprazole, atorvastatin
Current Illness:
Preexisting Conditions: Sarcoidosis
Allergies: Amoxicillin
Diagnostic Lab Data: Home test- Rapid test on 12/29/2021- PCR test on 1/03/2022.
CDC Split Type:

Write-up: Received 3 doses of Moderna. A month after the 3rd dose I started with symptoms of Covid-19.


VAERS ID: 1883131 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2021-11-12
Onset: 2021-11-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acoustic stimulation tests abnormal, Deafness, Inner ear inflammation
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Humira, Zyrtec, Fish Oil, Centrum
Current Illness:
Preexisting Conditions: Ulcerative Colitis, Autoimmune Ear Disease
Allergies: None
Diagnostic Lab Data: Hearing test
CDC Split Type:

Write-up: Severe Inflammation in the inner left ear, hearing loss. Undergoing treatment with oral steroid and steroid shot in ear. As of this reporting dat not yet under complete control though made some progress.


VAERS ID: 1880854 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-10-27
Onset: 2021-10-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Inappropriate schedule of product administration
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was offered Pfizer COVID-19 booster in conjunction with an employee flu shot clinic. She was not adequately screened to determine that it had not yet been 6 months since her 2nd dose, making her ineligible to receive a booster yet. It was given anyway.


VAERS ID: 1872403 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2021-10-15
Onset: 2021-10-23
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NO BATCH NUMBER / UNK LA / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK RA / OT

Administered by: Pharmacy       Purchased by: ?
Symptoms: Deafness
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Omeprazole
Current Illness: Drug allergy
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSEQIRUS202105515

Write-up: Sudden total hearing loss in left ear; This spontaneous case was received on 05-Nov-2021 from other non-health professional (consumer) via Pfizer (reference number: 202101440993) with additional information (being processed together) received on the same communication (reference number: SEQW21-05120) and concerned a 49-year-old male patient. The patient''s concurrent condition included codeine allergy. The patient''s concomitant medications included omeprazole for unknown indication. The patient''s previously received two doses of Pfizer BioNTech COVID-19 vaccine after which the patient did not developed any adverse event. On 15-Oct-2021, the patient was vaccinated with Afluria Quadrivalent (influenza vaccine; anatomical location: right arm, dose, route of administration and indication: not reported). The batch number was not reported. On the same day, the patient was vaccinated with non-company co-suspect Pfizer BioNTech COVID-19 vaccine (tozinameran; anatomical location: left arm, route of administration, dose, batch number and indication: not reported). On 23-Oct-2021, eight days after administration of Afluria Quadrivalent and Pfizer BioNTech COVID-19 vaccine, the patient experienced sudden total hearing loss in left ear. The patient was treated with high dose of steroids. At the time of initial report on 05-Nov-2021, the patient had not recovered from the event. The reporter did not provide a causality assessment. The event of ''hearing loss'' was assessed as serious due to disability and was also considered to be medically significant by a Physician from facilitating company. Company comment: A 49-year-old, male patient was vaccinated with the suspect Afluria Quadrivalent and non-company co-suspect Pfizer BioNTech COVID-19 vaccine. Eight days after vaccination the patient developed sudden total hearing loss in left ear. Information regarding the related diagnostic findings has not been provided. Due to limited information provided, causality is unassessable.; Sender''s Comments: A 49-year-old, male patient was vaccinated with the suspect Afluria Quadrivalent and non-company co-suspect Pfizer BioNTech COVID-19 vaccine. Eight days after vaccination the patient developed sudden total hearing loss in left ear. Information regarding the related diagnostic findings has not been provided. Due to limited information provided, causality is unassessable.


VAERS ID: 1916932 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-11-14
Onset: 2021-11-16
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3P3TY / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: astigmatism; bronchospasms; constipation; seasonal allergies
Allergies: n/a
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received the COVID vaccine on 11/14/21. No reactions noted after vaccine administration. Patient had a nurse visit on 11/16/21 at physicians office and received the Flulaval vaccine on 11/16/21. After the flu vaccine was administered, patient made it outside to the car and dad reported that patient was c/o increase arm pain (left) and then dad reported patient no longer was talking or responding. Dad took patient back to the pediatric office to haver MD evaluate. Patient left office stable on 11/16/2021 after monitoring for an adequate amount of time. Patient had an in office appointment on 12/2/21 for multiple dizzy episodes and one major passing out episode.


VAERS ID: 1855328 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2021-11-03
Onset: 2021-11-06
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 032F / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS K45Z2 / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Epistaxis
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Omeprazole, Metformin.
Current Illness: None
Preexisting Conditions: Overweight, GER
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Significant nose bleed multiple times; stopped after 10 min the first time and ~5 min following days with tissue


VAERS ID: 1922528 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Connecticut  
Vaccinated: 2021-12-02
Onset: 2021-12-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030H21B / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Eye swelling, Hypersensitivity, Lip swelling, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Unithroid, estradiol, medroxyprogesterone acetate, sertraline, digestive advantage for lactose intolerance, claritin
Current Illness: None
Preexisting Conditions: Hashimoto''s Disease, premature ovarian failure
Allergies: seasonal allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Allergic reaction- hives, swelling of eyes and lips. Prescribed steroids and epi pen


VAERS ID: 1782870 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: Connecticut  
Vaccinated: 2021-10-11
Onset: 2021-10-12
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN JANSSEN/J&J / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR FLUZONE HD / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Interchange of vaccine products
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Not sure
Current Illness: Patient was previously experiencing a rash, totally unrelated to the vaccine
Preexisting Conditions: None that we are aware
Allergies: NKA
Diagnostic Lab Data: None that we know of.
CDC Split Type:

Write-up: The patient made an appt for the J&J vaccine (only vaccine we were giving on 10/11/21), but meant to make an appt for his Pfizer booster. He was inadvertently given a J&J vaccine instead of the Pfizer booster he was looking for. He did not have symptoms, but happened to have an appt with his physician for a rash (totally unrelated to the vaccines). The physician called the pharmacy and informed us of what happened. I talked to the patient. He feels fine, is just concerned about whether the J&J will work as a booster or if he should still get a Pfizer booster shot.


VAERS ID: 1820434 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Male  
Location: D.C.  
Vaccinated: 2021-10-20
Onset: 2021-10-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ741AC / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: unknown
Diagnostic Lab Data: unknown
CDC Split Type:

Write-up: In vaccination clinic, patient presented for two vaccination, Fluzone-HD and Covid-19 booster, shots. While in preparation to give the vaccinations, I had patient to repeat what vaccines he was going to received that day. He said that he wanted the Flu and Covid-19 booster. Then, I processed to vaccinate. When processing, I saw that he had previously received this shots.


VAERS ID: 2575169 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Male  
Location: D.C.  
Vaccinated: 2022-11-02
Onset: 2022-11-05
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-02-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chest pain, Dizziness, Dyspnoea, Echocardiogram, Electrocardiogram, Electrocardiogram ambulatory, Palpitations
SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Finasteride
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: EKG in mid-November, Holter Monitor worn for a week in early December, and echo cardiogram on January 4, 2023,
CDC Split Type:

Write-up: After several days, I developed strong and frequent heart palpitations, shortness of breath, chest pain, and lightheaded feeling. Shortness of breath and lightheaded feeling dissipated after about a week. Heart palpitations and chest pain decreased over time in terms of frequency and intensity. Ten weeks later, I still have heart palpitations mostly at night while lying in bed. The heart palpitations are less frequent and less intense.


VAERS ID: 2032160 (history)  
Form: Version 2.0  
Age: 13.0  
Sex: Male  
Location: D.C.  
Vaccinated: 2022-01-13
Onset: 2022-01-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3P3TY / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient was given wrong dose of vaccine that was ordered. Misunderstanding of which vaccine dosage to give to Pediatric patients.


VAERS ID: 2607377 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: D.C.  
Vaccinated: 2022-12-22
Onset: 2022-12-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2587 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 244L3 / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: omeprazole 20mg
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Wrong vaccine administered. Pt was due for a bivalent formulation and received a monovalent. Pt counselled by clinician.


VAERS ID: 2003179 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Male  
Location: D.C.  
Vaccinated: 2021-12-19
Onset: 2021-12-30
   Days after vaccination: 11
Submitted: 0000-00-00
Entered: 2022-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Mechanical urticaria, Oesophageal discomfort, Pruritus
SMQs:, Anaphylactic reaction (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin D3 B12 tablets Restasis
Current Illness: None
Preexisting Conditions: Dry eyes
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Extreme itchiness accompanied with dermatographia on most of my body. Additionally light tightness in asophagus


VAERS ID: 2609933 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: D.C.  
Vaccinated: 2022-10-02
Onset: 2022-11-04
   Days after vaccination: 33
Submitted: 0000-00-00
Entered: 2023-04-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA DONT HAVE IT WI / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR NONE / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Alanine aminotransferase increased, Aspartate aminotransferase increased, Autoimmune hepatitis, Blood alkaline phosphatase normal, Blood bilirubin normal, Ceruloplasmin normal, Full blood count normal, Gene mutation identification test negative, Hepatitis A virus test, Hepatitis B virus test, Hepatitis C test negative, Laboratory test normal, Metabolic function test abnormal, Serum ferritin increased, Ultrasound abdomen normal, Ultrasound scan normal
SMQs:, Liver related investigations, signs and symptoms (narrow), Hepatitis, non-infectious (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamin D3; Timolol Eye Drops; Cetirizine; Rosuvastatin
Current Illness: N/A
Preexisting Conditions: Mild Osteoporosis; Chron Urticaria
Allergies: Sulfa; Pollin
Diagnostic Lab Data: Complete metabolic panel except elevated AST/ALT Bilirubin alkaline phosphatase normal; Complete Blood count normal; Test for Hepatitis A-B: HCV negative; Test for immune mediator negative; Ceruloplasmin negative; Dene Screening for Hemochromatosis negative; Abdominal ultrasound normal
CDC Split Type: vsafe

Write-up: AST and ALT check one month after vaccination abnormal. A full workup the elevated results didn''t disclose the cause. I also had elevated ferritin level. Ultrasounds were normal. Liver biopsy not done but I have and appointment April 19. The presumptive diagnosed is autoimmune hepatitis. Initial AST 144IU/L and ALT 185 IU/L Values peak on FEB 23, 2023, AT AST 341. ALT peak on January 25 at 482.Most recent April 3 AST 293 ALT 373.


VAERS ID: 2699945 (history)  
Form: Version 2.0  
Age: 4.0  
Sex: Female  
Location: D.C.  
Vaccinated: 2023-10-21
Onset: 2023-10-22
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5509B / 3 LG / SYR
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS PM35E / UNK LG / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site erythema, Injection site swelling, Injection site warmth, Vomiting
SMQs:, Acute pancreatitis (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Simultaneously received flu vaccine.
Current Illness: Cold
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Child received flu vaccine in one thigh and COVID vaccine in the other thigh. At site of one of these injections (unsure which vaccine), large 2-2.5? diameter), slightly raised, and warm-to-the-touch redness/swelling occurred (about 27 hours after vaccine). At about 35 hours post vaccine, child experienced vomiting.


VAERS ID: 2523139 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Male  
Location: D.C.  
Vaccinated: 2022-12-02
Onset: 2022-12-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 1 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / UNK - / -
HEPA: HEP A (VAQTA) / MERCK & CO. INC. - / UNK - / -
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. - / UNK - / -
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR - / UNK - / -
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / UNK - / -
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR - / UNK - / -
TD: TD ADSORBED (TDVAX) / MASS. PUB HLTH BIOL LAB - / UNK - / -
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK - / -

Administered by: School       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: On 12/02/2022, patient given initial dose of Pfizer 12+ monovalent COVID vaccine from refrigerator. Upon documenting administration, manufacturing date on vial found to be 12/2021, so called CDC, Pfizer, and LPN to clarify expiration date. MD informed; per provider, MD called and informed patient father. Vaccine administered at 0945 AM. RN called CDC on 12/02/2022, who advised to contact Pfizer, as they did not have any data on the stability of the vaccine; CDC website states that dose should be repeated. Called Pfizer medical information, who advised that they did not have any data on the stability of the vaccine after expiration, but did confirm that the expiration date was 11/30/2022, so vaccine was given two days out of date. contact confirmed the same on 12/05/2022. Enquiry form completed by RN and submitted to Pfizer for further information. Patient in no apparent distress upon leaving Facility.


VAERS ID: 2466626 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: D.C.  
Vaccinated: 2022-09-29
Onset: 2022-09-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Back pain, Crying, Discomfort, Lymph node pain, Pain, Sciatica
SMQs:, Retroperitoneal fibrosis (broad), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Small, stable brain aneurysm diagnosed Oct 2019.
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: On the night of Sept 30 around 11 PM while getting ready for bed I noticed the lymph node in my armpit was really tender on the left side, same side I got my COVID shot on. On Oct 1 I woke up at 7 AM experiencing such bad pain at my sciatic nerve that I was crying. I couldn''t find a comfortable position in bed and when I stood up I could feel blood rush down both legs and the pain was awful. I applied ice packs to both sides of my low back where the pain was most acute and took a warm shower, and that plus 400mg of Advil got me feeling better. If my primary care clinic had been open I''d have gone in but they are closed on weekends.


VAERS ID: 1939387 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: D.C.  
Vaccinated: 2021-12-10
Onset: 2021-12-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 334RL / 1 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Product preparation issue
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pfizer-BioNTech was mixed with too little diluent


VAERS ID: 2509454 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: D.C.  
Vaccinated: 2022-11-11
Onset: 2022-11-12
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / N/A RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / N/A RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Fatigue, Hypersensitivity, Swelling face, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: welbutrin, Mirena IUD, aleve
Current Illness: none
Preexisting Conditions: none
Allergies: allergic to sulfa, bananas, avocados
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Was exhausted and couldn''t keep my eyes open for more than four hours until Tuesday, experienced severe facial swelling and hives on neck and chest consistent with an allergic reaction begining on Satuday through Tuesday morning despite taking OTC antihistamines. Saught medical treatment Tuesday morning where I received a 6-day sterioid treatment. Hives continued through Tuesday night and swelling / skin seems to have gone back to 80% normal by Wednesday morning.


VAERS ID: 1757449 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Male  
Location: Delaware  
Vaccinated: 2021-10-03
Onset: 2021-10-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3590 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. PI00347995 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Loss of consciousness, Unresponsive to stimuli
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient states they "blacked out" soon after vaccination. Patient was unresponsive for approximately 3 minutes. Patient also states they felt "Dizzy" soon after vaccination.


VAERS ID: 1794720 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Male  
Location: Delaware  
Vaccinated: 2021-10-15
Onset: 2021-10-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 2 - / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 334RL / UNK - / IM

Administered by: Military       Purchased by: ?
Symptoms: Dizziness, Nausea
SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: none
Preexisting Conditions: none
Allergies: nkda
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt received flu and covid vaccine together; approx 8 minutes later pt complained of lightheadedness and nausea. Provider was immediately notified; pt was lowered to the floor and legs were elevated and a ice pack was placed behind his neck. Pt v/s were within normal limits


VAERS ID: 1804621 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Delaware  
Vaccinated: 2021-10-21
Onset: 2021-10-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3590 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ763AC / UNK RA / IM
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH DL2861 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: patient came in for a pneumonia vaccine our immunization selection tool recommended pneumovax 23 but patient got Prevnar 13


VAERS ID: 2592538 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Female  
Location: Delaware  
Vaccinated: 2022-04-22
Onset: 2023-02-23
   Days after vaccination: 307
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH CH969U / 4 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UNKNOWN / N/A AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Headache, Neck pain, Oropharyngeal pain, Strawberry tongue, Streptococcus test positive
SMQs:, Oropharyngeal infections (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Arthritis (broad), Infective pneumonia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Womens Multivitamin with Fiber; Vitamin D3; Probiotic; Latanoprost; Telmisartan; Atorvastatin; Pepcid; Metoprolol; Novolog; Levemir
Current Illness: N/A
Preexisting Conditions: Diabetes; High Cholesterol; High Blood
Allergies: N/A
Diagnostic Lab Data: Strep Test
CDC Split Type: vsafe

Write-up: I was having a sore neck and neck pain. I thought it may have to do some dental work I had done but then it did not go away. Then I started a sore throat and I ended up going to urgent care and I was tested for Strep and it was positive. The provider said I also had "strawberry tongue" and that is how they knew it was strep. I also had a horrible headache during this. The sore throat and all that is gone but my neck still hurts.


VAERS ID: 2722837 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Male  
Location: Delaware  
Vaccinated: 2023-10-05
Onset: 2023-10-13
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2023-12-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Bell's palsy, Borrelia test, Computerised tomogram head normal, Differential white blood cell count, Facial paralysis, Full blood count, Lipids, Magnetic resonance imaging head normal, Metabolic function test
SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Rosuvastatin 10mg
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: CT (10/13) and MRI (10/14) of head; CBC with diff; metabolic and lipid panels (10/13); Lyme Antigen Assay (10/19)
CDC Split Type:

Write-up: Woke up with facial paralysis on morning of 10/13/23. Went to emergency room at Hospital, CT scan on 10/13 negative for stroke; admitted to hospital; MRI on 10/14 negative for stroke; final diagnosis is Bell''s Palsy; condition unchanged as of 12/11/23


VAERS ID: 2068496 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Male  
Location: Delaware  
Vaccinated: 2022-01-26
Onset: 2022-01-26
   Days after vaccination: 0
Submitted: 2022-01-26
   Days after onset: 0
Entered: 2022-01-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1614 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3A9ZG / 1 LA / IM

Administered by: Other       Purchased by: Public
Symptoms: Anxiety, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE KNOWN
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: POST-IMMUNIZATION SYNCOPAL EPISODE; CALLED - EMS; LOCAL EMT RESPONDED AND EVALUATED PT.; URGED FATHER TO SEEK DEFINITIVE MEDICAL EVALUATION; FATHER TOOK PATIENT HOME. PER MOTHER ANXIOUS, BUT RESTING.


VAERS ID: 2076901 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Male  
Location: Delaware  
Vaccinated: 2022-01-31
Onset: 2022-01-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1614 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS ZG474 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Head injury, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Flu vaccine
Current Illness:
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient passed out and hit head on ground about 5 minutes after recieving vaccine. EMS was called. Patient refused transport to ER.


VAERS ID: 2032197 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Delaware  
Vaccinated: 2022-01-13
Onset: 2022-01-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031H21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ778AB / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Face injury, Fall, Lip swelling, Scratch, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Angioedema (narrow), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: none
Preexisting Conditions: none
Allergies: NKDA
Diagnostic Lab Data: checked BP and result 122/91 with HR of 67
CDC Split Type:

Write-up: Patient was sitting in a chair outside the pharmacy for 15 minutes post vaccination. While sitting in the chair, patient fainted and fell onto floor resulting into scrapes on her face and swollen lip. Pharmacist asked patient if she had difficulty breathing, but patient did not have any issues with breathing. Provided patient with paper towel to wipe face, bottle of water, and ice pack to alleviate symptoms. Also checked blood pressure and had patient elevate feet until she was able to leave pharmacy. Patient did not need additional medical attention


VAERS ID: 1833220 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Delaware  
Vaccinated: 2021-10-29
Onset: 2021-10-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 3203080 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Diarrhoea, Dizziness, Fatigue, Myalgia, Nausea, Pyrexia, Sleep terror, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Oxycodone, oxycontin, gabapentin, Robaxin, protonix, Zoloft, Buspar, doxycycline
Current Illness: MRSA vertebral myelitis
Preexisting Conditions: Crohn''s disease
Allergies: Droperidol, macrolide antibiotics
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fever up to 103.2, chills, muscle aches, diarrhea, nausea, vomiting, fatigue, night terrors, dizziness All lasted over 72hrs


VAERS ID: 2701283 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: Delaware  
Vaccinated: 2023-10-18
Onset: 2023-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG4671 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8043AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Condition aggravated, Gait disturbance, Irritable bowel syndrome, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Noninfectious diarrhoea (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: no
Preexisting Conditions:
Allergies: nka
Diagnostic Lab Data:
CDC Split Type:

Write-up: patient reports swollen right hand and swollen right foot that resolved after a few days. He also reports his IBS acting up, and and unsteady gait and felt weak walking for a few days after receiving vaccines


VAERS ID: 2718072 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-09-29
Onset: 2023-10-02
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-11-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Back pain, Chest pain, Fatigue, Insomnia, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Excedrin for Migraine (occasional, as needed), Benadryl (for allergies, as needed)
Current Illness: None
Preexisting Conditions: Pollen allergies, not very severe; chronic migraines
Allergies: None known
Diagnostic Lab Data:
CDC Split Type:

Write-up: Severe muscular and joint pain, sharp/strong chest and back pain, difficulty sleeping due to said pain, worst fatigue of my life (pains began the Monday following the shot, on October 2nd, and STILL continue to this day, 11/27/23). No treatments received, concerned about cost of going to a doctor. I believe it was the COMBINATION of receiving the flu shot with the Moderna Covid shot on the SAME DAY.


VAERS ID: 1778819 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-01
Onset: 2021-10-06
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Chills, Condition aggravated, Contusion, Eye contusion, Fatigue, Headache, Memory impairment, Nasal oedema, Skin laceration, Suture insertion, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Hostility/aggression (broad), Cardiomyopathy (broad), Depression (excl suicide and self injury) (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: experienced chills, headache with dose 2
Other Medications: ASA 81 mg Omeprazole 20 mg Lutein 20 mg Amlodipine 2.5 mg Ambien 10 mg Gabapentin 100-300 mg bisphosphonate calcium/vitamin D azelastine flonase
Current Illness: none
Preexisting Conditions: insomnia osteopenia degenerative disc disease back
Allergies: nka
Diagnostic Lab Data: Dr at walk-in clinic gave me a tetanus-diphtheria
CDC Split Type:

Write-up: Wednesday night I started experiencing pretty severe chills (had happened with dose #2 so I was expecting it). Chills off and on through Thursday. Headaches. Tiredness. At some point Friday I fainted (had not happened before), but do not remember many details. I called a friend to pick me up & take me to walk in clinic. I do not remember much from that visit. My friend would be very happy to provide additional details as my memory is foggy. The gash required 3 stitches which come out Thursday. I have a black eye, swollen nose (not broken), contusions on both elbows, and a huge bruise on one hip. My permanent damage will be an unsightly scar across my forehead.


VAERS ID: 2718887 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-10-31
Onset: 2023-11-02
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-11-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031281 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT81551A / UNK LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Laboratory test normal, Sedation, Staring, Unresponsive to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Reported Symptoms: 10010300:CONFUSION; 10039897:SEDATION; Narrative: Per caregiver (daughter), patient was admitted 11/02/23 due to "possible stroke". She states that "he was out of it, just starring off unresponsive for 8-10 min" Ambulance was called and patient stayed at hospital until discharged on 11/04/23. States that the work up was negative for stroke, seizures, UTI. He is back home resting comfortably, at baseline cognition and function. She had concerns that symptoms may have been due to flu and covid vaccines having been given 48 hrs prior. No updated records to review from other facility therefore unable to confirm complete course of tx. Other Relevant Hx: Per caregiver (daughter), patient was admitted 11/02/23 due to "possible stroke". She states that "he was out of it, just starring off unresponsive for 8-10 min" Ambulance was called and patient stayed at hospital until discharged on 11/04/23. Stated that the work up was negative for stroke, seizures, UTI. He is back home resting comfortably, at baseline cognition and function. She had concerns that symptoms may have been due to flu and covid vaccines having been given 48 hrs prior. No updated records to review from other facility therefore unable to confirm complete course of tx. Other:


VAERS ID: 1759824 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-01
Onset: 2021-10-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hyperhidrosis, Lethargy, Nausea
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: PATIENT CAME BACK INTO THE PHARMACY TODAY COMPLAINING OF POURING SWEAT, NAUSEA AND LETHARGIA AFTER RECEIVING VACCINES


VAERS ID: 1878032 (history)  
Form: Version 2.0  
Age: 88.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-14
Onset: 2021-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ730AAD / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Axillary pain, Injected limb mobility decreased, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: none yet
CDC Split Type:

Write-up: patient received both flu and covid booster in left arm during at a clinic. She reports pain from armpit to elbow,muscle pain and cannot lift arm. Suggested patient check with physician.


VAERS ID: 1774822 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Florida  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U3261AA / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Rash, Somnolence, Swollen tongue, Tongue discolouration, Vaccination complication
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Anticholinergic syndrome (broad), Dementia (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SYNTHROID
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USSA2021SA323131

Write-up: swollen tongue; sleepiness; swollen tongue, with raised white puffy lines; had Fluzone Quad vaccination in 2009 and had a reaction and had the moderna COVID and had a reaction as well; rash; Initial information received on 27-Sep-2021 regarding an unsolicited valid non-serious case received from a consumer/non-health care professional via Global Media Information (under the reference 00787220). This case involves a 57 years old female patient who experienced swollen tongue, sleepiness (somnolence), swollen tongue, with raised white puffy lines (tongue discolouration), had fluzone quad vaccination in 2009 and had a reaction and had the moderna covid and had a reaction as well (vaccination complication) and rash after receiving INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] and COVID-19 VACCINE MRNA (MRNA 1273) (MODERNA COVID-19 VACCINE). The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included LEVOTHYROXINE SODIUM (SYNTHROID). In 2009, the patient received a dose of suspect FLUZONE QUADRIVALENT (0.5 ml, total, lot U3261AA and expiration date not provided) via unknown route in an unknown administration site for prophylactic vaccination. On an unknown date, the patient received a dose of suspect MODERNA COVID-19 VACCINE not produced by Sanofi Pasteur (lot number and expiration date not reported) via unknown route in an unknown administration site for prophylactic vaccination On an unknown date the patient developed a non-serious swollen tongue, sleepiness (somnolence), swollen tongue, with raised white puffy lines (tongue discolouration), had fluzone quad vaccination in 2009 and had a reaction and had the moderna covid and had a reaction as well (vaccination complication) and rash (unknown latency) following the administration of vaccines No laboratory data reported. The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]). At time of reporting, the outcome was Unknown for the reported events.


VAERS ID: 2123977 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-09-22
Onset: 2021-09-22
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 051E21A / 3 AR / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal discomfort, Asthenia, Chills, Fatigue, Headache, Hypersomnia, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Eliquis, Tresiba, Folic Acid, Metoprolol, Vytorin
Current Illness: None
Preexisting Conditions: Diabetes, A-fib, heart condition with stents, post transplant bone marrow, previous cancer skin, tongue, and leukemia
Allergies: Tetracycline
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: The next day after vaccine, I got very weak, fatigued, and slept about all day. Was sick to my stomach with headaches. I had chills and a possible fever. I took liquid Tylenol. These symptoms lasted 2-3 days.


VAERS ID: 2129263 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-09-11
Onset: 2021-10-01
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2022-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 062F21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Arthralgia, Injection site pain
SMQs:, Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: Possible Pneumonia
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Pt. states that after receiving the 1st dose of Moderna 09/11/2021, started experiencing symptoms that evening of joint pain (knee, shoulders, hips). 10/2021 progressive joint pain throughout of the body and injection site pain. 02/2022 Primary visit/communications with recommendations of no following vaccinations.


VAERS ID: 2707365 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-10-27
Onset: 2023-10-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026A21A / 4 AR / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / SYR

Administered by: Military       Purchased by: ?
Symptoms: Balance disorder, Disorientation, Mobility decreased, Nausea, Tremor
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Yes
Current Illness: Cancer
Preexisting Conditions: Cancer, Parkinson''s disease
Allergies: No
Diagnostic Lab Data: No
CDC Split Type:

Write-up: Nauseous, disoriented, my tremors in my hands got worse with more frequency and more amplitude later on in the evening and the next day it was even worse. Also had "freezing" where i sit and cant move around. Out of balance.


VAERS ID: 2707241 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-09-21
Onset: 2023-09-23
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK UN / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 UN / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Aphasia, Blood test, Cardiac monitoring abnormal, Cerebrovascular accident, Chest discomfort, Computerised tomogram, Fatigue, Impaired driving ability, Magnetic resonance imaging, Mobility decreased
SMQs:, Anaphylactic reaction (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Cardiomyopathy (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: 81 mg aspirin, Amlodipine.
Current Illness: None.
Preexisting Conditions: Diabetes and CHF.
Allergies: Amiodarone, Bee venom.
Diagnostic Lab Data:
CDC Split Type:

Write-up: He got his vaccines, the followoing day he had a sore arm. The next day he was driving his car and he knew somethign was wrong. He came to a rotary and did not go around it and went over it. He did not hit anything, knew that he was in trouble. He went to a gas station and got half out of the car, and grabbed the steering wheel and could not move his arm. Attendend asked him if he was OK and he could not answer, he called 911 and he was taken to the hospital by ambulance. He went to Hospital. Once he got to the ER in about 3 hours he could speak and he could move his arm. They informed him that he had had a stroke. He was admitted to the hospital, and was there for 4 days. He did have blood work, MRI''s and CAT scans. He was put on Plavix for 21 days and then they wanted him to wear a heart monitor for 30 days, but he was going to travel in 20 days and he was told to see his cardiologist and he was put on a 14 day heart monitor and still has 6 days to go with the heart monitor. He is feeling tired at this point, more tired than he usually is. He did have some chest discomfort that is recorded on the event monitor that he is wearing.


VAERS ID: 1876876 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-16
Onset: 2021-11-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 006D21A / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS T93SR / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Nausea, Urticaria
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: albuterol, breo ellipta, albuterol
Current Illness: none
Preexisting Conditions: asthma
Allergies: morphine and penicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: generalized urticarial and nausea 15 min post administrations. IM solumedrol, IM Benadryl, PO Zofran administered. patient monitored for 1 hr post medications administrations, vss, symptoms resolved, pt sent home.


VAERS ID: 2703826 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-10-25
Onset: 2023-10-26
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Balance disorder, Blood test, Computerised tomogram, Dysgraphia, Gait disturbance, Motor dysfunction, Pyrexia, Sleep disorder
SMQs:, Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Akathisia (broad), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Metorolol ER succinate.
Current Illness: None.
Preexisting Conditions: SVT attacks.
Allergies: None.
Diagnostic Lab Data: CAT scan, blood work.
CDC Split Type:

Write-up: She got her vaccines, she started running a fever once they got home. At 3:00 PM yesterday the fever went away, then she mentioned to her husband that it was gone, and then she got up and then she realized that she started to loose her balance, and her motor skills on her right side, right arm and right leg were adversely affected and started to loose control of it, had trouble walking. They felt that it might be something that was going to go away, she could not sleep all night and she called him this morning and she needed help to get up and get around. Her husband called pharmacy and he explained what was going one, and she informed him that it could be a stroke. He called Medical Center and explained what he was e explaining to me, and they felt that it might be a stroke, and they told him to bring her to the ER. In the ER at 8:00 AM this morning, and they did a CAT scan, the doctor came in and told them it was not a stroke, and that they recommended that she see a neurologist. They indicated that one would be in during rounds, they waited 2 hours and nobody talked to them, and they decided since she did not have a stroke that they needed to go home. Her husband did bring it up that he had seen that peripheral neuropathy was a cause of the vaccine, but nobody wanted to talk about that. He had an article that showed what treatment and prescription and they stated that they had never heard of it. His wife has never had any health issues, and she has never had such issues like this prior to the vaccine. He feels it was due to the vaccine and if they had known what type of reaction she could potentially have that she would not have had the vaccine. The pharmacist said that they were going to file a report. She has feeling in her arm and leg, she has strength, has good hand strength but she has difficulty writing her signature, but she can hold a pen, but controlling it the way her mind wants to is difficult for her, which is exactly what the peripheral neuropathy is.


VAERS ID: 1833744 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-28
Onset: 2021-10-29
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Eye pain, Feeling abnormal, Headache, Neck pain, Rash
SMQs:, Anaphylactic reaction (broad), Dementia (broad), Glaucoma (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: same as above 72 10/28/2021 Merderna
Other Medications: potassium gabapenton serline levothoroxin lasex
Current Illness: none
Preexisting Conditions: neropathy
Allergies: vancamicien
Diagnostic Lab Data: none
CDC Split Type:

Write-up: headache neckpain rash on arm eye pain joint pain brain fog


VAERS ID: 2021560 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-09
Onset: 2021-12-30
   Days after vaccination: 82
Submitted: 0000-00-00
Entered: 2022-01-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / N/A RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Cough, Ear pain, Head discomfort, Headache, Lymphadenopathy, Musculoskeletal stiffness, Neck pain, Rhinorrhoea, SARS-CoV-2 test positive, Sneezing
SMQs:, Anaphylactic reaction (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hypersensitivity (broad), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Benicar, Vitamin D, C; Biotin
Current Illness: N/A
Preexisting Conditions: Obesity, Hypertension
Allergies: Thimerosal Preservative
Diagnostic Lab Data: Covid-19 Positive 12/7/2021, Dose 1 03/03/2021 EN6198, Dose 2:03/24/2021 EP7534
CDC Split Type: vsafe

Write-up: I started to have a runny nose overnight. My nose was running, and my ears hurt. I was sneezing and it felt like my head was under pressure. My neck hurt and my Lymph Nodes were swollen. I went to get tested at the city site and I tested positive. The next day I still felt extreme pressure in my head. I still had a headache and the runny nose and coughing. It has been four days and I have started to feel a little better. The headache is milder, but my Lymph Nodes are still swollen, and my neck is stiff. My nose is still running.


VAERS ID: 1651429 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-08-18
Onset: 2021-08-19
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-08-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain upper, Chills, Influenza like illness, Malaise, Paraesthesia, Pyrexia
SMQs:, Acute pancreatitis (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Losartan, Triamterene, Verapamil, Trazodone, Omega3 Acid Ethyl Esters, Vitamins : D, C, B complex
Current Illness: none
Preexisting Conditions: Arthritis,
Allergies: Nitrofurantoin, Amox-clav, Ciprofloxacin,
Diagnostic Lab Data:
CDC Split Type:

Write-up: Started to get very sick like bad flu. Shivers, prickly skin, fiver, stomac problems


VAERS ID: 1657730 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Florida  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-08-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Pain, Product administered at inappropriate site, Tendon disorder
SMQs:, Drug abuse and dependence (broad), Tendinopathies and ligament disorders (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: COVID VACCINE (NOS)
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USGLAXOSMITHKLINEUS202117

Write-up: administered in the hip; This case was reported by a consumer via call center representative and described the occurrence of vaccine administered at inappropriate site in a female patient who received Flu Seasonal QIV Dresden (Influenza vaccine Quadrivalent unspecified season) for prophylaxis. Previously administered products included Fluad with an associated reaction of tendon injury (received on 10th September 2019 (National Drug Code: 70461-0019-03)). Concomitant products included VIRAL VACCINES (COVID VACCINE (NOS)). On an unknown date, the patient received Influenza vaccine Quadrivalent unspecified season. On an unknown date, unknown after receiving Influenza vaccine Quadrivalent unspecified season, the patient experienced vaccine administered at inappropriate site. On an unknown date, the outcome of the vaccine administered at inappropriate site was unknown. Additional details were provided as follows: The patient reported the case for herself (reporter was a massage therapist). The patient received the Fluad 2019-2020 syringe flu shot was given at a pharmacy by a pharmacist and the patient believed that the pharmacist injected her too high on the upper arm/deltoid. This resulted in a visit to the emergency room and 7 months of severe pain and the use of prescription pain medications due to tendon damage. Since then patient had requested that all of her immunizations to be done in non-deltoid shots such as thigh or hip. The patient got a subsequent unspecified flu shot in the hip rather than the deltoid to avoid the risk of having the same shoulder tendon problem occur again, which led to vaccine administered at inappropriate site and her Covid shot(s) in the thigh. The reporter provided limited information


VAERS ID: 1989224 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-12-22
Onset: 2021-12-23
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Fatigue, Nausea, Pain, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Bupropion
Current Illness: NA
Preexisting Conditions: NA
Allergies: Sulfa, latex
Diagnostic Lab Data: NA
CDC Split Type:

Write-up: At 2 am following the vaccines I woke up with chills, body aches and a fever. I had those symptoms plus, extreme fatigue, nausea and vomiting for the next 4 days


VAERS ID: 1683255 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-09-08
Onset: 2021-09-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7316LA / UNK - / -
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. T029523 / 1 LA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U6984AA / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Aphasia, Blood pressure measurement, Dizziness, Heart rate, Hyperhidrosis, Pallor
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: NONE
Allergies: NONE
Diagnostic Lab Data: 9/8/21 4:20pm BP 97/45. P=44 9/8/21 4:22pm BP 99/48. P=44 9/8/21 4:24PM BP 101/51. P=50 9/8/21 4:26PM BP 109/58. P=57 9/8/21 4:30pm BP 112/66. P=65 9/8/21 4:35pm BP 113/69. P=63
CDC Split Type:

Write-up: Vasovagal Syncope was suspected. Patient felt lightheadedness and appeared pale a few minutes after receiving the vaccine. He was sweating profusely. 911 was called and patient was helped to lay down flat on the floor with his feet raised. His blood pressure was 97/45 with pulse of 44. Patient was responsive. Ammonium salt was given for patient to inhale to keep patient from fainting. Blood pressure and pulse was continually monitored. After about 10 minutes, patient was able to speak. His blood pressure was improving to 109/58 with pulse of 57. After about 15 minutes, patient was able to sit in a chair and appear alert. 911 has not arrived and patient was eager to leave. Final BP 115/69 with pulse of 63. Patient left store after about 20 minutes. 911 was cancelled.


