|
VAERS ID: |
2548111 (history) |
Form: |
Version 2.0 |
Age: |
19.0 |
Sex: |
Male |
Location: |
Ohio |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
AS7171B / N/A |
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: Unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: NKA Diagnostic Lab Data: n/a CDC Split Type: Write-up: Patient was administer bivalent dose in error. He still needs to complete the primary series. |
|
VAERS ID: |
2548161 (history) |
Form: |
Version 2.0 |
Age: |
92.0 |
Sex: |
Female |
Location: |
Virginia |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 5 |
LA / IM |
FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
346335 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Heart rate increased, Hypertension, Palpitations, Rash SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Hypertension (narrow), Cardiomyopathy (broad), 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Palpitation through out the body, increased heart beat, rash on her face Given Diphenhydramine 25 mg. Checked blood pressure and it was high 148, and 160 then went down to 128. Patient said she did not feel palpitation anymore after 10-15 min. Patient was told to monitor blood pressure at home and would feel drowsy due to allergy medication. She was sent to home with her son. |
|
VAERS ID: |
2548164 (history) |
Form: |
Version 2.0 |
Age: |
12.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
042H22A / 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: 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 given bivalent dose when they were expecting first dose in the series. |
|
VAERS ID: |
2548178 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR6965B / UNK |
LA / IM |
FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
348384 / UNK |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Client and family came by to receive the Bi-valent booster made by Moderna. They received the mono-valent booster in error. The family has been notified, and advised about potential adverse reactions such as a sore arm in the morning. The family was also advised to wait 2 months before getting the bivalent booster in accordance with current recommendations. The family members seemed frustrated, but understanding and appreciative of the pharmacy?s openness with them regarding the situation. Contributing factors include high volume, similarities between the two packages, improper workflow by the pharmacist, and storage of the two similar medications directly next to each other. |
|
VAERS ID: |
2548191 (history) |
Form: |
Version 2.0 |
Age: |
51.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2023-01-01 |
Onset: |
2023-01-02 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR6965B / UNK |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Client and family came by to receive the Bi-valent booster made by Moderna. They received the mono-valent booster in error. The family has been notified, and advised about potential adverse reactions such as a sore arm in the morning. The family was also advised to wait 2 months before getting the bivalent booster in accordance with current recommendations. The family members seemed frustrated, but understanding and appreciative of the pharmacy?s openness with them regarding the situation. Contributing factors include high volume, similarities between the two packages, improper workflow by the pharmacist, and storage of the two similar medications directly next to each other. |
|
VAERS ID: |
2548207 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Female |
Location: |
Kansas |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR6965B / UNK |
LA / IM |
FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
348384 / N/A |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Client and family came by to receive the Bi-valent booster made by Moderna. They received the mono-valent booster in error. The family has been notified, and advised about potential adverse reactions such as a sore arm in the morning. The family was also advised to wait 2 months before getting the bivalent booster in accordance with current recommendations. The family members seemed frustrated, but understanding and appreciative of the pharmacy?s openness with them regarding the situation. Contributing factors include high volume, similarities between the two packages, improper workflow by the pharmacist, and storage of the two similar medications directly next to each other. |
|
VAERS ID: |
2548216 (history) |
Form: |
Version 2.0 |
Age: |
50.0 |
Sex: |
Female |
Location: |
Kansas |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR6965B / UNK |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Client and family came by to receive the Bi-valent booster made by Moderna. They received the mono-valent booster in error. The family has been notified, and advised about potential adverse reactions such as a sore arm in the morning. The family was also advised to wait 2 months before getting the bivalent booster in accordance with current recommendations. The family members seemed frustrated, but understanding and appreciative of the pharmacy?s openness with them regarding the situation. Contributing factors include high volume, similarities between the two packages, improper workflow by the pharmacist, and storage of the two similar medications directly next to each other. |
|
VAERS ID: |
2548409 (history) |
Form: |
Version 2.0 |
Age: |
38.0 |
Sex: |
Female |
Location: |
Hawaii |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
017H22A / 2 |
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: Patient received Moderna Bivalent booster instead of Moderna (primary series) for second dose. Called patient to notify of mix up and patient came back to get Moderna second dose. |
|
VAERS ID: |
2548411 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Female |
Location: |
Hawaii |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
017H22A / 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient came in to get Moderna Primary series (first dose), but technican gave Moderna Bivalent booster . |
|
VAERS ID: |
2548412 (history) |
Form: |
Version 2.0 |
Age: |
52.0 |
Sex: |
Male |
Location: |
Kentucky |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
- / 5 |
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: Pt did not think that he had the pfizer bivalent booster yet- did not think he had his vaccine card with him. Said that his last vaccine was over 2 months ago and that it was Pfizer but the first 2 vaccine he got were Moderna. Vaccine given, then patient found documentation stating that he had the pfizer bivalent booster already exactly 2 months ago. Informed pt that he got an additional dose of the bivalent booster when it was not needed and gave him documentation to take home with him stating that he got that vaccine at my clinic given by me on todays date. |
|
VAERS ID: |
2548416 (history) |
Form: |
Version 2.0 |
Age: |
65.0 |
Sex: |
Female |
Location: |
Maine |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FR2583 / 4 |
- / 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? 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 THE ORIGINAL PFIZER MONO VALENT INSTEAD OF THE PFIZER BIVALENT DUE TO MY ERROR , PATIENT WILL HAVE TO RETURN TO US FOR ANOTHER VACCINE IN 2 MONTHS |
|
VAERS ID: |
2548863 (history) |
Form: |
Version 2.0 |
Age: |
11.0 |
Sex: |
Male |
Location: |
New Jersey |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9703 / 3 |
LA / IM |
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. |
WOOO244 / 1 |
RA / IM |
MNQ: MENINGOCOCCAL CONJUGATE (MENQUADFI) / SANOFI PASTEUR |
U7576AB / UNK |
RA / IM |
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
2ZF9N / 1 |
LA / IM |
Administered by: Public 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: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: Zofran Diagnostic Lab Data: n/a CDC Split Type: Write-up: This child was given Pfizer Bivalent 12 and up dose (0.3ml) instead of Pfizer Bivalent 5-11 years (0.2ml) |
