이상반응 보고

VAERS ID	1452697
성별	여성
나이
주 코드	FR
제약회사	PFIZER\BIONTECH
로트 번호
예방접종 횟수	2
접종일
발병일	2021-04-29
상태

증상

• 자연 낙태(Abortion spontaneous)

이환 중 질병

지병

Comments: Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test Patient is not enrolled in clinical trial

기타 의료

이전 예방접종

알레르기

임상 검사

증상 상세

Miscarriage of pregnancy; This is a spontaneous report from a contactable consumer.
This report is received from the Regulatory Agency (RA).
The regulatory authority report number is GB-MHRA-WEBCOVID-202106221233114910-Q16SV, Safety Report Unique Identifier is GB-MHRA-ADR 25520067.
A female patient of an unspecified age received bnt162b2 (COVID-19 MRNA VACCINE BIONTECH, Solution for injection, Lot Number: Not reported), dose 2 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization.
The patient medical history and concomitant medications were not reported.
The patient had not had symptoms associated with COVID-19, not had a COVID-19 test, and was not enrolled in any clinical trial.
The patient previous vaccine included bnt162b2 (COVID-19 MRNA VACCINE BIONTECH, Solution for injection, Lot Number: Not reported), dose 1 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization.
On 29Apr2021, the patient had a miscarriage of pregnancy.
The outcome of the event was recovered with sequelae.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.