VAERS ID: 2735216 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Florida  
Vaccinated: 2024-01-17
Onset: 2024-01-18
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2024-01-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Dizziness, Headache, Injection site pain, Malaise, Pain, Pyrexia, Rash
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: allergic rhinitis
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received COVID 19 and influenza vaccine on 01/17/24 at the pharmacy. Patient received both vaccines on the same day and the vaccine were administer in the same arm. Patient reported feeling sick with body aches, fever, headache, dizziness, pain at injection site and a rash to the left upper arm on 01/18/24.


VAERS ID: 1905944 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-29
Onset: 2021-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 330308D / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4L97X / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Vision blurred
SMQs:, Anticholinergic syndrome (broad), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient felt faint and had blurred vision. Resolved on its own. Patient was given a bottle of water. Patient went home ambulatory.


VAERS ID: 2000413 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-08
Onset: 2021-11-10
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 32030BD / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 312879 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: General physical health deterioration, Loss of consciousness, Memory impairment, Respiratory rate decreased
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Acute central respiratory depression (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Respiratory failure (narrow), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: none
Preexisting Conditions: none
Allergies: Maybe Eggs
Diagnostic Lab Data: Contact hospital. The shots she got at the same time in 2 different arms were Pfizer Covid 19 and FLAUD Quad 2021-2022 Syringe Flu ,single dose at pharmacy store
CDC Split Type:

Write-up: After she had both flu and Covid booster shots on the same day she had to rest for 2 days. After then her memory started to deteriorate. I took her to the ER on November27 where they did a battery of test and could find nothing wrong. Her condition continued to deteriorate over the next 3 weeks so I had her admitted to the Sarasota Memorial Hospital on Dec 17 . Again they could find nothing wrong and she was deteriorating rapidly She was moved to hospice on 27 Dec where she is now basically unconscious with very slow breathing.


VAERS ID: 1708859 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-09-15
Onset: 2021-09-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-09-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9JD9K / N/A RA / IM

Administered by: Military       Purchased by: ?
Symptoms: Anticoagulant therapy, Arthralgia, COVID-19 pneumonia, Computerised tomogram thorax abnormal, Condition aggravated, Cough, Dehydration, Fibrin D dimer increased, Headache, Interchange of vaccine products, Lung consolidation, Lung opacity, Nausea, Pulmonary embolism, Tachycardia, Vomiting
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Haemorrhage laboratory terms (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Embolic and thrombotic events, venous (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Medication errors (broad), Infective pneumonia (narrow), Dehydration (narrow), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None but he did get the flu vaccine at the same time as the Covid vaccine on 15 Sep 2021
Current Illness: Covid-19 diagnosed 30 Aug 2021
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: CTPE on 16 Sep 21: 1. Acute pulmonary embolism involving the left upper and lower lobar arteries with more significant thrombus burden in the left upper lobe. No evidence of right heart strain. 2. Multifocal patchy groundglass opacities and consolidative changes of the lungs bilaterally which are similar in distribution in comparison to prior, but have progressed in the interim. There are also more confluent changes in the left upper lobe. These findings may reflect progression of the patient''s known Covid pneumonia, although superimposed pulmonary infarct involving the left upper lobe cannot be excluded. 3. Similar mediastinal and hilar adenopathy which are likely reactive in etiology
CDC Split Type:

Write-up: Patient presented to the ED for 15 episodes of emesis in the morning of 16 Sep. The patient tested positive for COVID on August 30th. He was seen in the ED on 1 Sept and had a CT PE that was negative for clots at that time. He states that his main symptom of COVID was loss of appetite and he had lost approximately 15 lb in the past 3 weeks due to loss of appetite. He completed his quarantine and returned to work. On Wednesday 15 Sep 21, he received the first Pfizer vaccine as well as a Fluarix flu shot. He had a Headache and arthralgias after the shot. On 16 Sep 21 he woke up and vomited numerous times. He states that he has a mild cough still from Covid, but denies chest pain, shortness of breath dizziness or light headedness. He has been making urine and stooling appropriately though he has felt dehydrated on 16 Sep 21. In the ED on 16 Sep 21, the patient was found to have an elevated d-dimer of 3.13 and he underwent a new CTPE. This was positive for multiple pulmonary emboli in the left upper and lower lobar arteries. His nausea/tachycardia and clinical dehydration resolved with anti-emetics and intravenous fluids. He was started on heparin and then Xarelto for his pulmonary emboli. He never had shortness of breath or dyspnea on exertion. He was discharged home in about 24hrs after ED visit.


VAERS ID: 2001393 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-01-03
Onset: 2022-01-04
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Headache, Myalgia, Night sweats, Oropharyngeal pain, Pyrexia, Tremor
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Effexor and seroquel
Current Illness: Asthma
Preexisting Conditions: AsthmA
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Severe shakes, fever, sore throat, severe muscle aches, severe headache, night sweats, chills


VAERS ID: 2001429 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-01-06
Onset: 2021-02-28
   Days after vaccination: 53
Submitted: 0000-00-00
Entered: 2022-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026L20A / 1 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. 33332-0321-01 / 1 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Acoustic stimulation tests, Balance disorder, Computerised tomogram, Confusional state, Disorientation, Dizziness, Hyperacusis, Laboratory test, Magnetic resonance imaging, Motion sickness, Nausea, Photophobia, Vertigo, Vestibular function test, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Corneal disorders (broad), Retinal disorders (broad), Hearing impairment (narrow), Vestibular disorders (narrow), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: none
Preexisting Conditions: sleep apnea
Allergies: now
Diagnostic Lab Data: labs and CT scan 9/25/21 MRI 10/14/21 Hearing testing October 21 Vestibular testing 11/11/21
CDC Split Type:

Write-up: Everyday dizziness/vertigo, nausea/vomiting, balance problems, extreme motion sensitivity, disoriented, confused, unsteady, sensitive to light and sound.


VAERS ID: 1713590 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-09-18
Onset: 2021-09-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal pain upper, Dizziness, Dyspnoea, Rash
SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Also received the Flu shot at the same time as the Vaccine
Current Illness: None
Preexisting Conditions: None
Allergies: Not Sure
Diagnostic Lab Data: None we would like to further tests on my daughter to see what she is allergic to
CDC Split Type:

Write-up: After a minute starting having issues with breathing stomach pain and dizziness. Broke out with rash store nurse gave my daughter Benadryl and we waited about 20 minutes she started to feel better and the symptoms went away.


VAERS ID: 1951792 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-12-09
Onset: 2021-12-13
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2021-12-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 331308A / 1 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 49281-0421-50 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Body temperature increased, Erythema, Headache, Myalgia, Nausea, Pain of skin, Swelling, Urticaria
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CBD, Ashwaganda, St Johns Wart, multi-vitamin
Current Illness:
Preexisting Conditions: obesity
Allergies: nickel, latex, ampicillin, lactose
Diagnostic Lab Data:
CDC Split Type:

Write-up: Headache and general pain across skin and throughout muscles, as well as nausea on the first day after injection. Elevated body temperature. Beginning on the 13th, 4 days after injection, there was slight swelling on the right side of the lower back, with redness surrounding the area by about 2 inches. On the morning of the following day, hives covered the entire body, primarily on the upper torso and arms. Treatment began in the afternoon on the 14th with diphenhydramine hydrochloride, 25mg. Hives persist.


VAERS ID: 2032631 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-01-08
Onset: 2022-01-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL0007 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7378LA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Hyperhidrosis, Pallor, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NA
Current Illness: NA
Preexisting Conditions: NA
Allergies: NKA
Diagnostic Lab Data: NA
CDC Split Type:

Write-up: Patient became lightheaded about 5 minutes after vaccine administration. She then started to sweat and turn white and finally fainted. After lying her on the floor she woke up almost immediately. No further complications after that


VAERS ID: 2039124 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Male  
Location: Florida  
Vaccinated: 2022-01-16
Onset: 2022-01-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003J21A / 2 RA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 49281042150 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Nausea, Pain
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Nausea, body aches, tiredness


VAERS ID: 2722180 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-12-07
Onset: 2023-12-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (NOVAVAX)) / NOVAVAX - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Blood magnesium, Chest X-ray, Differential white blood cell count, Electrocardiogram, Extrasystoles, Full blood count, Metabolic function test, Troponin T
SMQs:, Tachyarrhythmia terms, nonspecific (narrow), Hypokalaemia (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Covid Moderna 2nd shot
Other Medications: Enepril, Hydrochlorothiazide, Norcor, Metformin, Tuarine, Saw Palemto, multi vitamin
Current Illness: Nothing
Preexisting Conditions: Idiopathic peripheral neuropathy, HBP, obesity
Allergies: None
Diagnostic Lab Data: ECG 12 lead Xray chest 1 View CBC and Differential Comprehensive metabolic panel Magnesium Troponin T Quant High Sensitivity
CDC Split Type:

Write-up: Heart rate was 120-130 BPM and skipping beats within an hour of taking the shot.


VAERS ID: 1745712 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-08-26
Onset: 2021-08-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3183 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal pain, Diarrhoea, Nausea, Pyrexia, Retching
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Glimepiride 2mg, omeprazole 40mg, estradiol 2mg, ropinerole 2 mg, montelukast 10mg, magnesium 250mg, multiple vitamin,
Current Illness: None
Preexisting Conditions: Diabetes, excema, asthma
Allergies: Levaquin, codeine
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Severe abdominal cramps, diarrhea, nausea, dry heaves, fever over 102


VAERS ID: 2721002 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-11-27
Onset: 2023-11-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Investigation, Joint swelling, Mobility decreased, Pain in extremity, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Allopurinol 100 mg, Indapamide tablets 0.75 mg, Rosuvastatin 10 mg., baby aspirin.
Current Illness: None.
Preexisting Conditions: Arthritis, high cholesterol, gout.
Allergies: None.
Diagnostic Lab Data: Screening for blood clots.
CDC Split Type:

Write-up: He got his vaccine, his arm was hurting, which it has never hurt before when he gets a vaccine. Then about 4-5 hours later he started to get both of his wrists on both hands started to swell, and became very difficult to use due to the pain. He called his doctor, was taking Tylenol for the pain 8 hour type, and may have taken an Advil, which helped only a little. The only thing that works for him is Colchicine, which he got from his doctor. This attach was brutal and went to the walk-in clinic and they did a screen on him checking for blood clots, wanted a blood test for this and they would not do it, which is the way to find out you have a gout flare, which he did not have one since July a and the first time he had a diagnosis was 12 years ago. He took the Colchicine for 3 days, and stopped as it scares him to take it as it is so strong. The pain is now tolerable, and back to it''s normal baseline annoying pain. He would like it known that if people have gout/arthritis conditions that they inform them before they have a vaccine that they may have an adverse reaction due to this.


VAERS ID: 1749473 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-02-01
Onset: 2021-09-16
   Days after vaccination: 227
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9263 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6200 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Grip strength decreased, Hypoaesthesia, Muscle spasms
SMQs:, Peripheral neuropathy (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: no
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Shortly after receiving FLU vaccine in left arm, start to develop mussel spasms in left shoulder, numbness in fingers, and weak grip strength in left hand. FLU vax site is same site as COVID 19 vax site.


VAERS ID: 1753227 (history)  
Form: Version 2.0  
Age: 67.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-09-24
Onset: 2021-09-27
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NOT SURE OF TYP / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Nausea, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Losartan Potassium (100mg) Amlodipine Besylate (5 mg) Rosuvastatin (40 mg) Janumet (50mg/150mg) Tadalafil (5 mg) Allopurinol (300 mg) Preservision ARED x2 Vitamin B12 (2500mcg) Folic Acid (1mg) Aspirin (81 mg)
Current Illness:
Preexisting Conditions: Diabetes (type 2)
Allergies: Lisinopril
Diagnostic Lab Data: Must note that I had flu shot at same time (different arm) as COVID shot.
CDC Split Type:

Write-up: Chills (severe shivering), fever (102), nausea, vomiting. Worst symptoms over in 2-3 hours. Back to normal after 10 hours.


VAERS ID: 2068698 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-10-04
Onset: 2022-01-12
   Days after vaccination: 100
Submitted: 0000-00-00
Entered: 2022-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939903 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Bronchitis, COVID-19, Chills, Cough, Productive cough, Pyrexia, SARS-CoV-2 test negative, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metformin 1000 mg, Tamsulosin .4 mg, Crestor 5 mg, Lisinopril 5 mg, Pantoprazole 40 mg
Current Illness: None
Preexisting Conditions: Diabetes
Allergies: Ampicillin, Levaquin
Diagnostic Lab Data: Covid test on 1/13- sample size was not sufficient. Covid test on 1/18- positive. Covid antigen test on 1/24- negative. Covid PCR test on 1/24- positive.
CDC Split Type: vsafe

Write-up: On 1/12/2022 I started feeling like I had bronchitis, I had some chills, fever, and wet coughing. I was coughing up phlegm. I did a teleconference with a doctor and she prescribed antibiotics and cough medicine and asked me to do a Covid-19 test. I did the Covid-19 test on 1/13 but the sample size was not sufficient. I had to retest on 1/18 and it came back positive. I did 2 tests on 1/24, negative antigen immediate test and the PCR came back positive. When I had the second test I did not have any symptoms except the cough. I still have the cough and I am still coughing up phlegm.


VAERS ID: 1952028 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-08
Onset: 2021-11-17
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2021-12-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939905 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Angioedema, Chest discomfort, Erythema, Inflammation, Oesophageal discomfort, Pruritus, Rash erythematous, Rash pruritic, Scratch, Swelling, Swollen tongue, Urticaria
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Cheers brand liver support supplement
Current Illness: none.
Preexisting Conditions: none.
Allergies: codeine. no food or other allergies.
Diagnostic Lab Data: none
CDC Split Type:

Write-up: 9 days after receiving the booster on Nov 17th overnight, broke out in hives, extreme itching. Started in head, but also moving to torso, waistline, groin. Also had a tight feeling in esophagus like a swallowed a pill, which coincided with MINOR swelling of tongue. These symptoms continued badly for 4 days all over body in random spots coming and going, plus chest tightness coming and going always with tongue sides swollen slightly. Nov 20 doctor gave a steroid shot and prednisolone 5 day pack of pills which helped a lot, but symptoms have continued still. Today is 4 weeks since the initial hives outbreak. Since the steroid shot/pills, the symptoms now are not big hives, maybe just minor, but itching red bumps, itching and scratching red inflamed lines, all different body parts, comes and goes, some days better than others. Taking Zyrtec most days. Benadryl some nights. Hydrocortisone cream if it itches a lot. Seems like I am keeping the bumps and itches from turning in to the huge welts and hives by staying on antihistamine and cream. If I have a mild day and go off for a day, the next day it is back. Just read on this case of dozens of others with same delayed symptoms after booster: https://www.cureus.com/articles/69363-chronic-spontaneous-urticaria-after-covid-19-vaccine?open_comments=true#article-comments-section


VAERS ID: 2069086 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-12-20
Onset: 2021-12-29
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2022-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041J21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Pruritus
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: HBP
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Pt. states that after receiving the 3rd dose of Moderna 12/20/2021 (Influenza Quad Right Arm), started experiencing symptoms 12/29/2021 on itchiness on the soles of both feet and itchiness in both palms of hands. Also itchiness continuing to spread throughout the Left thigh, back area, and Left arm. No noted Primary visit/communications.


VAERS ID: 1893660 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-11-19
Onset: 2021-11-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1620 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS N34CK / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Headache, Insomnia, Lymphadenopathy, Pain, Pain in extremity, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 2nd shot of Pfizer covid shot on 04/19/2021
Other Medications: buproprion xl 300 mg
Current Illness: none
Preexisting Conditions: depression
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: I received both vaccines simultaneously on 11/19/2021 shortly after 11 AM. 12 hours later around 11 PM the following symptoms occurred - extensive body aches, fever, headache, fatigue, inability to sleep, sore arms. These symptoms continued for the next two days. Also very noticeable are swollen lymph nodes under both arms. Fatigue continues as of today, 11/23/2021.


VAERS ID: 1846051 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-11-01
Onset: 2021-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 939906 / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Diarrhoea, Dizziness, Headache, Hyperhidrosis, Myalgia, Pyrexia, Syncope, Tremor
SMQs:, Torsade de pointes/QT prolongation (broad), Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Both Moderna COVID Injections
Other Medications: Prednisone 5mg Pantoprazole 50mg Atenolol 100mg LoDose Aspirin Vision Vitamin Hydrocodone 10mg 3/day Calcium D3 1000mg Potassium Chloride 10meq Morphine Sulfate ER 15mg 2/day Atrovastatin 40 mg Melatonin 10mg Tylenol PM 2/day
Current Illness: None
Preexisting Conditions: Rheumatoid Arthritis
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Uncontrolled Diarrhea Heavy Sweating Shaking Fever of 101 Weakness Dizziness Muscle Pain Throughout Body Headache Fainting


VAERS ID: 1853645 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-08-27
Onset: 2021-09-29
   Days after vaccination: 33
Submitted: 0000-00-00
Entered: 2021-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 002A21A / 1 AR / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 036B21A / 2 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ687AA / 1 AR / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Bell's palsy
SMQs:, Hearing impairment (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Fentanyl, Lisinopril, Abilify, Fenofibrate
Current Illness: HTN, Musular Dystrophy,
Preexisting Conditions: Muscle AMP Deaminise Deficiency
Allergies: Vancomycin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Bells palsy (R) face appeared 9/29/21 slowly improving, appears to be possible related to obtaining flu shot shortly after Covid vaccine.


VAERS ID: 2329647 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-23
Onset: 2021-11-27
   Days after vaccination: 4
Submitted: 0000-00-00
Entered: 2022-06-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 069F21A / UNK AR / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / UNK AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Herpes zoster
SMQs:, Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Albuterol; Lexapro; Alprazolam.
Current Illness: None.
Preexisting Conditions: Asthma; Generalized Anxiety Disorder.
Allergies: Thimerosal.
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: Moderate case of shingles on thighs and buttocks.


VAERS ID: 2593971 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-03-03
Onset: 2023-03-04
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Mobility decreased, Pain in extremity
SMQs:, Parkinson-like events (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Jardiance, Lisinopril, Rybelsus, Glypizide, Atorvastatin, Carvedilol.
Current Illness: None
Preexisting Conditions: Diabetes
Allergies: No
Diagnostic Lab Data:
CDC Split Type:

Write-up: extreme pain in right hand. Unable to close or open pinky finger. Pain at base of finger.


VAERS ID: 1848918 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-01
Onset: 2021-11-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7384JA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Back pain, Breast swelling, Discomfort, Erythema, Lymphadenopathy, Pain in extremity, Rash, Skin irritation
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Retroperitoneal fibrosis (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient had left underarm swelling and redness (near lymph node area). Swelling traveled to left breast and a visible rash with irritation appeared. Patient also had left leg pain, inner thigh pain, some back pain and discomfort.


VAERS ID: 2582963 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Male  
Location: Florida  
Vaccinated: 2022-11-03
Onset: 2022-11-01
Submitted: 0000-00-00
Entered: 2023-02-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9702 / 5 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: ENT 12/2022 & 02/2023
CDC Split Type:

Write-up: Tinnitus both ears


VAERS ID: 2440762 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-09-06
Onset: 2022-09-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-09-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS7144B / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, Immunisation reaction, Infection, Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth, Pain
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatin; Advair Inhaler; Levothyroxine; Estradiol vaginal cream; Multivitamin with iron; Turmeric; Calcium with Magnesium; Glucosamine: Vitamin D3; Wall zinc; Biotin; Probiotics
Current Illness: None
Preexisting Conditions: Asthma; High Cholesterol; Hypothyroid
Allergies: Codeine; Opioids; Lactose Intolerance
Diagnostic Lab Data: None
CDC Split Type: vsafe

Write-up: I received my fifth dose of my Moderna vaccine at the same time as receiving my flu shot. I had the soreness that I always have, but suddenly the injection site on my left arm got really red and swollen and hot and then it spread down to the top of my elbow and up toward my armpit and my left breast. I was in a lot of pain for a few days. I had a telehealth appointment where my doctor indicated that I either had an infection from the person not cleaning the area properly or a reaction to the vaccine. He put me on prednisone and Cephalexin on 09/09/2022. From 09/09/2022 to 09/11/2022 I noticed during that time that my blood pressure would get high, and thing were worse when I laid down. There were two nights where I would wake up and when I got up, I was in a lot of pain. As of today, my swelling has gone away, and I have a bit of tenderness but only in the localized area of the injection and it is very light.


VAERS ID: 2579413 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-03-05
Onset: 2023-01-31
   Days after vaccination: 697
Submitted: 0000-00-00
Entered: 2023-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026A21A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 002B21A / 2 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 069H21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7424LA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test abnormal, Contusion, Fatigue, Platelet count decreased
SMQs:, Haematopoietic thrombocytopenia (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Systemic lupus erythematosus (broad), Accidents and injuries (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: none
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: 2/2/23 low platelets
CDC Split Type:

Write-up: 1/31/2023 reported to HCP for bruising, fatigue, contusions. Blood drawn and results on 2/2/23 showed critically low platelets. Unsure if related to vaccinations.


VAERS ID: 1846215 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-07
Onset: 2021-10-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 RA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NOT SURE TYPE O / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chills, Fatigue, Hyperhidrosis, Muscular weakness, Myalgia, Night sweats
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atenolol, Atorvastin, Byetta, Hydrochlorothiazide, Spironolactone, Alosetron, Dycichlomine, Synthroid, Cytomel, Librax, Omega 3, AREDS, Centrum
Current Illness: None
Preexisting Conditions: IBS-D, Diabetes Type 2, Hashimotos
Allergies: Silicon
Diagnostic Lab Data: None. I called the Urgent Care and they told me that they didn''t take Covid reactions.
CDC Split Type:

Write-up: 9:00 PM woke up with shivers, 11:00 PM tried to get up and my legs did not work, 1:00 AM night sweats so bad I had to change nightgown. Fatigued for 2 days. My legs didn''t work for 48 hours. Then just as suddenly as they did not work, they started to work. My thigh muscles were sore and it felt like I had done squats for the whole day. no cough, no fever,


VAERS ID: 2573684 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-02-01
Onset: 2023-02-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7136 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3AH4A / 1 LA / IM
HEP: HEP B (HEPLISAV-B) / DYNAVAX TECHNOLOGIES CORPORATION 941054 / 1 LA / IM
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS 9ZK5T / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Blood glucose normal, Blood pressure decreased, Dizziness, Dysphagia, Gait disturbance, Hyperhidrosis, Orthostatic hypotension, Pallor, Pharyngeal hypoaesthesia, Trendelenburg position
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pt is not on any medication.
Current Illness: Pt reported no prior illness.
Preexisting Conditions: Pt reports no chronic illness.
Allergies: N.K.D.A
Diagnostic Lab Data: GLUCOSE POC DONE RESULTING 110.
CDC Split Type:

Write-up: 15:45 PM: PATIENT RECEIVED VACCINATIONS AFTER COMPLETING HER HEALTH ASSESSMENTS: TDAP, HEP-B, COVID-19 & FLU 15:55 PM: PATIENT WAS D/C HOME AND DENIED FEELING ANY S/S OF NAUSEA, VOMITING LIGHTHEADNESS. 16:00 PM: PATIENT REPORTED FEELING LIGHTHEAD AND DIZZY AND NEEDED TO SIT DOWN. PATIENT WAS FOUND BY AN EMPLOYEE IN THE ELEVATOR SITTING ON THE FLOOR OF THE ELEVATOR. PATIENT WAS AWAKE AND ALERT. 16:02PM: PATIENT WAS ABLE TO WALK WITH ASSISTANCE TO A CHAIR NEAR THE ELEVATOR. 16:03 PM: STAT VITAL SIGNS TAKEN: B/P: 86/55, P: 62, SAT: 100% & T: 97.7F. LUNGS SOUNDS CLEAR AND NO ECTOPIC HEART TONES NOTED. 16:06 PM: PATIENT STARTED TO REPORT NUMBNESS TO HER THROAT AND SLIGHT DIFFICULTY SWALLOWING. PALLOR NOTED AND DIAPHORESIS NOTED. 16:09 PM: PATIENT GIVEN DIPHENHYDRAMINE 25MG IM X 1 TO L DELTOID. 16:15 PM: REPEAT SET OF VS: B/P: 109/80, P;82 & 100%, BLOOD SUGAR: 110. LUNGS CLEAR-BILATERAL. 16:20 PM PATIENT STATES SHE WAS FEELING BETTER AND NO LONGER FELT HER THROAT NUMBNESS OR DIFFICULTY SWALLOWING. 16:30PM: PATIENT WAS STABLE AND LEFT SITTING IN THE CHAIR WITH ROUTINE V/S TAKEN. 16:50 PM: ATTEMPTED TO HAVE PATIENT STAND UP WITH ASSISTANCE AND PATIENT EXPERIENCED ORTHOSTATIC HYPOTENSION. B/P DROPPED TO 75/55, P: 100. 16:51 PM: PATIENT WAS ASSISTED TO FLOOR AND PLACE IN TRENDELENBURG POSITION. B/P RECHECKED: 92/70, P: 84 O2 SAT: 100%. 16:52 PM: EMS ACTIVATED 16:53 PM: VS REASSESSED: 79/60, P: 72 & O2 SAT: 82% 16:54 PM: VS: REASSESSED: 90/62, P: 76 & O2 SAT: 100%. PATIENT WAS DENYING FEELING SICK OR SHORT OF BREATH. DENIED CHEST PAIN. 17:03 PM: EMS ARRIVED 17: 10PM: EMS COMPLETED ASSESSMENT AND OFFERED TO TRANSPORT TO MEDICAL FACILITY FOR FURTHER MEDICAL EVALUATION AND TREATMENT. PATIENT AND SPOUSE REFUSED. PATIENT STATED SHE FELT MUCH BETTER AND WANTED TO GO HOME. 17:1PM: EMS ESCORTED PATIENT AND SPOUSE TO PERSONNEL VEHICLE. 17:20 PM: NO FURTHER INCIDENT NOTED.


VAERS ID: 1813583 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-21
Onset: 2021-10-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 RA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Chills, Fatigue, Headache, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Same symptoms with nausea, Pfizer Covid #1
Other Medications: Losartan, sertraline, trazadone
Current Illness: None
Preexisting Conditions: Hypertension
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Severe chills, fever, headache, muscle aches, fatigue


VAERS ID: 2563335 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-12-28
Onset: 2022-12-31
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2023-01-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (NOVAVAX)) / NOVAVAX - / 1 - / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / IM

Administered by: Military       Purchased by: ?
Symptoms: Migraine, Nausea, Phonophobia, Photophobia, Vomiting
SMQs:, Acute pancreatitis (broad), Noninfectious meningitis (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Corneal disorders (broad), Retinal disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: New onset of migraine headaches with nausea, vomiting, photo and phonophobia 3 days after vaccine administration. No history of migraines perviously


VAERS ID: 1943646 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-10-26
Onset: 2021-10-26
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1822811 / 2 RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Decreased appetite, Erythema, Headache, Hyperhidrosis, Impaired work ability, Injection site pruritus, Migraine, Nausea, Pain, Rash, Rash pruritic
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Candesartan - 2 milligrams nightly, Chlorthalidone - 25 milligrams in am, Januvia- 100milligrams - am, Jardiance- 10 milligrams am, Rosuvastatin - 5 milligram pm
Current Illness: Spider bite in Oct2021
Preexisting Conditions: Pre Diabetic
Allergies: Novocain, Spider bite
Diagnostic Lab Data: No test yet
CDC Split Type: vsafe

Write-up: Had spider bite in Oct 2021 Between 1st and Dose 2 before and after the 2nd dose. Went to ER after the spider bite. They drained it and followed up with dermatologist. 10/26/2021 booster and flu both on the same arm I think - headache, nausea and body aches in 5 mins after leaving the pharmacy. No appetite, headache with an hour. Laid down, body sweats, migraine. That night it got worst. In the am hit me like a ton of brinks and rash immediately and all over the body and back of the arms and legs got better and still very itchy and went in bed and did not go to work. Large redness and was itchy yet. The itching the next day. From the elbow to shoulder on right and bicep, Then legs from right leg from ankle onwards. Its getting better. Dermatologist changed meds to ointment. Seem to help with itching and the redness is till there and was steroid shot which helped with the itchy.


VAERS ID: 2558773 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-10-11
Onset: 2022-12-05
   Days after vaccination: 55
Submitted: 0000-00-00
Entered: 2023-01-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 5 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hypertension
SMQs:, Neuroleptic malignant syndrome (broad), Hypertension (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamin, Calcium 600+D3
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Don''t think this is reportable, or because of the vaccine, but I have recently been prescribed medication for high blood pressure. The form asked if my health situation has changed since the vaccine and I answered "yes". Was discovered after regular annual wellness check-up.


VAERS ID: 2544975 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-11-21
Onset: 2022-12-18
   Days after vaccination: 27
Submitted: 0000-00-00
Entered: 2022-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH G56738 / 4 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cough, Headache, Influenza virus test negative, Neck pain, Oropharyngeal pain, Pain, Respiratory syncytial virus test negative, Respiratory tract congestion, SARS-CoV-2 test negative, Secretion discharge, Upper-airway cough syndrome
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Arthritis (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec; Zoloft
Current Illness: None
Preexisting Conditions: FCG; Anxiety; Depression
Allergies: Seasonal Allergies
Diagnostic Lab Data: 28DEC2022 COVID-19 Test-Negative
CDC Split Type: vsafe

Write-up: After 1 week later the 4th dose I had headache that lasted for several days. It was very annoying. I was getting the headache almost every day. On 12/18/2022 in the morning I had a post nasal drip and a sore throat. The next few days I had body aches ( neck was sore ), chest congestions, cough, and severe headache. I went to the Urgent Care on 12/21/2022. Before I went to the Urgent care I was negative. In the Urgent Care they tested negative COVID-19, Flu, and RSV. They prescribed me with a cough pill Benzonatate which I only took it for 2 days because I kept getting headaches. As of today I am recovering . I still have mucus from my cough but my throat doesn''t hurt like before.


VAERS ID: 2535338 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-12-15
Onset: 2022-12-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-12-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Blood culture, Blood lactic acid, Chest X-ray, Chest pain, Condition aggravated, Dyspnoea, Fibromyalgia, Laboratory test
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: pt presented to ED with c/o of chest pain and SOB. pt also endorsing worsening fibromyalgia and states "it is worse then it has ever been, it doesnt feel like my normal pain". pt currently being worked up for a CP and infectious work up, This includes blood cultures, lactic acid, standard labs, checs xray, and medications. outcome unknown at the time of this report.


VAERS ID: 2457032 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: Florida  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-09-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U3261AA / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Rash, Somnolence, Swollen tongue, Tongue discolouration, Vaccination complication
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Anticholinergic syndrome (broad), Dementia (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SYNTHROID
Current Illness:
Preexisting Conditions: Comments: No medial history was reported
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20216

Write-up: swollen tongue; Sleepiness; swollen tongue, with raised white puffy lines; vaccination complication; Rash; This spontaneous case was reported by a patient and describes the occurrence of SWOLLEN TONGUE (swollen tongue), SOMNOLENCE (Sleepiness), TONGUE DISCOLOURATION (swollen tongue, with raised white puffy lines), VACCINATION COMPLICATION (vaccination complication) and RASH (Rash) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE QUADRIVALENT) for Prophylactic vaccination. No medial history was reported. Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for an unknown indication. In 2009, the patient received dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE QUADRIVALENT) (unknown route) .5 milliliter. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced SWOLLEN TONGUE (swollen tongue), SOMNOLENCE (Sleepiness), TONGUE DISCOLOURATION (swollen tongue, with raised white puffy lines), VACCINATION COMPLICATION (vaccination complication) and RASH (Rash). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at a dose of 1 dosage form. At the time of the report, SWOLLEN TONGUE (swollen tongue), SOMNOLENCE (Sleepiness), TONGUE DISCOLOURATION (swollen tongue, with raised white puffy lines), VACCINATION COMPLICATION (vaccination complication) and RASH (Rash) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in.


VAERS ID: 2527969 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-12-05
Onset: 2022-12-06
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-12-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Eye pain, Injection site pain, Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Glaucoma (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: First Moderna shot. slight fever and body aches lasting 1 day after
Other Medications: Stiolto
Current Illness:
Preexisting Conditions: COPD, Emphysema
Allergies: Iodine, Sulfa drugs
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fever, body aches, injection site pain, 4 days later? Not sure which shot produced the lasting side effects. Days 3 and 4 pain behind both eyes upon waking and getting up. subsides as morning goes on. If this continues, I will see my MD on Monday.


VAERS ID: 1821299 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-26
Onset: 2021-10-27
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test, Chest X-ray, Computerised tomogram, Dizziness, Face injury, Headache, Immunodeficiency, Loss of consciousness, Nausea
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Synthroid Protonix Wellbutrin Buspar Prazosin Clonazepam Emtricitabine/tenof Multivitamin Trazadone
Current Illness: None
Preexisting Conditions: Barrett?s disease Partial thyroid to your PTSD Depression
Allergies: Sulfa and shellfish
Diagnostic Lab Data: 10/27/21 Emergency Room Stitches, CT scan, Cxr, IV, blood tests
CDC Split Type:

Write-up: Passed out, hit chin on kitchen cabinet and split open, nausea, dizziness, headache


VAERS ID: 2513878 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-10-17
Onset: 2022-10-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ2524 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Diarrhoea, Feeling abnormal, Haemorrhage, Influenza like illness, Nausea, Needle issue, Vomiting
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Dementia (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Embree; Folid Acid; Hydroxychloroquine; Metoprolol; Hydrocodone; Atorvastatin; Eliquis; Prednisone
Current Illness: N/A
Preexisting Conditions: Arthritis
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type: vsafe

Write-up: When I sat down, they started giving me the vaccine and the needle broke and my arm started bleeding. The nurse then went and got another dose and gave it. My arm bleeds a little but not too much. Ago a hour later I started to feel nausea and I had diarrhea, and I went home to lay down. I had to contact my doctor to get medication to stop the vomiting. I then started having bad chills. I felt like I had the flu. The doctor prescribed ondansetron the pharmacist didn?t want to fill the medication because I have arthritis medication. The doctor sent me a lower dose, and, in the meantime, I was at home with flu like symptoms and I felt horrible. I started taking the medication and most of the stuff started going away.


VAERS ID: 2467495 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Male  
Location: Florida  
Vaccinated: 2022-10-01
Onset: 2022-10-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7138 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7681LA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood glucose, Dizziness, Loss of consciousness, Muscle rigidity, Musculoskeletal stiffness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dystonia (broad), Parkinson-like events (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Arthritis (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Patient verbalized that he always have the same reaction to injections due to his fears to injections
Other Medications:
Current Illness: None
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient arrived to the pharmacy requesting the covid vaccine (primary dose). After talking to the patient , he agreed to receive the influenza vaccine as well. Patient entered the immunization room with a friend. the 2 vaccines were administered to the patient in the right deltoid. Around half a minute of receiving the vaccine, patient said he was going to pass out and then he passed out. Patient was rigid (stiff) and his friend helped me placed the patient on the floor, while that was occurring I told my technicians to call EMS. After the patient was placed on the floor, he became awake and aware of his surroundings, that lasted less than 1 minute. He said that this always happens to him when he gets injections. EMS arrived and checked the patient and no signs of injury were observed. EMS pricked the patient finger to check his sugar and patient had the same reaction he had after receiving the vaccines. Patient then was cleared by EMS and left the pharmacy walking without need for assistance. The event was concluded to be due to his phobia to injections.


VAERS ID: 2494866 (history)  
Form: Version 2.0  
Age: 0.5  
Sex: Male  
Location: Florida  
Vaccinated: 2022-10-27
Onset: 2022-10-28
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 1 RL / IM
DTAPIPVHIB: DTAP + IPV + HIB (PENTACEL) / SANOFI PASTEUR U7331AA / 3 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9LC58 / 1 LL / IM
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH FX0078 / 3 LL / IM
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 1892788 / 3 MO / PO

Administered by: Private       Purchased by: ?
Symptoms: Injection site bruising, Petechiae, Platelet count decreased
SMQs:, Haematopoietic thrombocytopenia (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Systemic lupus erythematosus (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Probiotic
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: NKDA
Diagnostic Lab Data: 10/31 Platelet ct 15K, PT 13.7/PTT 44.3 see attached lab results
CDC Split Type:

Write-up: Petechial rash beginning 10/28/22 1 day after vaccination & significant bruising on body on body @ injection site. Twin sibling vaccinated same day (not identical) is fine.


VAERS ID: 1833452 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-09-30
Onset: 2021-10-10
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2021-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Ageusia, SARS-CoV-2 test negative
SMQs:, Taste and smell disorders (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Quinapril 10 mg. Rosuvastating 10mg.
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Tested negative for Covid 19, two times. First time using Rapid test on 10/16/2021. Second time using Lab SARS-COV-2 RNA, QL NAAT, RT PCR/TMA (COVID-19) on 10/19/2021 also came back neative.
CDC Split Type:

Write-up: Loss of taste. I can still smell ok, but I can not taste foods, such as sweet, salt spicy, bitter, etc.


