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Life Threatening? No
Write-up: This is a spontaneous report from a contactable consumer received via COVID-19 Adverse Event Self-Reporting. The patient was a non-pregnant 81-year-old female. It was not reported whether the patient received any other vaccines within 4 weeks prior to the COVID vaccine or any other medications within 2 weeks of vaccination. It was unknown whether the patient was diagnosed with COVID-19 prior to vaccination. The patient had no allergies to medications, food, or other products. Other medical history included oedema and neuralgia. On 02Jun2021 at 10:30 (the day of vaccination), the patient received the first single dose of BNT162b2 (COMIRNATY, Solution for injection, Lot number FA7338, Expiration date 30Sep2021) via an unspecified route of administration in the left arm for COVID-19 immunization. On 03Jun2021 (1 day after the vaccination), the patient experienced death. It was unknown if autopsy was done. The outcome of the event was fatal without treatment. It was unknown whether the patient the patient had been tested for COVID-19 since the vaccination.; Reported Cause(s) of Death: Death
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