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|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||FF3622 / 1||- / -|
Administered by: Other Purchased by: ??
Symptoms: Arrhythmia, Blood pressure increased, Body temperature, Epilepsy, Oxygen saturation, Presyncope, Seizure, Syncope, Blood pressure measurement
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Diagnostic Lab Data: Test Date: 20210906; Test Name: Blood pressure; Result Unstructured Data: Test Result:150/110 mmHg; Test Date: 20210906; Test Name: Body temperature; Result Unstructured Data: Test Result:36.9 Centigrade; Comments: before vaccination; Test Date: 20210906; Test Name: Spo2; Test Result: 98 %; Comments: room air
CDC 'Split Type': JPPFIZER INC202101170665
Write-up: Arrhythmia; Epilepsy; Blood pressure 150/110 mmHg; Convulsion for 30 seconds/hands and legs developed movement like Convulsion; Syncope; vasovagal reflex; This is a spontaneous report from a contactable physician received from the regulatory authority. Regulatory authority report number is v21126088. A 24-year-old male patient (also reported as 24-year and 4-month-old) received BNT162b2 (COMIRNATY, Solution for injection), via an unspecified route of administration on 06Sep2021 at 13:30 (Batch/Lot Number: FF3622; Expiration Date: 30Nov2021) (at the age of 24-years-old) as dose 1, single for COVID-19 immunisation. Body temperature before vaccination was 36.9 degrees Centigrade. The patient had no family history. There were no points to be considered on the vaccine screening questionnaire (primary diseases, allergies, vaccinations and illnesses within the last one month, medications the patient was taking, past adverse effect history, growth status). On 06Sep2021 at 13:35 (5 minutes after the vaccination), the patient experienced Convulsion for 30 seconds, Syncope, and vasovagal reflex. On 06Sep2021 (the day of the vaccination), the outcome of the event was recovering. The course of the event was as follows: The patient experienced Syncope several minutes after the vaccination and the same time, his hands and legs developed movement like Convulsion. Blood pressure 150/110 mmHg. Opened eyes in the normal position of the eyeball, lips and mouth were not seen. The patient recovered consciousness after reposed. SpO2 98% (room air), no symptoms. The events were considered as vasovagal reflex but with movement like Convulsion. The reporting physician classified the event as non-serious and assessed that the causality between the event and BNT162b2 as unassessable. Other possible cause(s) of the event such as any other diseases were Arrhythmia, Epilepsy. The reporting physician commented as follows: it was not sure whether the event was vasovagal reflex caused by vaccination or accidentally developed Convulsion. No follow-up attempts are possible. No further information is expected.; Reporter''s Comments: It was not sure whether the event was vasovagal reflex caused by vaccination or accidentally developed Convulsion.
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