VAERS ID: 2302598 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-26
Onset: 2021-12-01
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2022-05-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 0274421B / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Chills, Erythema, Fatigue, Illness, Influenza like illness, Pain, Pruritus, Pyrexia, SARS-CoV-2 test positive, Scratch, Skin swelling, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Accidents and injuries (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin - occasionally
Current Illness: Cold & sinus infection - couple weeks prior
Preexisting Conditions: N/A
Allergies: amoxicillin (hives - as toddler)
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Within approx. 6 hours of receiving vaccines patient experienced flu-like symptoms (fever, chills, aches); recovered within a day. Has never had an adverse reaction to prior Moderna vaccines (1st - 4/5/21, 2nd 6/3/21). Within approx 10-14 days after receiving Moderna booster, began to experience an intense itch (at first in groin area - mistook for yeast infection but creams only seemed to make worse), then the itch spread to any & all body parts as an intensely itchy, red & raised welts (hives). Seemed to be no pattern to where hives would occur except that simply scratching the skin could instigate raised hives & continued scratching makes it much worse. If ignored, will fade within the hour or less but will recur elsewhere without respite; some form of global migrating dermatographic urticaria? All areas of body seem susceptible (including scalp, soles, palms, ears - excepting does not occur directly on the face - no eyelids/cheeks/lips, forehead...) Most OTC antihistamines did not mitigate the hives, but just 1/2 zyrtec (generic) almost made them disappear when taken daily; if this does is missed, hives become apparent again & gradually worsen as when first appeared. Patient tired of taking Zyrtic daily due to perceived side effects & discontinued in April 2022 - hives were still present & just bearable if itching resisted. In May 2022, family tested postive at home for Covid-19 (patient was asymptomatic except for tiredness), but hives all but ceased to exist during the week of illness in the household. Within a week of illness in the household, hives have now returned, but at a lesser intensity. Patient manages without medication at the moment.


VAERS ID: 2151555 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-08-25
Onset: 2022-01-26
   Days after vaccination: 154
Submitted: 0000-00-00
Entered: 2022-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FA7485 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 3SE27 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2022-02-01
   Days after onset: 6
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vaccinated patient hospitalized with COVID-19.


VAERS ID: 2155350 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-03-03
Onset: 2022-03-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 033K21-2A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS TG723 / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Cystic fibrosis carrier
SMQs:, Congenital, familial and genetic disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: carrier of cystic fibrosis gene mutation
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Moderna booster administered 2 months early. First and second dose given 11/2021.


VAERS ID: 2698384 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-10-15
Onset: 2023-10-15
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030592 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8094DA / 1 LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS KD424 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Mobility decreased, Musculoskeletal stiffness, Pain in extremity
SMQs:, Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: rabies shot 60 years ago
Other Medications: advil 200mg, lisinopril, omeprazole
Current Illness: none
Preexisting Conditions: high blood pressure
Allergies: sulfa, rabies vaccine, finasteride
Diagnostic Lab Data: Nothing to date
CDC Split Type:

Write-up: The morning following vaccinations, patient experienced stiff neck, and can''t turn or nod head due to pain. Today is Thursday and patient still cannot move neck. Sore arm, on left side more than right after 24 hours.


VAERS ID: 1869029 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-10-30
Onset: 2021-10-31
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS CA599 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Asthenia, Atelectasis, Brain natriuretic peptide normal, Chest pain, Computerised tomogram thorax abnormal, Echocardiogram abnormal, Fibrin D dimer increased, Full blood count, Inflammatory marker increased, Left ventricular dysfunction, Lung consolidation, Myocardial necrosis marker normal, Pericardial effusion, Pleural effusion, Respiratory rate increased, Sinus tachycardia, Spinal X-ray, Ultrasound Doppler, White blood cell count normal
SMQs:, Cardiac failure (broad), Haemorrhage laboratory terms (broad), Systemic lupus erythematosus (broad), Supraventricular tachyarrhythmias (narrow), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Dehydration (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Losartan 25mg daily
Current Illness: none
Preexisting Conditions: Anxiety, ADHD, Bipolar, dilated aortic root, bicuspid aortic valve
Allergies: None
Diagnostic Lab Data: CBC, CTA chest x 2, Echo, Venous Ultrasound bilateral lower extremities, Spinal Xray, D-Dimer
CDC Split Type:

Write-up: He was admitted on 11/5/2021, until 11/7/2021. He had presented to the emergency department after his mother reported to us about the onset of increased breathing, followed by development of left-sided chest pain, and decreased energy several days after his Covid vaccine booster. He was afebrile, denied any cough, presyncope, syncope, complications. The symptoms of chest pain lasted for several days, and the rate of breathing continue to increase. During evaluation emergency department, he was found to have an elevated D-dimer, with a normal white blood cell count, and sinus tachycardia. He had a chest CT that was initially nondiagnostic, and subsequently repeated after being admitted. During the evaluation, he was found to have a left lower lobe consolidation/atelectasis concerning for effusion. Cardiac enzymes were negative, including a BNP that was normal. Chest CT repeat again demonstrated pleural effusion, with atelectasis, but no pulmonary embolus. Inflammatory markers were obtained, that were elevated. In addition echocardiogram was obtained, that demonstrated trivial pericardial effusion, with mildly decreased LV systolic function (baseline LVEF was 55% from 3/2021, decreased to approximately 51%) and no change of his bicuspid aortic valve function. He was started on NSAIDs and burst steroids. He was given a single dose of IV Lasix. With initiation of NSAIDs, he started to have less chest pain, and subsequent improved further before leaving the hospital.


VAERS ID: 2192252 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-12-03
Onset: 2022-01-02
   Days after vaccination: 30
Submitted: 0000-00-00
Entered: 2022-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 3 AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 AR / IM

Administered by: Military       Purchased by: ?
Symptoms: COVID-19, Cough, Fatigue, Respiratory symptom, Rhinorrhoea, SARS-CoV-2 test positive, Sneezing
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer and Flu shot, arm soreness.
Other Medications: Keppra
Current Illness: None
Preexisting Conditions: Epilepsy
Allergies: None
Diagnostic Lab Data: Positive COVID-19 PCR test.
CDC Split Type: vsafe

Write-up: I first got symptoms of tiredness, runny nose, sneezing, and cough. The cough was persistent and a dry cough but not very deep, more like an irritated upper respiratory issue. I received a positive COVID-19 test at a testing facility. The coughing lasted for 2-3 weeks.


VAERS ID: 2694050 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-09-30
Onset: 2023-09-30
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 204F23-2A / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8137DA / 1 RA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS 75BS5 / 1 LA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR U7869AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blister, Malaise, Swelling face
SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: METOPROLOL; LIPITOR; SYNTHROID
Current Illness: NOT KNOWN ILLNESS
Preexisting Conditions: HYPERTENSION
Allergies: NKDA
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: PATIENT HAD BLISTERS ON FACE; SWOLLEN FACE; SHE STARTED FELLING ILL IN THE SAME EVENING SHE GOT THE VACCINES;


VAERS ID: 2203983 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-19
Onset: 2022-01-03
   Days after vaccination: 45
Submitted: 0000-00-00
Entered: 2022-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 32030BD / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Fear, Illness, Influenza like illness, Injection site swelling, Mobility decreased, Nausea, Pain, Pyrexia, SARS-CoV-2 test positive
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: estridiol
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Covid-19 Nasal/Nasopharynx: Positive for 2019-nCoV. Speciman taken January 3, 2022 Test taken at Facility by Dr. T
CDC Split Type:

Write-up: Severe swelling on upper left arm at injection point that lasted 5 days. Severe Flu-like symptoms (fever, aches, nausea)for nearly 6 days. On January 3, 2022 I tested positive for Covid-19. I was severely sick for 10 days. I was given steroids and antibiotics. I was bedridden for 9 days but did not go to the hospital because I was scared.


VAERS ID: 2692331 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-10-06
Onset: 2023-10-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG2282 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8137DA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Aspirin, Clopidogrel
Current Illness: None
Preexisting Conditions: Dermatological disorders
Allergies: No known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient recieved COVID-19 and Flu shots on 10/06/2023. According to immunizer pharmacy technician, after vaccinated patient did not bleed. After a few minutes, patient presented to pharmacy counter with excessive bleeding from right arm. Patient stated that she is taking Aspirin and Clopidogrel. Patient was taken inside the immunitazion room once again and pressure was applied to the injection site until patient stopped bleeding.


VAERS ID: 1861412 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-11-10
Onset: 2021-11-11
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Exposure during pregnancy, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: 14 weeks pregnant. Hx of morning sickness
Preexisting Conditions: Na
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnant 14 weeks due May 8th2022 Experiencing intense and unrelenting vomiting


VAERS ID: 2691399 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-10-04
Onset: 2023-10-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG2282 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS H4297 / 1 LA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH GY1934 / 1 RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS TF9F4 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Laboratory test, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: Asthma, fibromyalgia, neuralgia
Preexisting Conditions: Asthma, fibromyalgia, neuralgia
Allergies: None
Diagnostic Lab Data: Currently 5/10/2023, the patient is in the hospital where he is undergoing testing.
CDC Split Type:

Write-up: After administering the 4 vaccines, the patient fainted. She was always breathing, EMS was called and they took her to the hospital.


VAERS ID: 2216076 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-10-08
Onset: 2021-10-20
   Days after vaccination: 12
Submitted: 0000-00-00
Entered: 2022-04-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30145BA / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS FPSXD / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Cerumen removal, Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Mirtazapine
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Had ear wax removal with no improvement at clinic express at the beginning of March 2022. Subsequently, I has another appt. with Physician who examined and ordered auditory examination. I am still waiting for that to be scheduled
CDC Split Type:

Write-up: Started hearing ringing in ears that would come and go from October through December. Since the beginning of the year the ringing (Tinnitus) has been a constant high pitch ring


VAERS ID: 1940725 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-12-09
Onset: 2021-12-10
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7411NA / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Heart rate increased
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Vestibular disorders (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Crestor 20mg, Iron supplement, Vitamin D supplement
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Measured on personal health monitoring device.
CDC Split Type:

Write-up: Elevated heart rate. Resting heart rate normally 72. First identified elevated heart rate at noon the day after injection. Recorded at 105. At 9 pm measured at 86 bpm. Standing heart rate rose to 115 bpm at 9 pm. Lightheaded when standing. No other symptoms noted.


VAERS ID: 2311667 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-04-25
Onset: 2022-06-01
   Days after vaccination: 37
Submitted: 0000-00-00
Entered: 2022-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ4959 / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Chills, Cough, Dyspnoea, Headache, Pain, Paranasal sinus discomfort, Pyrexia, Rhinorrhoea, SARS-CoV-2 test positive, Upper-airway cough syndrome
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamins
Current Illness: None
Preexisting Conditions: Stage 3 Kidney Disease, Brest Cancer Survivor
Allergies: Omnicef, Sudafed, Codeine
Diagnostic Lab Data: COVID-19 test - positive
CDC Split Type: vsafe

Write-up: I started getting symptoms of postnasal drip, runny nose, sinus pressure, headache. Then I stared getting chills, body aches, and fever. I took 2 at home COVID-19 test and it was positive. I then went to an urgent care walk in clinic and brought in my results. I was prescribed Molnupiravir, albuterol, and cough medication. Those medications did not help right away. The coughing is the worse and was hard to breath. I finished the antiviral drug and now I do feel somewhat normal.


VAERS ID: 2608499 (history)  
Form: Version 2.0  
Age: 78.0  
Sex: Male  
Location: Florida  
Vaccinated: 2022-09-30
Onset: 2022-10-01
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH G1194 / 5 LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR N/A / 1 - / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test abnormal, Diarrhoea, Lymphocyte count decreased, Mobility decreased, Muscular weakness, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Haematopoietic leukopenia (narrow), Peripheral neuropathy (broad), Systemic lupus erythematosus (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Acetaminophen; Alendronate; erythromycin; Destovy; Ezetimibe; Mirabegron; Prezista; Ritonavir; Pravastatin; Bactrim; Tivicay ; Valganciclovir; Vitamin B12; Vitamin D; Zen pep
Current Illness: N/A
Preexisting Conditions: HIV 1985; AIDS 2019; Stenosis of lower spine; Arthritic Hip
Allergies: Penicillin; Pollen; Trees
Diagnostic Lab Data: 10/03/2023 Blood Panel T Cells decreased
CDC Split Type: vsafe

Write-up: I had my vaccination on 09/30/2022. On 10/01/2022 I woke up from a nap and I could not move both legs as they were too weak. On 10/02/2022 that evening I vomited with an episode of diarrhea. I was having blood work done every 2 weeks. On 10/03/2023 my blood panel showed that my T Cells had decreased. Nothing was provided in regard to HIV medications. I was provided compassion care for when HIV medication does not work and this course of treatment worked. It is 2 injections administered twice a year. The results were favorable and increased my T Cells.


VAERS ID: 1798733 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Florida  
Vaccinated: 2021-10-01
Onset: 2021-10-15
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2021-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthma, Chest X-ray, Chest discomfort, Chest pain, Computerised tomogram abdomen, Computerised tomogram head, Computerised tomogram thorax, Condition aggravated, Dyspnoea, Echocardiogram, Headache
SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: ASTHMA, ANEMIA, OBESITY
Allergies: NONE
Diagnostic Lab Data: CT SCAN OF HEAD, CHEST, AND STOMACH 10/18/2021 XRAY OF CHEST 10/18/2021 ECHOCARDIOGRAM 10/18/2021 BREATHING TREATMENTS 10/16/2021 OXYGEN FROM 10/17/2021-10/19/2021
CDC Split Type:

Write-up: CHEST PAIN, CONSTANT HEADACHE, TROUBLE BREATHING, CHEST TIGHTNESS, ASTHMA WORSENED.


VAERS ID: 2684494 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Male  
Location: Florida  
Vaccinated: 2023-09-19
Onset: 2023-09-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 AR / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 AR / IM
RSV: RSV (ABRYSVO) / PFIZER/WYETH - / 1 AR / IM

Administered by: Private       Purchased by: ?
Symptoms: Gait inability, Muscular weakness
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: bilateral lower extremity weakness - unable to ambulate


VAERS ID: 2685832 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-09-17
Onset: 2023-09-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-09-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 7+ LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Chills, Computerised tomogram, Echocardiogram, Head injury, Hypotension, Loss of consciousness, Pyrexia, Suture insertion, X-ray
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: SERTRALINE TAB 50 mg, Baby Asprin
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: CatScan, X-Rays, Echocardiogram
CDC Split Type:

Write-up: Wife had fever and chills started 6 hours after vaccination. Temp of 99 degrees. Following morning she passed out in shower. Taken to Urgent Care - she had low blood pressure of 85/55. Needed 2 staples on head. Taken to ER. Low BP continued. She was admitted and spent the night. BP initially very low but started to improve. Discharges at 4pm.. Got flu & COVIS shot at same time


VAERS ID: 2688538 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-09-28
Onset: 2023-09-28
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-09-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 204F232A / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8132AA / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Amnesia, Aphasia, Mobility decreased, Pyrexia, Tremor, Urinary tract infection
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: BUTRANS 20MCH/HR PERCOCET 7.5/325 XARELTO 10 MG TRELEGY ELLIPTA KETOCONAZOLE SHAMPOO DULOXETINE 60 MG CAPSULE MONTELUKAST 10 MG TAB FENOFIBRATE 145MG TAB AMLODIPINE 10MG LISINOPRIL 40 MG LEVOTHYROXINE 150 MG TAB HYDROCHLOROTHIAZIDE 12.5
Current Illness: PT HAD UTI AT TIME OF HOSPITALIZATION
Preexisting Conditions: THYROID CHOLESTEROL CHRONIC PAIN COPD HYPERTENSION VENOUS THROMBUS EMBOLISM HX
Allergies: NO ALLERGIES LISTED
Diagnostic Lab Data: PT WAS DIAGNOISED WITH UTI AND HIGH FEVER
CDC Split Type:

Write-up: VACCINES WERE GIVE AROUND 09:38 AM ON 09/28/23. PT DID NOT EXPIERENCE EVENTS UNTIL AROUND 5:00 PM ON 09/28/23. PT HUSBAND EXPLAINED PT HAD SHAKING AND COULD NOT MOVE BODY OR TALK. AMBULANCE WAS CALLED AND PT WAS ADMITTED. SHE ALSO WAS DIAGNOISED WITH A UTI AT TIME OF EMERGENY ROOM VISIT .ALSO HAD HIGH FEVER WHEN ADMITTED TO HOSPITAL. PT WAS DISCHARGED AROUND 10:00PM 09/28/2023. EVENTS REPORTED BY HUSBAND PT EXPLAINED COULD NOT REMEMBER WHAT HAPPENED, PT ALSO EXPLAINED HX OF CHRONIC UTI''S.


VAERS ID: 2241217 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Florida  
Vaccinated: 2022-04-19
Onset: 2022-04-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-04-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1855835 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7378NA / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Loss of consciousness, Seizure, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prozac 20mg, prozac 10 mg, olanzapine 2.5mg, hydroxyzine 10 mg
Current Illness: NONE
Preexisting Conditions: Anxiety
Allergies: NONE
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient fainted, lost consciousness and seized for 10 secs. Then regained full consciousness with the help of alcohol. BP check was normal, no suspected pregnancy, possible result of anxiety/panic


VAERS ID: 2689431 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Florida  
Vaccinated: 2023-10-01
Onset: 2023-10-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA ? / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. ? / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Flank pain, Musculoskeletal chest pain, Pain in extremity, Pain in jaw, Skin warm, Sleep disorder, Trismus, Vertigo
SMQs:, Retroperitoneal fibrosis (broad), Dystonia (narrow), Vestibular disorders (narrow), Osteonecrosis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: hydroxyzine, clonazepam, zolpidem, citalopram,carbpcusteome, mirabegron, vitamin C, Red Yeast Rice, Vit D, celebrik.
Current Illness: LPR
Preexisting Conditions: LPR
Allergies: keflex sulfa
Diagnostic Lab Data: None as of yet. If I do not have relief by tomorrow will see my primary care doctor or ER.
CDC Split Type:

Write-up: Around 7pm left arm was sore and warm. At 3 AM woke up in excruciating pain on left side that was under ribs. Lowered the bed flat. Tried to get comfortable, couldn''t. Had a hydrocodone tablet left over from a prescription given in March. Took one. No relief. Got up at 5:20 tried to eat my cereal and jaw hurt too much to chew and room started spinning. My husband had too almost carry me back to bed because I was in so much pain on left side. Took an Excedrin migraine, no relief, got up at 10AM in pain. Husband gave me one of his tramadol. Pain eased somewhat. Took a Tylenol at 2pm. Pain on left side only, lower ribs, inside body cavity to around the side to back.


VAERS ID: 2216090 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Male  
Location: Florida  
Vaccinated: 2021-09-30
Onset: 2022-01-30
   Days after vaccination: 122
Submitted: 0000-00-00
Entered: 2022-04-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301458A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ716AC / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Biopsy skin, Rash, Rash erythematous, Rash pruritic
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CARTIA XT; ELIQUIS; ROPINIROLE HCL; OMEPRAZOLE; MIRTAZAPINE; SYNTHROID (LEVOTHYROXINE);VITAMINS;Shaklee Optiflora Probiotic; Bifidubacterium Longum;Lactobacillus Acidophilus ;Shaklee Nutriferon Tablets; Interferon Boosting Plant Extracts;
Current Illness:
Preexisting Conditions: Afib; Restless Legs; Depression; Acid Reflux-Barrets Esophagus.
Allergies: Bactrim.
Diagnostic Lab Data: Biopsy of Rash.
CDC Split Type:

Write-up: On about 3/30/22, Itchy rash, red bumps, on body, back, chest, arms, legs. Went to Dermatologist and got Rx on 2/5/22 for Methylprednisolone, 4 mg dspk, qty 21,d ays 6: Day 1: 6 , Day 2: 5, Day 3: 4. Day 4: 3, Day 5: 2. Day 6: 1. TRIAMCINOLONE 0.1% CREAM 2X A DAY. Rash went away after a day. Rash reappeared on 3/10/22 and got Rx: PREDNISONE 10 MG TAB 4/day for 4 days, 3/day for 4 days, 2/day for 4 days, 1/day for 4 days, ? a day for 4 days (Rash) 3/10-3/29/22.


VAERS ID: 1928220 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-11-16
Onset: 2021-11-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 1F10014A / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Herpes zoster
SMQs:, Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1911119 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-11
Onset: 2021-11-01
Submitted: 0000-00-00
Entered: 2021-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Platelet count decreased, Pulmonary embolism, Pulmonary sepsis, Pyrexia, Respiratory rate, Respiratory rate increased, SARS-CoV-2 test
SMQs:, Haematopoietic thrombocytopenia (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Embolic and thrombotic events, venous (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (narrow), Sepsis (narrow), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1891732 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-11-12
Onset: 2021-11-13
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / UNK - / SYR
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Fatigue, Lethargy, Medication error, Pain, Rash, Sensitive skin
SMQs:, Anaphylactic reaction (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypersensitivity (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1883389 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-10-30
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5475 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Pruritus, Rash pruritic, SARS-CoV-2 test
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: COVID-19 VACCINE ASTRAZENECA; FEXOFENADINE; FLUAD
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1883287 (history)  
Form: Version 2.0  
Age: 56.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-06
Onset: 2021-11-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Dyspnoea, Palpitations, Vaccination site erythema, Vaccination site swelling
SMQs:, Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1883095 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-03-17
Onset: 2021-11-05
   Days after vaccination: 233
Submitted: 0000-00-00
Entered: 2021-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH SCWF7 / UNK - / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW2239 / UNK - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET183 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Acute kidney injury, Blood creatinine, Blood culture positive, Escherichia sepsis, Fibrin D dimer, Multiple organ dysfunction syndrome, Platelet count, Pyrexia, Thrombocytopenia
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Haematopoietic thrombocytopenia (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow), Dehydration (broad), Sepsis (narrow), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-11-10
   Days after onset: 5
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: AMLODIPINO; ESOMEPRAZOLE; LORMETAZEPAM NORMON; FUROSEMIDA; ADIRO; EUTIROX; BOI-K COMPRIMIDOS
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1878251 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2021-10-16
Onset: 2021-10-01
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood electrolytes, Blood urea, Brain natriuretic peptide, Chest X-ray, Dyspnoea, Liver function test, Oedema, Oxygen saturation, Pain in extremity, Platelet count, SARS-CoV-2 test, Swelling face, Thrombocytopenia, Troponin, Urine analysis
SMQs:, Cardiac failure (broad), Anaphylactic reaction (narrow), Angioedema (narrow), Haematopoietic thrombocytopenia (narrow), Systemic lupus erythematosus (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1872607 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-10-01
Onset: 2021-10-25
   Days after vaccination: 24
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Confusional state, Severe acute respiratory syndrome, Speech disorder
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: BLOPRESID; BISOPROLOL FUMARATE; CARDIOASPIRIN
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1851570 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-05-03
Onset: 2021-05-01
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Superficial vein thrombosis, Varicose vein
SMQs:, Embolic and thrombotic events, venous (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUSEQIRUS202104489

Write-up: Painful varicose pain; Thrombophlebitis superficial / deep vein thrombosis; This spontaneous case from a country was retrieved on 26-Oct-2021 from a regulatory authority (TGA, reference number: AU-TGA-0000579072), reported by other non-healthcare professional (consumer) and concerned a 57-year-old, female patient. The patient''s medical history and concomitant medications were not reported. The patient had no allergies. On 03-May-2021, at 12:00 am, the patient was vaccinated with Afluria Quad (influenza vaccine; route of administration: intramuscular, dose and anatomical location: not reported) for unknown indication. The batch number was not reported. On the same day, at 12:00 am, the patient was vaccinated with non-company co-suspect COVID-19 Vaccine AstraZeneca (COVID-19 vaccine NRVV Ad (ChAdOx1 nCoV-19); dose, route of administration and anatomical location: not reported) for unknown indication. The batch number was not reported. On an unspecified date in Mar-2021, about 14 days after receiving Afluria Quad and suspect COVID-19 Vaccine AstraZeneca, the patient experienced first time painful varicose pain. The patient also experienced superficial thrombophlebitis and deep vein thrombosis (DVT). At the time of initial reporting, the patient had not recovered from the event of varicose vein and the outcome for the event of ''superficial vein thrombosis'' was unknown. The reporter did not provide a causality assessment. The Regulatory Authority assessed the event as possibly related to Afluria Quad. The events of varicose vein and ''superficial vein thrombosis'' were considered to be medically significant by a Physician within a regulatory authority. Company comment: A 57-year-old, female patient was vaccinated with the suspect product Afluria Quad and non-company co-suspect COVID-19 Vaccine AstraZeneca. The patient developed thrombophlebitis and deep vein thrombosis 14 days after vaccination. Information regarding the underlying medical history, related diagnostic findings and concomitant medications has not been provided. Causality is significantly confounded by concurrent administration of co-suspect vaccine. Causality is assessed as not related based on presented confounder and biological implausibility.; Sender''s Comments: A 57-year-old, female patient was vaccinated with the suspect product Afluria Quad and non-company co-suspect COVID-19 Vaccine AstraZeneca. The patient developed thrombophlebitis and deep vein thrombosis 14 days after vaccination. Information regarding the underlying medical history, related diagnostic findings and concomitant medications has not been provided. Causality is significantly confounded by concurrent administration of co-suspect vaccine. Causality is assessed as not related based on presented confounder and biological implausibility.


VAERS ID: 1849741 (history)  
Form: Version 2.0  
Age: 18.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-03-31
Onset: 2021-05-11
   Days after vaccination: 41
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Anti-platelet factor 4 antibody test, C-reactive protein, Electrocardiogram, Fibrin D dimer, Platelet count, Pulmonary embolism, Thrombosis with thrombocytopenia syndrome, Troponin I
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Immune-mediated/autoimmune disorders (narrow), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Anaemia
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202105; Test Name: Anti Pf4 antibodies - Acustar; Result Unstructured Data: Negative; Test Date: 202105; Test Name: Anti PF4 antibodies (ELISA); Result Unstructured Data: Positive; Test Date: 202105; Test Name: CRP; Result Unstructured Data: 147; Test Date: 202105; Test Name: ECG; Result Unstructured Data: Sinus tachycardia no evidence of right heart strain; Test Date: 202105; Test Name: D dimer; Result Unstructured Data: 59.9; Test Date: 202105; Test Name: Platelets; Result Unstructured Data: 42; Comments: less then; Test Date: 202105; Test Name: TnI; Result Unstructured Data: 1
CDC Split Type: AUSEQIRUS202104402

Write-up: Thrombosis with thrombocytopenia syndrome (TTS)/Pulmonary embolism; Thrombosis with thrombocytopenia syndrome (TTS)/Pulmonary embolism; This spontaneous case was retrieved on 26-Oct-2021 from regulatory authority (reference number: AU-TGA-0000554179), reported by other health professional and concerned an 18-year-old, female patient. The patient''s concurrent condition included anaemia. The patient''s concomitant medications were not reported. On 31-Mar-2021, the patient was vaccinated with non-company, co-suspect COVID-19 vaccine AstraZeneca (ChAdOx1 nCoV-19; dose reported as one, indication, route of administration, anatomical location: not reported). The batch number was not reported. On 06-May-2021, the patient was vaccinated with Afluria Quad (influenza vaccine; dose, route of administration and anatomical location: not reported) as a flu vaccination. The batch number was not reported. As reported, the patient was not ill prior vaccination. On 11-May-2021, five days after receiving Afluria Quad and 41 days after receiving co-suspect COVID-19 vaccine AstraZeneca, the patient developed right sided rib and chest pain managed by general practitioner (GP) for shortness of breath and pneumonia. Also, the patient reported pain in her calves and back. On 13-May-2021, unspecified laboratory test was positive. On 14-May-2021, thrombosis including pulmonary embolism and deep vein thrombosis was suspected and was admitted at Redcliffe hospital. On the same day, the patient was diagnosed with pulmonary embolism and thrombocytopenia and started corrective treatment with intravenous (IV) immunoglobulin and steroids. It was reported that the patient developed thrombosis with thrombocytopenia possibly vaccine induced heparin-induced thrombocytopenia (HIT) (as reported), however results of antibody absorption (ABS) test was pending. Also, heparin platelet factor 4 (PF4) enzyme-linked immunosorbent assay was pending. On 17-May-2021, unspecified laboratory analysis revealed unspecified results in micrograms. On the same day, the patient was clinically stable, and she was discharged from hospital on blood thinners and with a referral to Haematology. On an unspecified date in May-2021, laboratory analysis revealed platelet count (plt) at 42, D-dimer at 59.9, C-reactive protein (CRP) at 147 and troponin I (TnI) at 1 (units and reference ranges were not reported). Also, electrocardiogram (ECG) revealed sinus tachycardia with no evidence of right heart strain. Additionally, the patient was positive for anti PF4 antibodies performed via regulatory authority and negative for anti Pf4 antibodies performed via regulatory authority. On 19-May-2021, in accordance with laboratory analysis and symptoms thrombosis with thrombocytopenia syndrome (TTS) was confirmed. The outcome of the events was unknown. The reporter assessed the events to be related to Afluria Quad. As reported, the patient was not ill prior vaccination and thrombosis with thrombocytopenia was possibly vaccine induced HIT. The Regulatory Authority assessed the event as possibly related to Afluria Quad. The events of thrombosis with thrombocytopenia syndrome and pulmonary embolism were assessed as serious due to seriousness criteria of hospitalization and medical significance. Company comment: A 18-year-old female patient developed thrombosis with thrombocytopenia syndrome (TTS) with associated pulmonary embolism five days after vaccination with the suspect product Afluria Quad. Non-company co-suspect AstraZeneca COVID-19 vaccine was administered 41 days prior to events onset which is within the risk window for TTS described in literature. As reported TTS was confirmed in accordance with laboratory analysis and symptoms. Causality is significantly confounded by administration of co-suspect COVID-19 vaccine. Based on provided information, causality is assessed as not related due to presented confounder.; Reporter''s Comments: As reported, the patient was not ill prior vaccination and thrombosis with thrombocytopenia was possibly vaccine induced HIT.; Sender''s Comments: A 18-year-old female patient developed thrombosis with thrombocytopenia syndrome (TTS) with associated pulmonary embolism five days after vaccination with the suspect product Afluria Quad. Non-company co-suspect AstraZeneca COVID-19 vaccine was administered 41 days prior to events onset which is within the risk window for TTS described in literature. As reported TTS was confirmed in accordance with laboratory analysis and symptoms. Causality is significantly confounded by administration of co-suspect COVID-19 vaccine. Based on provided information, causality is assessed as not related due to presented confounder.


VAERS ID: 1836072 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-09-29
Onset: 2021-09-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Arthralgia, Limb discomfort, Pain in extremity, Paraesthesia, Product administered at inappropriate site, Toothache
SMQs:, Peripheral neuropathy (broad), Drug abuse and dependence (broad), Guillain-Barre syndrome (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1796281 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2019-10-11
Onset: 2019-10-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER UNK / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Body temperature, Body temperature decreased, Dehydration, Erythema, Fatigue, Feeling cold, Memory impairment, Nausea, Off label use, Poor venous access, Transfusion
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Depression (excl suicide and self injury) (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: VITAMIN B12
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1780362 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-10-05
Onset: 2021-10-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3712 / UNK - / SYR
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS FG3712 / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Bowel movement irregularity, Headache, Muscle fatigue, Pain, Poor quality sleep
SMQs:, Rhabdomyolysis/myopathy (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Depression (excl suicide and self injury) (broad), Noninfectious diarrhoea (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PARACETAMOL; PROGESTERONE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1774970 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-10-07
Onset: 2021-10-08
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2590 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Axillary pain, Extra dose administered, Injection site pain, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: -citalopram 30mg qd -multivitamin qd
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: **very sore left armpit, tender to the touch, can''t palpate it to feel if swollen lymph node. Still very sore on day 3, whereas all other symptoms have subsided (searched online and this was listed for moderna, but I got pfizer so I wanted to report it) -this was dose 3 of Pfizer. I had NO side effects or reaction after dose 1 and dose 2 -I also had a flu shot at the same time as dose 3 -typical sore arm at injection site for one day -did experience fever but that lasted just for a few hours the next day -large muscle groups (back, legs) felt sore/achy/heavy the next day (few hours) -joint pain in *right* elbow and fingers (probably unrelated?)


VAERS ID: 1424541 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-04-27
Onset: 2021-04-30
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-06-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK - / -
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER UNK / UNK - / SYR
MMR: MEASLES + MUMPS + RUBELLA (NO BRAND NAME) / UNKNOWN MANUFACTURER UNK / UNK - / SYR
VARCEL: VARICELLA (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Deep vein thrombosis, Joint swelling, Limb discomfort, Lymphadenopathy, Malaise, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: DESOGESTREL
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2756383 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2024-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Body temperature abnormal, Bone pain, Fall, Malaise
SMQs:, Accidents and injuries (narrow), Osteonecrosis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: BISOPROLOL; FUROSEMIDE; METFORMIN; RIVAROXABAN; ROSUVASTATIN; TELMISARTAN; TENOFOVIR
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CASA2024SA086754

Write-up: bone pain; body temperature abnormal; malaise; fall; Initial information received on 14-Mar-2024 regarding an unsolicited valid serious case received from Pharmacist via Health Authorities under reference 001069982. This case involves an unknown age male patient who experienced bone pain, fall, body temperature abnormal and malaise after receiving Spikevax and Influenza Quadrival A-B High Dose Hv Vaccine [Fluzone High-Dose Quadrivalent]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. It is unknown if the patient had any medical history, concomitant disease or risk factor. Concomitant medications included Bisoprolol ; Furosemide ; Metformin; Rivaroxaban ; Rosuvastatin ; Telmisartan ; and Tenofovir . On an unknown date, the patient received a unknown dose of suspect Influenza Quadrival A-B High Dose Hv Vaccine suspension (lot number, strength, expiry date not reported via intramuscular route in unknown administration site for Influenza Immunization and also received a unknown dose of suspect Spikevax not produced by Sanofi Pasteur(formulation, strength, expiry date, lot number not reported) via intramuscular route in unknown administration site for COVID-19 immunization. There will be no information available on batch number for this case. On an unknown date the patient developed bone pain , fall , body temperature abnormal and malaise (unknown latency) following the administration of Influenza Quadrival A-B High Dose Hv Vaccine and Spikevax. It is unknown if there were lab data/results available. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events (body temperature abnormal, bone pain, fall, malaise). At time of reporting, the outcome was Recovered / Resolved on an unknown date for all the events. Seriousness Criteria : Hospitalized for all the events.; Sender''s Comments: Sanofi Company Comment dated 19-Mar-2024 : This case involves an unknown age male patient who experienced bone pain, fall, body temperature abnormal and malaise after receiving Spikevax and Influenza Quadrival A-B High Dose Hv Vaccine [Fluzone High-Dose Quadrivalent].Further information regarding Past medical history, concurrent condition, allergic history, laboratory investigations excluding alternative etiologies for the reported events are needed to fully assess this case. Based upon the reported information, the role of a vaccine cannot be assessed.


VAERS ID: 2702245 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2023-10-24
Onset: 2023-10-25
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 7+ RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Deafness unilateral, Ear discomfort, Tinnitus
SMQs:, Hearing impairment (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: BP Telemisartin, cholesterol meds,
Current Illness: None
Preexisting Conditions: None
Allergies: penicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Tinitis and loss of hearing in right ear. Feels plugged but won?t clear. Started less than 24 hrs of Vax. Is this permanent??


VAERS ID: 2622977 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-11-08
Onset: 2022-11-01
Submitted: 0000-00-00
Entered: 2023-04-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cardiac stress test, Chest X-ray, Echocardiogram, Electrocardiogram, Myocarditis, Pericarditis, Troponin, Troponin increased
SMQs:, Systemic lupus erythematosus (broad), Myocardial infarction (narrow), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: None
Allergies:
Diagnostic Lab Data: Test Name: Stress testing; Result Unstructured Data: No evidence of inducible regional motion abnormality either at rest or at peak exercise; Test Name: CXR; Result Unstructured Data: NAD; Test Name: Echocardiogram; Result Unstructured Data: NAD (normal); Test Date: 202211; Test Name: Echocardiogram; Result Unstructured Data: Confirmed diagnosis of pericarditis; Test Name: Resting echocardiogram; Result Unstructured Data: No evidence of inducible regional motion abnormality either at rest or at peak; Test Name: ECG; Result Unstructured Data: NAD; Test Name: Troponin; Result Unstructured Data: Mild to moderately elevated at around 150 mmol/L; Test Date: 202211; Test Name: Troponin; Result Unstructured Data: Leak, confirmed diagnosis of pericarditis
CDC Split Type: AUSEQIRUS202302577

Write-up: Myocarditis (level 3)/Pfizer induced myocarditis; Troponin leak/elevated troponin at around 150 mmol/L; Symptoms of pericarditis; This spontaneous case from Regulatory Authority was retrieved on 24-Apr-2022 from Regulatory Authority, reported by other healthcare professional and concerned a 27-year-old, female patient. The patient''s medical history and concomitant medications were not reported. The patient the no previous vaccine reactions. On 08-Nov-2022, the patient was vaccinated with Afluria Quad (influenza vaccine inact sag 4v; dose, route of administration, anatomical location, and indication: not reported). The batch number was not reported. On the same day, the patient was vaccinated with non-company co-suspect Pfizer BioNTech COVID-19 vaccine (tozinameran; dose, route of administration, anatomical location, and indication: not reported). The batch number was not reported. On an unspecified date in Nov-2022, within 24 hours after receiving Afluria Quad and non-company, co-suspect Pfizer BioNTech COVID-19 vaccine, the patient developed symptoms of pericarditis. The diagnosis was confirmed with admission to the hospital with troponin leak and echocardiogram. On an unspecified date, the patient had review by cardiologist in two weeks (as reported). The patient was on regular colchicine and ibuprofen. On an unspecified date, the patient was admitted to Hospital emergency department (ED) and echocardiogram, electrocardiogram (ECG) and chest x-ray (CXR) was performed, and all were with no abnormality detected. Results were reviewed by cardiology review who advised myocarditis (level three). On an unspecified date, the patient presented to the hospital with a mild to moderately elevated troponin at around 150 mmol/L. Echocardiogram at the time was normal. The patient was discharged on ibuprofen and colchicine. Resting echocardiogram and stress testing were performed with no evidence of inducible regional motion abnormality either at rest or at peak exercise. At the time of initial reporting, the patient was recovering from ''pericarditis'' and ''myocarditis''. As reported, the patient''s symptoms are slowly getting better. The outcome for event ''troponin increased'' was unknown. The reporter assessed the event of ''myocarditis'' not to be related to Afluria Quad. As reported, she referred with Pfizer induced myocarditis. The Regulatory Authority assessed the events as possibly related to the Afluria Quad vaccine. The events ''pericarditis'' and ''myocarditis'' were considered to be medically significant by a Physician within Regulatory Authority. Company comment: A 27-year-old female patient developed symptoms of pericarditis within 24 hours after vaccination with Afluria Quad and non-company, co-suspect Pfizer BioNTech COVID-19 vaccine. Reportedly, the patient was admitted to hospital where electrocardiogram and chest X-ray were performed, however there were no abnormalities detected. The results from cardiology review, ''in two weeks'' as reported, advised myocarditis. The patient also had troponin increased. Information regarding the underlying medical history and concomitant medications has not been provided. Despite confounding with the co-suspect vaccine, causality is assessed as possibly related for all three events (pericarditis, myocarditis and troponin increased) based on plausible temporal relationship.; Sender''s Comments: A 27-year-old female patient developed symptoms of pericarditis within 24 hours after vaccination with Afluria Quad and non-company, co-suspect Pfizer BioNTech COVID-19 vaccine. Reportedly, the patient was admitted to hospital where electrocardiogram and chest X-ray were performed, however there were no abnormalities detected. The results from cardiology review, ''in two weeks'' as reported, advised myocarditis. The patient also had troponin increased. Information regarding the underlying medical history and concomitant medications has not been provided. Despite confounding with the co-suspect vaccine, causality is assessed as possibly related for all three events (pericarditis, myocarditis and troponin increased) based on plausible temporal relationship.