|
VAERS ID: |
2548995 (history) |
Form: |
Version 2.0 |
Age: |
69.0 |
Sex: |
Female |
Location: |
Iowa |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
- / UNK |
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: N/A Current Illness: n/a Preexisting Conditions: n/a Allergies: nka Diagnostic Lab Data: n/a CDC Split Type: Write-up: Pt did not have an adverse event. However, pt presented for the newest Covid Booster. After giving pt Pfizer bivalent she presented cards that showed she already received Covid bivalent on 09/20/22 from her Dr. office. So pt accidently received a 2nd Pfizer bivalent booster dose. |
|
VAERS ID: |
2549030 (history) |
Form: |
Version 2.0 |
Age: |
44.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-03 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3274 / 3 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Chest pain, Palpitations SMQs:, Arrhythmia related investigations, signs and symptoms (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: thyroid np/levothyroxine Current Illness: cough reported 12/19 per medication history; visit to urgent care Preexisting Conditions: hypothyroidism Allergies: N/A Diagnostic Lab Data: CDC Split Type: Write-up: PER PATINET, AWOKE OVERNIGHT WITH HEART PALPITATIONS/MILD CHEST PAIN THAT HAS CONTINUED TO PRESENT TIME |
|
VAERS ID: |
2549054 (history) |
Form: |
Version 2.0 |
Age: |
70.0 |
Sex: |
Male |
Location: |
Idaho |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GL0446 / UNK |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Unevaluable 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: M/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: Write-up: N/A |
|
VAERS ID: |
2549106 (history) |
Form: |
Version 2.0 |
Age: |
80.0 |
Sex: |
Male |
Location: |
Nevada |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
011H22A / 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient received second bivalent booster |
|
VAERS ID: |
2549116 (history) |
Form: |
Version 2.0 |
Age: |
11.0 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3270 / 3 |
RA / IM |
Administered by: Pharmacy 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: CDC Split Type: Write-up: Both patients (twin brothers) were given the pfizer bivalent (gray cap) instead of the pediatric version. They are 11 years and 3 months but not old enough to receive this vaccine yet. Upon speaking to the mother the following day, the patients both are doing fine and not experiencing any side effects from their vaccination. |
|
VAERS ID: |
2549128 (history) |
Form: |
Version 2.0 |
Age: |
66.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-01 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 4 |
LA / IM |
Administered by: Public 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: Preexisting Conditions: N/A Allergies: None Diagnostic Lab Data: N/A CDC Split Type: Write-up: Patient received an extra dose of the Pfizer Bivalent Booster. Her original Bivalent was given on 10/4/2022 but was not entered on her CDC card |
|
VAERS ID: |
2549161 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Ohio |
Vaccinated: |
2023-01-01 |
Onset: |
2023-01-03 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
352491 / 1 |
RA / SYR |
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? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: UNKNOWN Current Illness: NONE Preexisting Conditions: UNKNOWN Allergies: NO KNOWN ALLERGIES Diagnostic Lab Data: UNKNOWN CDC Split Type: Write-up: PATIENT BEGAN TO PASS OUT AND IT IS AMBIGUOUS IF HE PASSED OUT OR HAD A MINOR SEIZURE. |
|
VAERS ID: |
2549354 (history) |
Form: |
Version 2.0 |
Age: |
19.0 |
Sex: |
Male |
Location: |
Colorado |
Vaccinated: |
2023-01-01 |
Onset: |
2023-01-01 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 1 |
RL / IM |
FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
997A5 / UNK |
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? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none reported on var Current Illness: none reported on var Preexisting Conditions: none reported on var Allergies: none reported on var Diagnostic Lab Data: CDC Split Type: Write-up: pt reeived the bivalent covid vaccine in error. patient came to pharmacy for primary series dose#1 |
|
VAERS ID: |
2549364 (history) |
Form: |
Version 2.0 |
Age: |
56.0 |
Sex: |
Female |
Location: |
Virginia |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS7170B / UNK |
LA / IM |
FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
AS3617B / N/A |
RA / IM |
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
397B5 / N/A |
RA / IM |
VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS |
7KG39 / 1 |
LA / 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: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: passed out after vaccinations were administered. regained consciousness after approximately 1 minute |
|
VAERS ID: |
2549474 (history) |
Form: |
Version 2.0 |
Age: |
24.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (NOVAVAX)) / NOVAVAX |
4302MF023 / 1 |
RA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Immediate post-injection reaction, Muscular weakness, Nausea, Paraesthesia SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (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: Write-up: Almost immediately after given vaccine client began to feel nausea, tingling in both arms and weakness, client placed in anti-gravity chair and water client began to feel better. |
|
VAERS ID: |
2549478 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Alaska |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9702 / 4 |
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? 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 was given a vaccine that was over 24 hours in room temperature. The advised temperature is no more than 12 hours in room temperature |
|
VAERS ID: |
2549481 (history) |
Form: |
Version 2.0 |
Age: |
67.0 |
Sex: |
Female |
Location: |
Alaska |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9702 / 4 |
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? 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: Thimerosol, sulfa Diagnostic Lab Data: None CDC Split Type: Write-up: Patient was given vaccine that was over 24 hours in room temperature. Patient will follow up with primary care doctor. |
|
VAERS ID: |
2549488 (history) |
Form: |
Version 2.0 |
Age: |
35.0 |
Sex: |
Male |
Location: |
Oregon |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-04 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3274 / 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: NO APPARENT ADVERSE REACTION, BIVALENT VACCINE ADMINISTERED FOR DOSE 1 INSTEAD OF MONOVALENT VACCINE. |
|
VAERS ID: |
2549506 (history) |
Form: |
Version 2.0 |
Age: |
7.0 |
Sex: |
Male |
Location: |
New Mexico |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
019H22A / 4 |
LA / IM |
FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT7682JA / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Headache, Nausea, 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: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: n/a CDC Split Type: Write-up: Patient mother reports headache , nausea and vommiting. Patient advised to maintain hydration. Acetominophen for headaches. |
|
VAERS ID: |
2550087 (history) |
Form: |
Version 2.0 |
Age: |
14.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-01 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
GJ6796 / 3 |
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? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: seasonal allergies Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: Developed fever 12 hours after vaccination, then significant bodyaches all over 24 hours later. Fever resolved after 48 hours, but bodyaches still persisting after 48 hours. |
|
VAERS ID: |
2550089 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Idaho |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
063B22A / 2 |
