이상반응 보고
| VAERS ID | 1767502 |
|---|---|
| 성별 | 여성 |
| 나이 | 48세 |
| 주 코드 | LA |
| 제약회사 | PFIZER\BIONTECH |
| 로트 번호 | ER8729 |
| 예방접종 횟수 | |
| 접종일 | 2019-10-01 |
| 발병일 | 2021-04-30 |
| 상태 | 회복 |
증상
- 자궁 출혈(Uterine haemorrhage)
- 심한 월경 출혈(Heavy menstrual bleeding)
- 자궁 염증(Uterine inflammation)
이환 중 질병
지병
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
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증상 상세
Heavy bleeding and inflammation where IUD was; Heavy bleeding and inflammation where IUD was; Her period was very heavy, moreso than ever, and the next month and the month after was worse; This is a spontaneous report from a contactable consumer (patient).
A 48-year-old female patient received bnt162b2 (BNT162B2), intramuscular administered in Arm Left on 14Apr2021 15:00, at the age of 48-years-old, (Lot Number: ER8729; Expiration Date: 31Jul2021) as DOSE 2, 0.
3 ML SINGLE for covid-19 immunisation; intrauterine contraceptive device (PARAGARD), via an unspecified route of administration from Oct2019 (Batch/Lot number was not reported) for Birth control.
Historical vaccine includes dose 1 of Comirnaty, lot number: EP6955, expiration date: 30Jun2021, 30mcg, injected in left arm in the muscle.
The patient also previously received flu vaccine in which her arm hurt and felt tired.
The patient's medical history includes none.
Concomitant medication is none.
On 30Apr2021 12:00, the patient stated she started having Heavy bleeding and inflammation where IUD was.
It kept getting worse.
The patient stated her Paraguard causes heavy bleeding anyway, so she really did not put it together at that time.
Her period was very heavy, moreso than ever, and the next month and the month after was worse.
In Aug 2021, she was only without a cycle for 5 days and it was horrible.
Her IDU was removed a week after the hurricane.
She had it done in the doctor's office and had no effects.
She is fine now.
She doesn't know if it had some sort of reaction with the copper.
She is healthy and has no issues now.
The events involved physician office visit and emergency room visit.
The action taken for the event INTRAUTERINE CONTRACEPTIVE DEVICE (PARAGUARD) was unknown.
The outcome of the events was recovered.
Treatment was received for the events.
Follow-up attempts are completed.
No further information is expected.