이상반응 보고

VAERS ID	1760052
성별	여성
나이	34세
주 코드	FR
제약회사	PFIZER\BIONTECH
로트 번호
예방접종 횟수	2
접종일	2021-07-31
발병일
상태	회복

증상

• 자연 낙태(Abortion spontaneous)
• 임신 중 모성 노출(Maternal exposure during pregnancy)

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임상 검사

증상 상세

spontaneous miscarriage; pregnant female patient received bnt162b2; This is as spontaneous report received from a contactable consumer downloaded from the regulatory authority-WEB.
The regulatory authority report number is FR-AFSSAPS-PS20212091.
The same reporter reported events after both vaccine doses for the mother and the fetus.
This is the first report for the second dose, for the mother.
A 34-year-old pregnant female patient received bnt162b2 (COMIRNATY), intramuscular, administered in the left arm on 31Jul2021 (at the age of 34-years-old) (Batch/Lot Number: Unknown) as dose 2, single for COVID-19 immunisation.
Pregnancy information included 48 days gestation period.
Medical history and concomitant medications were not reported.
No history of COVID.
On an unspecified date, the patient experienced spontaneous miscarriage.
The event was described as follows: Report of a spontaneous miscarriage 13 days after the second injection of the Comirnaty vaccine.
There is a strong coincidence between the date of the stop of growth of the embryo given by the doctor and the date of this second injection.
The embryo stopped at 6 WA + 6 days.
The patient recovered from spontaneous miscarriage on an unspecified date.
Spontaneous miscarriage was considered serious, medically significant by the regulatory authority.
"Accountability score (s) established without prejudice to the elements of investigation which could be carried out within the framework of legal or amicable compensation procedures" Official Bulletin No follow-up attempts possible.
No further information expected.
; Sender's Comments: Linked Report(s) : FR-PFIZER INC-202101239544 Fetal case