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: No medications Current Illness: None Preexisting Conditions: None Allergies: No known allergies Diagnostic Lab Data: N/A CDC Split Type: Write-up: No adverse reactions noted - Vaccines BUD date was 12/28/2022 - Vaccine given on 01/03/2023 5 days past BUD date |
|
VAERS ID: |
2550108 (history) |
Form: |
Version 2.0 |
Age: |
29.0 |
Sex: |
Female |
Location: |
Utah |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
- / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Dizziness, Dysgeusia, Eye irritation, Lacrimation increased, Nausea, Pharyngeal swelling, Swelling, Swelling face, Swollen tongue SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis (broad), Angioedema (narrow), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Corneal disorders (broad), Vestibular disorders (broad), Lacrimal 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? Yes Hospitalized? No Previous Vaccinations: Other Medications: Na Current Illness: Na Preexisting Conditions: Na Allergies: Penicillin Diagnostic Lab Data: I am going in to urgent care now. CDC Split Type: Write-up: Within 15 minutes of receiving the COVID19 Pfizer vaccination, I began feeling a swollen feeling near my left carotid artery, and it began radiating out through the left side of my face. My throat and tongue now feels swollen, and my eyes are burning and watery. I have a metalic taste in my mouth, and as of the last 5 minutes (2:41 pm) feel lightheaded and slightly nauseous. |
|
VAERS ID: |
2550113 (history) |
Form: |
Version 2.0 |
Age: |
34.0 |
Sex: |
Female |
Location: |
Maine |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6739 / 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: Bivalent booster was given for 1st dose in primary series |
|
VAERS ID: |
2550114 (history) |
Form: |
Version 2.0 |
Age: |
6.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
GD1857 / 3 |
LA / IM |
Administered by: Public 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: nka Diagnostic Lab Data: CDC Split Type: Write-up: Brief Description Patient presents to clinic to receive second dose Pfizer Covid 19 vaccine, parent present.. Parent provided Covid 19 Vaccination Record Card that showed 1st dose Pfizer was given. Parent requesting second dose of Pfizer Covid 19 vaccine. Upon documentation, it was discovered that patient had received second dose of Pfizer Covid 19 vaccine. Parent advised that patient had received second dose in the past. Parent continued to deny vaccine was given. Parent requesting for Covid 19 Pfizer second dose to be given today.. |
|
VAERS ID: |
2550115 (history) |
Form: |
Version 2.0 |
Age: |
9.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
GD1857 / 3 |
RA / IM |
Administered by: Public 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: n/a Current Illness: unknown Preexisting Conditions: unknown Allergies: Rice and Chocolate concentrate Diagnostic Lab Data: CDC Split Type: Write-up: Patient presented, accompanied by parent, for Second dose Pfizer COVID 19 vaccine. Parent presented vaccination card with only first dose vaccine administration. Parent stated patient had not received her second dose COVID 19 vaccine and denied ever receiving second dose COVID 19 vaccine. Parent advised of previously administered second dose COVID 19 vaccine. Parent continued to deny second dose COVID 19 vaccine was administered and continued requesting second dose COVID 19 vaccine to be administered on 1/03/23. |
|
VAERS ID: |
2550128 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Utah |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FT9142 / 2 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product preparation issue 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: None Preexisting Conditions: None Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: Vial of Covid 19 6m-4yr vaccine was not diluted with sodium chloride and all 10 doses were given to the patient in one injection. |
|
VAERS ID: |
2550141 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Female |
Location: |
Utah |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FT9142 / 2 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product preparation issue 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: NONE Current Illness: Hand Foot and Mouth (B08.4) 11/20/2022 Preexisting Conditions: NONE Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: Vial of Covid 19 6m-4yr vaccine was not diluted with sodium chloride and all 10 doses were given to the patient in one injection. |
|
VAERS ID: |
2550143 (history) |
Form: |
Version 2.0 |
Age: |
65.0 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
023H22A / 5 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Blood pressure increased, Dizziness, Heart rate increased, Laboratory test, Muscular weakness, Nausea SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypertension (narrow), Cardiomyopathy (broad), Vestibular disorders (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: unknown Current Illness: unknown Preexisting Conditions: Leukemia Allergies: codeine, Vicodin, ciprofloxacin, hydrocodone, lactulose, Latex Diagnostic Lab Data: Lab work was done at local hospital unknown results at this time CDC Split Type: Write-up: Patient experienced weakened muscles, rapid heart rate, elevated blood pressure, dizziness, nausea |
|
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FT9142 / 2 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product preparation issue 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: None Current Illness: None Preexisting Conditions: None Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: Vial of Covid 19 6m-4yr vaccine was not diluted with sodium chloride and all 10 doses were given to the patient in one injection. |
|
VAERS ID: |
2550154 (history) |
Form: |
Version 2.0 |
Age: |
30.0 |
Sex: |
Female |
Location: |
Indiana |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3274 / 2 |
LA / IM |
Administered by: Public 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: Not known Current Illness: NA Preexisting Conditions: NA Allergies: NKA Diagnostic Lab Data: CDC Split Type: Write-up: Patient did not have any adverse reactions to vaccine. |
|
VAERS ID: |
2550166 (history) |
Form: |
Version 2.0 |
Age: |
76.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
GH9702 / 2 |
LA / IM |
Administered by: Other 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: Aspirin Centrum Silver Duloxetine Metformin Rosuvastatin Calcium solifenacin succinate Tramadol Current Illness: None Preexisting Conditions: Hypertension Type 2 diabetes mellitus Fatty Liver Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Patient received COVID Booster, Pf Bivalent Booster, instead of 2nd dose of Pfizer vaccine in initial series. Patient did not exhibit adverse reaction and no treatment needed. |
|
VAERS ID: |
2550168 (history) |
Form: |
Version 2.0 |
Age: |
53.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
063B22A / 2 |
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? 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: The Patient was unintentionally provided an expired dose of this vaccine. The patient had no symptoms or adverse reactions. The patient was notified of the error and plans to return in 8 weeks to be revaccinated per CDC and the manufacturer guidelines. |
|
VAERS ID: |
2550171 (history) |
Form: |
Version 2.0 |
Age: |
74.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
GH9702 / 2 |
LA / IM |
Administered by: Other 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: Eliquis Atorvastatin Cyanocobalamin Lisinopril Meclizine Metoprolol tartrate omeprazole paroxetine polyethylene glycol promethazine tramadol Current Illness: None Preexisting Conditions: Hypertension Obstructive sleep apnea Reflux esophagitis Chronic Kidney Disease Allergies: Amlodipine Besylate Diagnostic Lab Data: none CDC Split Type: Write-up: Patient was administered Bivalent booster instead of 1st dose of COVID vaccine in initial series. |
|
VAERS ID: |
2550188 (history) |
Form: |
Version 2.0 |
Age: |