VAERS ID: 2401467 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 2022-04-27
Submitted: 0000-00-00
Entered: 2022-08-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Loss of consciousness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUMODERNATX, INC.MOD20226

Write-up: Loss of consciousness; This regulatory authority case was reported by an other health care professional and describes the occurrence of LOSS OF CONSCIOUSNESS (Loss of consciousness) in a 64-year-old male patient who received mRNA-1273 (Spikevax) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (AFLURIA QUAD) for an unknown indication. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE INACT SPLIT 4V (AFLURIA QUAD) (unknown route) 1 dosage form. On 27-Apr-2022, the patient experienced LOSS OF CONSCIOUSNESS (Loss of consciousness) (seriousness criterion medically significant). At the time of the report, LOSS OF CONSCIOUSNESS (Loss of consciousness) had resolved. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. No treatment information was provided. The RA reference number was reported as AU-TGA-740034. Company comment: This regulatory case concerns a 64-year-old male patient, with no reported medical history, who experienced the unexpected serious (medically significant) event of Loss of consciousness after receiving the dose of mRNA-1273 vaccine. The vaccination date was not reported. Clinical course and treatment details were not reported. The outcome of event was reported as resolved. Patient received Influenza vaccine (date not reported) which was reported as a co-suspect drug, could be considered as a confounder. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender''s Comments: This regulatory case concerns a 64-year-old male patient, with no reported medical history, who experienced the unexpected serious (medically significant) event of Loss of consciousness after receiving the dose of mRNA-1273 vaccine. The vaccination date was not reported. Clinical course and treatment details were not reported. The outcome of event was reported as resolved. Patient received Influenza vaccine (date not reported) which was reported as a co-suspect drug, could be considered as a confounder. The benefit-risk relationship of mRNA-1273 is not affected by this report.


VAERS ID: 2386079 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-12-06
Onset: 2022-05-23
   Days after vaccination: 168
Submitted: 0000-00-00
Entered: 2022-07-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 017G21A / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA632BA / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Aortic aneurysm rupture, Cognitive disorder, Malaise, Pyrexia, Sepsis
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Sepsis (narrow), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2626058 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Generalised tonic-clonic seizure
SMQs:, Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAMODERNATX, INC.MOD20237

Write-up: Generalised tonic-clonic seizure; This regulatory authority case was reported by a pharmacist and describes the occurrence of GENERALISED TONIC-CLONIC SEIZURE (Generalised tonic-clonic seizure) in a 52-year-old female patient who received mRNA-1273 BIVALENT .222 (SPIKEVAX BIVALENT (ORIGINAL / OMICRON BA.4/5)) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLULAVAL TETRA) for Antiviral prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 BIVALENT .222 (SPIKEVAX BIVALENT (ORIGINAL / OMICRON BA.4/5)) (Intramuscular) .5 milliliter and dose of INFLUENZA VACCINE INACT SPLIT 4V (FLULAVAL TETRA) (Intramuscular) .5 milliliter. On an unknown date, the patient experienced GENERALISED TONIC-CLONIC SEIZURE (Generalised tonic-clonic seizure) (seriousness criteria hospitalization and medically significant). At the time of the report, GENERALISED TONIC-CLONIC SEIZURE (Generalised tonic-clonic seizure) outcome was unknown. For mRNA-1273 BIVALENT .222 (SPIKEVAX BIVALENT (ORIGINAL / OMICRON BA.4/5)) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not reported. Company comment. This regulatory authority case concerns a 52 ? year ? old female patient, with no medical history reported, who received a dose of mRNA ? 1273.222 (Original/Omicron BA.4/5) vaccine and experienced the unexpected, serious (medically significant and hospitalization) AESI generalised tonic-clonic seizure. Latency cannot be properly assessed since exact onset date and vaccination date were not provided. No further clinical details were provided for medical reviewing. Co ? suspect product included Influenza vaccine (Flulaval tetra) which remains as confounder. The benefit-risk relationship of mRNA ? 1273.222 (Original/Omicron BA.4/5) vaccine is not affected by this report.


VAERS ID: 2372229 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-07-08
Onset: 2022-07-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-07-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Product use issue, Seizure, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Medication errors (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202200957668

Write-up: Seizure; Syncope; BNT162B2 and influenza vaccine on 08/Jul/2022; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: 744066 (RA). A 17-year-old female patient received BNT162b2 (COMIRNATY), on 08Jul2022 as dose 1, single (Batch/Lot number: unknown) at the age of 17 years for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX TETRA), on 08Jul2022 (Batch/Lot number: unknown). The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 08Jul2022, outcome "unknown", described as "BNT162B2 and influenza vaccine on 08/Jul/2022"; SEIZURE (medically significant) with onset 08Jul2022, outcome "unknown"; SYNCOPE (medically significant) with onset 08Jul2022, outcome "unknown". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2242465 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-12-04
Onset: 2021-12-04
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3005294 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS AFLBA607AA / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Activated partial thromboplastin time, Activated partial thromboplastin time prolonged, Anaemia, Computerised tomogram normal, Condition aggravated, Coombs direct test, Haematoma, Haemoglobin, Oedema peripheral
SMQs:, Cardiac failure (broad), Angioedema (broad), Haematopoietic erythropenia (broad), Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhage laboratory terms (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2630950 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2022-10-28
Onset: 2022-12-12
   Days after vaccination: 45
Submitted: 0000-00-00
Entered: 2023-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ2541 / 4 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Dyshidrotic eczema, Morphoea
SMQs:, Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SIMVASTATINA; METFORMIN; INDAPAMIDE RETARD
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2202589 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Agitation, Apnoea, Breath sounds abnormal, Cheyne-Stokes respiration, Erythema, Haematoma, Hypotension, Jugular vein distension, Lethargy, Moaning, Oedema peripheral, Pulmonary embolism, Stupor, Tachypnoea
SMQs:, Cardiac failure (broad), Anaphylactic reaction (narrow), Angioedema (broad), Asthma/bronchospasm (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Dementia (broad), Embolic and thrombotic events, venous (narrow), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CASA2022SA101718

Write-up: agitation; apnoea; breath sounds abnormal; Cheyne-Stokes respiration; erythema; haematoma; hypotension; jugular vein distension; moaning; oedema peripheral; pulmonary embolism; stupor; tachypnoea; Lethargy; Initial information received on 23-Mar-2022 regarding an unsolicited valid serious case received from Health Authorities under reference 000974506. This case involves an 85 year old female patient (175 cm and 43 kg) who experienced agitation, apnoea, breath sounds abnormal, cheyne-stokes respiration, erythema, haematoma, hypotension, jugular vein distension, moaning, oedema peripheral, pulmonary embolism, stupor, tachypnoea and lethargy while receiving vaccine influenza quadrival a-b high dose hv vaccine [Fluzone high-dose quadrivalent] and while treated with elasomeran [Spikevax]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient started taking elasomeran vial (containing 10 doses of 0.5 mL), once (1X) (with an unknown batch number and expiry date: unknown) for Prophylactic vaccination. On an unknown date, the patient received an unknown dose of suspect influenza quadrival a-b high dose hv vaccine (lot number and expiry date: not reported) via unknown route in unknown administration site as prophylactic vaccination. Information on batch number was requested. On unknown dates, the patient developed serious events of agitation, apnoea, breath sounds abnormal, cheyne-stokes respiration, erythema, haematoma, hypotension, jugular vein distension, moaning, oedema peripheral, pulmonary embolism, stupor, tachypnoea and lethargy (unknown latency) following the administration of elasomeran and (unknown latency) following the administration of influenza quadrival a-b high dose hv vaccine. These events were leading to death. Additionally, events of apnoea, Cheyne-Stokes respiration and pulmonary embolism were assessed as medically significant. It is unknown if an autopsy was done. The cause of death was reported as Agitation, Apnoea, Breath sounds abnormal, Cheyne-Stokes respiration, Erythema, Haematoma, Hypotension, Jugular vein distension, Lethargy, Moaning, Oedema peripheral, Pulmonary embolism, Stupor and Tachypnoea. Final diagnosis was (fatal) lethargy, (fatal) tachypnoea, (fatal) stupor, (fatal) pulmonary embolism, (fatal) oedema peripheral, (fatal) moaning, (fatal) jugular vein distension, (fatal) hypotension, (fatal) haematoma, (fatal) erythema, (fatal) cheyne-stokes respiration, (fatal) breath sounds abnormal, (fatal) apnoea and (fatal) agitation. Action taken with quadrivalent influenza vaccine (Fluzone high-dose quadrivalent) and elasomeran (Spikevax) was not applicable. It was not reported if the patient received a corrective treatment for the events (agitation, apnoea, breath sounds abnormal, Cheyne-Stokes respiration, erythema, haematoma, hypotension, jugular vein distension, Lethargy, moaning, oedema peripheral, pulmonary embolism, stupor, tachypnoea). At time of reporting, the outcome was Fatal for all the events.; Sender''s Comments: Sanofi company comment dated 25-Mar-2022: This case concerns an 85 year old female patient who experienced agitation, apnoea, breath sounds abnormal, cheyne-stokes respiration, erythema, haematoma, hypotension, jugular vein distension, moaning, oedema peripheral, pulmonary embolism, stupor, tachypnoea and lethargy and died due to these events after receiving vaccine influenza quadrival a-b high dose hv vaccine [Fluzone high-dose quadrivalent] and elasomeran [Spikevax]. A significant temporal relationship cannot be established due to lack of information on event onset date and product start date and hence, causal role of suspect vaccine cannot be excluded in occurrence of the events. Further information such as condition at the time of vaccination, medical history, concomitants, autopsy report would be needed to rule out alternative etiologies. Based on the reported information, the role of an individual vaccine cannot be assessed.; Reported Cause(s) of Death: Agitation; Apnoea; Autopsy-determined Cause(s) of Death: Breath sounds abnormal; Cheyne-Stokes respiration; Erythema; Haematoma; Hypotension; Jugular vein distension; Lethargy; Moaning; Oedema peripheral; Pulmonary embolism; Stupor; Tachypnoea


VAERS ID: 2636587 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-05-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Feeling hot, Loss of consciousness, Nausea, Seizure, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAGSKCA2023AMR073184

Write-up: Loss of consciousness; Seizure; Feeling hot; Nausea; Vomiting; This serious case was reported by a pharmacist via regulatory authority and described the occurrence of loss of consciousness in a 16-year-old female patient who received Flu Seasonal QIV Quebec (FluLaval Tetra) for prophylaxis. Co-suspect products included TOZINAMERAN (COMIRNATY) for prophylaxis. On an unknown date, the patient received FluLaval Tetra (intramuscular) .5 ml and COMIRNATY (intramuscular) .3 ml. On an unknown date, an unknown time after receiving FluLaval Tetra, the patient experienced loss of consciousness (Verbatim: Loss of consciousness) (serious criteria GSK medically significant), seizure (Verbatim: Seizure) (serious criteria GSK medically significant), feeling hot (Verbatim: Feeling hot), nausea (Verbatim: Nausea) and vomiting (Verbatim: Vomiting). The outcome of the loss of consciousness, seizure, feeling hot, nausea and vomiting were resolved. It was unknown if the reporter considered the loss of consciousness, seizure, feeling hot, nausea and vomiting to be related to FluLaval Tetra and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device. It was unknown if the company considered the loss of consciousness, seizure, feeling hot, nausea and vomiting to be related to FluLaval Tetra and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 23-MAY-2023 The pharmacist reported that the patient received a dose of FluLaval tetra multi-dose vial with preservative once along with Comirnaty once. It was unknown if the reporter considered the adverse events to be related to Comirnaty. This report was one of several cases received as part of a line-listing, each containing minimal information. The follow up would not possible as no contact details were available.


VAERS ID: 2200109 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-04-23
Onset: 2021-09-29
   Days after vaccination: 159
Submitted: 0000-00-00
Entered: 2022-03-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER PV46674 / 2 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Chest pain, Influenza like illness
SMQs:, Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2166376 (history)  
Form: Version 2.0  
Age: 85.0  
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Agitation, Apnoea, Breath sounds abnormal, Cheyne-Stokes respiration, Erythema, Haematoma, Hypotension, Jugular vein distension, Lethargy, Moaning, Oedema peripheral, Pulmonary embolism, Stupor, Tachypnoea
SMQs:, Cardiac failure (broad), Anaphylactic reaction (narrow), Angioedema (broad), Asthma/bronchospasm (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Dementia (broad), Embolic and thrombotic events, venous (narrow), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAMODERNATX, INC.MOD20225

Write-up: Agitation; Apnoea; Breath sounds abnormal; Cheyne-Stokes respiration; Erythema; Haematoma; Hypotension; Jugular vein distension; Lethargy; Moaning; Oedema peripheral; Pulmonary embolism; Stupor; Tachypnoea; This case was received via Regulatory Authority (Reference number: 000974506) on 07-Mar-2022 and was forwarded to Moderna on 07-Mar-2022. This regulatory authority case was reported by a nurse and describes the occurrence of AGITATION (Agitation), APNOEA (Apnoea), BREATH SOUNDS ABNORMAL (Breath sounds abnormal), CHEYNE-STOKES RESPIRATION (Cheyne-Stokes respiration), ERYTHEMA (Erythema), HAEMATOMA (Haematoma), HYPOTENSION (Hypotension), JUGULAR VEIN DISTENSION (Jugular vein distension), LETHARGY (Lethargy), MOANING (Moaning), OEDEMA PERIPHERAL (Oedema peripheral), PULMONARY EMBOLISM (Pulmonary embolism), STUPOR (Stupor) and TACHYPNOEA (Tachypnoea) in an 85-year-old female patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19 immunisation. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) for an unknown indication. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) .5 milliliter and dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) (Intramuscular) .5 milliliter. On an unknown date, the patient experienced AGITATION (Agitation) (seriousness criterion death), APNOEA (Apnoea) (seriousness criterion death), BREATH SOUNDS ABNORMAL (Breath sounds abnormal) (seriousness criterion death), CHEYNE-STOKES RESPIRATION (Cheyne-Stokes respiration) (seriousness criterion death), ERYTHEMA (Erythema) (seriousness criterion death), HAEMATOMA (Haematoma) (seriousness criterion death), HYPOTENSION (Hypotension) (seriousness criterion death), JUGULAR VEIN DISTENSION (Jugular vein distension) (seriousness criterion death), LETHARGY (Lethargy) (seriousness criterion death), MOANING (Moaning) (seriousness criterion death), OEDEMA PERIPHERAL (Oedema peripheral) (seriousness criterion death), PULMONARY EMBOLISM (Pulmonary embolism) (seriousness criterion death), STUPOR (Stupor) (seriousness criterion death) and TACHYPNOEA (Tachypnoea) (seriousness criterion death). It is unknown if an autopsy was performed. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No treatment information was provided. Company comment: This regulatory authority case concerns a 85-year-old female with no reported medical history who experienced the serious (Death), unexpected events of Agitation, Apnoea, Breath sounds abnormal, Cheyne-Stokes respiration , Erythema, Haematoma, Hypotension, Jugular vein distension, Lethargy, Moaning, Oedema peripheral, Pulmonary embolism (AESI), Stupor and Tachypnoea presumably sometime time after and unknown dose of mRNA-1273. Testing and treatment are not reported. The outcome is death. The risk-benefit relationship of mRNA-1273 vaccine is not affected by this report. Very scant information is available and no more is expected.; Sender''s Comments: This regulatory authority case concerns a 85-year-old female with no reported medical history who experienced the serious (Death), unexpected events of Agitation, Apnoea, Breath sounds abnormal, Cheyne-Stokes respiration , Erythema, Haematoma, Hypotension, Jugular vein distension, Lethargy, Moaning, Oedema peripheral, Pulmonary embolism (AESI), Stupor and Tachypnoea presumably sometime time after and unknown dose of mRNA-1273. Testing and treatment are not reported. The outcome is death. The risk-benefit relationship of mRNA-1273 vaccine is not affected by this report. Very scant information is available and no more is expected.


VAERS ID: 2751424 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2023-10-18
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2024-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA MD20026A / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8130BA / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Erythema multiforme
SMQs:, Severe cutaneous adverse reactions (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2637152 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-05-11
Onset: 2023-05-16
   Days after vaccination: 5
Submitted: 0000-00-00
Entered: 2023-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Pulmonary embolism
SMQs:, Embolic and thrombotic events, venous (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300200841

Write-up: Pulmonary embolism; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number. A 78-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (COMIRNATY), on 11May2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX TETRA), as dose number unknown, single (Batch/Lot number: unknown). The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunisation. The following information was reported: PULMONARY EMBOLISM (medically significant) with onset 16May2023, outcome "not recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2707515 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-05-17
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Muscle spasms, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Dystonia (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300342392

Write-up: Syncope; Muscle spasms; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from Regulatory Authority. Regulatory number: NZ-Medsafe-151866 (Medsafe). A 36-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 17May2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 17May2023 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for COVID-19 immunisation. The following information was reported: SYNCOPE (medically significant), outcome "recovered"; MUSCLE SPASMS (non-serious), outcome "recovered". Additional Information: case was assessed non-serious by Regulatory Authority. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2469146 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-07-10
Onset: 2021-12-01
   Days after vaccination: 144
Submitted: 0000-00-00
Entered: 2022-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / 1 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Interchange of vaccine products, Malaise, Pain, Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2646729 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 2023-06-11
Submitted: 0000-00-00
Entered: 2023-06-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Seizure, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300222803

Write-up: Seizure; Syncope; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: 777288 (RA). A female patient received BNT162b2, BNT162b2 omi ba.4-5 (COMIRNATY), as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), as dose number unknown, single (Batch/Lot number: unknown) for influenza immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: SEIZURE (medically significant) with onset 11Jun2023, outcome "recovered"; SYNCOPE (medically significant) with onset 11Jun2023, outcome "recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2129521 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-12-06
Onset: 2022-02-02
   Days after vaccination: 58
Submitted: 0000-00-00
Entered: 2022-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / 2 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood test, Chest pain, Computerised tomogram, Computerised tomogram thorax, Dyspnoea, Fatigue, Palpitations, Pericarditis lupus, Pyrexia, SARS-CoV-2 test, Systemic lupus erythematosus, Tachycardia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (narrow), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad), Immune-mediated/autoimmune disorders (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2649220 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-05-26
Onset: 2023-05-27
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-06-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Acute generalised exanthematous pustulosis
SMQs:, Severe cutaneous adverse reactions (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300228756

Write-up: Acute generalised exanthematous pustulosis; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: 777565 (RA). A 53-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (COMIRNATY), on 26May2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 26May2023 as dose number unknown, single (Batch/Lot number: unknown) for influenza immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunisation. The following information was reported: ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS (medically significant) with onset 27May2023, outcome "unknown". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2659195 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-04-26
Onset: 2023-05-10
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2023-07-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Ear pain, Facial paralysis, Ocular discomfort
SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300253998

Write-up: Facial paralysis; Ear pain; Ocular discomfort; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: 781013 (RA). A 53-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (COMIRNATY), on 26Apr2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX TETRA), on 26Apr2023 as dose number unknown, single (Batch/Lot number: unknown) for influenza immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunisation. The following information was reported: EAR PAIN (non-serious) with onset 10May2023, outcome "not recovered"; FACIAL PARALYSIS (medically significant) with onset 10May2023, outcome "not recovered"; OCULAR DISCOMFORT (non-serious) with onset 10May2023, outcome "not recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2661841 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2023-07-18
Onset: 2023-07-20
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-07-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Electrocardiogram abnormal, Pericarditis, Pleuritic pain
SMQs:, Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300261170

Write-up: Pericarditis; Electrocardiogram abnormal; Pleuritic pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: (TGA ADR#). A 56-year-old male patient received BNT162b2, BNT162b2 omi ba.1 (COMIRNATY), on 18Jul2023 as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 18Jul2023 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: ELECTROCARDIOGRAM ABNORMAL (non-serious) with onset 20Jul2023, outcome "unknown"; PERICARDITIS (medically significant) with onset 20Jul2023, outcome "unknown"; PLEURITIC PAIN (non-serious) with onset 20Jul2023, outcome "unknown". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2129517 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-10-08
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2022-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal discomfort, Dizziness, Menstruation delayed, Ovarian cyst ruptured, Pregnancy test, Pyrexia, Weight
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Fertility disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2103001 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-09-18
Onset: 2021-12-12
   Days after vaccination: 85
Submitted: 0000-00-00
Entered: 2022-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: COVID-19, Multiple sclerosis relapse, SARS-CoV-2 test
SMQs:, Optic nerve disorders (broad), Demyelination (narrow), Infective pneumonia (broad), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (narrow), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2085102 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-01
Onset: 2021-12-24
   Days after vaccination: 53
Submitted: 0000-00-00
Entered: 2022-02-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / N/A LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Facial pain, Trigeminal neuralgia
SMQs:, Glaucoma (broad), Demyelination (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine 50 mcg norethindrome 0.35 mg
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: MRI will be performed on February 14, 2022.
CDC Split Type:

Write-up: Intense pain on the right side of the face that started with some crisis in the day of Dec 23, 2021 and then evolved to a lot of extremely painful crisis each day. After a week of seeing different doctor/urgent care visits, I was diagnosed with trigeminal nerve neuralgia. I was given Pregabalin (generics of Lyrica) which helps with the pain. I''m now waiting for a cerebral MRI, and an appointment with a neurologist to try and find the cause of the neuralgia.


VAERS ID: 2081843 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-05-12
Onset: 2021-12-18
   Days after vaccination: 220
Submitted: 0000-00-00
Entered: 2022-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / UNK - / -
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Ageusia, COVID-19, Migraine, Oropharyngeal pain, Rhinorrhoea, SARS-CoV-2 test
SMQs:, Taste and smell disorders (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2701129 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2023-04-11
Onset: 2023-04-27
   Days after vaccination: 16
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Bell's palsy
SMQs:, Hearing impairment (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300336031

Write-up: Bell''s palsy; This is a spontaneous report received from a contactable reporter(s) (Physician) from Regulatory Authority. Regulatory number: NZ-Medsafe-152035 (Medsafe). A 77-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 11Apr2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 11Apr2023 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for COVID-19 immunisation. The following information was reported: BELL''S PALSY (medically significant) with onset 27Apr2023, outcome "not recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2072457 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-04-08
Onset: 2021-04-15
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2022-01-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Alopecia, Arthralgia, Basophil degranulation test, Chronic spontaneous urticaria, Contusion, Feeling abnormal, Reynold's syndrome, Skin test, Somnolence, Urticaria
SMQs:, Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Anaphylactic reaction (broad), Angioedema (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Dementia (broad), Biliary tract disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210922; Test Name: BAT testing; Result Unstructured Data: BAT negative to Pfizer Comirnaty; Test Date: 2021; Test Name: IDT; Result Unstructured Data: Histamine control negative; Test Date: 2021; Test Name: SPT; Result Unstructured Data: Histamine control negative
CDC Split Type: AUSEQIRUS202200338

Write-up: Hives; Possible Reynold''s syndrome; Chronic hives/Urticaria/Knee felt hot/Entire leg appreared red/welts along legs arms face/dermatographism/Blotchy/Rash has spread to feet/Itch/Ongoing itch/Likely dg of chronic spontaneous urticaria; Losing more hair than usual; Bruising along thighs and legs; Drowsiness; Sensitive joints; Fogginess; This spontaneous case retrieved on 21-Jan-2022 from Regulatory Authority (reference number: AU-TGA-0000646046), reported by physician and concerned a 41-year-old female patient. The patient had no significant prior medical history and was not taking any concomitant medications regularly. The patient''s historical drugs included morphine/opioids with immediate reaction of itch and Tramacet (paracetamol, tramadol hydrochloride) in 2014 with associated reaction of itch, but no wheeze, shortness of breath (SOB), welts or urticaria. On 08-Apr-2021, the patient was vaccinated with Afluria Quad (influenza vaccine; route of administration: intramuscular; dose, anatomical location and indication: not reported). The batch number was not reported. This was the patient''s first flu vaccine ever. On 15-Apr-2021, one week after receiving Afluria Quad, the patient developed hives. Thought initially it was mould (as reported), but was tested negative and also tested negative to coeliac screening. On 15-Jul-2021 prior to Pfizer vaccination, the patient saw dermatologist and was diagnosed with ''chronic hives''. On 29-Jul-2021, Thursday, the patient received first dose of non-company co-suspect vaccine Comirnaty (tozinameran; route of administration: intramuscular; dose, anatomical location and indication: not reported). The batch number was not reported. On the same day, within 30 minutes after receiving Comirnaty, the patient developed severe urticaria. On her way home her knee felt hot and she developed itch. When she arrived home entire leg appeared red with itch. There was no wheeze, SOB or lightheadedness. The patient took Zyrtec (cetirizine hydrochloride) and later that evening Phenergan (promethazine hydrochloride). The patient trailed Zyrtec to up to four a day and Phenergan two per night. On an unspecified date in 2021, the patient was also prescribed montelukast by dermatologist at a dose of 10 mg daily, but it did not help. The patient then tried Deptran (doxepin hydrochloride) at a dose of 10 mg for 14 days which did not help and then increased the dose to 20 mg three times a day (tds). On an unspecified date in 2021, the patient experienced significant fogginess/drowsiness. The patient used Eurax HC cream (crotamiton, hydrocortisone) and Bioderma DS, but still had blotches and at other times was itchy. On an unspecified date in 2021, the patient visited her general physician (GP) and brought photos in with her - welts noted along legs, arms, face, dermatographism; bruising along thighs and legs dated two days following vaccine. She had ongoing itch every day and used Zyrtec, Phenergan or lotion/creams - taking 1-2 daily. The patient also had a blood test at clinical labs. It was noted that patient possibly had Reynold''s, she was losing more hair than usual and had sensitive joints. After consultation with another specialist the patient tried a skin prick test (SPT)/intradermal test (IDT) and blood tests. Histamine control was negative on SPT/IDT. On 22-Sep-2021, after discussion with another specialist the patient underwent basophil activation test (BAT) testing, which was negative to Pfizer Comirnaty and the plan was to proceed with next dose of Pfizer Comirnaty. It was considered that first dose reaction was unlikely related given pre-existing possible chronic spontaneous urticaria. The patient was given significant medical therapy - almost maximal and the plan was to consider monoclonal antibodies. Impression after blood autoimmune tests was a likely diagnosis of chronic spontaneous urticaria. The patient was prescribed nizatidine at a dose of 150 mg twice a day (bid) in addition to Zyrtec four times a day and was provided urticaria activity score questionarries. On 30-Sep-2021, the patient was vaccinated with second dose of non-company co-suspect Comirnaty vaccine (tozinameran; dose, route of administration, anatomical location and indication: not reported). The batch number was not reported. On 07-Oct-2021, a week after receiving the second dose, the symptoms which were previously improving with treatment, reoccurred and exacerbated, rash had now spread to feet. The patient spoke with her GP who advised to contact immunisation clinic. The outcome of the events was unknown. The reporter did not provide a causality assessment. The Regulatory Authority assessed the events as possibly related to Afluria Quad. The event of ''Reynold''s syndrome'' was considered to be medically significant by a Physician within Seqirus'' Pharmacovigilance and Risk Management Department. Company comment: A 41-year-old female patient experienced urticaria 1 week after receiving Afluria Quad vaccine. Besides, the patient was diagnosed with chronic spontaneous urticaria 3 months after vaccination. On the other hand, the patient experienced arthralgia and chronic spontaneous urticaria on the same day after receiving first dose of non-company co-suspect vaccine Comirnaty, and more than 3 months after receiving Afluria Quad vaccine. And on an unspecified date, the patient experienced bruising, alopecia, somnolence, foggy feeling in head and possible Reynold''s syndrome. As reported, symptoms exacerbated after receiving a second dose of non-company co-suspect vaccine Comirnaty, which was administered approximately 5 months after Afuria Quad administration. Causality for urticaria is assessed as possibly related due to plausible temporal relationship. Causality for bruising, alopecia, somnolence, foggy feeling in head and Reynold''s syndrome is unassessable due to lack of information regarding chronology. Based on implausible temporal relationship, causality for chronic spontaneous urticaria and arthralgia is assessed as not related.; Sender''s Comments: A 41-year-old female patient experienced urticaria 1 week after receiving Afluria Quad vaccine. Besides, the patient was diagnosed with chronic spontaneous urticaria 3 months after vaccination. On the other hand, the patient experienced arthralgia and chronic spontaneous urticaria on the same day after receiving first dose of non-company co-suspect vaccine Comirnaty, and more than 3 months after receiving Afluria Quad vaccine. And on an unspecified date, the patient experienced bruising, alopecia, somnolence, foggy feeling in head and possible Reynold''s syndrome. As reported, symptoms exacerbated after receiving a second dose of non-company co-suspect vaccine Comirnaty, which was administered approximately 5 months after Afuria Quad administration. Causality for urticaria is assessed as possibly related due to plausible temporal relationship. Causality for bruising, alopecia, somnolence, foggy feeling in head and Reynold''s syndrome is unassessable due to lack of information regarding chronology. Based on implausible temporal relationship, causality for chronic spontaneous urticaria and arthralgia is assessed as not related.


VAERS ID: 2675516 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2018-04-17
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-08-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. B4960101302 / UNK - / OT
HEPAB: HEP A + HEP B (TWINRIX) / GLAXOSMITHKLINE BIOLOGICALS NO BATCH NUMBER / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Chest discomfort, Chest pain, Colonoscopy, Dehydration, Dyspepsia, Endoscopy upper gastrointestinal tract, Erosive oesophagitis, Gastric mucosal lesion, Oesophagitis, Skin lesion
SMQs:, Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Gastrointestinal ulceration (narrow), Gastrointestinal nonspecific inflammation (narrow), Gastrointestinal nonspecific dysfunction (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Dexamphetamine; Cipramil; Nexium
Current Illness: Asperger''s disorder; Autism spectrum disorder
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Colonoscopy; Result Unstructured Data: Bowel was full of lesions; Test Date: 2018; Test Name: Gastroscopy; Result Unstructured Data: Revealing severe esophagitis.; Test Date: 2018; Test Name: Gastroscopy; Result Unstructured Data: Esophagus had improved remarkably since last week. Still inflamed but much better.
CDC Split Type: AUSEQIRUS202302986

Write-up: The lesions started on the spot where she got the needle and spread to various areas on her body; Bowel was full of lesions; Chest pains when eating/ Pain when eating and drinking. Pain became so bad didn''t want to even drink; Heart burn; Dehydrated; Esophagitis/Still inflamed; Esophagus was full of lesions; Tight chest; This spontaneous case was received on 30-May-2023 from other non-healthcare professional (patient''s mother) via Medical Information (reference number: AU23-001408) and concerned an adult, female patient (at the time of vaccination 33-year-old). The patient''s concurrent conditions included autism spectrum disorder (ASD) and Asperger tendencies. The patient''s concomitant medications included Dexamphetamine (dexamfetamine sulfate), Cipramil (citalopram hydrochloride) and Nexium (esomeprazole sodium), all used for an unreported indication. On 17-Apr-2018, the patient was vaccinated with Afluria Quad (influenza vaccine inact split 4v; anatomical location: arm; dose, route of administration, and indication: not reported). The batch number reported was B4960101302 (Seqirus batch number unable to be matched). On an unspecified date in 2018, within a couple of weeks after receiving Afluria Quad, the patient experienced a major reaction. The patient started having chest pains when eating. The patient thought it was just heartburn so she continued with Nexium. Problem gradually became worse with pain when eating and drinking. Pain became so bad the patient didn''t want to even drink. The patient was advised not to receive any more influenza vaccines. On 26-May-2018, the patient finally attended a doctor and was immediately put in the hospital, severely dehydrated. On an unspecified date in 2018, initially the patient was investigated for heart problems. Eventually a gastroscopy was done revealing severe esophagitis. Esophagus was full of lesions. The surgeon mentioned she had only seen one case as bad before. The patient received acyclovir, unspecified intravenous (IV) antibiotics and unspecified anti reflux medication. On an unspecified date in 2018, on second gastroscopy, surgeon commented ''esophagus had improved remarkably since last week. Still inflamed but much better''. On 09-Jun-2018, the patient was discharged from the hospital. On an unspecified date, the patient recovered from the events of chest pain, heartburn, dehydration, esophagitis and ''esophageal erosions''. On the unspecified date, subsequently, the patient received a first doses of Twinrix (hepatitis a vaccine inact; hepatitis b vaccine rhbsag (yeast); dose, route of administration, anatomical locationa and indication: not reported) and COVID-19 vaccine (Brand not specified; dose, route of administration, anatomical locationa and indication: not reported). The batch number was not reported. On an unspecified date, with the first dose, the patient experienced a tight chest. On an unspecified date, the patient received a second dose of Twinrix (hepatitis a vaccine inact; hepatitis b vaccine rhbsag (yeast); dose, route of administration, anatomical locationa and indication: not reported) and COVID-19 vaccine (Brand not specified; dose, route of administration, anatomical locationa and indication: not reported). The batch number was not reported. On an unspecified date, after her second dose of Twinrix, the patient had a similar reaction, only the lesions started on the spot where she got the needle and spread to various areas on her body. Also, her bowel became problematic and a colonoscopy showed her bowel was full of lesions. The reporter did not provide a causality assessment for tight chest, ''skin lesion NOS'' and ''gastric mucosal lesion NOS''. The reporter assessed the events of chest pain, heartburn, dehydration, esophagitis and ''esophageal erosions'' as related to Afluria Quad. As reported, patient received Afluria Quad vaccine in 2018 and experienced a major reaction. The events of chest pain, heartburn, dehydration, esophagitis, ''esophageal erosions'', ''skin lesion NOS'' and ''gastric mucosal lesion NOS'' were assessed as serious due to the seriousness criterion of hospitalization. Additionally, the event of ''esophageal erosions'' was considered to be medically significant by a Physician within Department. Additional information received on 07-Aug-2023 from other non-healthcare professional (the patient''s mother): Report type changed from ''invalid'' to ''spontaneous''. Age at vaccination added. Medical history added (autism spectrum disorder, asperger''s disorder). Patient notes changed from ''none'' to null flavor UNK. Lab data was added (gastroscopy and colonoscopy). Concomitant added (Dexamphetamine, Cipramil and Nexium) and treatment medications (Acyclovir) added. Co-suspect vaccines COVID-19 and Twinrix added. Vaccination start date was amended from ''?2018'' to ''17-Apr-2018''. Vaccination anatomical location was changed from ''unknown'' to ''arm''. The events of tight chest, ''chest pain'', ''heartburn'', ''dehydration'', ''esophagitis'', ''esophageal erosions'', ''skin lesion NOS'' and ''gastric mucosal lesion NOS'' were added. Case outcome amended from ''recovered/resolved'' to ''not reported''. The narrative was amended accordingly. Company comment: An adult, female patient was vaccinated with Afluria Quad. Within a couple of weeks after receiving Afluria Quad, the patient experienced a major reaction, as reported. The patient started having chest pain when eating. The patient thought it was just heartburn so she continued with Nexium. The pain gradually became worse when eating, till the patient didn''t want to even drink. On 26-May-2018, the patient was admitted to the hospital, severely dehydrated. A gastroscopy revealed severe esophagitis. The patient received acyclovir, unspecified intravenous (IV) antibiotics and unspecified anti reflux medication. On the unspecified date, subsequently, the patient received a first doses of Twinrix (hepatitis a vaccine inact; hepatitis b vaccine rhbsag (yeast)) and COVID-19 vaccine. After the first dose, the patient experienced a tight chest. After receiving a second dose of Twinrix, the lesions started on vaccination site and spread to various areas of her body. Also, a colonoscopy revealed a bowel was full of lesions. Causality was highly confounded by patient''s concomitant medications, citalopram and esomeprazole. The event of skin lesions is assessed as not related to the suspect vaccine, based on anatomical implausibility, and Twinrix provided alternative aetiology. For the remaining events (chest pain, dyspepsia, esophagitis/erosive esophagitis, dehydration, tight chest, gastric mucosal lesion NOS) causality is assessed as not related, since temporal relationship is unsuggestive and patient''s medical history and Twinrix confounded causality.; Reporter''s Comments: Patient received Afluria Quad vaccine in 2018 and experienced a major reaction.; Sender''s Comments: An adult, female patient was vaccinated with Afluria Quad. Within a couple of weeks after receiving Afluria Quad, the patient experienced a major reaction, as reported. The patient started having chest pain when eating. The patient thought it was just heartburn so she continued with Nexium. The pain gradually became worse when eating, till the patient didn''t want to even drink. On 26-May-2018, the patient was admitted to the hospital, severely dehydrated. A gastroscopy revealed severe esophagitis. The patient received acyclovir, unspecified intravenous (IV) antibiotics and unspecified anti reflux medication. On the unspecified date, subsequently, the patient received a first doses of Twinrix (hepatitis a vaccine inact; hepatitis b vaccine rhbsag (yeast)) and COVID-19 vaccine. After the first dose, the patient experienced a tight chest. After receiving a second dose of Twinrix, the lesions started on vaccination site and spread to various areas of her body. Also, a colonoscopy revealed a bowel was full of lesions. Causality was highly confounded by patient''s concomitant medications, citalopram and esomeprazole. The event of skin lesions is assessed as not related to the suspect vaccine, based on anatomical implausibility, and Twinrix provided alternative aetiology. For the remaining events (chest pain, dyspepsia, esophagitis/erosive esophagitis, dehydration, tight chest, gastric mucosal lesion NOS) causality is assessed as not related, since temporal relationship is unsuggestive and patient''s medical history and Twinrix confounded causality.


