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Write-up: acute kidney injury; Covid pneumonitis/Covid postive; Covid pneumonitis/Covid postive; Acute diarrhea; This is a spontaneous report from a contactable physician. This is a report received from the Regulatory Agency (MHRA). Regulatory authority report number GB-MHRA-EYC 00241369, Safety Report Unique Identifier GB-MHRA-ADR 24791249. An 84-year-old male patient receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL0739), intramuscular on 14Jan2021 at 0.3 mL, single for COVID-19 immunisation. The patient medical history was not reported. Concomitant medications included allopurinol, atorvastatin calcium, bisoprolol fumarate, furosemide sodium, lisinopril anhydrous, warfarin, lisinopril. The patient experienced acute diarrhea (death) on 15Jan2021, covid pneumonitis/covid postive (death, medically significant) on 30Jan2021, acute kidney injury (death, hospitalization, medically significant) on 20Jan2021. The patient underwent lab tests and procedures which included COVID-19 virus test: negative on 21Jan2021, COVID-19 virus test: negative on 24Jan2021, COVID-19 virus test: negative on 26Jan2021, COVID-19 virus test: negative on 28Jan2021, COVID-19 virus test: positive on 30Jan2021, Virus stool test: negative on 26Jan2021. The patient died on 08Feb2021. It was not reported if an autopsy was performed. The outcome of the events was fatal. The clinical course was reported as follows: Developed Diarrhoea. Diagnosis with acute kidney injury on 20Jan2021 and admitted to hospital. Died on 08Feb2021. Covid pneumonitis. Reporter was aware patient died of covid -but impact of vaccine on possible cause of admission reporter wish to report. No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: Covid pneumonitis/Covid postive; Acute kidney injury; Covid pneumonitis/Covid postive; Acute diarrhea
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