11.0 |
Sex: |
Male |
Location: |
Kentucky |
Vaccinated: |
2023-01-01 |
Onset: |
2023-01-03 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 3 |
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: Unknown Current Illness: Unknown Preexisting Conditions: Unknown Allergies: Unknown Diagnostic Lab Data: None CDC Split Type: Write-up: No adverse reactions. Patient received pfizer booster bivalent on 1/3/23, 3rd dose, however it was beyond use date. Placed in fridge on 10/17/22, beyond use on 12/26/22. |
|
VAERS ID: |
2550192 (history) |
Form: |
Version 2.0 |
Age: |
58.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / IM |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
LA / IM |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 3 |
LA / IM |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
- / 4 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Atrial fibrillation, Condition aggravated 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? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Atrial Fibrillation. Lasted about a couple hours, needed to take medication. Had not had an episode in several months and was feeding good. |
|
VAERS ID: |
2550198 (history) |
Form: |
Version 2.0 |
Age: |
8.0 |
Sex: |
Female |
Location: |
Virginia |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product preparation issue 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: none known Diagnostic Lab Data: None at this time CDC Split Type: Write-up: The nurse administered the Bivalent COVID vaccine without first diluting it. |
|
VAERS ID: |
2550200 (history) |
Form: |
Version 2.0 |
Age: |
54.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1415B / 5 |
LA / IM |
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? 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: Moderna infant dose was given to 54 yo patient |
|
VAERS ID: |
2550233 (history) |
Form: |
Version 2.0 |
Age: |
9.0 |
Sex: |
Female |
Location: |
Connecticut |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 1 |
UN / IM |
Administered by: Private Purchased by: ? Symptoms: Headache, Immunisation reaction, 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: no known allergies Diagnostic Lab Data: CDC Split Type: Write-up: Pfizer bivalent 12 and up was administered to 9 year old in error. Dose administered was 0.2ml. Parent notified, child had normal expected reaction following vaccine. 01/04/2023 child had mild headache. Also received influenza vaccine same day. |
|
VAERS ID: |
2550241 (history) |
Form: |
Version 2.0 |
Age: |
7.0 |
Sex: |
Female |
Location: |
Puerto Rico |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GL1657 / 3 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Expired product administered, Fatigue, Injection site reaction, Malaise 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 an expired pfizer bivalent dose (Beyond used date: 12/27/2022; administered on 01/02/2023). Spoke to patient''s mother and she said patient feels Injection site reactions, tired, and overall malaise. |
|
VAERS ID: |
2550260 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Arkansas |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-01 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: I was informed by the MA administering the vaccine that she did not dilute the vaccine prior to vaccination. No known adverse effects at this time. Patient''s mother was notified about error. She is going to keep an eye on the patient and will present to ER if any symptoms occur and will follow up with doctor. |
|
VAERS ID: |
2550277 (history) |
Form: |
Version 2.0 |
Age: |
77.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
055F22B / 6 |
RA / SYR |
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: CALCIUM, ESTRADIOL, HYDROXYCHLOROQUINE, JARDIANCE, LORATADINE, MUTLIVITAMIN, ROSUVASTATIN, SYNTHROID, TYLENOL ARTHRITIS Current Illness: NONE Preexisting Conditions: Allergies: FLAGYL Diagnostic Lab Data: NOTHING PATIENT IS FINE CDC Split Type: Write-up: PATIENT RECEIVED BIVALENT BOOSTER DOSE 1/3/2023 - HOWEVER WHEN SHE GOT HOME SHE HAD CARD THAT SHE HAD ALREADY GOTTEN DOSE ON 11/3/2022 WHICH WAS NEVER DOCUMENTED IN MEDICAL RECORD OR UPLOADED TO LOCAL CENTER. IMAGE FOUND AFTER PHONE CALL. PATIENT GOT TWO BIVALENT DOSES 2 MONTHS APART. |
|
VAERS ID: |
2550287 (history) |
Form: |
Version 2.0 |
Age: |
31.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
- / 3 |
RA / 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: Current Illness: Preexisting Conditions: MS Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: Vaccine given 1 day early, earliest due was 1/5/23 and vaccine was given 1/4/23. |
|
VAERS ID: |
2550314 (history) |
Form: |
Version 2.0 |
Age: |
69.0 |
Sex: |
Female |
Location: |
Puerto Rico |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
042H22A / 5 |
RA / IM |
Administered by: Pharmacy 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: WAS ADMINISTERED 1ML INSTEAD OF 0.5ML |
|
VAERS ID: |
2550335 (history) |
Form: |
Version 2.0 |
Age: |
29.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
FR2583 / 2 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Immediate post-injection reaction, 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? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none per patient, but reports she has had some issues with anesthesia in the past. Diagnostic Lab Data: none CDC Split Type: Write-up: patch of hives on right lower face and on left bend of arm immediately after injection. No shortness of breath, dizziness, or any other symptoms. monitored patient for 30 minutes after. |
|
VAERS ID: |
2550349 (history) |
Form: |
Version 2.0 |
Age: |
0.58 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
GD1857 / 2 |
RL / SYR |
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? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: poly trim drops Current Illness: none Preexisting Conditions: prematurity 29 weeks Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: The patient received the 5 -11 year old COVID 19 Pfizer vaccine instead of the 6 months - 4years vaccine |
|
VAERS ID: |
2550356 (history) |
Form: |
Version 2.0 |
Age: |
72.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 5 |
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 Pfizer Bivalent vaccine in October of this 2022 and scheduled another dose today 01/04/2023. We missed the previous dose and administered a second dose of Bivalent vaccine today. |
|
VAERS ID: |
2550359 (history) |
Form: |
Version 2.0 |
Age: |
1.75 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
GD1857 / 2 |
LL / SYR |
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? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: patient was given the 5 - 11 year COVID 19 vaccine and should have received the 6 months - 4 years vaccine |
|
VAERS ID: |
2550484 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
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 |
- / 3 |
- / IM |
Administered by: Private 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? 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: No adverse effects. CDC Split Type: Write-up: Wrong manufacturer given. This child should have received the Moderna Bivalent booster but was given the Pfizer Bivalent 3rd dose. This child got the Moderna 1st and 2nd dose primary series. |
|
VAERS ID: |
2550804 (history) |
Form: |
Version 2.0 |
Age: |
47.0 |
Sex: |
Male |
Location: |
Nevada |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FW1330 / 3 |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Pt was given monovalent instead of bivalent as a booster. |
|
VAERS ID: |
2550806 (history) |
Form: |
Version 2.0 |
Age: |
49.0 |
Sex: |
Female |
Location: |
Nevada |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FW1330 / 3 |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Pt was given monovalent instead of bivalent booster shot |
|
VAERS ID: |
2550807 (history) |
Form: |
Version 2.0 |
Age: |
52.0 |
Sex: |
Male |
Location: |
