Your Health. Your Family. Your Choice.
|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: Respiratory failure, Vaccination complication
Life Threatening? Yes
Birth Defect? No
Permanent Disability? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days:
Write-up: Pulmonary failure; serious health/medical complications (vaccination adverse reaction); This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority-WEB. Regulatory authority report number is CZ-CZSUKL-21001570. A 31-year-old female patient received first dose of BNT162B2 (COMIRNATY; Solution for injection, unknown lot number and expiration), intramuscular on 29Dec2020 at a single dose for COVID-19 immunisation. Medical history included cystic fibrosis, lung transplant in Dec2007, and kidney transplant in 2015, all ongoing. The patient''s concomitant medications were not reported. Few hours after the vaccination, the patient experienced serious health/medical complications (vaccination adverse reaction) on 30Dec2020 which needed immediate medical care, patient was hospitalized. Pulmonary failure developed later on unspecified date, and the patient was transferred to Department of Anesthesiology, Resuscitation and Intensive Medicine, where she died on 03Feb2021. The attending physician was contacted. No further information and are waiting for results from indicated tests and autopsy report. Whole report will be sent with complete information. Outcome of serious health/medical complications (vaccination adverse reaction) was unknown. The patient died of pulmonary failure on 03Feb2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Pulmonary failure
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