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Write-up: joint pain; High temperature; Injection site muscle pain; Generalized joint pain; Headache; Decreased appetite; This is a spontaneous report from a contactable consumer received from the regulatory authority report number is GB-MHRA-WEBCOVID-202106051430043410-ENHLB, Safety Report Unique Identifier GB-MHRA-ADR 25425944.A 34-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 04Jun2021 (Lot number was not reported) as 1st dose, single dose for covid-19 immunisation. Medical history included Lactation decreased, cold, Common cold. Had a cold ongoing for 3 weeks at time of vaccine being administered. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not pregnant, Patient is not currently breastfeeding.Concomitant medication(s) included paracetamol, phenylephrine hydrochloride (LEMSIP MAX) taken for nasopharyngitis from 16May2021 to an unspecified stop date. The patient experienced joint pain on an unspecified date with outcome of unknown, high temperature on 04Jun2021 with outcome of not recovered, injection site muscle pain on 04Jun2021 with outcome of not recovered, generalized joint pain on 04Jun2021 with outcome of not recovered, headache on 04Jun2021 with outcome of recovering, decreased appetite on 04Jun2021 with outcome of not recovered.The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 26May2021, No - Negative COVID-19 test. Case Narrative: The joint pain and headache are sufficient that she cannot move without significant difficulty. Patient has not tested positive for COVID-19 since having the vaccine. All events were marked as medically significant. No follow-up attempts are possible, information about batch number cannot be obtained. No further information is expected.
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