Nevada |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FW1330 / 3 |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient was given monovalent instead of bivalent booster shot |
|
VAERS ID: |
2550809 (history) |
Form: |
Version 2.0 |
Age: |
49.0 |
Sex: |
Female |
Location: |
Nevada |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FW1330 / 3 |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Gave patient monovalent booster instead of bivalent booster. |
|
VAERS ID: |
2550830 (history) |
Form: |
Version 2.0 |
Age: |
43.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-03 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
043H22A / 4 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site erythema, Injection site inflammation, Injection site swelling, Injection site warmth 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: UNKNOWN Current Illness: UNKNOWN Preexisting Conditions: UNKNOWN Allergies: NO KNOWN DRUG ALLERGIES Diagnostic Lab Data: NONE CDC Split Type: Write-up: PAIENT REPORTED THAT HER ARM (AROUND THE SITE OF INJECTION) WAS SWOLLEN, RED AND WARM TO THE TOUCH. SHE RECEIVED HER MODERNA BIVALENT COVID VACCINE BOOSTER 2 DAYS AGO AND HER SYMPTOM BEGAN THE MORNING AFTER AND HAD INCREASED IN AREA ON THE SECOND DAY. THE AREA APPEARED INFLAMMED ABOUT 2.5 INCHES X 2.5INCHES. PT WAS ADVISED TO CONTACT HER HEALTHCARE PROVIDER TO GET IT EVALUATED AND TO GO TO THE ER IF IT WORSENS. THE INFLAMMATION APPEARED LIKE A "COVID ARM" AND SHE WAS ALSO ADVISED IN THE MEANTIME TO APPLY COLD COMPRESS AND TAKE SOME TYLENOL FOR PAIN RELIEF. |
|
VAERS ID: |
2551032 (history) |
Form: |
Version 2.0 |
Age: |
1.58 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2023-01-02 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
215K22A / UNK |
- / OT |
Administered by: Unknown 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: USMODERNATX, INC.MOD20236 Write-up: rash on the abdomen and chest; This spontaneous case was reported by a physician and describes the occurrence of RASH (rash on the abdomen and chest) in an infant female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 215K22A) for COVID-19 prophylaxis. Previously administered products included for COVID-19 prophylaxis: Moderna COVID-19 Vaccine on 24-Jun-2022 and Moderna COVID-19 Vaccine on 29-Jul-2022. Past adverse reactions to the above products included No adverse event with Moderna COVID-19 Vaccine and Moderna COVID-19 Vaccine. On 02-Jan-2023 at 5:03 PM, 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. On an unknown date, the patient experienced RASH (rash on the abdomen and chest). At the time of the report, RASH (rash on the abdomen and chest) had not resolved. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. Patient did not received any other vaccines in the 4 weeks prior to COVID-19 vaccine. The parent reported a rash on the abdomen and chest starting 4 hours after the vaccine administration. Concomitant medication was not provided. Treatment medication information was not provided by the reporter. |
|
VAERS ID: |
2551310 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Female |
Location: |
Indiana |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
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 |
FP7136 / 3 |
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: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: NKA Diagnostic Lab Data: None CDC Split Type: Write-up: Patient was due to 3rd dose of COVID 19 vaccination. Consent and screening completed per mom. Pfizer COVID 19 Bivalent 12+ was ordered and RN gave Pfizer COVID 19 Monovalent 12+. Patient, parent, physician, and management notified of error. Patient waited in office 15 minutes after administration of vaccination with no adverse effects. |
|
VAERS ID: |
2551334 (history) |
Form: |
Version 2.0 |
Age: |
69.0 |
Sex: |
Female |
Location: |
Florida |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
AS7171B / UNK |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Contusion, Hypoaesthesia SMQs:, Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Guillain-Barre syndrome (broad), Accidents and injuries (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: nexium Current Illness: none Preexisting Conditions: none known. Allergies: nka Diagnostic Lab Data: CDC Split Type: Write-up: patient had brusing and numbness in there entire arm for days. |
|
VAERS ID: |
2551338 (history) |
Form: |
Version 2.0 |
Age: |
47.0 |
Sex: |
Female |
Location: |
Alabama |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-05 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ5342 / 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: Unknown; patient does not regularly fill at our pharmacy Current Illness: Unknown Preexisting Conditions: Unknown Allergies: Phenazopyridine Diagnostic Lab Data: None CDC Split Type: Write-up: Patient''s husband called 1/5/23 to report the patient had broken out in hives after receiving the Pfizer Bivalent Covid booster vaccine. I counseled him to give the patient two 25 mg Benadryl tablets to alleviate the hives and to go the the emergency room if symptoms worsen. |
|
VAERS ID: |
2551341 (history) |
Form: |
Version 2.0 |
Age: |
28.0 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-01 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FR2587 / 2 |
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: N/A Current Illness: Preexisting Conditions: Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: 2nd dose of Pfizer was given one day early |
|
VAERS ID: |
2551365 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 3 |
LL / IM |
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: None Current Illness: None Preexisting Conditions: GERD Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Patient was administered undiluted Pfizer 6mo-4yr Bivalent vaccine and was noticed after family left the office. Staff notified Supervisor. Pfizer contacted. Dr. will be contacting family today to notify them of incident. |
|
VAERS ID: |
2551411 (history) |
Form: |
Version 2.0 |
Age: |
10.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 1 |
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? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NONE NOTED Current Illness: NONE NOTED Preexisting Conditions: NONE NOTED Allergies: NONE NOTED Diagnostic Lab Data: NO CDC Split Type: Write-up: Patient came into the office with parent for 2nd dose of Peds Pfizer Vaccine, CVPP and I pulled the wrong vaccine, CVPO and administered to patient in the right deltoid which is the Peds Pfizer Bivalent dose; we do not have in stock; I immediately reported to my Nurse Manager, spoke with parent about vaccine error; obtained V/S normal (P94, R18, BP 112/78; T98, O2 98%); monitored patient for an hour; no distress noted; no S/S of any adverse effects; no swelling noted; no SOB; denies pain at site at this time; patient is alert/oriented; smiling, talking with her parents, and playing on her mobile device; parent verbalized understanding; I advised parent/patient someone will be in touch with her within 24 hours for follow up with the child |
|
VAERS ID: |
2551416 (history) |
Form: |
Version 2.0 |
Age: |
59.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
021H22A / UNK |
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? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None noted Current Illness: unknown Preexisting Conditions: unknown Allergies: unknown Diagnostic Lab Data: Patient was counseled and kept in the office for a longer observation period. CDC Split Type: Write-up: Patient was given a 2.5ml dose instead of a 0.5ml dose of the Moderna bivalent covid booster. |
|
VAERS ID: |
2551428 (history) |
Form: |
Version 2.0 |
Age: |
21.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