VAERS ID: 2067395 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 2021-12-12
Submitted: 0000-00-00
Entered: 2022-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Cardiac arrest, Fatigue, Immunisation, Influenza, Pyrexia, SARS-CoV-2 test
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (broad), Cardiomyopathy (broad), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2677038 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-08-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -
HEPAB: HEP A + HEP B (TWINRIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Chest discomfort, Chest pain, Dehydration, Dyspepsia, Erosive oesophagitis, Gastric mucosal lesion, Oesophagitis, Skin lesion
SMQs:, Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Gastrointestinal ulceration (narrow), Gastrointestinal nonspecific inflammation (narrow), Gastrointestinal nonspecific dysfunction (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CIPRAMIL [CITALOPRAM HYDROBROMIDE]; NEXIUM [ESOMEPRAZOLE SODIUM]; DEXAMFETAMINE SULFATE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300283750

Write-up: Erosive oesophagitis; Chest discomfort; Chest pain; Dehydration; Dyspepsia; Gastric mucosal lesion; Oesophagitis; Skin lesion; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: (TGA ADR#). A 30-year-old female patient received BNT162b2 (COVID-19 VACCINE NOS MANUFACTURER UNKNOWN), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), as dose number unknown, single (haemagglutinin) (Batch/Lot number: unknown) for influenza immunisation; hepatitis a vaccine inact, hepatitis B vaccine rhbsag (yeast) (TWINRIX), as dose number unknown, single (adult 720/20 formulation) (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history was not reported. Concomitant medication(s) included: CIPRAMIL [CITALOPRAM HYDROBROMIDE]; NEXIUM [ESOMEPRAZOLE SODIUM]; DEXAMFETAMINE SULFATE. The following information was reported: EROSIVE OESOPHAGITIS (medically significant), outcome "unknown"; CHEST DISCOMFORT (non-serious), outcome "unknown"; CHEST PAIN (non-serious), outcome "unknown"; DEHYDRATION (non-serious), outcome "unknown"; DYSPEPSIA (non-serious), outcome "unknown"; GASTRIC MUCOSAL LESION (non-serious), outcome "unknown"; OESOPHAGITIS (non-serious), outcome "unknown"; SKIN LESION (non-serious), outcome "unknown". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1930888 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-22
Onset: 2021-11-23
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3005884 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA632BA / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Arthralgia, Back pain, Chest pain, Influenza like illness, Musculoskeletal chest pain
SMQs:, Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: EUTIROX;
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2541020 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-11-17
Onset: 2022-11-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ2541 / 4 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Herpes zoster, Interchange of vaccine products, Investigation, Off label use, Pain, Pain in extremity, Product use issue, Rash vesicular
SMQs:, Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2545041 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-12-15
Onset: 2022-12-01
Submitted: 0000-00-00
Entered: 2022-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. 3017378 / UNK LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Dermatitis atopic, Laryngeal oedema, Rash
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2545934 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2022-11-08
Onset: 2022-11-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ4535 / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR W3E831V / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Aphasia, Asthenia, Blindness unilateral, Body temperature, Cerebrovascular accident, Computerised tomogram, Conjunctivitis, Echocardiogram, Endocarditis, Paralysis, Product use issue, Pyrexia
SMQs:, Severe cutaneous adverse reactions (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Glaucoma (broad), Optic nerve disorders (broad), Retinal disorders (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Conjunctival disorders (narrow), Ocular infections (broad), Hypersensitivity (broad), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2548742 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2022-11-07
Onset: 2022-11-07
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9851 / 4 LA / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA678DA / UNK RA / OT

Administered by: Other       Purchased by: ?
Symptoms: Off label use, Product use issue, Vertigo
SMQs:, Vestibular disorders (narrow), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2539647 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2022-11-01
Onset: 2022-11-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9715 / UNK LA / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA671DB / UNK RA / OT

Administered by: Other       Purchased by: ?
Symptoms: Aspartate aminotransferase, Blood calcium, Blood potassium, Blood sodium, Blood thyroid stimulating hormone, C-reactive protein, Full blood count, Gamma-glutamyltransferase, Off label use, Product use issue, Vasculitis
SMQs:, Vasculitis (narrow), Medication errors (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2524439 (history)  
Form: Version 2.0  
Age: 10.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Lethargy, Neutropenia, Off label use, Product use issue, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Agranulocytosis (broad), Haematopoietic leukopenia (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202201340805

Write-up: Off label use; Product use for unapproved combination; Neutropenia; Lethargy; Pyrexia; Vomiting; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: 759210. A 10-year-old female patient received BNT162b2 (COMIRNATY), on 21Nov2022 as dose 1 (orange cap), single (Batch/Lot number: unknown) at the age of 10 years for covid-19 immunisation; pneumococcal 13-val conj vac (dipht CRM197 protein) (PREVENAR 13), on 21Nov2022 as dose number unknown, single (Batch/Lot number: unknown) at the age of 10 years for immunisation; influenza vaccine inact split 4v (FLUARIX TETRA), on 21Nov2022 (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: LETHARGY (non-serious) with onset 21Nov2022, outcome "unknown"; NEUTROPENIA (medically significant) with onset 21Nov2022, outcome "unknown"; OFF LABEL USE (medically significant) with onset 21Nov2022, outcome "unknown"; PRODUCT USE ISSUE (medically significant) with onset 21Nov2022, outcome "unknown", described as "Product use for unapproved combination"; PYREXIA (non-serious) with onset 21Nov2022, outcome "unknown"; VOMITING (non-serious) with onset 21Nov2022, outcome "unknown". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2518618 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-29
Onset: 2021-12-01
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3001942 / 3 - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / 1 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Antinuclear antibody, Balance disorder, Blood immunoglobulin M, Cardiovascular examination, Chronic fatigue syndrome, Cognitive disorder, Dermatologic examination, Dizziness, Ear, nose and throat examination, Erythema, Face oedema, Investigation, Magnetic resonance imaging head, Neurological examination, Oedema peripheral, Paraesthesia, Vertigo positional
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (narrow), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Vestibular disorders (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: BILOL; AMLODIPINE BESILATE + PERINDOPRIL TOSILATE; ELIQUIS; JODETTEN HENNING; NEO-MERCAZOLE
Current Illness: Allergy (contact allergy to balsam of Peru, balsam of tolu, turpentine and arnica); Atrial fibrillation paroxysmal (since March 2019, CHADSVASc score 3 points); Dizziness; Drug allergy (pyrazinamide, lornoxicam, piroxicam and questionable Bactrim (sulfamethoxazole/trimethoprim)); Drug hypersensitivity (allergies to pyrazinamide, lornoxicam, piroxicam and questionable Bactrim (sulfamethoxazole)); Hashimoto''s thyroiditis; Hypertensive heart disease (since December 2013); Iodine deficiency goitre; Penicillin allergy; Tremor (pre-existing dystonic postural and action tremor of the right hand)
Preexisting Conditions: Medical History/Concurrent Conditions: Angiography (in July 2021, coronary angiography); Aortic valve replacement (Aortic valve replacement (TAVI) in July 2021, good function in cardiological follow-up); Aortic valve stenosis (from December 2013 to July 2021); Craniocerebral injury (in June 2022, stage 1 craniocerebral trauma)
Allergies:
Diagnostic Lab Data: Test Date: 20220119; Test Name: ANA; Result Unstructured Data: (Test Result:no result,Unit:unknown,Normal Low:,Normal High:); Comments: ANA, ANCA, Complement C3, C4, IgE Total, Trypt; Test Date: 20220524; Test Name: IgM; Result Unstructured Data: (Test Result:no result,Unit:unknown,Normal Low:,Normal High:); Comments: for CMV, VZV, TBE, Coxsackie, measles, duck; Test Date: 20220325; Test Name: Cardiology; Result Unstructured Data: (Test Result:properly functioning aortic artery,Unit:unknown,Normal Low:,Normal High:); Test Date: 20220302; Test Name: Dermatological; Result Unstructured Data: (Test Result:Recurrent erythema with angioedema in the,Unit:unknown,Normal Low:,Normal High:); Test Date: 20220119; Test Name: ENT; Result Unstructured Data: (Test Result:Vertebral positional vertigo in back view,Unit:unknown,Normal Low:,Normal High:); Test Date: 20220921; Test Name: Covid consultation hour; Result Unstructured Data: (Test Result:Psychometry Clinically r,Unit:unknown,Normal Low:,Normal High:); Test Date: 20220207; Test Name: MR skull native; Result Unstructured Data: (Test Result:Chronic ischemia,Unit:unknown,Normal Low:,Normal High:); Test Date: 20220204; Test Name: Neurological examination; Result Unstructured Data: (Test Result:Mainly cerebral ischemia,Unit:unknown,Normal Low:,Normal High:); Comments: LabComments: ANA 19-JAN-22: ANA, ANCA, Complement C3, C4, IgE Total, Trypt, IgM 24-MAY-22: for CMV, VZV, TBE, Coxsackie, measles, duck
CDC Split Type: CHGSKCH2022173739

Write-up: Vertigo positional; increasing dizziness; swelling of the face; Burning and tingling paresthesias in both legs and feet; Chronic fatigue and exercise intolerance; Cognitive deficits with concentration disorders; Balance disorder with unsteady gait and falls; Reddening of the skin on the face; Swellings on both forearms; This case was reported by a physician via regulatory authority and described the occurrence of vertigo positional in a 74-year-old female patient who received Flu Seasonal QIV Dresden (Fluarix Tetra 2021-2022 season) for prophylaxis. Co-suspect products included flu seasonal qiv dresden pre-filled syringe device (Influenza Vaccine Quadrivalent Pre-Filled Syringe Device) injection syringe for prophylaxis and ELASOMERAN (SPIKEVAX) (batch number 3001942, expiry date unknown) for prophylaxis. The patient''s past medical history included aortic valve stenosis (from December 2013 to July 2021), aortic valve replacement (Aortic valve replacement (TAVI) in July 2021, good function in cardiological follow-up) and angiography (in July 2021, coronary angiography). Previously administered products included Spikevax (1st dose received on 1st February 2021, batch number: 300042460, dose 50 ?g) and Spikevax (2nd dose received on 15th March 2021, batch number: 300042460, dose 25 ?g). Concurrent medical conditions included hypertensive heart disease (since December 2013), atrial fibrillation paroxysmal (since March 2019, CHADSVASc score 3 points), hashimoto''s thyroiditis, craniocerebral injury (in June 2022, stage 1 craniocerebral trauma), dizziness, tremor (pre-existing dystonic postural and action tremor of the right hand), iodine deficiency goitre, drug hypersensitivity (allergies to pyrazinamide, lornoxicam, piroxicam and questionable Bactrim (sulfamethoxazole)), penicillin allergy, drug allergy (pyrazinamide, lornoxicam, piroxicam and questionable Bactrim (sulfamethoxazole/trimethoprim)) and allergy (contact allergy to balsam of Peru, balsam of tolu, turpentine and arnica). Concomitant products included bisoprolol fumarate (Bilol), amlodipine besilate + perindopril tosilate, apixaban (Eliquis), carbimazole (Neo-Mercazole) and potassium iodide (Jodetten Henning). On 29th November 2021, the patient received the 1st dose of Fluarix Tetra 2021-2022 season (intramuscular) 1 dosage form(s), Influenza Vaccine Quadrivalent Pre-Filled Syringe Device and the 3rd dose of SPIKEVAX (intramuscular) 25 ?g. In December 2021, less than 2 months after receiving Fluarix Tetra 2021-2022 season and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device, the patient experienced vertigo positional (serious criteria other: serious as per reporter), dizziness aggravated (serious criteria other: serious as per reporter), face edema (serious criteria other: serious as per reporter), paraesthesia lower limb (serious criteria other: serious as per reporter), chronic fatigue syndrome (serious criteria other: serious as per reporter), cognitive impairment (serious criteria other: serious as per reporter), balance disorder (serious criteria other: serious as per reporter), erythema (serious criteria other: serious as per reporter) and oedema peripheral (serious criteria other: serious as per reporter). The patient was treated with pimecrolimus (Elidel Cream). On an unknown date, the outcome of the vertigo positional, dizziness aggravated, face edema, paraesthesia lower limb, chronic fatigue syndrome, cognitive impairment, balance disorder, erythema and oedema peripheral were not recovered/not resolved. The reporter considered the vertigo positional, dizziness aggravated, face edema, paraesthesia lower limb, chronic fatigue syndrome, cognitive impairment, balance disorder, erythema and oedema peripheral to be possibly related to Fluarix Tetra 2021-2022 season and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device. This report was made by GSK without prejudice and did not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 22-Nov-2022. Reporter''s Comments: The patient had swelling of the face, burning and tingling paresthesias in both legs and feet, increasing dizziness, chronic fatigue and exercise intolerance, cognitive deficits with concentration disorders, balance disorder with unsteady gait and falls and reddening of the skin on the face. Time to onset with respect to SPIKEVAX for all the events was less than 2 months. The 3rd Spikevax immunization was given about 2 weeks after a presumably viral infection with flu symptoms, nausea and pronounced general weakness at the same time as the first influenza vaccination I.M. (Fluarix Tetra). There was no loss of sense of smell. A swab for Sars-CoV-2 was not carried out. There was no knowing contact with Covid 19- positive people. After a week, the acute symptoms of infection had subsided. Around mid- late December 2021 (3 to 4 weeks after the vaccination), persistent symptoms of exhaustion with accompanying dizziness began. The patient was already familiar with dizziness when standing up. However, a different, undirected dizziness had now occurred, which occured with movement and exertion. In the context of dizziness, there were balance disorders. The patient felt unsteady when walking and had fallen several times since, with no loss of consciousness. She noticed a lack of strength in her legs and intermittent tingling paresthesias in her hands and soles of her feet. In the evening the arms were often red and swollen. In the 2nd half of December a reddening/rash appeared on the face. Physical performance was significantly reduced. Even after small exertions like making coffee in the morning, the patient had to sit down again to recover. The patient could usually sleep well at night but has recently had to lie down several times during the day. In addition, she often noticed concentration problems, increased forgetfulness and word-finding difficulties. The symptoms also affected the patient''s psyche. Often she could no longer be happy and tends to withdraw because she was immediately exhausted by any activity. The symptoms were still persistent. The following could be summarized as to the history: The 1st immunization with Spikevax I.M. (lot no. 300042460, specified as 50 ?g) was carried out on 1st February 2021, the 2nd (lot no. 300042460, specified as 25 ?g) on 15th March 2021 I.M. The patient tolerated the first two Covid19 vaccinations without any problems. Nicotine consumption was suspended 40 years ago, she rarely consumes beer and had no kidney or liver diseases. Various clarifications of the symptoms that had occurred since December 2021 have resulted in the following findings: ENT clarification on 8th December 2021 and follow-up on 19th January 2022: History of dizziness, especially in the morning and with fast movements and when bending over and looking up. No dizziness or nystagmus could be triggered during positioning tests. Diagnosis of a vertebral tympanic ventilation disorder bilateral positional vertigo. Dermatological clarification 30th January 2022 and follow up 2nd March 2022 because of a rash on the face: Initial suspected perioral dermatitis DD erythematous rosacea, in the course of suspected diagnosis of a recurrent erythema with angioedema on the face after booster vaccination. ANA, ANCA, complement C3, C4, IgE total, tryptase unremarkable. History of redness and swelling at follow-up examination only in the evening, improvement since taking Elidel cream (pimecrolimus). Neurological examination on 4th February 2022: Anamnestic malaise throughout the day, swollen knees and burning sensation as well as loss of strength in the legs and consecutive falls since the end of January 2022. The clinical neurological examination revealed a well-known slight tremor of the right hand, which was accentuated at rest, a slight paresis in the right leg with thermal hypesthesia in the legs and hypalgesia in the right leg. No evidence of polyradiculitis, polyneuropathy or myopathy in ENG/EMG. A duplex sonography of the cerebral vessels on 4th February 2022 showed a progressive, approx. 50 % exit stenosis of the right internal carotid artery. An MRI of the lumbar spine was largely age-appropriate. In the case of suspected cerebral ischemia, an MRI of the skull was performed on 7th, 2022 February which showed chronic infarction scars on both sides of the cerebellum, questionable postischemic gliotic parenchymal changes in the pons on both sides and questionable small ischemia in the area of the pons. An endocrinological follow up on 16th March 2022 did not result in a renewed indication for Neo-Mercazole with stable findings. Cardiological follow-up March 2022: Echocardiographically no indication of the source of the embolism, normal function of the TAVI prosthesis. Long Covid consultation hours July 2021 and 21st September 2022: Etiologically, an immunologically triggered genesis in the context of the most likely viral infection as well as the double vaccination carried out shortly thereafter was fundamentally possible. Whether it was a post-Covid syndrome could not be assessed retrospectively if there was no evidence of Covid. In principle, however, postviral fatigue could also occur to a lesser extent after other virus infections. A connection with the booster vaccination was also conceivable, although a post-infectious genesis was much more common. Under combined pacing therapy and dizziness training, there was no symptom improvement until September 2022. The dizziness and the unsteady gait could basically be explained in the context of the cerebellar ischemia that took place. Findings: Sympathicotonic orthostatic hypotension in the Schellong test, MoCA test (Montreal Cognitive Assessment Test) unremarkable, EQ-5D-5L: severe problems, current health VAS: 23/100 points, HADS anxiety: severe symptoms, depression: Very severe symptoms, ISI (sleep): clinically subthreshold, FSS (fatigue): clinically relevant disease value, IES-R (trauma): indication of post-traumatic stress disorder. Between October 2021 and September 2022, unremarkable laboratory parameters (blood count, liver and kidney function, CRP, haematogram) were repeatedly determined by laboratory chemistry. In May 2022 there were no indications of an acute viral genesis (IgM for CMV, VZV, TBE, Coxsackie, measles, enterovirus, herpes simplex 1+2, mumps each negative). In July 2022 BSR of 24 mm/h (norm less than 12), therefore clarification of endocarditis lenta still in planning. They did not have any other relevant information about the case. Judgement: According to the drug information from Spikevax, fatigue (less than 10%) could occur very frequently under Elasomeran. It was described that fatigue was one of the adverse drug reactions (ADRs), which were usually only mild to moderate and subside again after a short time. Rash was common (1 to 10%), dizziness was uncommon (0.1 to 1%) and hypoesthesia and paraesthesia were rare (0.01 to 0.1%). Facial swelling was listed as a rare ADR (0.01 to 0.1%), explaining that two serious adverse events in the form of facial swelling were reported in vaccine recipients who had a history of dermatological filler injections. The onset of swelling was reported to had been reported on day 1 and day 3 post-vaccination. Swelling/edema/burning of the limbs, apart from swelling in the area of the injection site, were not mentioned as ADRs. The occurrence of angioedema, concentration or memory disorders as well as balance or gait disorders were also not explicitly listed as adverse drug reactions in the drug information. Persistent symptoms or chronic fatigue syndrome were also not explicitly documented as ADRs. Since 2021, out of a total of 869,278 individual case safety reports on elasomeran, the WHO pharmacovigilance database had included 146,850 cases of fatigue (PT), 241 cases of chronic fatigue syndrome (PT), 222 cases of chronic fatigue (LLT), 62,862 cases of dizziness (PT), 22,046 cases of paraesthesia (PT), 83 cases of burning legs/burning sensation lower legs (LLT), 39,327 cases of Rash (PT), 90 cases of Facial rash (LLT), 1,925 cases of Angioedema (PT), 770 cases of Cognitive disorder (PT), 1,954 cases of Memory impairment (PT), 938 cases of Concentration impairment/impaired (LLT), and 3,446 cases of Balance disorder (PT). According to the safety report of the Regulatory Agency (reporting period December 27th, 2020 to June 30th, 2022) of September 7th, 2022, in view of the spontaneous reports, no signal for ongoing symptoms associated with fatigue after COVID19 vaccination could be detected in the international context either became. According to the drug information from Fluarix Tetra, the influenza virus vaccine could very frequently (more than 10%) lead to exhaustion, occasionally (0.1 to 1%) to skin rash and dizziness and rarely (0.01 to 0.1%) to erythema and angioedema. Paraesthesia, swelling (except at the injection site)/ edema/ burning sensation in the limbs, impaired concentration or memory, and impaired balance or gait were not mentioned as ADRs. Persistent symptoms or chronic fatigue syndrome were not explicitly documented as ADRs for Fluarix Tetra either. In the WHO pharmacovigilance database since 2013, out of a total of 13,481 individual case safety reports on Fluarix Tetra, 710 cases of fatigue (PT), 0 cases of chronic fatigue syndrome (PT), 2 cases of chronic fatigue (LLT), 802 cases of Dizziness (PT), 442 cases of Paraesthesia (PT), 0 cases of burning legs/burning sensation lower legs (LLT), 785 cases of Rash (PT), 0 cases of Facial rash (LLT), 41 cases of Angioedema (PT), 10 cases of Cognitive disorder (PT), 19 cases of Memory impairment (PT), 0 cases of Concentration impairment /impaired (LLT), and 57 cases of Balance disorder (PT). Influenza A (H1N1) infection was associated with a more than two-fold increased risk of chronic fatigue syndrome (CSF)/myalgic encephalomyelitis (ME) in a national Norwegian cohort study, while no evidence of an increased risk of CFS/ME after Vaccination with individual vaccines (Pandemrix and Celvapan) could be detected. In more than two thirds of those affected by ME/CFS, a temporal relationship between the onset of symptoms and an infectious disease could be identified. Fatigue and exercise intolerance were cardinal symptoms of ME/CF and the diagnosis of ME/CFS was considered when there was new onset, otherwise unexplained, pervasive fatigue that persists for at least 6 months. The complex and variable symptomatology of ME/CFS also includes, among other things: neurocognitive complaints (concentration and memory disorders, word-finding and articulation disorders, slurred speech), headache and/or muscle or joint pain and signs of autonomic dysfunction or a Orthostatic intolerance with the symptoms of tachycardia, dizziness, drowsiness, shortness of breath on light exertion, intermittently cold extremities with reduced perfusion of the acral muscles and generalized edema formation (bloated face, tense calves, difficult clenching of the fist). There was a temporal connection between the symptoms and the immunizations with Spikevax and Fluarix tetra. However, if the complaints persist at the time of reporting, the abatement of the symptoms could not be evaluated in the sense of a positive dechallenge. In principle, there was also a temporal connection to the onset of the symptoms with the use of Bilol (bisoprolol), perindopril-amlodipine-Mepha, Eliquis (apixaban) and in particular with Neo-Mercazole (carbimazole) and Jodetten Henning (potassium iodide). In the case of therapy that had been in place for more than 2 years (Bilol, Perindopril-Amlodipin-Mepha, Eliquis) or in the case of negative dechallenge (Neo-Mercazole, Jodetten), they consider a causal connection with these drugs to be etiologically less likely. In summary, they assess the causality between the Use of Spikevax and Fluarix Tetra and the symptoms: swelling and redness of the skin on the face and both forearms, burning and tingling paresthesias in both legs and feet, dizziness and balance disorders, fatigue and exercise intolerance, cognitive deficits and concentration disorders according to WHO/CIOMS criteria formal as a whole and individually as possible. In particular, the infection that occurred shortly before the vaccinations comes into question as a differential diagnostic cause of the symptoms; the dizziness, the unsteady gait and the paraesthesia could also be explained by the ischaemia in the cerebellum and in the area of the pons. WHO causal assessment was reported as possible in association to dizziness aggravated, face edema, paraesthesia lower limb, chronic fatigue syndrome, cognitive impairment, balance disorder, erythema oedema peripheral and vertigo positional for Fluarix Tetra 2021-2022 season and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device and SPIKEVAX. The reporter considered the dizziness aggravated, face edema, paraesthesia lower limb, chronic fatigue syndrome, cognitive impairment, balance disorder, erythema, oedema peripheral and vertigo positional to be possibly related to SPIKEVAX. Additional Supportive Information: The concomitant vaccine was reported as COVID-19 VACCINE MODERNA however, from reported dates both the doses were captured as historical vaccines. From narrative information considering possible diagnosis vertigo positional was captured as an event. More clear information expected upon follow up.


VAERS ID: 2518400 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-10-14
Onset: 2022-10-31
   Days after vaccination: 17
Submitted: 0000-00-00
Entered: 2022-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA UNK / 4 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Diarrhoea, Dizziness, Nasopharyngitis, Palpitations, Postmenopausal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CHGSKCH2022173738

Write-up: Diarrhoea; racing heart; Serious cold, runny nose and cough; spotting; 1. Dizziness; This case was reported by a consumer via regulatory authority and described the occurrence of postmenopausal spotting in a 76-year-old female patient who received Flu Seasonal QIV Dresden (Fluarix Tetra 2022-2023 season) for prophylaxis. Co-suspect products included ELASOMERAN (SPIKEVAX) for prophylaxis. On 14th October 2022, the patient received Fluarix Tetra 2022-2023 season (unknown) and the 4th dose of SPIKEVAX (unknown). On 31st October 2022, 17 days after receiving Fluarix Tetra 2022-2023 season, the patient experienced postmenopausal spotting (serious criteria disability, GSK medically significant and other: serious as per reporter), light headedness (serious criteria disability and other: serious as per reporter), heart racing (serious criteria disability and other: serious as per reporter) and cold symptoms (serious criteria disability and other: serious as per reporter). On 16th November 2022, the patient experienced diarrhoea (serious criteria disability and other: serious as per reporter). On an unknown date, the outcome of the postmenopausal spotting, light headedness, diarrhoea, heart racing and cold symptoms were not recovered/not resolved. The reporter considered the postmenopausal spotting, light headedness, diarrhoea, heart racing and cold symptoms to be possibly related to Fluarix Tetra 2022-2023 season. Additional Information: Receipt Date: 22-NOV-2022 Reporter''s Comments: This spontaneous report was received from a Consumer or other non health professional. This report was serious - disabling. The patient''s medical history and concurrent conditions were not reported. The patient received COVID-19 Vaccine Moderna (Spikevax) 4th vaccination, unknown dosage. The patient received Fluarix tetra (Influenza vaccine inact split virion 4v), unknown dosage. No concomitant medications were reported. As per event verbatim, the patient had dizziness, tachycardia, severe cold, cold and cough and spotting. The time to onset for the events postmenopausal spotting, light headedness, heart racing and cold symptoms was 17 days with SPIKEVAX. The time to onset for the event diarrhoea was 33 days with Fluarix Tetra 2022-2023 season and SPIKEVAX. It was unknown if the reporter considered the postmenopausal spotting, light headedness, diarrhoea, heart racing and cold symptoms to be related to SPIKEVAX. scale causal assessment was reported as possible in association to postmenopausal spotting, light headedness, diarrhoea, heart racing and cold symptoms with Fluarix Tetra 2022-2023 season and SPIKEVAX. Due to the temporal relationship, causality was considered possible. The reactions heart racing, cold symptoms and postmenopausal spotting are not listed in the product information for Spikevax and the labeling was not considered adequate. In addition, according to the prescribing information for Fluarix tetra, the reactions heart racing and postmenopausal spotting are not labeled and the labeling was also considered inadequate. Additional supportive information: The date of birth of the patient was captured from the reporters comment. In dosage text of SPIKEVAX it was reported as 2 dose. However, no information had been pulled as it was not clear if it was dose number.


VAERS ID: 2723090 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2023-10-18
Onset: 2023-10-19
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH8656 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA754AE / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Leukocytosis, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2723761 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2023-11-29
Onset: 2023-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HJ3093 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA786AB / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Circumoral oedema, Eye irritation, Sneezing
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Corneal disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Naproxen; GINKGO BILOBA LEAF; METFORMINA GENERIS
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2514335 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2022-10-18
Onset: 2022-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ4535 / 4 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Dyspnoea, Ear, nose and throat examination, Interchange of vaccine products, Myalgia, Product use issue, Rash erythematous, Rash pruritic, Saliva altered, Tongue discomfort
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: ADIRO; OMEPRAZOL; ATACAND PLUS; CYMBALTA; EFENSOL; DIAZEPAM
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2724754 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2022-09-16
Onset: 2022-09-26
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2023-12-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 1 RL / -
DTAPIPVHIB: DTAP + IPV + HIB (UNKNOWN) / UNKNOWN MANUFACTURER X9HS4 / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4RK3C / 1 LL / -
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH FJ4070 / 3 LL / -
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. W002561 / 3 MO / PO

Administered by: Unknown       Purchased by: ?
Symptoms: Cardiac disorder, Death, Pulse absent, Shock
SMQs:, Anaphylactic reaction (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Hypovolaemic shock conditions (narrow), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypoglycaemic and neurogenic shock conditions (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2022-09-26
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: FAMOTIDINE; Omeprazole
Current Illness: Otitis media
Preexisting Conditions: Medical History/Concurrent Conditions: Gastroesophageal reflux; Comments: No Allergies
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAGSKCA2023AMR174988

Write-up: Death; Shock associated circulatory; Pulseless in crib/ Pulse absent; Cardiac condition; This serious case was reported by a consumer via market research programs and described the occurrence of unknown cause of death in a 6-month-old male patient who received Flu Seasonal QIV Quebec (FluLaval Tetra 2022-2023 season) (batch number 4RK3C) for prophylaxis. Co-suspect products included DTPa-IPV+Hib (DTPa-IPV-HIB) (batch number X9HS4) for prophylaxis, Tozinameran (Pfizer BioNTech COVID-19 vaccine) (batch number FT9142) for prophylaxis, PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) (batch number FJ4070) for prophylaxis and ROTAVIRUS VACCINE LIVE REASSORT ORAL 5V (ROTATEQ) (batch number W002561) for prophylaxis. The patient''s past medical history included gastroesophageal reflux. Concurrent medical conditions included otitis media. Additional patient notes included No Allergies. Concomitant products included famotidine and omeprazole sodium (Omeprazole). On 16-SEP-2022, the patient received the 1st dose of FluLaval Tetra 2022-2023 season (left thigh), the 1st dose of DTPa-IPV-HIB (intramuscular, right thigh), the 1st dose of Pfizer BioNTech COVID-19 vaccine (right thigh), the 3rd dose of PREVNAR 13 (left thigh) and the 3rd dose of ROTATEQ (oral). On 26-SEP-2022, 10 days after receiving FluLaval Tetra 2022-2023 season and DTPa-IPV-HIB, the patient experienced unknown cause of death (Verbatim: Death) (serious criteria death and GSK medically significant), shock circulatory (Verbatim: Shock associated circulatory) (serious criteria GSK medically significant), pulse absent (Verbatim: Pulseless in crib/ Pulse absent) and heart disorder (Verbatim: Cardiac condition). The outcome of the shock circulatory, pulse absent and heart disorder were not reported. The patient died on 26-SEP-2022. The reported cause of death was unknown. The reporter considered the unknown cause of death, shock circulatory, pulse absent and heart disorder to be possibly related to FluLaval Tetra 2022-2023 season, Influenza Vaccine Quadrivalent Pre-Filled Syringe Device and DTPa-IPV-HIB. The company considered the unknown cause of death, shock circulatory, pulse absent and heart disorder to be possibly related to FluLaval Tetra 2022-2023 season, Influenza Vaccine Quadrivalent Pre-Filled Syringe Device and DTPa-IPV-HIB. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt date: 13-DEC-2023 It was reported that 6 month old boy had childhood vaccines. It was reported that unexpected death took place of patient while taking a nap in the afternoon and was found pulseless in crib. The standardize medra query reported was shock associated circulatory or cardiac conditions (excluding torsade de pointes).; Reported Cause(s) of Death: Unknown cause of death


VAERS ID: 2717167 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2023-10-16
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-11-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA MD20026A / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8130BA / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Arthralgia, Asthenia, Diplopia, Dizziness, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Ocular motility disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: IBUMETIN; CLOPIDOGREL [CLOPIDOGREL BISULFATE]; PARACETAMOL; BISOPROLOL; LERCANIDIPINE HYDROCHLORIDE; ATORVASTATIN
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2560506 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2018-01-22
Onset: 2022-08-10
   Days after vaccination: 1661
Submitted: 0000-00-00
Entered: 2023-01-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / 5 - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UNK / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Diverticulitis, Dysphonia, Erythema, Fall, Gastrointestinal infection, Headache, Inappropriate schedule of product administration, Kidney infection, Loss of consciousness, Oropharyngeal pain, Pain in extremity, Peripheral swelling, Pneumonia, Product dose omission issue, Pyrexia
SMQs:, Torsade de pointes/QT prolongation (broad), Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific inflammation (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: SYMBICORT; SALBUTAMOL; SEEBRI; METOPROLOL; COMBIVENT; Mepolizumab
Current Illness: Chronic obstructive pulmonary disease
Preexisting Conditions: Medical History/Concurrent Conditions: Stent placement; Comments: Patient history: Comorbidities
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAGSKCA2022AMR133664

