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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||- / -|
Administered by: Other Purchased by: ??
Symptoms: Circulatory collapse, Dyspnoea
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': DEPFIZER INC2021795798
Write-up: Acute circulatory failure; Dyspnea; This is a spontaneous report from a non-contactable physician downloaded from the Regulatory Authority. The regulatory authority number DE-PEI-202100113103. A 51-years-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on 22Jun2021 (Batch/Lot Number: Unknown) as dose number unknown, single for Covid-19 immunisation. The patient''s weight and height were not reported. The patient medical history and concomitant medications were not reported. On 22Jun2021, five hours after vaccination the patient experienced dyspnea, acute circulatory failure, and had a resuscitation. The events were reported as fatal. The patient died on 22Jun2021. It was not reported if an autopsy was performed. Event assessment : Comirnaty/ all events/Result of Assessment: Unclassifiable No follow-up attempts are possible, information on batch/lot number cannot be obtained. No further information expected.; Reported Cause(s) of Death: dyspnea; Acute circulatory failure
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