057A22A / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Dizziness, Fall SMQs:, Anticholinergic syndrome (broad), Accidents and injuries (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: Write-up: *Dose #1 Moderna Monovalent covid vaccine given at 10:46 am in left deltoid.Pt waited 15 minutes for observation; no problems noted. When he got up to leave, he fell on the floor. Pt stated no apparent injuries, but he felt dizzy. Pt denies having breakfast this morning. Pt able to ambulate with assistance; placed on stretcher. VS monitored for 1 hour by RN. At 10:55 am, bp=128/70, HR=80, Pulse ox=100%, skin cool and damp. At 11:15 am, BP=130/80, HR=86, Pulse ox=98%. Pt stated he felt much better, head of stretcher elevated.At 11:30am, BP=128/76, HR=76. Laughing, talkiing, skin is dry, denies discomfort.at 11:55 am, BP=127/72, HR=76. * Plan: Plan Pt left for home with wife; ambulatory. Denies dizziness or any symptoms. Advised to contact his PCP for any further concerns. |
|
VAERS ID: |
2551431 (history) |
Form: |
Version 2.0 |
Age: |
8.0 |
Sex: |
Female |
Location: |
Puerto Rico |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 3 |
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? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Asthma Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Dose administered past the expiration date |
|
VAERS ID: |
2551447 (history) |
Form: |
Version 2.0 |
Age: |
11.0 |
Sex: |
Female |
Location: |
Puerto Rico |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 3 |
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? 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: Dose administered past the expiration date |
|
VAERS ID: |
2551464 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Oregon |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 2 |
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: none Current Illness: None Preexisting Conditions: None Allergies: NKDA Diagnostic Lab Data: None CDC Split Type: Write-up: Pt was given Bivalent Pfizer 6mo - 4yr vaccine instead of the monovalent Pfizer 6mo - 4yr. |
|
VAERS ID: |
2551470 (history) |
Form: |
Version 2.0 |
Age: |
5.0 |
Sex: |
Male |
Location: |
Oregon |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
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 |
FT9142 / 2 |
RA / 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: None Current Illness: None Preexisting Conditions: None Allergies: NKDA Diagnostic Lab Data: None CDC Split Type: Write-up: Pt received the Pfizer monovalent 6mo - 4yr vaccine instead of the 5-11yr Monovalent vaccine for dose #2 |
|
VAERS ID: |
2551473 (history) |
Form: |
Version 2.0 |
Age: |
24.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
015B22A / 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: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: Patient had received the primary J&J vaccine and was considered fully vaccinated and was due for bivalent dose monovalent vaccine incorrectly administered for a booster dose. Per CDC recommendations patient will be scheduled for bivalent booster in 2 months |
|
VAERS ID: |
2551478 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 4 |
RA / 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Dose in Series Given Too Early- |
|
VAERS ID: |
2551483 (history) |
Form: |
Version 2.0 |
Age: |
10.0 |
Sex: |
Female |
Location: |
Puerto Rico |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 3 |
RA / 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? 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: Dose administered past the expiration date. |
|
VAERS ID: |
2551504 (history) |
Form: |
Version 2.0 |
Age: |
39.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6796 / 4 |
RA / IM |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 1 |
LA / IM |
Administered by: Public 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: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Patient received bivalent Pfizer( lot # GK1667)(age 6months-4 years) vaccine 0.2ml. inadvertently instead of the Pfizer (lot # GJ6796) adult vaccine dose(0.3ml). Clinical nurse consultant was contacted immediately and instructed to vaccinate patient immediately with correct vaccine for adult (12+). |
|
VAERS ID: |
2551505 (history) |
Form: |
Version 2.0 |
Age: |
9.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, Product preparation issue 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: dose was administer UNDILUTED, no side effects yet |
|
VAERS ID: |
2551523 (history) |
Form: |
Version 2.0 |
Age: |
38.0 |
Sex: |
Female |
Location: |
Missouri |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-03 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6742 / 4 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Chills, Feeling hot, Lymph node pain, Lymphadenopathy, Night sweats, Oral herpes, Pain, Petechiae SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Oropharyngeal infections (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: COVID Pfizer #2 5/2021 had similar reaction Other Medications: Adderall; Yaz; Venlafaxine; Zyrtec. Current Illness: NONE Preexisting Conditions: NONE Allergies: Garlic Diagnostic Lab Data: N/A CDC Split Type: Write-up: That night I had severe body aches and muscle spasms and during the night developed tender/swollen LEFT axillary lymph nodes. FYI: I''ve never had cosmetic fillers before. Tuesday during the day I felt feverish with chills (although had a normal temperature), worsening swelling to LEFT axillary lymph nodes, and night sweats. Wednesday, I continued to be achy, have tender/swollen lymph nodes and night sweats, and also developed petechiae on my face. Today on Thursday, I developed cold sore on my lip. |
|
VAERS ID: |
2551526 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
- / 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? 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: Patient completed a monovalent Pfizer primary series 10/22. Pt was in office for covid booster bivalent. Pt given Moderna bivalent in error as our office does not supply Pfizer under 5 yrs. |
|
VAERS ID: |
2551541 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 2 |
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: AUGEMENTIN ES-600 MG 5 ML BID UNTIL 01/06/2023 SINGULAR 4 MG QD HYDROXYZINE HCL 10 MG/5ML 4 ML Q HS FLOVENT HFA 110 MCG/2 PUFFS TWICE A DAY Current Illness: ACUTE SINUSITIS 12/27/22- TREATED WITH AUGMENTIN ES-600 FOR 10 DAYS Preexisting Conditions: MILD PERSISTENT ASTHMA Allergies: NO KNOWN ALLERGIES Diagnostic Lab Data: NONE CDC Split Type: Write-up: NO ADVERSE REACTION, NO TREATMENT OTHER THAN OBSERVATION FOR 15". PHYSICIAN NOTIFIED OF VACCINE GIVEN. HEALTH DEPT NOTIFIED |
|
VAERS ID: |
2551555 (history) |
Form: |
Version 2.0 |
Age: |
34.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-01 |
Onset: |
2023-01-04 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
015H22A / 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? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: LITHIUM CARBONATE 300MG TWICE DAILY, PALIPERIDONE ER 9MG ONCE DAILY, TRAZODONE 100MG TWICE DAILY Current Illness: NONE Preexisting Conditions: NONE Allergies: CYCLOBENZAPRINE, HYDROCODONE, MORPHINE Diagnostic Lab Data: NONE CDC Split Type: Write-up: WEDNESDAY, 1/4/2023, PATIENT RECEIVED 0.5ML MODERNA BI-VALENT BOOSTER WITHOUT HAVING RECEIVED THE PRIMARY, MONOVALENT SERIES. THURSDAY, 1/5/2023, WE CONTACTED HEALTH DEPARTMENT AND WE WERE ADVISED TO GIVE THE FIRST MONOVALENT VACCINE IMMEDIATELY. WE DO NOT HAVE THE MONOVALENT VACCINE IN STOCK SO THE PATIENT HAS MADE AN APPOINTMENT WITH HEALTH DEPARTMENT TO RECEIVE HIS FIRST MONOVALENT VACCINE ON WEDNESDAY, 1/11/2023. PATIENT HAS NO ADVERSE REACTIONS TO REPORT. |
|
VAERS ID: |
2551556 (history) |
Form: |
Version 2.0 |
Age: |
55.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
010H22A / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Lymph node pain, 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? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: topiramate, multivitamin, cetirizine, biotin, acetaminophen Current Illness: none Preexisting Conditions: prediabetes, obesity Allergies: nka Diagnostic Lab Data: NA - physical exam only. CDC Split Type: Write-up: lymphadenopathy on left side of neck, tenderness |
|
VAERS ID: |
2551563 (history) |