Write-up: Infection of the lungs; Infection of the kidneys; Infection of the intestines; Diverticulitis; pain, redness and swelling in his arm; redness in his arm; swelling in his arm; voice is hoarse; severe sore throat; fell,Patient fell down; loss of consciousness; Headache for a few hours; Injection outside the 7-day treatment window; Missed dose; arm. He says having had a fever,he had a fever; This case was reported by a nurse via patient support programs and described the occurrence of lung infection in a 73-year-old male patient who received mepolizumab solution for injection in pre-filled pen (batch number 7U4F, expiry date February 2025) for eosinophilic asthma. Co-suspect products included mepolizumab autoinjector device administration system (batch number 7U4F, expiry date February 2025) for eosinophilic asthma, mepolizumab solution for injection in pre-filled pen (batch number A75M, expiry date March 2025) for eosinophilic asthma, mepolizumab autoinjector device administration system (batch number A75M, expiry date March 2025) for eosinophilic asthma, mepolizumab solution for injection in pre-filled pen (batch number EC7Y, expiry date 28th February 2025) for eosinophilic asthma, mepolizumab autoinjector device administration system (batch number EC7Y, expiry date 28th February 2025) for eosinophilic asthma, Flu Seasonal QIV Quebec (influenza vaccine Quadrivalent 2022-2023 season) for prophylaxis and COVID-19 VACCINE (COVID 19 VACCINE) for prophylaxis. The subject''s past medical history included stent placement. Concurrent medical conditions included chronic obstructive pulmonary disease. Additional subject notes included Patient history: Comorbidities. Concomitant products included budesonide + formoterol fumarate (Symbicort), salbutamol, glycopyrronium bromide (Seebri), metoprolol and ipratropium bromide + salbutamol sulfate (Combivent). On 22nd January 2018, the patient started mepolizumab (subcutaneous) 100 mg (see dose text), mepolizumab autoinjector device, mepolizumab (subcutaneous) 100 mg (see dose text), mepolizumab autoinjector device, mepolizumab (subcutaneous) 100 mg (see dose text) and mepolizumab autoinjector device. On 7th November 2022, the patient received influenza vaccine Quadrivalent 2022-2023 season. On 2nd December 2022, the patient received the 5th dose of COVID 19 VACCINE. On 10th August 2022, 1661 days after starting mepolizumab, mepolizumab autoinjector device, mepolizumab, mepolizumab autoinjector device, mepolizumab and mepolizumab autoinjector device and not applicable after receiving influenza vaccine Quadrivalent 2022-2023 season, the patient experienced missed dose. On 14th September 2022, the patient experienced drug dose administration interval too long. On 8th November 2022, the patient experienced headache. On 3rd January 2023, the patient experienced loss of consciousness (serious criteria GSK medically significant), sore throat and fall. On 4th January 2023, the patient experienced hoarse voice. On an unknown date, the patient experienced lung infection (serious criteria hospitalization and GSK medically significant), kidney infection (serious criteria hospitalization and GSK medically significant), ill-defined intestinal infections (serious criteria hospitalization and GSK medically significant), diverticulitis (serious criteria hospitalization and GSK medically significant), pain in arm, erythema of extremities, swelling arm and fever. The subject was treated with azithromycin. Mepolizumab was continued with no change. Mepolizumab was continued with no change. Mepolizumab was continued with no change. On 8th November 2022, the outcome of the headache was recovered/resolved. On an unknown date, the outcome of the missed dose, drug dose administration interval too long, loss of consciousness, sore throat, fall, hoarse voice, lung infection, kidney infection, ill-defined intestinal infections, diverticulitis, pain in arm, erythema of extremities, swelling arm and fever were unknown. It was unknown if the reporter considered the lung infection, kidney infection, ill-defined intestinal infections, diverticulitis, loss of consciousness, headache, pain in arm, erythema of extremities, swelling arm, fever, hoarse voice, sore throat and fall to be related to mepolizumab, mepolizumab autoinjector device, mepolizumab, mepolizumab autoinjector device, mepolizumab and mepolizumab autoinjector device. It was unknown if the reporter considered the loss of consciousness, headache, pain in arm, erythema of extremities, swelling arm, fever, hoarse voice, sore throat and fall to be related to influenza vaccine Quadrivalent 2022-2023 season. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Linked case(s) involving the same patient: CA2018GSK009324, CA2018GSK112298, CA2018GSK168403, CA2018GSK232416, CA2019AMR178826, CA2019GSK089243, CA2020AMR125587, CA2020AMR255608, CA2021AMR139166, CA2021AMR177020, CA2022166158, CA2022AMR068571, CA2022AMR081188 Additional Information: GSK Receipt: 14 Sep 2022, 16 Sep 2022 Reporter comments: Patient was taking antibiotics since your last infusion/injection. A query was sent to the Nurse for further information. Patient was hospitalized for about 2 weeks for infection of the lungs, kidneys and intestines. Patient does not know exactly, also talks about diverticulitis. Patient missed the scheduled dose of injection on 10-Aug-2022. Patient''s current injection on 14- Sep-2022 falls outside the 7-day treatment window. Last dose of Nucala was administered on 13-Jul- 2022. No further information provided. As per email received, form the RN, Patient had been taking azithromycin 3x/week regularly for years. No further information provided. Follow-up information received on 12-Oct-2022. Reporter''s Comments: Case was received via, Patient Support Program. On questioning, Are you taking or have you taken antibiotics since your last infusion/injection, response was Yes. Patient had been taking azithromycin 3 times per week regularly for years. Questioned, Did the patient report an adverse event, was marked as a Yes. Query was sent to the registered nurse RN for further information. No further information provided. The drug mepolizumab used y patient was Nucala with frequency every 4 weeks. Summary of Changes: Product details updated. Follow-up information received on 9-Nov-2022. Reporter''s Comments: Case was received via PSP201500007, Nucala Patient Support Program. Post injection Report: Flu vaccine received on 07 Nov 2022, he had a headache for a few hours, yesterday (1 day after vaccination). Visit to his MD this morning. Stable condition. Combivent since summer 2017. No further information Summary of changes: Historical condition, suspect and concomitant, event and narrative were updated. Follow up information was received on 9 Dec 2022 Reporters comment-Patient had the 5th dose of COVID-19 on 02/12/2022 and he had pain, redness and swelling in his arm. He says having had a fever for 2 days. No further information provided. It was unknown if the reporter considered the pain in arm, redness, swelling arm and fever to be related to Covid 19 vaccine. Summary of changes-co suspect covid vaccine added, event added. Follow-up information received on 04 Jan 2023. Reporter''s Comments: As per the email received, patient called this morning (04 Jan 2023) to tell that he had a fever last night and that his voice was hoarse this morning. He wanted to postpone his appointment until next week. Nurse would call him back on Sunday to check when he wants the visit for his Nucala injection. No further information provided. On 03 Jan 2023, patient experience Fever. It was unknown if the reporter considered the hoarse voice to be related to Covid 19 vaccine. Time to onset of headache was 1 day and hoarse voice, 58 days with Flu vaccine. Time to onset of pain in arm, redness, swelling arm and fever was less than 2 months with Flu vaccine. Time to onset of pain in arm, redness, swelling arm and fever was unknown and time to onset of hoarse voice was 33 days with Covid 19 vaccine. Summary of changes: Event added hoarse voice and narrative were updated. Follow-up information received on 09 Jan 2023 Reporter''s Comments: Patient said he had a fever and severe sore throat on the night of 03 Jan 2023 and when agent called him to confirm the appointment on 04 Jan 2023 he refused the visit. He fell as a loss of consciousness in the evening of 03 Jan 2023. The paramedics picked him up and took his vital signs but he refused to go to the hospital. He was doing better on reporting day. It took a few days before the fever stopped. Patient takes Antibiotics continuously (Monday-Wednesday-Friday). No further information provided. Time to onset of loss of consciousness, sore throat and fall was 57 days with Flu vaccine and 32 days with Covid 19 vaccine. It was unknown if the reporter considered the loss of consciousness, sore throat and fall to be related to Covid 19 vaccine. Summary of Changes: Events and suspect drug details updated. Narrative updated.; Sender''s Comments: Pneumonia, kidney infection, Gastrointestinal infection, Diverticulitis and Loss of consciousness are unlisted events which are considered unrelated to GSK study drug Mepolizumab and Mepolizumab autoinjector device. CA-GSK-CA2018GSK009324:Same patient CA-GSK-CA2018GSK112298:Same patient CA-GSK-CA2018GSK168403:Same patient CA-GSK-CA2018GSK232416:Same patient CA-GLAXOSMITHKLINE-CA2019AMR178826:Same patient CA-GLAXOSMITHKLINE-CA2019GSK089243:Same patient CA-GSK-CA2020AMR125587:Same patient CA-GSK-CA2020AMR255608:Same patient CA-GSK-CA2021AMR139166:Same patient CA-GSK-CA2021AMR177020:Same patient CA-GSK-CA2022AMR068571:Same patient CA-GLAXOSMITHKLINE-CA2022AMR081188:Same patient


VAERS ID: 1938229 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-10-01
Onset: 2021-11-01
   Days after vaccination: 31
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG7898 / 3 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ750AA / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Cerebrovascular accident
SMQs:, Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ACETYLSALICYLSYRA; IMPUGAN [FUROSEMIDE]; CLOPIDOGREL; ESOMEPRAZOL ACTAVIS; OLANZAPIN SANDOZ; OLANZAPINE; METOPROLOL SANDOZ [METOPROLOL SUCCINATE]; BETOLVEX [CYANOCOBALAMIN]; ALIMEMAZIN EVOLAN; KALIUMKLORID; SPIRONOLAKTON; AKINETON [BIPERIDE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2512688 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2022-04-27
Onset: 2022-04-27
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Loss of consciousness, Road traffic accident
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUSEQIRUS202207664

Write-up: Transient loss of consciousness; Car accident; This spontaneous case was retrieved on 13-Nov-2022 from Regulatory Authority (RA) (reference number: AU-TGA-0000740034), reported by pharmacist and concerned a 64-year-old, male patient. The patient''s medical history and concomitant medications were not reported. The patient had no reactions to previous vaccines. On 27-Apr-2022, the patient was vaccinated with Afluria Quad (influenza vaccine inact split 4v; route of administration, indication, dose and anatomical location: not reported). The batch number was not reported. On the same date, the patient was vaccinated with non-company co-suspect Spikevax (elasomeran; route of administration, indication, dose and anatomical location: not reported). The batch number was not reported. On the same date, 30 minutes after receiving Afluria Quad and non-company co-suspect Spikevax, while driving, the patient lost consciousness which resulted in a car accident. As reported, he experienced transient loss of consciousness. The patient recovered, had no further episodes and no ongoing issues. The reporter did not provide causality assessment. The Regulatory Authority assessed the events as possibly related to the Afluria Quad vaccine. The event ''transient loss of consciousness'' was considered to be medically significant by a Physician within Seqirus'' Pharmacovigilance and Risk Management Department. Company comment: A 64-year-old, male patient was vaccinated with Afluria Quad. Thirty minutes after vaccination, while driving, the patient lost consciousness which resulted in a car accident. As reported, he experienced transient loss of consciousness. The patient recovered and had no further episodes and no ongoing issues. The patient''s medical history and concomitant medications were not reported. The patient had no reactions to previous vaccines. Information regarding relevant diagnostic findings was not provided. Causal role of the suspect vaccine is assessed as not related for the event car accident, considering that event developed due to loss of consciousness. Causal role of the suspect vaccine is assessed as possibly related for the event loss of consciousness, with the currently available information and plausible temporal relationship.; Sender''s Comments: A 64-year-old, male patient was vaccinated with Afluria Quad. Thirty minutes after vaccination, while driving, the patient lost consciousness which resulted in a car accident. As reported, he experienced transient loss of consciousness. The patient recovered and had no further episodes and no ongoing issues. The patient''s medical history and concomitant medications were not reported. The patient had no reactions to previous vaccines. Information regarding relevant diagnostic findings was not provided. Causal role of the suspect vaccine is assessed as not related for the event car accident, considering that event developed due to loss of consciousness. Causal role of the suspect vaccine is assessed as possibly related for the event loss of consciousness, with the currently available information and plausible temporal relationship.


VAERS ID: 2710119 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-10-24
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2023-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HD9871 / 1 - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 1134847 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Blood pressure measurement, Body temperature, Condition aggravated, Dementia Alzheimer's type, Heart rate, Oxygen saturation, SARS-CoV-2 test
SMQs:, Dementia (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2023-10-25
   Days after onset: 24
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2707521 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2023-06-27
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-10-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Cardiac flutter, Chest pain
SMQs:, Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Tachyarrhythmia terms, nonspecific (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300342398

Write-up: Cardiac flutter; Chest pain; This is a spontaneous report received from a contactable reporter(s) (Physician) from Regulatory Authority. Regulatory number: NZ-Medsafe-152454 (Medsafe). A 31-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 27Jun2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 27Jun2023 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for COVID-19 immunisation. The following information was reported: CARDIAC FLUTTER (medically significant), outcome "recovering"; CHEST PAIN (non-serious), outcome "recovering". Additional Information: case was assessed non-serious by Regulatory Authority. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2560507 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2023-01-08
Onset: 2023-01-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-01-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GK0926 / 4 LA / OT
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 395K7 / 1 RA / -

Administered by: Other       Purchased by: ?
Symptoms: Asthenia, Feeling hot, Loss of consciousness, Nausea, Off label use, Pallor, Product use issue, Seizure, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Medication errors (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAPFIZER INC202300014579

Write-up: pale; weak; her body was hot; nauseated; vomited; Convulsions and lost conscious for 10-15 seconds; Convulsions and lost conscious for 10-15 seconds; vaccine received same date: FLULAVAL TETRA; vaccine received same date: FLULAVAL TETRA; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 16-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Jan2023 at 16:00 as dose 4 (booster), single (Lot number: GK0926) at the age of 16 years intramuscular, in left arm for covid-19 immunisation; influenza vaccine inact split 4v (FLULAVAL TETRA), on 08Jan2023 as dose 1, single (Lot number: 395K7), in right deltoid for influenza immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, single), for COVID-19 immunization; Covid-19 vaccine (Dose 2, single), for COVID-19 immunization; Covid-19 vaccine (Dose 3 (Booster), single), for COVID-19 Immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 08Jan2023, outcome "unknown" and all described as "vaccine received same date: FLULAVAL TETRA"; SEIZURE (medically significant), LOSS OF CONSCIOUSNESS (medically significant) all with onset 08Jan2023 at 16:00, outcome "recovered" (2023) and all described as "Convulsions and lost conscious for 10-15 seconds"; PALLOR (non-serious), outcome "unknown", described as "pale"; ASTHENIA (non-serious), outcome "unknown", described as "weak"; FEELING HOT (non-serious), outcome "unknown", described as "her body was hot"; NAUSEA (non-serious), outcome "unknown", described as "nauseated"; VOMITING (non-serious), outcome "unknown", described as "vomited". The events "convulsions and lost conscious for 10-15 seconds", "pale", "weak", "her body was hot", "nauseated" and "vomited" required emergency room visit. It was unknown if therapeutic measures were taken as a result of seizure, loss of consciousness. Clinical course: Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. The patient not received any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination was Not applicable. Prior to vaccination, was the patient was not diagnosed with COVID-19. Reported that, shortly after receiving the 2 vaccines and while in the waiting area she had convulsions and lost conscious for 10-15 seconds then recovered but was pale and weak and complained her body was hot . she got nauseated and vomited. The adverse event resulted in Emergency room/department or urgent care. Since the vaccination, has the patient been tested for COVID-19 was Unknown.; Sender''s Comments: Based on the available information in the case, the causal association between the events OFF LABEL USE, PRODUCT USE ISSUE, SEIZURE, LOSS OF CONSCIOUSNESS, PALLOR, FEELING HOT, NAUSEA, VOMITING and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 2729060 (history)  
Form: Version 2.0  
Age: 87.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2023-11-20
Onset: 2023-11-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 0000048 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS ASLBA764AE / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Dizziness, Electroencephalogram, Fall, Fatigue, Incorrect route of product administration, Investigation, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug abuse and dependence (broad), Accidents and injuries (narrow), Vestibular disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 15 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Acute pyelonephritis (Since April 2020); Chronic kidney disease; Disease Parkinson''s; Hypertension; Pyelonephritis (since 2004); Renal agenesis; Spinal claudication; Unilateral renal agenesis (right)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: EEG in the appendix; Result Unstructured Data: (Test Result:Not reported,Unit:unknown,Normal Low:,Normal High:); Test Name: Test; Result Unstructured Data: (Test Result:Not reported,Unit:unknown,Normal Low:,Normal High:); Comments: See screenshot of laboratory; Comments: LabComments: Test : See screenshot of laboratory
CDC Split Type: CHGSKCH2023180059

Write-up: General physical decline and reduced alertness after the covid/flu vaccinations; Dizziness; Tiredness; Fever; Intramuscular formulation administered by other route; This serious case was reported by a pharmacist via regulatory authority and described the occurrence of fall in a 87-year-old male patient who received Flu Seasonal QIV Dresden (Fluarix Tetra 2023-2024 season) (batch number ASLBA764AE) for prophylaxis. Co-suspect products included ELASOMERAN (SPIKEVAX) (batch number 0000048) for prophylaxis. Concurrent medical conditions included disease parkinson''s, spinal claudication, hypertension, renal agenesis, acute pyelonephritis (Since April 2020), unilateral renal agenesis (right), chronic kidney disease and pyelonephritis (since 2004). On 20-NOV-2023, the patient received Fluarix Tetra 2023-2024 season (intraarticular) 60 ?g and SPIKEVAX (intramuscular) .5 ml. On 20-NOV-2023, less than a day after receiving Fluarix Tetra 2023-2024 season, the patient experienced fever (Verbatim: Fever) (serious criteria hospitalization and other: Serious as per reporter) and intramuscular formulation administered by other route (Verbatim: Intramuscular formulation administered by other route). On 21-NOV-2023, the patient experienced fall (Verbatim: General physical decline and reduced alertness after the covid/flu vaccinations) (serious criteria hospitalization and other: Serious as per reporter), dizziness (Verbatim: Dizziness) (serious criteria hospitalization and other: Serious as per reporter) and tiredness (Verbatim: Tiredness) (serious criteria hospitalization and other: Serious as per reporter). On 23-NOV-2023, the outcome of the fever was resolved (duration 3 days). On 05-DEC-2023, the outcome of the fall was resolved (duration 15 days). The outcome of the dizziness, tiredness and intramuscular formulation administered by other route were unknown. The reporter considered the fall, dizziness, tiredness and fever to be possibly related to Fluarix Tetra 2023-2024 season and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device. The company considered the fall, dizziness, tiredness and fever to be possibly related to Fluarix Tetra 2023-2024 season and Influenza Vaccine Quadrivalent Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 26-DEC-2023. The suspect was reported as Spikevax monovalent Omicron XBB.1.5. On 20-NOV-2023, unknown time after receiving Fluarix Tetra 2023-2024 season, the patient experienced intramuscular formulation administered by other route. On 21-NOV-2023, 1 day after reciving Fluarix Tetra 2023-2024 season and Spikevax monovalent Omicron XBB.1.5 the patient experienced fall, dizziness and tiredness. On 20-NOV-2023, less than a day after receiving Spikevax monovalent Omicron XBB.1.5, the patient experienced fever. From 2023 till 2023 for 15 days the patient was hospitalized for the event fall, dizziness, tiredness and fever. The reporter considered the fall, dizziness, tiredness and fever to be possibly related to Spikevax monovalent Omicron XBB.1.5. This spontaneous report was received from a pharmacist and concerns an 87 year old male polimorbid patient who suffered from Parkinson''s disease, hypertension, chronic kidney disease, spinal claudication, pyelonephritis (2004) and renal agenesis. In the report recieved it was informed that the patient took an antihypertensive medication at home, although the name of the medication was not given. There was also no information regarding the patient''s blood pressure upon the paramedic''s arrival. This patient recieved the Spikevax vaccine along with Flaurix Tetra. On the day of the vaccination the patient experienced fever as a symptom although this was not medically confirmed. On the day after the vaccination the patient referred to the onset of dizziness and tiredness, after which he fell, leading to the hospital admission. For this reason the case had been deemed as medically serious since it led to a hospital admission which lasted 15 days. Emergency assignment by paramedic. The patient reported collapsing in the shower on the morning of reporting. The patient had received flu and Covid vaccinations from his family doctor the day before. He had felt a little weak and had slight dizziness since last night. During the night there was a fever. Showered on the morning of reporting and then lost strength in the shower, the patient wasn''t unconscious and didn''t hit his head. ''Fever'' and ''tiredness'' were both labelled in the Regulatory database as adverse events for both Spikevax and Fluarix and thus these adverse reactions could had been assessed as ''possibile'' (according to the WHO causality assesment) especially due to the clear temporality between the vaccine and these symptoms. It was not know if the symptoms of dizziness and tiredness had resolved. ''Dizziness'', however, was not labelled for the Spikevax vaccine (albeit present on the UptoDate list of adverse effects for mRNA vaccinations -1) but it was labelled as a rare adverse effect for the Fluarix vaccine. It was important to note that this was a case of a polimorbid patient who took antihypertensive therapy (unknown drug name, referred to ) and it was possible that the patient might had been hypotensive at the time of the fall, although they did not had it. The same goes for the adverse event ''fall'' which was not listed in the Regulatory database as a known adverse event but may have been a result of a combination of the above mentioned symptoms. It is therefore also ''possibile'' according to the WHO causality assessment that all of the above mentioned adverse reaction was caused by the two vaccinations received. It was also important to recall the fact that this patient has multiple risk factors for falls (age, lives alone, blood-pressure lowering medication, ) and whilst it is possible that the vaccine had a possibile impact on the fall, the fall itself was likely multifactorial and it would not be possibile to say which vaccine was most implicated as the cause of the fall. The patient received Fluarix Tetra 2023-2024 season Intraarticular instead of intramuscular route. Hence, intramuscular formulation administered by other route was captured as an additional event.


VAERS ID: 2564361 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2022-12-15
Onset: 2022-12-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-01-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS1414B / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5ES77 / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2022-12-16
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAGSKCA2023AMR006833

Write-up: died; This case was reported by a medical representative and described the occurrence of death in a 2-year-old female patient who received Flu Seasonal QIV Quebec (FluLaval Quadrivalent 2022-2023 season) (batch number 5ES77, expiry date unknown) for prophylaxis. Co-suspect products included COVID-19 VACCINE MODERNA (batch number AS1414B, expiry date unknown) for prophylaxis. On 15th December 2022, the patient received FluLaval Quadrivalent 2022-2023 season and COVID-19 VACCINE MODERNA. On 16th December 2022, 1 days after receiving FluLaval Quadrivalent 2022-2023 season, the patient experienced death (serious criteria death and GSK medically significant). On an unknown date, the outcome of the death was fatal. The patient died on 16th December 2022. The reported cause of death was death. It was unknown if the reporter considered the death to be related to FluLaval Quadrivalent 2022-2023 season. Additional Information: GSK Receipt Date: 16-JAN-2023 Reporter''s Comment: The reporter reported that patient was vaccinated with Flulaval vaccine and was died on 16th December 2022. The flu vaccine was given with covid-19 vaccine from moderna. It was unknown if the reporter considered the death to be related to COVID-19 Vaccine moderna. 1 days after receiving COVID-19 Vaccine moderna, the patient experienced death (serious criteria death and GSK medically significant).; Reported Cause(s) of Death: Death


VAERS ID: 2567913 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2022-04-20
Onset: 2022-04-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-01-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. - / UNK - / -
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cellulitis, Chest pain, Electrocardiogram abnormal, Malaise, Nausea, Pericarditis
SMQs:, Acute pancreatitis (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AU0095075132301AUS008055

Write-up: chest pain; electrocardiogram a; malaise; nausea; pericarditis; cellulitis; Information was obtained from a health professional on a request by The Company from the agency via a (Public Case Detail) concerning a 17-years-old male patient. No information was provided regarding the patient''s concomitant medications. History (Hx): Nil "MPCODECDC2" Client presented to clinic on 20-APR-2022, for covid-19 vaccine tozinameran (COMIRNATY) (Pfizer booster). Also administered childhood adolescence same day 20-APR-2022 (influenza vaccine inact split 4v (VAXIGRIP TETRA), pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23), and hpv rl1 6 11 16 18 31 33 45 52 58 vlp vaccine (yeast) (GARDASIL 9)). 2 days later, presented to clinic for adverse reaction symptoms include; nausea, malaise, chest pain, left deltoid erythema/cellulitis. Electrocardiogram (ECG) revealed pericarditis discussed with cardiology. Client sent to emergency department (ED) and admitted to general medical ward. Diagnosed with Pericarditis and cellulitis (onset date of cellulitis reported as 21-APR-2022 and for the rest of the events reported as 22-APR-2022). Started on intravenous antibiotics (IVABx) initially for cellulitis and stepped down to oral antibiotics (POABx). Started on colchicine and cardiology follow up with echography (ECHO) for pericarditis. The outcome of pericarditis was reported as not resolved (discrepant information, also reported as "stop date: 26-APR-2022"). The outcome of cellulitis was reported as resolving (discrepant information, also reported as "stop date: 27-APR-2022). The outcome of chest pain, nausea, malaise, and electrocardiogram abnormal was unknown. The reporter considered all the events to be possible related to HPV rL1 6 11 16 18 31 33 45 52 58 VLP vaccine (yeast)(GARDASIL 9) and Pneumococcal Vaccine, Polyvalent (23-valent)(PNEUMOVAX23).


VAERS ID: 2746638 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-04-20
Onset: 2021-06-23
   Days after vaccination: 64
Submitted: 0000-00-00
Entered: 2024-02-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NO BATCH NUMBER / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. NO BATCH NUMBER / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Arthritis, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Systemic lupus erythematosus (broad), Hypersensitivity (narrow), Arthritis (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZSEQIRUS202304916

Write-up: Arthritis; Urticaria; This spontaneous case was retrieved on 10-Oct-2023 from The Centre for Adverse Reactions Monitoring (reference number: 141948), reported by a physician, and concerned a 51-year-old, female patient. The patient''s medical history and concomitant medications were not reported. On 20-Apr-2021, the patient was vaccinated with a non-company, co-suspect Comirnaty (tozinameran; dose: 0.3 ml; route of administration: intramuscular; anatomical location and indication: not reported). The batch number was not reported. On 01-Jun-2021, the patient was vaccinated with Afluria Quad (influenza vaccine inact split 4v; dose: 0.5 ml, route of administration: intramuscular, anatomical location: not reported) due to a need for immunisation against influenza. The batch number was not reported. On 23-Jun-2021, 22 days after receiving Afluria Quad and two months and three days after receiving a non-company, co-suspect Comirnaty, the patient experienced arthritis and urticaria. On an unspecified date, the patient recovered from the events. The reporter did not provide a causality assessment. Both events were considered as serious due to the seriousness criterion of medical significance. Additional information was received on 05-Feb-2024 from The Centre for Adverse Reactions Monitoring (Medsafe), reported by a physician: Reporter type changed from ''Other healthcare professional'' to ''Physician''. Comirnaty vaccine added as a co-suspect product. Outcome updated from ''Not reported'' to ''Recovered / Resolved''. Medically significant seriousness criterion added for both events. Narrative was amended accordingly. Company comment: A 51-year-old patient was vaccinated with the suspect product Afluria Quad and non-company, co-suspect Comirnaty vaccine. The patient experienced arthritis and urticaria 22 days after receiving the suspect vaccine and two months and three days after receiving a non-company, co-suspect vaccine. The patient''s medical history, concomitant drugs, and diagnostic findings were not provided. Causal role of the suspect vaccine is assessed as not related for both events, due to implausible temporal relationship.; Sender''s Comments: A 51-year-old patient was vaccinated with the suspect product Afluria Quad and non-company, co-suspect Comirnaty vaccine. The patient experienced arthritis and urticaria 22 days after receiving the suspect vaccine and two months and three days after receiving a non-company, co-suspect vaccine. The patient''s medical history, concomitant drugs, and diagnostic findings were not provided. Causal role of the suspect vaccine is assessed as not related for both events, due to implausible temporal relationship.


VAERS ID: 2511024 (history)  
Form: Version 2.0  
Age: 82.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2022-10-18
Onset: 2022-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ2541 / 4 RA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Alanine aminotransferase, Blood albumin, Blood alkaline phosphatase, Blood bilirubin, Blood calcium, Blood cholesterol, Blood creatinine, Blood glucose, Blood lactate dehydrogenase, Blood potassium, Blood pressure measurement, Blood sodium, Blood thyroid stimulating hormone, Blood triglycerides, Blood urea, Blood uric acid, C-reactive protein, Cerebral haemorrhage, Chest X-ray, Electrocardiogram, Gamma-glutamyltransferase, Haematocrit, Haemoglobin, High density lipoprotein, Low density lipoprotein, Lymphocyte count, Neutrophil count, Off label use, Platelet count, Product use issue, Protein total, Red blood cell sedimentation rate, Scan brain, Thyroxine, White blood cell count
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Medication errors (broad)

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 2022-10-25
   Days after onset: 7
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2504687 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2022-10-14
Onset: 2022-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ4535 / 4 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Deafness unilateral, Off label use, Product use issue, Tinnitus
SMQs:, Hearing impairment (narrow), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2501408 (history)  
Form: Version 2.0  
Age: 1.08  
Sex: Male  
Location: Foreign  
Vaccinated: 2022-10-05
Onset: 2022-10-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR9236B / 2 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 424R7 / UNK RL / IM

Administered by: Other       Purchased by: ?
Symptoms: Injection site erythema, Injection site haemorrhage, Syringe issue, Underdose
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Client presented to a local Covid Vaccination site on 10/05/2022 to receive a Moderna COVID infant second dose vaccine Lot# AR9236B on left anterolateral thigh and Fluarix vaccine Lot#424R7 on right anterolateral thigh. At approximately 1258 nurse notified lead PHN that minor moved when injecting Fluarix vaccine and vaccine leaked out. Per vaccinator, about half the dose of Fluarix had been administered. Lead nurse assessed injection site. Redness around client?s injection site and a small drop of blood were observed. Client was crying. Mother expressed concerns that vaccinator did not position herself appropriately to administer Fluarix vaccine. Vaccinator reported she educated mother the need for and importance of proper stabilization of child to avoid injuries prior to vaccine. Interpreter reported she witnessed when vaccinator educated mother on proper stabilization and when incident occurred. Per interpreter, vaccinator properly administered vaccine however vaccine leaked when client moved. Client?s mother was upset of incident and expressed concern of injection site and if another Fluarix dose could be readministered. An ice pack was provided. Mother reported no known allergies, no medical conditions, and no adverse reactions to previous COVID and flu vaccines. Lead nurse communicated with client?s mother that a medical consult would be done via text message and recommended a 30 minute observation time. At 1310 a medical consult was sent via text message to Dr. to report incident and to advise if client needs another dose of Fluarix and if so when. A picture of client?s injection site was also sent via text message to Dr. At 1321 Dr. recommended to administer half a dose of flu vaccine. Client?s mother questioned how sure were we that half dose was given, where the doctor was, and that client?s injection site was red and irritated. At 1328 lead nurse communicated with Dr. via phone call to express mother?s concerns. Dr. communicated with lead nurse that the redness on injection site was expected after incident and that half a dose of flu was safe to administer. Client?s mother did not agree with Dr. recommendation and did not want her child to get poked again. Lead nurse advised mother to follow up with pediatrician, educated on possible side effects after vaccine and when to seek medical care. Mother verbalized understanding. Lead nurse reassessed client?s injection site. Redness had subsided around injection site. Another ice pack was provided to client?s mother. Mother stated she would come back in a month for another flu shot for client. At approximately 1402 mother left vaccination site with client in stroller. At 1427 lead nurse sent a text message to Dr. to communicate that mother denied half the flu vaccine today and would come back in a month for another flu shot. At 1429 Dr. replied with ?Yes full dose if/when she comes back.?


VAERS ID: 2474079 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2022-09-28
Onset: 2022-09-30
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 4 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Hypoaesthesia, Muscular weakness, Neuromuscular pain, Pain, SARS-CoV-2 test
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), COVID-19 (broad), Sexual dysfunction (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2588888 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2022-12-02
Onset: 2022-12-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9434 / 4 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR W3E793V / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Adenovirus test, Blood culture, Blood glucose, Blood test, Bradykinesia, Cognitive disorder, Computerised tomogram abdomen, Computerised tomogram head, Computerised tomogram thorax, Confusional state, Cytomegalovirus test, Electroencephalogram, Enterovirus test, Epstein-Barr virus test, Haemophilus test, Herpes simplex test, Lumbar puncture, Magnetic resonance imaging head, Microscopy, Nasopharyngeal swab, Neisseria test, Off label use, Product use issue, Protein total, Streptococcus test, Viral test
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Medication errors (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2023-02-08
   Days after onset: 68
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2611693 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2023-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA UNK / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Agraphia, Aphasia, Apraxia, Blood test, C-reactive protein, Condition aggravated, Electroencephalogram, Encephalitis autoimmune, Lumbar puncture, Malaise, Pain, Pleocytosis, Protein total, Pyrexia, Red blood cell sedimentation rate, White blood cell count
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (narrow), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2682311 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-08-25
Onset: 2023-08-26
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-09-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Anaphylactic reaction
SMQs:, Anaphylactic reaction (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202300299584

Write-up: Anaphylactic reaction; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority. Regulatory number: 785189. A 73-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 25Aug2023 as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 25Aug2023 as dose number unknown, single (Batch/Lot number: unknown). The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: ANAPHYLACTIC REACTION (medically significant) with onset 26Aug2023, outcome "recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2045201 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-02-23
Onset: 2021-02-24
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK0596 / 3 - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW4109 / 2 - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1741 / 1 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Arthralgia, Arthritis, Blood test, Joint swelling, Magnetic resonance imaging, Pain in extremity, Pain in jaw, Rheumatoid arthritis, Rheumatoid factor, Rheumatoid factor increased, SARS-CoV-2 test, X-ray
SMQs:, Systemic lupus erythematosus (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Osteonecrosis (broad), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2701105 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-05-09
Onset: 2023-05-10
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Axillary pain, Chest pain, Decreased appetite, Diarrhoea, Headache, Hyperhidrosis, Lethargy, Malaise, Migraine with aura, Nausea, Neck pain
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Pseudomembranous colitis (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Arthritis (broad), Noninfectious diarrhoea (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300336005

Write-up: Axillary pain; Chest pain; Hyperhidrosis; Malaise; Nausea; Migraine with aura; Decreased appetite; Diarrhoea; Headache; Lethargy; Neck pain; This is a spontaneous report received from a contactable reporter(s) (Physician) from Regulatory Authority. Regulatory number: NZ-Medsafe-152385 (Medsafe). A 45-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 09May2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 09May2023 (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunisation. The following information was reported: DECREASED APPETITE (medically significant) with onset 10May2023, outcome "recovering"; DIARRHOEA (medically significant) with onset 10May2023, outcome "recovering"; HEADACHE (medically significant) with onset 10May2023, outcome "recovering"; LETHARGY (medically significant) with onset 10May2023, outcome "recovering"; MIGRAINE WITH AURA (medically significant) with onset 10May2023, outcome "recovering"; NECK PAIN (medically significant) with onset 10May2023, outcome "recovering"; NAUSEA (medically significant) with onset 13May2023, outcome "recovering"; AXILLARY PAIN (medically significant), outcome "recovering"; CHEST PAIN (medically significant), outcome "recovering"; HYPERHIDROSIS (medically significant), outcome "recovering"; MALAISE (medically significant), outcome "recovering". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1996663 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-04-27
Onset: 2021-04-29
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET6956 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / -
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Malaise, Systemic lupus erythematosus
SMQs:, Systemic lupus erythematosus (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PLAQUENIL
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2701085 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-04-13
Onset: 2023-04-19
   Days after vaccination: 6
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Fatigue, Goitre, Heart rate increased, Rhinorrhoea, Sinus congestion, Thyroiditis subacute, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Hypothyroidism (broad), Hyperthyroidism (broad), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300335984

Write-up: Goitre; Tremor; Heart rate increased; Fatigue; Sinus congestion; Rhinorrhoea; Thyroiditis subacute; This is a spontaneous report received from a contactable reporter(s) (Nurse) from Regulatory Authority. Regulatory number: NZ-Medsafe-151918. A 44-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 13Apr2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 13Apr2023 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for COVID-19 immunisation. The following information was reported: THYROIDITIS SUBACUTE (medically significant) with onset 19Apr2023, outcome "not recovered"; RHINORRHOEA (medically significant) with onset 16May2023, outcome "not recovered"; SINUS CONGESTION (medically significant) with onset 16May2023, outcome "not recovered"; GOITRE (medically significant), outcome "not recovered"; TREMOR (medically significant), outcome "not recovered"; HEART RATE INCREASED (medically significant), outcome "not recovered"; FATIGUE (medically significant), outcome "not recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1994786 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-10-17
Onset: 2021-10-24
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2021-12-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / 3 - / SYR
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Body temperature, Pneumonia, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2045840 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-11-23
Onset: 2021-11-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3006322 / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS AFLBA632BA / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Back pain, Chest pain, Dyspnoea, Headache, Musculoskeletal pain, Tachycardia, Vertigo
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Retroperitoneal fibrosis (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Vestibular disorders (narrow), Tendinopathies and ligament disorders (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: PANTOPRAZOLE; ALLOPURINOL; DOBETIN; ATORVASTATIN; ADRONAT; OMEGA POLIENOICI; TARDYFER; COMPETACT
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1998803 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-02-15
Onset: 2021-02-16
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / 3 - / -
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER AB0012 / 1 - / IM
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER PN40041 / 2 - / IM
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Biopsy muscle, Blood test, Feeling abnormal, Full blood count, Headache, Interchange of vaccine products, Off label use, Polymyalgia rheumatica, Red blood cell count, Red blood cell sedimentation rate, Rheumatological examination, Ultrasound pelvis, Ultrasound scan, X-ray
SMQs:, Dementia (broad), Vasculitis (narrow), Medication errors (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1991136 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Local reaction
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CASA2021SA430313

Write-up: local reaction; Initial information received on 17-Dec-2021 regarding an unsolicited valid serious case received from a consumer/non-hcp. This case involves a 11 years old male patient who experienced local reaction while receiving vaccine Influenza Usp Trival A-B Vaccine - Unspecified [Fluzone Unsp] and while treated with Tozinameran [Comirnaty]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect Influenza Usp Trival A-B Vaccine - Unspecified (lot number not reported) via unknown route in unknown administration site as prophylactic vacination. On an unknown date, the patient started taking Tozinameran (with an unknown batch number dose, strength, route) for Immunisation. On an unknown date , it was reported patient caregiver wanted to vaccinate her child with Pfizer vaccine for covid , in 2020-2021, with Fluzone he had a local reaction (local reaction)(latency: unknown), the pharmacist thinks of tromethanol or polyethylene glycol sees in the ingredients it is in the Pfizer vaccine ,our opinion to get it. He had a local allergy on his arm for 2 weeks, they does not know exactly what he is allergic to, he has not seen an allergist. This event was assessed as medically significant. Action taken :not applicable It was not reported if the patient received a corrective treatment for the event (local reaction). At time of reporting, the outcome was Unknown for the event local reaction.; Sender''s Comments: Sanofi company comment dated 28-Dec-2021:This case concerns 11 years old male patient who had localised reaction after vaccination with Influenza Usp Trival A-B Vaccine - Unspecified [Fluzone Unsp] and Tozinameran [Comirnaty](not produced by Sanofi Pasteur). The time to onset is not reported with the role of the vaccine. Additional information regarding condition at the time of vaccination, lab data, past medical history excluding other predisposing etiologies would be needed for complete assessment of the case. Based upon the reported information, the role of an individual vaccine cannot be assessed.


