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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||- / 1||- / OT|
Administered by: Other Purchased by: ??
Symptoms: Sudden death
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
Other Medications: LERCANIDIPINE; MOXONIDIN; APIXABAN; PRAMIPEXOLE; L-DOPA; ISOSORBIDE; SIMVASTATIN; METOPROLOL
Preexisting Conditions: Medical History/Concurrent Conditions: Apoplexy; Artificial cardiac pacemaker user; Atrial fibrillation; AV block third degree; Cerebral ischaemia; COPD; Dementia; Hypertension arterial; Parkinson''s disease; Sick sinus syndrome
Diagnostic Lab Data:
CDC 'Split Type': DEPFIZER INC2021199863
Write-up: Sudden death; This is a spontaneous report from a non-contactable physician downloaded from the Medicines Agency (MA) Regulatory authority-WEB [DE-DCGMA-21188070]. A female patient of an unspecified age received the first dose of bnt162b2 (COMIRNATY), intramuscularly on 10Feb2021 at single dose for covid-19 immunisation. Medical history included AV block third degree, Parkinson''s disease, artificial cardiac pacemaker user, hypertension arterial, chronic obstructive pulmonary disease (COPD), sick sinus syndrome, cerebral ischaemia, dementia, apoplexy and atrial fibrillation, all from an unknown date and unknown if ongoing. Concomitant medication included lercanidipine, moxonidine (MOXONIDIN), apixaban, pramipexole, l-dopa, isosorbide, simvastatin and metoprolol. On 12Feb2021 after vaccination, the patient developed death sudden, lasted for unknown. Death cause was reported as sudden death. It was not reported if an autopsy was performed. Relatedness of drug to reactions/events assessed as D. Unclassifiable as PEI. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Sudden death
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