Form: |
Version 2.0 |
Age: |
62.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 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? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: aspirin, flonase, motrin, lisinopril, multivitamin, crestor, claritin, valtrex. Current Illness: Preexisting Conditions: hypertension, high cholesterol Allergies: penicillin, sulfa Diagnostic Lab Data: CDC Split Type: Write-up: Pt came in for primary dose of Covid vaccine. Pt was given bivalent dose instead of monovalent dose. |
|
VAERS ID: |
2551568 (history) |
Form: |
Version 2.0 |
Age: |
42.0 |
Sex: |
Male |
Location: |
Connecticut |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3274 / 3 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Blood test, Chest discomfort, Dyspnoea, Electrocardiogram, Lip swelling, Swelling face SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (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: Current Illness: Preexisting Conditions: Morbid Obesity; Obstructive Sleep Apnea; Type 2 Diabetes Mellitus; Hypertension; Pacemaker; Complete Heart Block; Major Depressive Disorder; Mild Persistent Asthma Osteoarthritis of Knee; PTSD; Dyspnea; Syncope. Allergies: Contrast Dye; Metrizamide; Ace Inhibitor; Avocado; Banana; Potassium Chloride; Kiwi; Tree Nut Latex. Diagnostic Lab Data: EKG and blood work done at ED. CDC Split Type: Write-up: Patient reported lip swelling, facial swelling, shortness of breath, chest tightness approximately 30 minutes after administration of vaccine. Patient was given one dose of Epi-pen 0.3 mg intramuscular injection and sent to ED via ambulance for observation. Patient was seen in ED and discharged home after 6 hour observation (pt given another dose of Epi-pen, steroids, Benadryl, Pepcid in the ED). |
|
VAERS ID: |
2551574 (history) |
Form: |
Version 2.0 |
Age: |
79.0 |
Sex: |
Female |
Location: |
Oregon |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
AS7166B / 7+ |
RA / IM |
Administered by: Public 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 was inadvertently given a second Moderna Bivalent Booster. She had one in October, then repeated on 1/4/23 |
|
VAERS ID: |
2551610 (history) |
Form: |
Version 2.0 |
Age: |
20.0 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-01 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1337 / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Anxiety, Dizziness, Facial paralysis, Paraesthesia SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad), Vestibular 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? Yes Hospitalized? No Previous Vaccinations: Other Medications: hydroxyzine (ATARAX) 25 MG tablet Sig - Route: Take 1 tablet by mouth every 8 hours as needed for Anxiety. - Oral Current Illness: Unknown Preexisting Conditions: Unknown Allergies: No known allergies Diagnostic Lab Data: Patient reported to urgent care 1/5/2023 CDC Split Type: Write-up: Patient was scheduled to receive her first primary dose of the Pfizer vaccine. She was given the Bivalent booster instead at 1407. She called back to the clinic about 45 minutes after leaving (after the 15 minute waiting period) to report "Patient reports upon returning home, felt "dizzy" then tingling sensation to limbs, face, may have droop to face as well." I called her again at 1600 and she reported that her symptoms had subsided and the urgent care felt her symptoms were anxiety induced. |
|
VAERS ID: |
2551626 (history) |
Form: |
Version 2.0 |
Age: |
40.0 |
Sex: |
Male |
Location: |
New Jersey |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-01 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6739 / 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Bivalent vaccine was accidentally given as a primary series first dose. |
|
VAERS ID: |
2551628 (history) |
Form: |
Version 2.0 |
Age: |
24.0 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
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 |
GJ6742 / 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: baclofen 10mg Current Illness: hyperthyroidism, obesity, hsv , chronic nonintractable headache, hidradenitis axillaris Preexisting Conditions: Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: physician ordered covid vaccine medical assistant wasn''t aware patient had never received primary dose so the booster vaccine was given and not the first dose patient is aware and understanding clinic manager was notified and she contacted pharmacist which stated this could be used as her primary dose |
|
VAERS ID: |
2551772 (history) |
Form: |
Version 2.0 |
Age: |
63.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-03 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
JJ3275 / 5 |
RA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Conjunctivitis, Vision blurred SMQs:, Severe cutaneous adverse reactions (broad), Anticholinergic syndrome (broad), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Conjunctival disorders (narrow), Ocular infections (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? No Hospitalized? No Previous Vaccinations: Shingrex 2--high fever Other Medications: Lisinopril 10 mg, Clonazepam .125 mg, Escitpralogram 5mg Current Illness: None Preexisting Conditions: High blood pressure Allergies: None Diagnostic Lab Data: None conducted. I called Dr. ''s office repeatedly and eventually walked in, but the clerk up front just handed me Systane and said it was likely a coincidence. Just after that I picked up my new glasses at my optician of many years and he looked at it, said he was quite sure it was conjunctivitis and that several of his older patients had had similar reactions to the bivalent. He encouraged me to file this report. CDC Split Type: Write-up: Blurred vision and Conjunctivitis in left eye beginning the day after the vaccine. I had no symptoms the day or week before and had not been anywhere to come in contact with the conjunctivitis. |
|
VAERS ID: |
2551799 (history) |
Form: |
Version 2.0 |
Age: |
14.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 4 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Gait disturbance, Pain in extremity SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: PT STATES HER left calf started hurting enough to make her limp. We elevated her leg for 15min and she said it felt better. advised guardian to watch and if worse see a DR |
|
VAERS ID: |
2551956 (history) |
Form: |
Version 2.0 |
Age: |
53.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
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 |
FP7140 / 4 |
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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: PATIENT WAS GIVEN THE MONOVALENT PFIZER COVID-19 BOOSTER INSTEAD OF THE BIVALENT BOOSTER. PATIENT DID NOT EXPERIENCE ANY IMMEDIATE SIDE EFFECTS OR ADVERSE EFFECTS, DISPLAYED NO SIGNS OR SYMPTOMS OF A REACTION. CALLED AND THEY SAID THAT PATIENT WILL JUST NEED TO COME IN TWO MONTHS FOR BIVALENT BOOSTER SHOT. |
|
VAERS ID: |
2551984 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6737 / 3 |
RA / 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Faint |
|
VAERS ID: |
2551986 (history) |
Form: |
Version 2.0 |
Age: |
38.0 |
Sex: |
Female |
Location: |
Michigan |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-05 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 3 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Chills, Headache, Incorrect product formulation administered, Malaise, Pain, Photophobia, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious meningitis (narrow), Glaucoma (broad), Corneal disorders (broad), Retinal 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: Prenatal vitamins, Fluoxetine 10 mg Current Illness: No Preexisting Conditions: Gerd, chest pains. Allergies: Sulpha Drugs Diagnostic Lab Data: None. I informed my doctor Dr. who recommended that I create a report on this site. CDC Split Type: Write-up: I was given the wrong booster dose yesterday. I had already got 3 COVID shots (primary series and monovalent booster). I was scheduled to receive 2nd booster which is the bivalent one that protects against omicron. I got my shot yesterday and fell sick today with ith fever, chills, body pain, headache and light sensitivity. To my horror, I received a call from pharmacy stating that they gave me the monovalent booster instead of the bivalent one that I was supposed to receive. They said I will not be able to get the bivalent booster till 10 th February. My fever and chills have subsided but I still have body pain and headache and light sensitivity. |