VAERS ID: 2032992 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2021-11-16
Onset: 2021-11-17
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-01-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER PW40167 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Asthenia, Blood pressure measurement, Chest pain, Fatigue, Heart rate, Hypotension, Palpitations
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2061184 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-06-10
Onset: 2021-10-07
   Days after vaccination: 119
Submitted: 0000-00-00
Entered: 2022-01-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER UNK / UNK - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Rheumatoid arthritis
SMQs:, Arthritis (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2701092 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-06-08
Onset: 2023-06-15
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Blood pressure increased, Heart rate increased
SMQs:, Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Hypertension (narrow), Cardiomyopathy (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300335991

Write-up: Heart rate increased; Blood pressure increased; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from Regulatory Authority. Regulatory number: NZ-Medsafe-152117 (Medsafe). An 81-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 08Jun2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 08Jun2023 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for COVID-19 immunisation. The following information was reported: BLOOD PRESSURE INCREASED (medically significant) with onset 15Jun2023, outcome "recovering"; HEART RATE INCREASED (medically significant) with onset 15Jun2023, outcome "recovering". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2755171 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 0000-00-00
Onset: 0000-00-00
Submitted: 0000-00-00
Entered: 2024-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Palpitations, Tachycardia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAPFIZER INC202400064841

Write-up: Palpitations; Tachycardia; This is a spontaneous report received from a Pharmacist from Regulatory Authority. Regulatory number: 001071631. A male patient received BNT162b2 (COMIRNATY NOS), as dose number unknown, single (Batch/Lot number: unknown) intramuscular for covid-19 immunisation; influenza vaccine inact split 4v (FLULAVAL TETRA) intramuscular for immunisation. The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: PALPITATIONS (medically significant), outcome "recovered"; TACHYCARDIA (medically significant), outcome "recovered". No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.


VAERS ID: 2701091 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated: 2023-05-17
Onset: 2023-05-24
   Days after vaccination: 7
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Chest pain, Musculoskeletal pain
SMQs:, Rhabdomyolysis/myopathy (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300335990

Write-up: Chest pain; Musculoskeletal pain; This is a spontaneous report received from a contactable reporter(s) (Physician) from Regulatory Authority. Regulatory number: NZ-Medsafe-152428 (Medsafe). A 44-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 17May2023 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 17May2023 as dose number unknown, single (Batch/Lot number: unknown). The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacture), for COVID-19 immunisation. The following information was reported: CHEST PAIN (medically significant) with onset 24May2023, outcome "not recovered"; MUSCULOSKELETAL PAIN (medically significant) with onset 24May2023, outcome "not recovered". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1942962 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-23
Onset: 2021-11-24
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNK / UNK - / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNK / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: C-reactive protein, Pericarditis
SMQs:, Systemic lupus erythematosus (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ENALAPRIL
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 1942963 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2021-11-02
Onset: 2021-11-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3739 / 3 - / -
FLU4: INFLUENZA (SEASONAL) (QIV DRESDEN) / GLAXOSMITHKLINE BIOLOGICALS AFLBAG/13AA / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Body temperature, Ecchymosis, Fall, Hypotension, Loss of consciousness, Pyrexia, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: TACHIPIRINA
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2701116 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Female  
Location: Foreign  
Vaccinated: 2023-06-01
Onset: 2023-06-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Arthralgia, Fatigue, Joint stiffness, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NZPFIZER INC202300336016

Write-up: Myalgia; Fatigue; Arthralgia; Joint stiffness; This is a spontaneous report received from a contactable reporter(s) (Physician) from Regulatory Authority. Regulatory number: NZ-Medsafe-152426 (Medsafe). A 69-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (COMIRNATY), on 01Jun2023 as dose number unknown (booster), single (Batch/Lot number: unknown) at the age of 69 years for covid-19 immunisation; influenza vaccine inact split 4v (AFLURIA QUAD), on 01Jun2023 as dose number unknown, single (Batch/Lot number: unknown). The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacture), for COVID-19 immunisation. The following information was reported: ARTHRALGIA (medically significant) with onset 01Jun2023, outcome "not recovered"; FATIGUE (medically significant) with onset 01Jun2023, outcome "not recovered"; JOINT STIFFNESS (medically significant) with onset 01Jun2023, outcome "not recovered"; MYALGIA (medically significant) with onset 01Jun2023, outcome "unknown". Additional information: Onset: 0min (as reported) was mentioned for events of Myalgia, Fatigue, Arthralgia, Joint stiffness. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1945612 (history)  
Form: Version 2.0  
Age: 94.0  
Sex: Male  
Location: Foreign  
Vaccinated: 2021-11-05
Onset: 2021-11-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH SCWF7 / 3 - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS UNKNOWN / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Immunisation, Lip oedema, Pruritus, Seizure, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Angioedema (narrow), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: APOCARD
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2754405 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated: 2023-10-11
Onset: 2023-10-01
Submitted: 0000-00-00
Entered: 2024-03-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8085BA / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abnormal behaviour, Body temperature, Cerebrovascular accident, Chest X-ray, Cognitive disorder, Computerised tomogram, Computerised tomogram liver, Depressed level of consciousness, Diarrhoea, Diplegia, Disorientation, Gait inability, Hepatic haemorrhage, Liver function test, Oxygen saturation, Pneumonia, Pyrexia, Speech disorder, Vasculitis, Vomiting
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (narrow), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Retroperitoneal fibrosis (broad), Dementia (broad), Pseudomembranous colitis (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Dystonia (broad), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Eosinophilic pneumonia (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Vasculitis (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (narrow), Dehydration (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: ALPRAZOLAM; AMITRIPTYLINE; CITALOPRAM; FLUCONAZOLE; LEFLUNOMIDE; METHOTREXATE; MORPHINE; OMEPRAZOLE; RIVAROXABAN; SUMATRIPTAN; VALACYCLOVIR [VALACICLOVIR]; VOLTAREN [DICLOFENAC]; PREDNISONE
Current Illness: Anxiety; Dementia (mild dementia, forget a name here and there and be a little mixed up, but 80-90% of the time; remember all close family, grandkids and close friends.); Depression; Fungal infection; Gastrooesophageal reflux disease; Memory impairment (little forgetful previously but was able to hold a conversation); Migraine; Rheumatoid arthritis
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20231011; Test Name: Body temperature; Test Result: 38.5 {DF}; Test Date: 20231012; Test Name: Chest X-ray; Result Unstructured Data: saw a shady spot; Test Date: 20231019; Test Name: Computerised tomogram; Result Unstructured Data: likely had a small stroke in hospital; Test Date: 20231023; Test Name: Computerised tomogram; Result Unstructured Data: showed no further strokes.; Test Date: 20231019; Test Name: Computerised tomogram liver; Result Unstructured Data: likely had a small stroke in hospital; Test Date: 20231014; Test Name: Liver function test; Result Unstructured Data: Elevated liver enzymes; Test Date: 202310; Test Name: Liver function test; Result Unstructured Data: high; blood was collecting in liver.; Test Date: 20231019; Test Name: Oxygen saturation; Test Result: 93 %
CDC Split Type: CASA2024SA077362

Write-up: Small stroke; Severe abdominal pain; Fever/ Pneumonia; diarrhoea; Severe internal bleeding/ bleed severely inside liver/Blood was collecting in liver/ damaged liver; Liver Vasculitis; severe decline in cognitive abilities/severely deteriorated cognitive ability; Partial paralysis in legs; Still not communicating well/saying one word that didn''t relate to anything every 3-5min and mumbling was also seeing things that weren''t there, picking fluff off clothes that wasn''t there, etc. didn''t know where was, who family; didn''t know where was, who family was, what name was, what month or even year it was; Throwing up; Ability to walk severely deteriorated/ was a little unsteady on feet but able to walk 100ft with little issues; Not completely non-responsive, but quite non-responsive/ was not getting out of bed; fever; was not able to talk or form words at all; Initial information received on 06-Mar-2024 regarding an unsolicited valid serious case received from other health professional. This case involves an unknown age female patient who experienced small stroke, partial paralysis in legs, severe internal bleeding/ bleed severely inside liver/blood was collecting in liver/ damaged liver, not completely non-responsive, but quite non-responsive/ was not getting out of bed, fever/ pneumonia, severe abdominal pain, severe decline in cognitive abilities/severely deteriorated cognitive ability, liver vasculitis, diarrhoea, was not able to talk or form words at all, ability to walk severely deteriorated/ was a little unsteady on feet but able to walk 100ft with little issues, still not communicating well/saying one word that didn''t relate to anything every 3-5min and mumbling was also seeing things that weren''t there, picking fluff off clothes that wasn''t there, etc. didn''t know where was, who family, didn''t know where was, who family was, what name was, what month or even year it was and throwing up after receiving vaccine Spikevax and Influenza Quadrival A-B High Dose HV vaccine [Fluzone High-Dose Quadrivalent]. The patient''s past medical treatment included Humira with used years ago. The patient''s past medical history, vaccination(s) and family history were not provided. At the time of the event, the patient had ongoing Rheumatoid arthritis on 21-JUL-1977, Memory impairment with little forgetful previously but was able to hold a conversation, Dementia with mild dementia, forget a name here and there and be a little mixed up, but 80-90% of the time; remember all close family, grandkids and close friends., Anxiety, Depression, Fungal infection, Gastrooesophageal reflux disease and Migraine. Concomitant medications included Alprazolam for Anxiety; Amitriptyline for Anxiety and Depression; Citalopram for Anxiety; Fluconazole for Fungal infection; Leflunomide for Rheumatoid arthritis; Methotrexate for Rheumatoid arthritis; Morphine for Rheumatoid arthritis; Omeprazole for Gastrooesophageal reflux disease; Rivaroxaban for Anticoagulant therapy; Sumatriptan for Migraine; Valacyclovir for Fungal infection; diclofenac (Voltaren [diclofenac]) for Rheumatoid arthritis and Myalgia; and Prednisone for Rheumatoid arthritis. On 11-Oct-2023, the patient received 1 DF dose (dose 1) of suspect Influenza Quadrival A-B High Dose HV vaccine of lot U8085BA (strength, formulation and expiry: unknown) via intramuscular route in unknown administration site for immunization. On the same day, the patient also received 1 DF dose of suspect SPIKEVAX not produced by Sanofi Pasteur (strength, formulation, lot number and expiry: not reported) via intramuscular route in unknown administration site as COVID-19 prophylaxis. On 11-Oct-2023, the patient developed not completely non-responsive, but quite non-responsive/ was not getting out of bed (depressed level of consciousness), fever/ pneumonia (pneumonia) (pyrexia), diarrhoea same day following the administration of Influenza Quadrival A-B High dose HV vaccine and SPIKEVAX. On 12-Oct-2023, the patient developed severe abdominal pain (abdominal pain), severe decline in cognitive abilities/severely deteriorated cognitive ability (cognitive disorder), partial paralysis in legs (diplegia), ability to walk severely deteriorated/ was a little unsteady on feet but able to walk 100ft with little issues (gait inability), throwing up (vomiting) 1 day following the administration of Influenza Quadrival A-B High Dose HV vaccine and SPIKEVAX. On 14-Oct-2023, the patient developed still not communicating well/saying one word that didn''t relate to anything every 3-5min and mumbling was also seeing things that weren''t there, picking fluff off clothes that wasn''t there, etc. didn''t know where was, who family (abnormal behaviour), didn''t know where was, who family was, what name was, what month or even year it was (disorientation), severe internal bleeding/ bleed severely inside liver/blood was collecting in liver/ damaged liver (hepatic haemorrhage), liver vasculitis (vasculitis) 3 days following the administration of Influenza Quadrival A-B High Dose HV vaccine and SPIKEVAX. On 19-Oct-2023, the patient developed small stroke (cerebrovascular accident) 8 days following the administration of Influenza Quadrival A-B High Dose HV vaccine and SPIKEVAX. On an unknown date in Oct-2023, the patient was not able to talk or form words at all (speech disorder) (latency: unknown) following the administration of Influenza Quadrival A-B High dose HV vaccine and SPIKEVAX. Relevant laboratory test results included: Body temperature - On 11-Oct-2023: 38.5 Cel Chest X-ray - On 12-Oct-2023: [saw a shady spot] Computerised tomogram - On 19-Oct-2023: [likely had a small stroke in hospital]; on 23-Oct-2023: [showed no further strokes.] Computerised tomogram liver - On 19-Oct-2023: [likely had a small stroke in hospital] Liver function test - On 14-Oct-2023: [Elevated liver enzymes]; in October 2023: [high; blood was collecting in liver.] Oxygen saturation - On 19-Oct-2023: 93 % Action taken was not applicable. The patient was treated with paracetamol (Tylenol) for Pyrexia and Surgery (4 hr surgery to correct damage on one side of liver on 16-Oct-2023) for Hepatic haemorrhage and for Vasculitis. It was unknown if patient received any treatment for rest of the events. At time of reporting, the outcome was Unknown for the event small stroke, diarrhoea, not completely non-responsive, but quite non-responsive/ was not getting out of bed, fever/ pneumonia, ability to walk severely deteriorated/ was a little unsteady on feet but able to walk 100ft with little issues, throwing up, didn''t know where was, who family was, what name was, what month or even year it was, was not able to talk or form words at all; was Not Recovered / Not Resolved for the event partial paralysis in legs, severe internal bleeding/ bleed severely inside liver/blood was collecting in liver/ damaged liver, severe decline in cognitive abilities/severely deteriorated cognitive ability, liver vasculitis; was Recovered / Resolved on an unknown date for the event severe abdominal pain; was Recovering / Resolving for the event still not communicating well/saying one word that didn''t relate to anything every 3-5min and mumbling was also seeing things that weren''t there, picking fluff off clothes that wasn''t there, etc. didn''t know where was, who family; and was Not Recovered / Not Resolved for the event and was Unknown for the event. Seriousness criteria: Medically significant for depressed level of consciousness, pneumonia, pyrexia, diplegia, hepatic haemorrhage, vasculitis and cerebrovascular accident. The patient was hospitalized on the same day the events pneumonia, pyrexia and diarrhoea occurred; the patient was already hospitalized when the events Cognitive disorder, diplegia, hepatic haemorrhage, vasculitis occurred. The patient was discharged on 08-Nov-2023 (hospitalization during 27 days). The patient was also hospitalized for the event cerebrovascular accident and abdominal pain.; Sender''s Comments: Sanofi company comment dated 12-Mar-2024: This case involves an unknown age female patient who experienced small stroke, partial paralysis in legs, severe internal bleeding/ bleed severely inside liver/blood was collecting in liver/ damaged liver, not completely non-responsive, but quite non-responsive/ was not getting out of bed, fever/ pneumonia, severe abdominal pain, severe decline in cognitive abilities/severely deteriorated cognitive ability, liver vasculitis, diarrhoea, was not able to talk or form words at all, ability to walk severely deteriorated/ was a little unsteady on feet but able to walk 100ft with little issues, still not communicating well/saying one word that didn''t relate to anything every 3-5min and mumbling was also seeing things that weren''t there, picking fluff off clothes that wasn''t there, etc. didn''t know where was, who family, didn''t know where was, who family was, what name was, what month or even year it was and throwing up after receiving vaccine Spikevax and Influenza Quadrival A-B High Dose HV vaccine [Fluzone High-Dose Quadrivalent]. At the time of the event, the patient had ongoing Rheumatoid arthritis on 21-JUL-1977, Memory impairment with little forgetful previously but was able to hold a conversation, Dementia with mild dementia, forget a name here and there and be a little mixed up, but 80-90% of the time; remember all close family, grandkids and close friends., Anxiety, Depression, Fungal infection, Gastrooesophageal reflux disease and Migraine. The time to onset was compatible with the role of vaccine. The clinical course of the event was not provided. Furthermore, information regarding role of medical history, lab data excluding other predisposing etiologies would be needed for complete assessment of the case. Based upon the reported information, the role of the suspect vaccine cannot be assessed.


VAERS ID: 2494983 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-09-19
Onset: 2022-09-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP7140 / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ899AA-CP / UNK RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pfizer monovalent booster given to patient.


VAERS ID: 2687683 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-09-26
Onset: 2023-09-01
Submitted: 0000-00-00
Entered: 2023-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Headache, Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Ramipril 15 MG, Toporlol 25 MG, vitamin D, Flintstone multivitamin with iron
Current Illness: Chronic Kidney Disease, Gastrointestinal virus with diarrhea that lasted about 10 days about 3 weeks before vaccine. Covid test was negative.
Preexisting Conditions: Chronic Kidney Disease and high blood pressure controlled with meds
Allergies: NA
Diagnostic Lab Data: Na
CDC Split Type:

Write-up: Severe headaches that Tylenol did not help with the pain. Chills. Arm soreness


VAERS ID: 2687015 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-09-19
Onset: 2023-09-27
   Days after vaccination: 8
Submitted: 0000-00-00
Entered: 2023-09-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK RA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, SARS-CoV-2 test negative
SMQs:, COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Blood Pressure and diabetes medication
Current Illness: None
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data: Covid-19 at home test retuned negative.
CDC Split Type:

Write-up: I am still having chills. I never had this effect and definitely this long. Few times a day. Started taking Ibuprofen since 9/26 (1 pill 3 times a day)


VAERS ID: 1821288 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-10-07
Onset: 2021-10-10
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal pain upper, Amylase, Bowel movement irregularity, Differential white blood cell count, Flank pain, Full blood count, Gastrointestinal hypomotility, Lipase, Nausea, Ultrasound abdomen, Vomiting
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Fexofenadine HCTZ Cymbalta 60mg Mobetric 50mg Vitamin D2 50000 IU Motegrity 2mg Potassium Citrate 10NEQ, Magnesium Oxide 400mg Fiber Choice 4mg Prilosec 40mg Montelukast 10mg
Current Illness: Sinusitis
Preexisting Conditions: Fibromyalgia Gastro Paresis Ovarian Fibroma and Cyst History of Pulmonary Embolism Chronic Gastritis Asthma, GERD Endometriosis Tachycardia Overactive Bladder
Allergies: NSAIDS Amoxicillin Penicillin Bees Wasps Ants Pistachios Fish
Diagnostic Lab Data: CBC differential Lipase and Amylase Test Abdominal Ultrasound
CDC Split Type: vsafe

Write-up: A few days after the vaccine early in the morning hours I woke up with extreme nausea and vomiting up undigested food that had been eaten 12hrs earlier. And my stomach and flank pain begin at that time. Over the next few days, I noticed further slowing of my gastric motility so I reached out to my PCP because I couldn''t get in to see my Gastrologist. I also noticed changes in my vomiting and bowel movements with further pain in the stomach and flank area. My PCP started me on 12.5mg of Promethazine as needed to help try to elevate the symptoms. I take Motergitiy for the motility issues but that may have to be changed. I have been referred to a Specialty clinic for further evaluation.


VAERS ID: 2495002 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-09-11
Onset: 2022-09-01
Submitted: 0000-00-00
Entered: 2022-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GH9694 / UNK AR / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / UNK AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test, Ear pain, Fatigue, Heart rate abnormal, Neck pain, Pain in jaw, Thyroiditis subacute, Ultrasound thyroid, Weight decreased
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Hypothyroidism (broad), Hyperthyroidism (broad), Osteonecrosis (broad), Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Slynd birth control, multi-vitamin, iron supplement, vitamin D
Current Illness: None
Preexisting Conditions: Endometriosis
Allergies: None
Diagnostic Lab Data: General examination, blood tests, specialist (ent and endocrinologist) visits to determine the issue. Ultrasound of thyroid.
CDC Split Type:

Write-up: Subacute thyroiditis beginning after vaccine, and ongoing. Lost 15lbs., pain in neck, jaw, and ear. Fatigue. Have been prescribed a beta blocker for heart rate.


VAERS ID: 1877578 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-11-17
Onset: 2021-11-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 019F21A / 1 LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7377KA / 1 RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Skin warm
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: unknown
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: patient felt warm to touch and requested a cooling pad and coke which was provided. Patient was then lowered to floor by husband and administering rph


VAERS ID: 1904389 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-11-06
Onset: 2021-11-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 071F21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. UNKNOWN / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Chills, Fatigue, Hyperhidrosis, Nausea, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lorazepam 1 mg twice a day Buproprion 300 mg QD loratadine 10mg QD
Current Illness: none
Preexisting Conditions: anxiety and depression
Allergies: none
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Chills approximately after 6 hours, fever after 8 hours gradually increasing through the night to reach 104. Chills, sweats, vomiting lasting all night. Fever went down to 102.5 after 12 hours, subsiding after 24 hours. No medication taken to reduce the fever. Fatigue and nausea lasted 48 hours. It was the first time I had a flu shot combined with another shot, and I think it maybe why I had such a strong reaction. I did not have strong reactions to the 1st and 2nd Covid vaccines (both Moderna), ans I usually do not have a reaction to the flu shot except for a sore arm for a few days.


VAERS ID: 2485176 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2022-10-13
Onset: 2022-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 063B22A / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ919AC / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Monovalent vaccine given as a booster. No known adverse effects reported at this time


VAERS ID: 2486376 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-10-19
Onset: 2022-10-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7680LA / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Conjunctival haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Conjunctival disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Asthma, migraines
Allergies: Demerol and phenergan IV
Diagnostic Lab Data:
CDC Split Type:

Write-up: Conjuntival hemorrhage


VAERS ID: 2709125 (history)  
Form: Version 2.0  
Age: 83.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-11-01
Onset: 2023-11-02
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9299 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8138BA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Burning sensation, Rash pruritic, Swollen tongue
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Peripheral neuropathy (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: PENICILLIN, sULFA
Diagnostic Lab Data:
CDC Split Type:

Write-up: PATIENT REPORTED SWELLING IN THE TONGUE, ITCHING AND BURNING RASH. WAS SEEN AT DOCTORS OFFICE 24 HOURS AFTER VACCINE AND PATIENT REPORTED BEING GIVEN BENADRYL AND EPINEPHRINE.


VAERS ID: 2485560 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-10-13
Onset: 2022-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 063B22A / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7680NA / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: monovalent vaccine given as a booster. no adverse symptoms reported at this time


VAERS ID: 1723082 (history)  
Form: Version 2.0  
Age: 54.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-09-03
Onset: 2021-09-03
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3182 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ685AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: none
Preexisting Conditions: none
Allergies: nka
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt came in to get the flu vaccine. The vaccine was processed incorrectly and the covid vaccine was given instead. The pt wanted to also get the flu vaccine, this covid dose would''ve been the 3rd dose ( 1st dose given on 4/6/21 and second dose was on 5/4/21). Pt didn''t have any adverse reaction when she left the store


VAERS ID: 1982097 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-10-24
Onset: 2021-11-02
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2021-12-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003F21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Acoustic stimulation tests abnormal, Balance disorder, Blood test, Deafness unilateral, Dizziness, Ear, nose and throat examination, Magnetic resonance imaging, Tinnitus
SMQs:, Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Hearing impairment (narrow), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Crestor - 10 mg/da Trimetheine-HCTZ - 37.5-25 mg/da Acetyl Carnitine - 1000 mg/da CoQ 10 - 200 mg/da Centrum Silver - 1/da Menaquinone-7 - 90 ug/da Fish Oil - 1400 mg/da (1000 mg omea-3) Niacin - 1250 mg/da
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Primary care provider - Evaluation/Exam and blood work (11/17/2021). Order for MRI. Referred to ENT. ENT - Exam, hearing test. (11/19/2021) MRI performed 12/19/2021.
CDC Split Type:

Write-up: Hearing Loss (left ear), tinnitus, dizziness, loss of balance.


VAERS ID: 2710137 (history)  
Form: Version 2.0  
Age: 91.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-10-10
Onset: 2023-10-12
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK UN / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 UN / IM
RSV: RSV (ABRYSVO) / PFIZER/WYETH - / 1 UN / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Amnesia, Aphasia, Blood test, Bradykinesia, Cerebrovascular accident, Cognitive disorder, Computerised tomogram abnormal, Dysstasia, Fall, Gait disturbance, Incoherent, Intensive care, Loss of personal independence in daily activities, Magnetic resonance imaging abnormal, Speech disorder, Walking aid user
SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Parkinson-like events (narrow), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 10 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: List not available, Zyrtec, Omeprazole, Hydrochlorothiazide.
Current Illness: None.
Preexisting Conditions: High cholesterole, high blood pressure.
Allergies: Lisinopril (cough), Peanuts.
Diagnostic Lab Data:
CDC Split Type:

Write-up: She had her vaccines, and on the night of the 12th her daughter heard a thump and she found her sitting on the floor in her bedroom basically mumbling and unable to stand. She had fallen. She was mumbling incoherently. Her daughter could not get her up, they called her 911, she went to Hospital ER. In the ER they did a CT scan on her and blood work, and they gave her the medication with their consent for the stroke tPA and subsequently they admitted her to ICU with FU CT''s and MRI''s that demonstrated the stroke, not a hemorrhagic stroke. She was in ICU for 5-6 days, and then she was moved to the stroke floor and she was discharged on 10/22/2023 to home. They did not do in-patient rehab, they are doing rehab at home with home health. She is slowly improving, still has aphasia, she has to have maximum assistance with activities of daily living, toiletering. She can feed herself with medium assistance. She is only walking minimal steps requiring maximum assistance. She has only been up twice since she has been home. She is having fairly slow to move and does not comprehend things very good. She was having some issues prior to the stroke, but knew what she did not remember. She was able to wash dishes, but they did not allow her to cook anymore. She was able to walk up and down 16 stairs to get in her bedroom, she exercised with her walker and was able to walk 15-20 minutes. She was attending to all of her activities of daily living other than not cooking. She has had a major set back since receiving the vaccines as she had the stroke. They saw on the news that there was a link in people receiving the new COVID and the flu vaccine the risk of stroke over 65 years old. They were not informed of that information and if they had known they would have deferred getting those vaccines a the same time. They are not happy that information was not released to the public at the time she had the vaccine. She would have had ample opportunity to ge taken back to get the vaccines at different times. They saw that there was 20-35% increase of strokes, where others were miniscule, but it outweighed people not getting the vaccine that were not optical as she could have been taking back at another time to get the other vaccines.


VAERS ID: 1880290 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-11-13
Onset: 2021-11-16
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 022C21A-B / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ764AA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Peripheral swelling, Pruritus
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 11/16/21 SWELLING AND ITCHING OF LEFT HAND 11/17/21 SWELLING AND ITCHING OF LEFT AND RIGHT HANDS TREATMENT BEGINNING ON 11/17/21 INDOMETHACIN 50MG TID X 7 DAYS HYDROXYZINE HCL 25MG BID PRN X 7 DAYS OUTCOME NOT DETERMINED YET


VAERS ID: 2485236 (history)  
Form: Version 2.0  
Age: 69.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2022-10-13
Onset: 2022-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP 7138 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ925AD / UNK LA / IM

Administered by: Public       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: PT IS A RESIDENT OF NURSING HOME FACILITY
Allergies: NKA
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: NO ADVERSE REACTIONS REPORTED


VAERS ID: 2699152 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-10-13
Onset: 2023-10-14
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Injected limb mobility decreased, Injection site bruising, Musculoskeletal stiffness, Neck pain, Pain in extremity, Peripheral swelling, X-ray normal
SMQs:, Cardiac failure (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Warfarin, Atorvastatin, Losartan, Amlodipine
Current Illness:
Preexisting Conditions: HBP, Sleep Apnea
Allergies: Adhesive Tape
Diagnostic Lab Data: Xray shows nothing
CDC Split Type:

Write-up: I had the flu vaccine in my left arm and the covid vaccine in my right arm on Friday 10/13/2023. The next day I had what I felt was normal soreness. Later that evening my left arm pain intensified beyond normal. By Sunday 10/15/2023, my arm was swollen, and I could not lift my arm above my head. The pain spread from my shoulder through my neck. On Monday I noted a large bruise covering my deltoid, and halfway through my bicep. Since then, the bruise has turned darker and covered my shoulder down to my elbow. As of Friday 10/20/2023 , I still have intense pain and stiffness with limited motion.


VAERS ID: 2727077 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-12-23
Onset: 2023-12-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-12-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG9498 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8111DA / 1 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: No adverse event, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received Fluzone High Dose incidentally rather than receiving Fluzone Quad. No adverse reaction at time of injection.


VAERS ID: 2477105 (history)  
Form: Version 2.0  
Age: 6.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-10-06
Onset: 2022-10-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 53Y2G / 3 RA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR V1A022M / 1 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Headaches
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient given an expired dose of the COVID19 Pfizer Biontech vaccine. Vaccine expiration date was 9/30/2022 and vaccine administered on 10/6/2022. No adverse reactions.


VAERS ID: 2636256 (history)  
Form: Version 2.0  
Age: 0.5  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-05-04
Onset: 2023-05-10
   Days after vaccination: 6
Submitted: 0000-00-00
Entered: 2023-05-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 214K22A / 1 LL / IM
DTAPIPVHIB: DTAP + IPV + HIB (PENTACEL) / SANOFI PASTEUR UJ808AB / 3 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7744KA / 1 RL / IM
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH GF1990 / 3 RL / IM
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 1968378 / 3 MO / PO

Administered by: Private       Purchased by: ?
Symptoms: Underdose
SMQs:, Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Received smaller dose of bivalent covid vaccine as first primary dose


VAERS ID: 2628376 (history)  
Form: Version 2.0  
Age: 1.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-01-03
Onset: 2023-01-05
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2023-05-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FX5095 / 2 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7744NA / 1 LL / IM
HEPA: HEP A (VAQTA) / MERCK & CO. INC. WO29899 / 1 LL / IM
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. W009750 / 1 LL / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. W018830 / 1 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Cough, Dyspnoea, Ear infection, Nasopharyngitis, Pyrexia, Respiratory tract congestion, SARS-CoV-2 test negative
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: Common Cold
Preexisting Conditions: N/A
Allergies: Cow''s Milk Protein
Diagnostic Lab Data: 19JANCOVID-19 Test - Negative; 16MAR2023 COVID-19 Test - Negative
CDC Split Type: vsafe

Write-up: On 1/17/23, he had a common cold with an ear infection. He had congestion, fever, coughing, and difficulty breathing. We contacted his doctor and was prescribed Albuterol and Amoxicillin. We had to take him back to the doctor because he wasn''t getting better, and they prescribed Cefdinir. This lasted until 2/6/23.


VAERS ID: 1813399 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-10-18
Onset: 2021-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 009C21A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7R9NM / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Unknown
Preexisting Conditions: Immunocompromised, medically managed by Hematologist per patient
Allergies: NKDA, NKA
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient was administered a Moderna Covid vaccine with published expiry date 10/15/2021. Pt. was monitored 15 min after injections. Pt. tolerated well. No complications or adverse reactions noted at this time.


VAERS ID: 1718891 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-09-14
Onset: 2021-09-15
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2588 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cough, Illness, Pyrexia, Respiratory tract congestion
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Paxil 10 mg, Rexulti .5 MG, testosterone 3 mg
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: None: pharmacist stated on Saturday 9/18 he doesn''t advise getting both at once so I am not sure why the tech there advised it.
CDC Split Type:

Write-up: I became sick the next afternoon with a low grade fever and cough. I have had body aches, a cough, congestion for a week. I have had no throat pain.


VAERS ID: 2628385 (history)  
Form: Version 2.0  
Age: 0.83  
Sex: Male  
Location: Georgia  
Vaccinated: 2022-11-02
Onset: 2022-11-22
   Days after vaccination: 20
Submitted: 0000-00-00
Entered: 2023-05-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT9142 / 1 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7761NA / 1 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Dehydration, Diarrhoea, Ear disorder, Ear infection, Hand-foot-and-mouth disease, Malaise, SARS-CoV-2 test negative
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Pseudomembranous colitis (broad), Oropharyngeal infections (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Dehydration (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: RSV
Preexisting Conditions: N/A
Allergies: Cow''s Milk Protein
Diagnostic Lab Data: 08NOV2022 COVID-19 Test - Negative; 02DEC2022 COVID-19 Test - Negative; 22DEC2022 COVID-19 Test - Negative
CDC Split Type: vsafe

Write-up: He got sick on 11/08/22. We took him to the doctor was diagnosed with an ear infection and was prescribed Amoxicillin. He still had the ear infection on 11/22/22, so we went back to the doctor, and he was also diagnosed with hands foot and mouth as well. He was prescribed Amoxicillin-Pot Clavulanate. He got better, then we went back on 12/2/23, because he was having ear trouble again and was having diarrhea. Due to being dehydrated, we stopped taking Amoxicillin until his stomach got better and then we started Amoxicillin again. This lasted until 12/31/22.


VAERS ID: 2694011 (history)  
Form: Version 2.0  
Age: 79.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-09-29
Onset: 2023-10-09
   Days after vaccination: 10
Submitted: 0000-00-00
Entered: 2023-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HD9876 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR U8132CA / 1 LA / IM
RSV: RSV (AREXVY) / GLAXOSMITHKLINE BIOLOGICALS KY322 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2023-10-09
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: unclear


VAERS ID: 1989451 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-09-27
Onset: 2021-11-11
   Days after vaccination: 45
Submitted: 0000-00-00
Entered: 2021-12-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Acute myocardial infarction, Brain natriuretic peptide increased, Catheterisation cardiac abnormal, Coronary arterial stent insertion, Coronary artery occlusion, Echocardiogram abnormal, Ejection fraction decreased, Electrocardiogram abnormal, Left ventricular failure, Myocardial infarction
SMQs:, Cardiac failure (narrow), Myocardial infarction (narrow), Arrhythmia related investigations, signs and symptoms (broad), Embolic and thrombotic events, arterial (narrow), Pulmonary hypertension (broad), Cardiomyopathy (narrow), Other ischaemic heart disease (narrow), Noninfectious myocarditis/pericarditis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Lisinopril,Prilosec, Tamsulosin, Tylenol, Vitamin D, Probiotic
Current Illness:
Preexisting Conditions: Hypertension, coronary artery disease
Allergies: Augmentin, doxycycline
Diagnostic Lab Data: 11/11/21 EKG: acute anteroseptal STEMI Cardiac cath: 100% occlusion LAD Echo: LVEF 20-25% BNP $g2000
CDC Split Type:

Write-up: Acute MI requiring emergent placement of stent, complicated by LV failure Discharged from hospital to home care and followup cardiac rehabilitation


VAERS ID: 1924608 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-12-03
Onset: 2021-12-05
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD0809 / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Rash macular
SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pepcid, singular, meloxicam, melatonin, lexapro
Current Illness: None
Preexisting Conditions: None
Allergies: PCN
Diagnostic Lab Data:
CDC Split Type:

Write-up: Splotchy rash has developed in injection arm as well as hands on other arm.


VAERS ID: 1876820 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-11-13
Onset: 2021-11-16
   Days after vaccination: 3
Submitted: 0000-00-00
Entered: 2021-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 3203080 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Ageusia, Anosmia, Fatigue, Headache, Nausea
SMQs:, Acute pancreatitis (broad), Taste and smell disorders (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Seroquel, Trazodone, Benzema
Current Illness: N/A
Preexisting Conditions: COPD
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Pt. states that after receiving the 1st dose of Phizer 11/13/2021, started experiencing symptoms 11/14/2021 of headache, nausea, fatigue, and loss of smell and taste. No noted Primary visit/communications. Still experiencing symptoms. Also received the Influenza 1st dose Left arm 11/13/2021.


VAERS ID: 1828246 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-10-18
Onset: 2021-10-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 009C21A / UNK - / OT
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7R9NM / 1 RA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Expired product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20213

Write-up: Expired vaccine used; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 44-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 009C21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLUARIX QUADRIVALENT) for an unknown indication. No Medical History information was reported. On 18-Oct-2021, the patient received first dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUARIX QUADRIVALENT) (Intramuscular) 1 dosage form. On 18-Oct-2021 at 11:50 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Oct-2021 at 11:50 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 18-Oct-2021 at 11:50 AM, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were reported. No Treatment details were reported.


VAERS ID: 2719952 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-11-29
Onset: 2023-11-30
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 303373 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8091MA / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Loss of personal independence in daily activities, Tremor
SMQs:, Neuroleptic malignant syndrome (broad), Dementia (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: uncontrolled shaking in arm both vaccine was give(Spikevax and Fluzone). unable to hold a glass of water. advised pt to go to urgent care to be seen.


VAERS ID: 1757476 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-10-01
Onset: 2021-10-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ732AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: no known
Current Illness: No known
Preexisting Conditions: No per PQCF
Allergies: NKDA
Diagnostic Lab Data: None so far
CDC Split Type:

Write-up: Redness, Swelling, Lump


VAERS ID: 2719959 (history)  
Form: Version 2.0  
Age: 84.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-11-22
Onset: 2023-11-28
   Days after vaccination: 6
Submitted: 0000-00-00
Entered: 2023-12-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030373 / UNK LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8131DA / UNK LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Large amount of swelling in the arm that recieved both vaccines. Advised pt follow up with PCP.


VAERS ID: 2504312 (history)  
Form: Version 2.0  
Age: 7.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-10-20
Onset: 2022-10-20
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FT1551 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 953Y2 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Cardiac murmur
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient received monovalent vaccine and should have received Bivalent


VAERS ID: 2731648 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2024-01-11
Onset: 2024-01-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU3832B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT8219NA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Nausea, Syncope, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: patient noted similar feelings with previous injections
Other Medications: sertraline 100mg, levothyroxine 50 mcg
Current Illness: none
Preexisting Conditions:
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Minutes after the injections the patient became faint, dizzy, and nauseous. He later vomited.


