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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||- / UNK||- / OT|
Administered by: Other Purchased by: ??
Symptoms: Cardiac arrest, Aortic rupture
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
Diagnostic Lab Data:
CDC 'Split Type': JPPFIZER INC202100987495
Write-up: aortic rupture; cardiac arrest; This is a spontaneous report from a contactable physician received via a Pfizer employee. A 93-year-old female patient received BNT162B2 (COMIRNATY, solution for injection, lot number and expiry date were not reported), intramuscularly on 04Jun2021 as dose number unknown, 0.3 mL single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient experienced aortic rupture and cardiac arrest on 20Jun2021. The clinical course was as follows: On 04Jun2021, the patient received Comirnaty. It had passed without any problems. On 20Jun2021, the patient died from cardiac arrest due to aortic rupture at the facility that the patient went for a short stay. The cause of death was aortic rupture. The patient died on 20Jun2021. It was not reported if an autopsy was performed and the reported causes of death were aortic rupture and cardiac arrest. The reporting physician commented as follows: It had passed more than two weeks after the vaccination, and the causality was unknown. The lot number for BNT162b2 was not provided and will be requested during follow up.; Reported Cause(s) of Death: aortic rupture; cardiac arrest
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