|
VAERS ID: |
2552136 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2023-01-02 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 3 |
LA / 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? 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: No adverse event - vaccine given 23 days too early |
|
VAERS ID: |
2552390 (history) |
Form: |
Version 2.0 |
Age: |
78.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2023-01-04 |
Onset: |
2023-01-04 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS7166B / UNK |
- / OT |
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: Bradycardia; Dementia; GERD Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20236 Write-up: No Adverse Event; Patient received a dose from a vial that was punctured a week ago; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial that was punctured a week ago) and NO ADVERSE EVENT (No Adverse Event) in a 78-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7166B) for COVID-19 prophylaxis. Concurrent medical conditions included GERD, Dementia and Bradycardia. On 04-Jan-2023, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .5 milliliter. On 04-Jan-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial that was punctured a week ago). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial that was punctured a week ago) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received a dose from a vial that was punctured a week ago). No concomitant medication details was reported. No other vaccine received 4 weeks prior to COVID-19 vaccine. No treatment medication details was reported. |
|
VAERS ID: |
2552399 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Hawaii |
Vaccinated: |
2023-01-02 |
Onset: |
2023-01-02 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1667 / 3 |
RL / IM |
Administered by: Other 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: Error: Wrong Vaccine/Product Administered- |
|
VAERS ID: |
2552409 (history) |
Form: |
Version 2.0 |
Age: |
19.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FR2587 / 2 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: No adverse event, 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: None reported Current Illness: None reported Preexisting Conditions: None reported Allergies: No known allergies Diagnostic Lab Data: None CDC Split Type: Write-up: Patient received a COVID vaccine that had been out of the refrigerator for longer than 12 hours. No adverse reaction reported. |
|
VAERS ID: |
2552419 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2023-01-05 |
Onset: |
2023-01-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3274 / 4 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Blood pressure increased, Dyspnoea SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Hypertension (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? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: apples Diagnostic Lab Data: CDC Split Type: Write-up: patient was administered covid pfizer bivalent booster vaccine and within minutes she had trouble breathing and holding her throat. pharmacist administered epinephrine and 911 was contacted. patient immediately improved after administration, her throat felt better and breathing improved. local county sheriff was in close proximity to pharmacy and came in while awaiting local ems and police to arrive. pt was stable and was assessed by local ems. she had elevated blood pressure due to epinephrine. mother opted not to transport to ER by ems. Patient and mother left the pharmacy about 7pm. Pharmacist followed up with parent next day 1/6 about 930am and mother stated she did take daughter local ER for further evaluation where she was given rx for benadryl, prednisone, and epinephrine |
|
VAERS ID: |
2552439 (history) |
Form: |
Version 2.0 |
Age: |
|
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2023-01-03 |
Onset: |
2023-01-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2023-01-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS7170B / 5 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Feeling abnormal, Immunisation reaction, Pain in extremity, Underdose SMQs:, Dementia (broad), Tendinopathies and ligament 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: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20236 Write-up: Light reaction she felt following injection; Little soreness in her arm; she suspected of the dosage administered/she hesitated about receiving a full dose/patient doubts about receiving a full dose of the vaccine; Did not feel the needle/ weird things happened following administration; This spontaneous case was reported by a patient and describes the occurrence of IMMUNISATION REACTION (Light reaction she felt following injection), FEELING ABNORMAL (Did not feel the needle/ weird things happened following administration), PAIN IN EXTREMITY (Little soreness in her arm) and UNDERDOSE (she suspected of the dosage administered/she hesitated about receiving a full dose/patient doubts about receiving a full dose of the vaccine) in a female patient of an unknown age who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7170B) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (Dose1, lot ER2630, Presented with symptoms not severe at all) on 19-Mar-2021, Pfizer (Doe 2, Lot EW0158, Presented with symptoms not severe at all) on 09-Apr-2021, Pfizer (Dose 3, Lot 32030BD, Presented with symptoms not severe at all) on 21-Oct-2021 and Flu shot (feeling something in her bones and migrating in the body in the lower back like a flu shot). Past adverse reactions to the above products included Vaccination adverse reaction with Flu shot, Pfizer, Pfizer and Pfizer. On 03-Jan-2023, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 03-Jan-2023, the patient experienced FEELING ABNORMAL (Did not feel the needle/ weird things happened following administration) and UNDERDOSE (she suspected of the dosage administered/she hesitated about receiving a full dose/patient doubts about receiving a full dose of the vaccine). On 04-Jan-2023, the patient experienced PAIN IN EXTREMITY (Little soreness in her arm). On an unknown date, the patient experienced IMMUNISATION REACTION (Light reaction she felt following injection). At the time of the report, IMMUNISATION REACTION (Light reaction she felt following injection), FEELING ABNORMAL (Did not feel the needle/ weird things happened following administration), PAIN IN EXTREMITY (Little soreness in her arm) and UNDERDOSE (she suspected of the dosage administered/she hesitated about receiving a full dose/patient doubts about receiving a full dose of the vaccine) outcome was unknown. No concomitant drug information was provided. Reporter reported that after second or third Pfizer dose, patient felt sleepy and always soreness in the injection site. It was reported that the following the Moderna vaccination, the patient felt nothing for hours, and didn''t feel any soreness at the injection site. Patient did not felt the needle and also after injection the needle was not put in the hazard bucket. Next day following the vaccination patient felt little soreness in the arm, not consisting for her with a full dose. Patient wanted to make a complaint, because she hesitated about receiving a full dose. No treatment drug information was provided. This case was linked to MOD-2023-694548 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 05-Jan-2023: Follow-up received contains non-significant information. |
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