VAERS ID: 2129218 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2022-02-17
Onset: 2022-02-19
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK9729 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ778AA / UNK RA / IM
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH DW2999 / 1 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR U6821AA / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chills, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: FEVER UP TO 105 WITH CHILLS


VAERS ID: 1993435 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-11-22
Onset: 2021-11-24
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2021-12-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR 7J2CA / N/A RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Blood test, Blood thyroid stimulating hormone normal, C-reactive protein normal, Condition aggravated, Crying, Emotional disorder, Epstein-Barr virus test, Fatigue, Full blood count normal, Headache, Metabolic function test, Red blood cell sedimentation rate normal, Serum ferritin decreased, Streptococcus test, Thyroxine free normal
SMQs:, Depression (excl suicide and self injury) (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: October 2021 had COVID illness- had brief fever and ST- symptoms lasted for 3-5 days.
Preexisting Conditions: None, but has ongoing ankle pain since summer 2021
Allergies: None known
Diagnostic Lab Data: Bloodwork obtained 12/30/21- CBCd, CMP, sed rate, CRP, TSH, FT4- all within normal range. Ferritin slight low at 15. EBV panel, ASO titer, antiDnaseB titer all pending.
CDC Split Type:

Write-up: Received COVID vaccine #1 (Pfizer for 5-11 yr) on 11/22/21 and two days later on 11/24/21, parents state when asked to perform simple task, he became significantly emotional, laid on garage cement floor, curled up and continued to cry for 2-3 hours. He has not had episodes like this previously. The emotional episodes has continue to reoccur since 11/24/21. He has previously had intermittent headaches for about a year and headaches have gradually worsened since 11/2021. He has had fatigue for the past several months that has worsened since 11/2021.


VAERS ID: 1906736 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-11-29
Onset: 2021-11-29
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL0007 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ68SAA / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: No adverse event, Product administration error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: n/a
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: vaccine error - no adverse events as of yet


VAERS ID: 2690323 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-10-02
Onset: 2023-10-02
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HG2282 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8150CA / 1 RA / IM
PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH GW7965 / 1 RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS 7S7MF / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Malaise, Pruritus, Rash, Rash erythematous, Rash pruritic
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: no known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient returned to pharmacy department today complaining of severe redness and rash on his right side from the clavicle to his lower abdomen. Patient presented a photo of rash and said it was red and itchy. Patient said he had gone home after vaccinations were administered and took a nap because he did not feel well. Patient stated he woke up to the redness and rash and tried Triamcinolone cream he had at home to stop itching but it did not resolve. Patient was looking for recommendation from pharmacist as to what he could do for rash. Pharmacist informed patient that he needed to contact his primary care physician because the rash looked severe and would need to be treated by physician. Patient understood and verbalized understanding. Patient said he would contact his primary care physician immediately.


VAERS ID: 1814778 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-10-14
Onset: 2021-10-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100350391 / UNK - / -

Administered by: Military       Purchased by: ?
Symptoms: Head discomfort, Immunodeficiency
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisinopril carvetolow
Current Illness:
Preexisting Conditions: unstable gate high blood pressure
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Since 10/14/21 pt complains of a fluid moving around in his head when he turns over in bed


VAERS ID: 1776081 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2021-08-31
Onset: 2021-08-31
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3182 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7315LA / N/A LA / IM
PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH AW7402 / N/A RA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS FZ7Z4 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fatigue, Movement disorder, Pain
SMQs:, Akathisia (broad), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: severe fatigue, body pain; pt reports not being able to move easily and was close to going to hospital


VAERS ID: 2696431 (history)  
Form: Version 2.0  
Age: 94.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-10-12
Onset: 2023-10-12
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HF9275 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UT8131DA / 1 LA / IM
RSV: RSV (ABRYSVO) / PFIZER/WYETH HF5023 / 1 LA / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Death, Feeling abnormal, Intensive care, Vomiting
SMQs:, Acute pancreatitis (broad), Dementia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: unknown
Allergies: none known
Diagnostic Lab Data: none
CDC Split Type:

Write-up: The 3 vaccines were administered to patient on 10/12/2023 at 11:39 a.m. She was instructed on common side effects and asked to remain in waiting area for 15 minutes. Patient then left area with no issues. That evening, she began feeling bad and saw the facility nurse the next morning for vomiting. The nurse kept an eye non her until Saturday morning when she was sent to hospital and admitted to ICU. She then died sometime between then and Monday morning.


VAERS ID: 2228789 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-10-28
Onset: 2021-11-06
   Days after vaccination: 9
Submitted: 0000-00-00
Entered: 2022-04-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3590 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT734KA / UNK LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Ataxia, CSF cell count normal, CSF protein increased, Endotracheal intubation, Guillain-Barre syndrome, Headache, Immunoglobulin therapy, Intensive care, Lumbar puncture, Neurological symptom, Pain, Paraesthesia, Plasmapheresis, Polymerase chain reaction
SMQs:, Angioedema (broad), Peripheral neuropathy (narrow), Anticholinergic syndrome (broad), Guillain-Barre syndrome (narrow), Noninfectious encephalitis (broad), Demyelination (narrow), Respiratory failure (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 21 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Anastrazole, Vitamin D2, tramadol
Current Illness: Severe acute headache
Preexisting Conditions: Breast Cancer s/p mastectomy
Allergies: NKA
Diagnostic Lab Data: LP on 11/11/2021 showed normal cells and high protein. Meningitis/encephalopathy PCR test on 11/11/2021 was negative.
CDC Split Type:

Write-up: Patient reported to the emergency department on 11/10/2021 with multiple neurological symptoms including paresthesis, weakness, ataxic gait, pain, and headache with symptoms prior to admission starting 11/06/2021. Patient was admitted to the ICU with Acute Inflammatory Demylenating Polyradiculopathy (AIDP). Treatment included gabapentin and IVIG treatment 11/11/2021 - 11/16/2021. Patient intubated from 11/15/2021-11/19/2021. Additional treatment included PLEX (plasmapheresis) therapy 11/16/2021-11/23/2021 . Patient was discharged to an acute rehabilitation facility on 12/1/21. Noted doing well clinically with ongoing weakness.


VAERS ID: 2595285 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2022-11-21
Onset: 2022-11-21
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GK1657 / UNK - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GK1657 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2995K / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: None
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given the incorrect Pfizer vaccine for dose 1 and 2. Patient was given Bivalent instead of the monovalent for dose 1 and 2. Patient received these on 11/21/2022 and 12/12/2022. The patients parents have been notified of the error at a follow up visit by the Physician in the office. Patient reported no concerns.


VAERS ID: 2238633 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-12-02
Onset: 2021-12-31
   Days after vaccination: 29
Submitted: 0000-00-00
Entered: 2022-04-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8762 / 3 AR / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Vaccine breakthrough infection
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metformin, prazosin, escitalopram, Allegra, isibloom
Current Illness:
Preexisting Conditions: Depression, anxiety, PTSD, kidney stones, PCOS
Allergies: Tamiflu, dust, pets, seasonal allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Breakthrough Covid-19 case


VAERS ID: 2692089 (history)  
Form: Version 2.0  
Age: 63.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2023-10-04
Onset: 2023-10-05
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027L21A / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8200BA / UNK RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Injection site pain, Limb discomfort, Oedema peripheral
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Estradiol 0.075 Ozempic 2 mg Pravastatin 40 mg Folic Acid 1 mg Synthroid 35 mg Krill oil Co q 10
Current Illness: Thyroid disease
Preexisting Conditions: Fibromyalgia Anemia
Allergies: Latex
Diagnostic Lab Data:
CDC Split Type:

Write-up: The day after vaccination injection site sore. On Friday morning soreness not as bad at injection site.I noticed discomfort in armpit later upon examining underarm area and noticed visible swelling in armpit. I contacted primary care physician via portal to ask if swelling was common. No response.


VAERS ID: 1829882 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-10-13
Onset: 2021-10-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8839 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ732AA / N/A RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Joint swelling, Thrombosis, Ultrasound scan
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NOT KNOWN
Current Illness: NOT KNOWN
Preexisting Conditions: NOT KNOWN
Allergies: NOT KNOWN
Diagnostic Lab Data: PATIENT STATES THAT ULTRASOUND WAS DONE AND BLOOD CLOT WAS CONFIRMED.
CDC Split Type:

Write-up: PATIENT STATES THAT AFTER ABOUT 2-3 HOURS OF VACCINATION STARTED TO HAVING SOME SWELLING IN HER LEFT ANKLE . SHE STATES THAT THE SWELLING WAS VERY BAD.


VAERS ID: 2729817 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: Georgia  
Vaccinated: 2023-11-09
Onset: 2023-11-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-01-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3897 / 5 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS JJ547 / UNK LA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS Y77XY / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Chest discomfort, Dyspnoea, Flushing, Pruritus
SMQs:, Anaphylactic reaction (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metoprolol, Simvastatin, and Levothyroxine
Current Illness:
Preexisting Conditions: Stem cell transplant for Non-Hodgkins Lymphoma in 2015.
Allergies: Allergy to Ragweed
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient states that he had trouble breathing with chest tightening and flushing for about 1 minute after initially receiving vaccines. About 5 days after vaccination patient states that he had itching that lasted for a few hours.


VAERS ID: 1942605 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Georgia  
Vaccinated: 2021-12-09
Onset: 2021-12-10
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ8757 / UNK - / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cheilitis, Facial discomfort, Headache, Lip blister, Oral mucosal blistering, Pyrexia, Stomatitis, Swelling face
SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamins, Zyrtec, Tylenol
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: High fever, severe headaches, sores and blisters around my mouth and lips, face swelling, discomfort on the left side of my face


VAERS ID: 2178558 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Guam  
Vaccinated: 2021-12-13
Onset: 2021-12-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 1 - / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5618 / 2 - / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS A2AK3 / N/A - / IM

Administered by: Military       Purchased by: ?
Symptoms: Biopsy lymph gland abnormal, Blood alkaline phosphatase increased, Chest X-ray abnormal, Eosinophil count increased, Full blood count abnormal, Hodgkin's disease, Monocyte count increased, Neoplasm of thymus, Neutrophil count increased, Rash, Swelling, Swelling face, Urine analysis abnormal, Urine leukocyte esterase positive, Vasodilatation, White blood cell count increased
SMQs:, Liver related investigations, signs and symptoms (broad), Anaphylactic reaction (broad), Angioedema (narrow), Haematopoietic leukopenia (broad), Neuroleptic malignant syndrome (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Biliary system related investigations, signs and symptoms (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Chronic kidney disease (broad), Hypersensitivity (narrow), Malignant lymphomas (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Haematological malignant tumours (narrow), Haematological tumours of unspecified malignancy (narrow), Infective pneumonia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: Possible itchy rash 2 weeks before vaccination
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Biopsy = Hodgkin Lymphoma CBC: WBC 14,700 Neuts 9,400 Monocyte 1,010 Eosinophils 1,400 Alk phos 192 (remainder LFTs NL) Urinalysis "small" Leuk Esterase culture = $g100,000 Lactobacillus
CDC Split Type:

Write-up: Mother of pt noted small rash about 2 weeks before first Covid-19 injection (about 1 week after Influenza vaccine). Similar rash with severe flare on day of the first Pfizer Covid-19 vaccine. Worsening of same rash right after second Pfizer vaccine. Rash resolved with oral steroids. Approx 1 month after rash began, patient was admitted for facial swelling and neck venous distention. CXR showed thymic mass. Biopsy proven Hodgkin Lymphoma stage IV


VAERS ID: 2757904 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Male  
Location: Hawaii  
Vaccinated: 2024-03-06
Onset: 2024-03-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2024-03-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031895 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8041AA / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Expired product administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Magnesium 250mg
Current Illness: Basal cell carcinoma
Preexisting Conditions: Hx of skin cancer
Allergies: NKDA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: The patient received an expired vaccine. No actual reaction occurred with the patient after administrating.


VAERS ID: 2717057 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Hawaii  
Vaccinated: 2023-11-20
Onset: 2023-11-21
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-11-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK LA / SYR
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Erythema, Peripheral swelling, Skin warm, Sleep disorder, Tenderness
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Fluoxetine 20mg 1xday; ibuprofen 800 mg 2x day; multivitamin
Current Illness: None
Preexisting Conditions: None
Allergies: Codeine
Diagnostic Lab Data: None
CDC Split Type:

Write-up: On left arm, Red swelling, about 3 inches wide by 1.5 inches high. Warm & very tender to touch. Wakes me up at night if I roll onto that arm. Taking 800 mg ibuprofen every 8 hours to relieve some tenderness. I?ve never had a reaction like this to any vaccine nor my previous Covid-19 shots & boosters (all by Pfizer)


VAERS ID: 2435987 (history)  
Form: Version 2.0  
Age: 8.0  
Sex: Male  
Location: Hawaii  
Vaccinated: 2022-08-20
Onset: 2022-08-22
   Days after vaccination: 2
Submitted: 0000-00-00
Entered: 2022-09-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AR6965B / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7681KA / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal discomfort, Axillary pain, Decreased appetite, Feeding disorder, Injection site pain, Nausea, Pain, Pain in extremity, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Pain at injection point and adjacent armpit. Pain throughout his arm and legs when picked up from school yesterday 8/22/2022, he also said his arms and legs hurt really bad all day whenever he moved. Pain throughout body is continuing today 8/23/2022. Loss of appetite. Pt. is normally the biggest eater in the family however, he is saying his stomach is bothering him and he is unable to eat. Nauseous: He woke up feeling nauseous and vomited. Decreased appetite for 1 week.


VAERS ID: 1735478 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Hawaii  
Vaccinated: 2021-09-25
Onset: 2021-09-25
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3952 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 9339N / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Arthralgia, Dizziness, Headache, Pain in extremity, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Vestibular disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Last covid vaccine similar symptoms but much more mild.
Other Medications: Luvox Gabapentin Depakote Nasal sprays
Current Illness: Oral hsv 1 week prior
Preexisting Conditions: Anxiety, depression, ocd
Allergies: Ceclor- rash
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Severe bilateral arm pain right greater than left, severe arthralgias, fever 101.9, headache, dizziness. Much more severe symptoms with booster than either other shot.


VAERS ID: 1713662 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Hawaii  
Vaccinated: 2021-08-18
Onset: 2021-08-18
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-09-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0172 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ686AA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Joint range of motion decreased
SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Should pain, loss of range of motion after injection.


VAERS ID: 2490034 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Hawaii  
Vaccinated: 2022-09-22
Onset: 2022-09-23
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH GJ2524 / 5 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / N/A RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Dyspnoea, Pyrexia, Quarantine, Respiratory tract congestion, SARS-CoV-2 test positive
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Metoprolol succinate ER; Triamterene-HCTZ; Metformin HCL; Glipizide; Xarelto; Jardiance; Omeprezole; Aspirin; Vitamin D; Vitamin B-12 ; Loratadine; Fish oil/Omega-3; Senior Multi-Vitamin
Current Illness: None
Preexisting Conditions: Atrial fibrillation; type-2 diabetes; hypertension; sleep apnea
Allergies: None
Diagnostic Lab Data: COVID TEST 09/24/2022
CDC Split Type:

Write-up: LAB-TESTED POSITIVE, 09/26/2022, FOLLOWING A NASAL SWAB 09/24/2022. SYMPTOMS INCLUDED UPPER CHEST CONGESTION AND MODERATE DIFFICULTY BREATHING. TREATED WITH MOLNUPIRAVIR DUE TO POTENTIAL INTERACTION WITH XARELTO. FEVER VARIED FROM 99.0? TO 103? FOR 3 DAYS. PER CDC GUIDELINES, HOME-ISOLATED 5 DAYS AND MASKED UP IN CROWDS FOR 2 WEEKS FOLLOWING DIAGNOSIS.


VAERS ID: 2293181 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Male  
Location: Hawaii  
Vaccinated: 2022-05-17
Onset: 2022-05-18
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2022-05-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK9894 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR - / UNK LA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Headache, Influenza A virus test positive, Myalgia, Oropharyngeal pain, SARS-CoV-2 test negative, Streptococcus test positive, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Rhabdomyolysis/myopathy (broad), Arrhythmia related investigations, signs and symptoms (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypotonic-hyporesponsive episode (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: HE WAS GIVEN IMMUNIZATIONS FOR INFLUENZA AND ALSO MEASLES, MUMPS, AND RUBELLA.
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: INFLUENZA A TEST POSITIVE. STREPTOCOCCUS TYPE A TEST POSITIVE. COVID TEST NEGATIVE.
CDC Split Type:

Write-up: HEADACHE, SYNCOPE, SORE THROAT, AND MUSCLE ACHES.


VAERS ID: 2524858 (history)  
Form: Version 2.0  
Age: 95.0  
Sex: Male  
Location: Hawaii  
Vaccinated: 2022-12-05
Onset: 2022-12-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 018C22A / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7681KA / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, Injection site pain
SMQs:, Extravasation events (injections, infusions and implants) (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Clotrimazole, Doxazosin, Finasteride, Furosemide, Levothyroxine, metoprolol succinate XL, multi-vitamins, rivaroxaban
Current Illness:
Preexisting Conditions: Atrial Fibrillation, CHF, Coronary artery disease, Persistent Sinus bradycardia, Lef inguinal hernia, BPH; Osteoperosis, Arthropathy of right hip, hypothyroidism, Megaloblastic anemia due to vit B12 deficiency, cataract of right eye
Allergies: No known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient requested/scheduled to received 0.5 ml of COVID 19 Moderna Bivalent booster. Patient was given 0.5ml of COVID 19 Moderna monovalent pediatric dosage for ages 5-11 years old. Patient reports arm tenderness at injection site, no other reported symptoms. Moderna Manufacturer notified of event, awaiting further instructions from manufacturer. Patient notified of event, and will be updated with further instructions for future COVID 19 vaccines doses, as per manufacturer instructions.


VAERS ID: 2524841 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Hawaii  
Vaccinated: 2022-12-05
Onset: 2022-12-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 018C22A / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7681KA / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, Injection site pain, Underdose
SMQs:, Extravasation events (injections, infusions and implants) (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Albuterol, ALprazolam, Atorvastatin, Baclofen, Dulaglutide,
Current Illness:
Preexisting Conditions: Chronic pain, OSA, Asthma, Benign Essential Hypertension, Diabetes, Depression
Allergies: No known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient requested/scheduled to received 0.5 ml of COVID 19 Moderna Bivalent booster. Patient was given 0.5ml of COVID 19 Moderna monovalent pediatric dosage for ages 5-11 years old. Patient reports arm tenderness at injection site, no other reported symptoms. Moderna Manufacturer notified of event, awaiting further instructions from manufacturer. Patient notified of event, and will be updated with further instructions for future COVID 19 vaccines doses, as per manufacturer instructions.


VAERS ID: 2586717 (history)  
Form: Version 2.0  
Age: 0.58  
Sex: Female  
Location: Hawaii  
Vaccinated: 2022-12-10
Onset: 2022-12-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS1415B / 2 RL / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UJ879AB / 2 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: No adverse event
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: No adverse effects.


VAERS ID: 2524852 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Hawaii  
Vaccinated: 2022-12-05
Onset: 2022-12-05
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 018C22A / 4 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7681KA / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Albuterol, Asmanex, Aspirin, Atenolol, Atorvastatin, Cilostazo Cilostazol, Clopidogrel, Ergocalciferol, Fluticasone, Glipizide, Hydroxyzine, Isosorbide Dinitrate, Loperamide, Nitroglycerin, Oxybutynin, Pramipexole, Prednisone,
Current Illness:
Preexisting Conditions: COPD, Intervertebral Disc Stenosis, Atrial fibrillation, Aneurysm of abdominal aorta, hypertention, PAD, stage 3 CKD, Diabetes type 2, Chronic lymphocytic leukemia, hyperlipidemia, sciatica
Allergies: Hydrocodone-Acetaminophen, Codeine, Hydrocodone
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient requested/scheduled to received 0.5 ml of COVID 19 Moderna Bivalent booster. Patient was given 0.5ml of COVID 19 Moderna monovalent pediatric dosage for ages 5-11 years old. Patient reports no symptoms at this time. Moderna Manufacturer notified of event, awaiting further instructions from manufacturer. Patient notified of event, and will be updated with further instructions for future COVID 19 vaccines doses, as per manufacturer instructions.


VAERS ID: 2711905 (history)  
Form: Version 2.0  
Age: 1.33  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-11-06
Onset: 2023-11-06
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HH3252 / 1 LL / IM
DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS YC239 / UNK LL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 5DYSA / UNK RL / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. X006983 / UNK RL / SC

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, Product administration error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: 11.6.23 Rec''d Pfizer 2023-2024 formulation of Covid Vaccine for 6m-4yr. Inadvertently received full vial after dilution ( Instead of recommended dose of 0.3 mL/3 ug). Administered by MA. Attending MD notified, ID consulted and notified regarding questions about expected adverse reactions, if any. Practice and office managers notified. Parent notified by telephone by office RN. Mother''s questions answered, in detail, regarding the actual vaccine administration error, measures being taken to address the administration error, and procedures that will be put into place to avoid this error again in the future. RN will call parent daily for the next three office days to check on status of child.


VAERS ID: 2719536 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-11-21
Onset: 2023-11-01
Submitted: 0000-00-00
Entered: 2023-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH HJ7224 / UNK RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Neck pain, Pain in extremity
SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: sore arm,shoulder and neck


VAERS ID: 2522004 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2022-10-01
Onset: 2022-10-01
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / 3 LA / SYR
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 1 UN / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: COVID-19, Chills, Decreased appetite, Influenza virus test negative, Infusion, Pyrexia, SARS-CoV-2 test positive
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: After all the COVID-19 vaccines I got sicker and sicker.
Other Medications: Aspirin; metformin; ACTOS; anti-depressants; lamotrigine; trazadone; fish oil; calcium B3; omeprazole; multivitamins; tramadol
Current Illness: None
Preexisting Conditions: GERD; CODP; Using 2 liters of Oxygen every day; Arthritis
Allergies: SYMBYAX; morphine; antibiotics
Diagnostic Lab Data: 02DEC2022 COVID-19 test positive
CDC Split Type: vsafe

Write-up: I had fever, chills, cough, loss of appetite, loss of taste. I didn''t know what was happening with me. I did a COVID-19 home test which was negative. I knew something was happening to me so I contacted my doctor. When I went to my doctor''s office he did a COVID-19 test. I was positive for COVID-19 but I was negative for flu. My doctor scheduled an appointment for me to go to the hospital to get infusion. After a few days of getting the infusion I felt better and I recovered from COVID-19 infection. I just wanted to let you know after each COVID-19 vaccines I''ve got sicker and sicker not sure why.


VAERS ID: 2507288 (history)  
Form: Version 2.0  
Age: 66.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2022-11-11
Onset: 2022-11-11
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 063B22A / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ925AC / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: tizanidine, lisinopril, metformin, simvastatin, tradjenta, hum
Current Illness:
Preexisting Conditions: vision changes, tinea pedia, right sciatica, GERD, right foot venous statis, proteinuria, allergic rhinitis, DM II, di
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented to his PCP for a follow up. Patient was offered covid booster and flu. Patient was given Moderna Monovalent instead of Moderna Bivalent for booster dose. No adverse reactions.


VAERS ID: 1897834 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2021-11-16
Onset: 2021-11-16
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 035C21A / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ512AB / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Product storage error
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given Fluzone HD PF 2020-2021. Expired vaccine from last influenza season. Expired 6-30-2021


VAERS ID: 2718651 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-11-28
Onset: 2023-11-28
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3031914 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS PPM35E / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient received a dose of Fluarix but came to pharmacy for Spikevax. Patient had already received a dose of Fluarix on 9/15/2023. Patient was immediately notified and received the correct vaccination. No treatment was necessary and the patient was comfortable still receiving the Spikevax.


VAERS ID: 2503121 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2022-11-08
Onset: 2022-11-08
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS Y72ZZ / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: metformin, atorvastatin, tamsulosin, lisinopril, Senna S, Vit
Current Illness:
Preexisting Conditions: alcohol use, CKD stage 2, DM type II, Microalbuminuria, Diabetic neuropathy, Peripheral neuropathy, Vit D Deficiency,.
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient had no history of Covid vaccines in EMR and did not have his covid vaccination card with him. Patient refused to go home and bring back card. Patient stated he had received a covid vaccine in the past. Nurse administered a monovalent Pfizer vaccine. When checking the vaccine log system patient patient had a documented J&J in March 2021. Patient should have received a bivalent booster dose.


VAERS ID: 2604143 (history)  
Form: Version 2.0  
Age: 3.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2023-03-23
Onset: 2023-03-23
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-03-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FL2757 / 2 LL / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS DM4FM / N/A RL / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event, Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: zyrtec
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: The covid vaccine intended for 5-11 yr old was given in error to this patient.; no adverse effects


VAERS ID: 1959183 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2021-12-17
Onset: 2021-12-17
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-12-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FJ1611 / 2 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR UT7377JA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Adverse event, Dizziness, Feeling abnormal, Hyperhidrosis, Hypotonia, Mydriasis, Pallor, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (narrow), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Took cranberry pills a few days ago for suspected UTI
Current Illness: None
Preexisting Conditions: None
Allergies: Bee stings
Diagnostic Lab Data: EMS took vitals (blood pressure, oxygen saturation, and pulse) which were within normal limits.
CDC Split Type:

Write-up: Patient received vaccine at 10:31 AM. He stated before receiving the shot he was anxious. Within a few minutes of receiving the vaccine and sitting down in a chair in the vaccination area, the patient suddenly dropped his phone and started sliding down the chair. His friend caught him before he fell out of the chair and was able to safely get him to the ground with no damage. He immediately laid down on the floor and I came over and noticed he was pale, sweating, and his pupils were enlarged. He stated he had been slightly dizzy before he fainted and had not eaten or drank anything today besides a coffee. I had the patient lay down and elevate his legs and we immediately got him water. 911 services were called and patient drank water and started eating some crackers before EMS arrived. EMS did a thorough medical evaluation including blood pressure , pulse, and oxygen which were normal. Patient was not diabetic and has no history of low blood sugars so they didn''t test his blood sugar. The patient stayed supine for about 30 minutes while drinking and eating. EMS ensured he was able to sit up before leaving. Patient finished 2 bottles of water and ate crackers during the 1 hour after the adverse event and his color returned to normal as well as pupils. Patient was provided a water bottle before leaving and I ensured he was okay walking and was feeling back to normal before leaving. I provided him information for follow up and patient was going to shop in store for a little longer and knew how to contact me right away. Patient was with family when he left and he was aware of need to continue to hydrate throughout day.


VAERS ID: 2700846 (history)  
Form: Version 2.0  
Age: 6.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2023-10-24
Onset: 2023-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AU5555B / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 7PB23 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: Augmentin, milk
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Patient was given 0.5mL instead of 0.25mL of Moderna Covid vaccine


VAERS ID: 1850389 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2021-10-14
Onset: 2021-10-15
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2593 / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4L97X / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Arthralgia, Blood creatine phosphokinase, Full blood count, Joint swelling, Myalgia, Red blood cell sedimentation rate
SMQs:, Rhabdomyolysis/myopathy (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Mulitvitamin, L-lysyne, Lexapro, Wellbutrin
Current Illness: No
Preexisting Conditions: No
Allergies: NKA
Diagnostic Lab Data: C-Kinase, Sed rate, CBC 11/2/2021
CDC Split Type:

Write-up: Extreme muscle pain, under arms, thighs especially. Right knee and ankle swelling and pain on week 2 after vaccination. Prednisone and antibiotic prescribed. Can still feel vague muscle aches and thinks pain will return at conclusion of prednisone.


VAERS ID: 2581518 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2023-02-13
Onset: 2023-02-13
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-02-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 071B22A / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS DM4FM / 1 LA / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. W023072 / 1 LA / SC
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS 2LG35 / 1 LA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. W018825 / 1 RA / SC

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: fatigue, back pain
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented for physical with provider. Patient was given his first covid vaccine of Pfizer on 01/17/2023. Patient was to complete his series with Pfizer but was given Moderna Monovalent vaccine instead of Pfizer. No adverse reactions noted.


VAERS ID: 1855102 (history)  
Form: Version 2.0  
Age: 9.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2021-11-09
Onset: 2021-11-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FK5127 / 1 LA / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. P100367901 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Fall, Loss of consciousness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Shortly after receiving his vaccines he was sitting on a chair and then started to pass out and fell to the floor. He was out for about 5 seconds. Pharmacist caught him and had him sit on the floor with his back to the wall, asked him questions such as name, where he was, who he was with. Provided water and a granola bar and had them stay in the pharmacy for an additional 30 minutes. Child was able to get up on his own and could walk by himself with no issues. Went home with family.


VAERS ID: 1780320 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2021-10-07
Onset: 2021-10-08
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF8841 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ741AB / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Dizziness, Headache, Musculoskeletal stiffness
SMQs:, Anticholinergic syndrome (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Starting 10/8 patient complained of headaches, lightheadedness, sleeping stiff and dizziness. He said the headaches, lightheadedness and dizziness improved by end of day 10/9 but he is still very stiff when sleeping as of 10/12.


VAERS ID: 2504668 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2022-11-10
Onset: 2022-11-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA AS1414B / 3 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS K7752 / N/A LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, Underdose
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Wellbutrin XL 300 mg po daily Omeprazole 40 mg. oral daily Halobetasol 0.05% cream nightly
Current Illness: no illness
Preexisting Conditions: anxiety/depression GERD
Allergies: Penicillin G
Diagnostic Lab Data: none Notified supervisor and physician
CDC Split Type:

Write-up: Incorrect dose administered. Gave her the Children''s Moderna.


VAERS ID: 2503317 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2022-11-09
Onset: 2022-11-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 063B22A / 2 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2A3H9 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: omeprazole, sertraline, vyvanse, red yeast rice, levothyroxine
Current Illness:
Preexisting Conditions: hypothyroidism, depression, asthma, ADHD, insomnia
Allergies: Erthromycin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient had started her covid 19 primary series. First vaccine given was Pfizer in June 2022. Patient received a Moderna Monovalent today instead of a Pfizer Monovalent to complete her primary series. No adverse reactions noted.


VAERS ID: 2712451 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-10-24
Onset: 2023-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA HG4633 / 5 LA / -
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR U8041BA / 1 RA / IM
HEPAB: HEP A + HEP B (TWINRIX) / GLAXOSMITHKLINE BIOLOGICALS 7X224 / 1 LA / IM
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS 97D52 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Influenza like illness, Injection site erythema, Injection site induration, Injection site pain, Injection site warmth, Malaise, Pruritus, Pyrexia, Rash macular
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: levothyroxine, gabapentin, combivent, clonazepam,duloxetine, quetiapine, omeprazole
Current Illness: none
Preexisting Conditions: hypothyroidism, lung disease
Allergies: latex, venlafaxine, sympathomimetics
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Pt reported feeling sick like she has the flu, redness and blotchy arm at site of injection on, soreness, hard to the touch, felt warm and was itchy all over and felt sick for 5 days. Patient reported taking some tylenol for her fever and some benadryl for the itching.


VAERS ID: 2690216 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-09-27
Onset: 2023-09-28
   Days after vaccination: 1
Submitted: 0000-00-00
Entered: 2023-10-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Axillary pain, Pyrexia, Vaccination site erythema, Vaccination site pain, Vaccination site swelling
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: JUNEL; SEROQUEL; WELLBUTRIN; VYVANSE; HYDROXYZINE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202300313059

Write-up: Pain in underarm/armpit on the side of the vaccine; Pain, swelling, redness, and fever at injection site/ Injection site pain; Pain, swelling, redness, and fever at injection site/ Injection site swelling; Pain, swelling, redness, and fever at injection site/ Injection site redness; Pain, swelling, redness, and fever at injection site/ Fever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30-year-old female patient (not pregnant) received bnt162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), on 27Sep2023 at 17:30 as dose 1, single (Batch/Lot number: unknown) at the age of 30 years, in right arm for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX QUADRIVALENT), on 27Sep2023 as dose 1, single (Batch/Lot number: unknown), in left arm for influenza immunisation. The patient''s relevant medical history was not reported. Concomitant medication(s) included: JUNEL; SEROQUEL; WELLBUTRIN; VYVANSE; HYDROXYZINE. Past drug history included: Cefzil, reaction(s): "Known allergies: Cefzil". Vaccination history included: bnt162b2 (Dose 1, Single, Vaccination site: Arm Left, Vaccine Administration Time: 05:00 PM), administration date: 25Jan2021, for COVID-19 immunisation; bnt162b2 (Dose 2, Single, Vaccination site: Arm Left, Vaccine Administration Time: 05:00 PM), administration date: 06Oct2021, for COVID-19 immunisation, reaction(s): "Inappropriate schedule of vaccine administered"; bnt162b2;bnt162b2 omi ba.4-5 (Dose 3 (Booster), Single, Vaccination site: Arm Left, Vaccine Administration Time: 05:00 PM), administration date: 17Oct2022, for COVID-19 immunisation. The following information was reported: AXILLARY PAIN (non-serious) with onset 28Sep2023 at 14:00, outcome "not recovered", described as "Pain in underarm/armpit on the side of the vaccine"; PYREXIA (non-serious) with onset 28Sep2023 at 14:00, outcome "not recovered", described as "Pain, swelling, redness, and fever at injection site/ Fever"; VACCINATION SITE PAIN (non-serious) with onset 28Sep2023 at 14:00, outcome "not recovered", described as "Pain, swelling, redness, and fever at injection site/ Injection site pain"; VACCINATION SITE ERYTHEMA (non-serious) with onset 28Sep2023 at 14:00, outcome "not recovered", described as "Pain, swelling, redness, and fever at injection site/ Injection site redness"; VACCINATION SITE SWELLING (non-serious) with onset 28Sep2023 at 14:00, outcome "not recovered", described as "Pain, swelling, redness, and fever at injection site/ Injection site swelling". Therapeutic measures were not taken as a result of axillary pain, vaccination site pain, vaccination site swelling, vaccination site erythema, pyrexia. The information on the batch/lot number for bnt162b2 omi xbb.1.5 has been requested and will be submitted if and when received.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-202300314962 same patient, different vaccine dose/event;


VAERS ID: 2533138 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Iowa  
Vaccinated: 2022-12-14
Onset: 2022-12-14
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-12-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FR2583 / 3 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 2A3H9 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect product formulation administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: lisinopril, levothyroxine, viagra, pantoprazole, atorvastatin, tramadol, IBU, methocarbamol
Current Illness:
Preexisting Conditions: paresthesia of limb, neck pain, shingles, thyroid nodule, hypothyroidism, muscle cramps, elevated liver enzymes, ED, lung nodule RLL, abdominal pain RLQ, bilat elbow pain, pain in right ankle and joints of right foot, HTN, hyperlipidemia, basal cell carcinoma of scalp, lumbar back pain, thoracic spine pain, GERD, begin esophageal stricture, hiatal hernia and obesity
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented for a nurse visit to get a covid vaccine. There were no prior covid vaccines documented in patient''s chart. Patient did not have card and denied every receiving covid vaccines prior. Then when immune coordinator was checking flags she noticed the system showed patient completed series of Pfizer back in 2021. Patient should have received a bivalent booster but was given a monovalent instead. No adverse reactions noted.


VAERS ID: 2050743 (history)  
Form: Version 2.0  
Age: 11.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2021-12-10
Onset: 2021-12-10
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2022-01-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3594 / 1 RA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR H3YZ4 / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Incorrect dose administered, No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was given the wrong vaccine. She was given the dose for 12 and older. She is only 11 but the size of an adult. She has no symptom to report. She felt fine as I called the Mother the next day.


VAERS ID: 1804698 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2021-10-19
Onset: 2021-10-19
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301358A / 4 LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR UJ768AC / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, No adverse event, Wrong product administered
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness:
Preexisting Conditions: Lupus Diverticulitis
Allergies: unknown
Diagnostic Lab Data:
CDC Split Type:

Write-up: Resident had completed Pfizer Covid 2 dose series plus 1 booster dose (Dates: 1/15/21; 02/15/21; 09/28/21). At clinic to receive a influenza vaccine. Vaccinator administered an additional Pfizer Covid in error. This would represent a 4th dose. Error realized. Patient notified. Correct vaccine (influenza High dose) was administered. Follow up with patient the next day. No adverse reactions.


VAERS ID: 2587018 (history)  
Form: Version 2.0  
Age: 0.75  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-01-25
Onset: 2023-02-08
   Days after vaccination: 14
Submitted: 0000-00-00
Entered: 2023-02-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FX5095 / 1 LG / IM
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. - / 2 LG / IM

Administered by: Private       Purchased by: ?
Symptoms: Cough, Diarrhoea, Influenza virus test negative, Pyrexia, SARS-CoV-2 test negative, Secretion discharge
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Flu and Covid test both negative
CDC Split Type:

Write-up: Yellow snot, cough, fever, and loose stool 3-5 days Motrin/Tylenol


VAERS ID: 2692756 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-10-09
Onset: 2023-10-09
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030536 / UNK LA / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS 4XY5D / UNK RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Hot flush, Immediate post-injection reaction, Muscle spasms, Rash
SMQs:, Anaphylactic reaction (broad), Dystonia (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: administered 25 mg benadryl
CDC Split Type:

Write-up: immediate reaction-- became flush, back spasm, rash noted bilaterally on arms


VAERS ID: 2702488 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: Iowa  
Vaccinated: 2023-10-24
Onset: 2023-10-24
   Days after vaccination: 0
Submitted: 0000-00-00
Entered: 2023-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3030535 / UNK AR / IM
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS - / UNK AR / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Extra dose administered, No adverse event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: No adverse events. Patient had already received a fluarix vaccination on 9/21/23.


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