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Life Threatening? No
Write-up: muscle pain; pins and needles; Muscle ache; muscle pain at the injection site; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106041141474890-Y3M1N. Safety Report Unique Identifier is GB-MHRA-ADR 25419676. A 50-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on 03Jun2021 (Lot Number: EW3143-L690) as single dose for COVID-19 immunisation. The patient medical history was not reported. Patient had not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. The patient''s concomitant medications were not reported. The patient experienced muscle pain on an unspecified date, pins and needles on an unspecified date, muscle ache on 03Jun2021. Started off with slight pins and needles in arm shortly after leaving vaccination center. After a few hours there was muscle pain at the injection site. This had remained during the following day. Patient had not tested positive for COVID-19 since having the vaccine. The events were reported as serious due to medically significant. The patient underwent lab tests and procedures which included COVID-19 virus test: Negative on 20May2021. The outcome of the event muscle ache and muscle pain at the injection site were not recovered, while the other events were recovering. No follow-up attempts are possible. No further information is expected.
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