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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, Incorrect route of product administration
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: Medical History/Concurrent Conditions: CPAP; Hypothyreosis; Ischemic heart disease; Percutaneous coronary intervention; Pulmonary embolism; Sleep apnea
Diagnostic Lab Data:
CDC 'Split Type': SEPFIZER INC2021389516
Write-up: Cardiac arrest; comirnaty administered via subcutaneous; This is a spontaneous report from a contactable physician downloaded from the Agency Regulatory Authority-WEB. The Regulatory Authority report number is SE-MPA-2021-023470, other case identifier number SE-MPA-1616707176996. A 78-year-old male patient received BNT162B2 (COMIRNATY, lot number and expiration date not reported), subcutaneous on 25Mar2021 as a single dose for COVID-19 immunisation. Medical history included ischemic heart disease, Hypothyreosis, sleep apnea uses CPAP (continuous positive airway pressure) at night, pulmonary embolism and previous percutaneous coronary intervention in 2005. The patient''s concomitant medications were not reported. According to a relative, the patient has been feeling well lately. On the same day that the patient was vaccinated with Comirnaty, on 25Mar2021, the patient experienced cardiac arrest in the evening. The patient died the same day despite CPR (cardiopulmonary resuscitation) for nearly 60 minutes. The patient died on 25Mar2021. It was not reported if an autopsy was performed. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Cardiac arrest
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