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Life Threatening? Yes
Write-up: Respiratory failure; Pneumonia; covid-19; This is a spontaneous report from a non-contactable physician downloaded from the Medicines Agency (MA) Regulatory Authority-WEB. The regulatory authority report number is DE-PEI-PEI2021001974. An 86-year-old female patient received BNT162B2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE), intramuscular on 16Jan2021 at single dose for covid-19 immunization. Medical history included dementia, stroke, and atrial fibrillation from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. The patient experienced covid-19 on 19Jan2021; the patient also experienced respiratory failure and pneumonia on an unspecified date, which were serious as they were life threatening, and lead to death. Details were as follows: covid-19 on 19Jan2021 was noted. Also reported unknown after vaccination, the patient developed respiratory failure and pneumonia, reported as lasting until 29Jan2021. The patient was dead and condition was reported as life threatening. Death cause was reported as respiratory failure and pneumonia. The patient died on 29Jan2021. It was not reported if an autopsy was performed. The patient under lab test include covid-19 virus test: covid-19 on 19Jan2021. The batch/lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up. Follow-up (15Feb2021): This follow-up is being submitted to notify that the batch number is not available, follow-up activities not applicable, information about lot/batch number cannot be obtained. Further follow-up information will be provided automatically upon availability via MA.; Reported Cause(s) of Death: pneumonia; respiratory failure
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