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Life Threatening? No
Write-up: Miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106290915153710-98QTS, Safety Report Unique Identifier is GB-MHRA-ADR 25562135. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 18May2021 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had not had symptoms associated with COVID-19, was not enrolled in clinical trial. The patient was pregnant at time of vaccination. The patient experienced miscarriage in 2021 with outcome of recovered. The patient underwent lab tests and procedures which included COVID-19 virus test was negative. Patient has not tested positive for COVID-19 since having the vaccine. The event was reported as serious and seriousness criteria was provided as other medically important condition. No follow-up attempts are possible; information about lot/batch number cannot be obtained.
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