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From the 5/31/2024 release of VAERS data:

Found 28,192 cases where Vaccine is COVID19 or COVID19-2 and Vaccination Date from '2023-01-01' to '2023-12-31'

Government Disclaimer on use of this data

Table

   
Event Outcome Count Percent
Death 472 1.67%
Life Threatening 547 1.94%
Permanent Disability 753 2.67%
Birth Defect 7 0.02%
Hospitalized 2,042 7.24%
Hospitalized, Prolonged 12 0.04%
Emergency Doctor/Room 1,652 5.86%
Emergency Room 2 0.01%
Office Visit 3,457 12.26%
Recovered 7,211 25.58%
None of the Above 15,665 55.57%
TOTAL † 31,820 † 112.87%
† Because VAERS cases can have multiple vaccinations, symptoms, and event outcomes, a single case can account for multiple entries in this table. This is why the Total Count is greater than 28,192 (the number of cases found), and the Total Percent is greater than 100.



Case Details

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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


VAERS ID: 2550147 (history)  
Form: Version 2.0  
Age: 2.0  
Sex: Male  
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: 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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