有害事象報告詳細
| VAERS ID | 1393259 |
|---|---|
| 性別 | 女性 |
| 年齢 | |
| 州コード | FR |
| 製薬会社 | 不明 |
| ロット番号 | |
| ワクチン接種回数 | |
| 接種日 | |
| 発生日 | |
| 状態 |
症状
- SARS-CoV-2テスト(SARS-CoV-2 test)
- 自然流産(Abortion spontaneous)
- 適応外使用(Off label use)
- 製品使用の問題(Product use issue)
罹患中の病気
持病
Medical History/Concurrent Conditions: Pregnancy (healthy pregnancies in the past)
その他医療
以前のワクチン接種
アレルギー
臨床検査
Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
症状詳細
miscarriage/ Miscarriage of pregnancy; Patient received BNT162B2 and COVID-19 VACCINE ASTRAZENECA; Patient received BNT162B2 and COVID-19 VACCINE ASTRAZENECA; This is a spontaneous report from a contactable consumer (patient).
This report was received from the Regulatory Agency (UK-MHRA).
The regulatory authority report number is GB-MHRA-WEBCOVID-202105261611038430-5A6DX,Safety Report Unique Identifier GB-MHRA-ADR 25365609.
A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Lot number was not reported) as UNKNOWN, SINGLE for COVID-19 immunisation; and COVID-19 vaccine astrazeneca (COVID-19 VACCINE ASTRAZENECA), via an unspecified route of administration on an unspecified date (Lot number was not reported) at unspecified dose for an unspecified indication.
Medical history included healthy pregnancies in the past.
It was unknown if patient was pregnant at time of vaccination.
The patient had no concomitant medications.
Patient has not had symptoms associated with COVID-19.
Patient was not enrolled in clinical trial.
The patient reported that after spending lots of time with vaccinated family members, she had a miscarrriage/ miscarriage of pregnancy on unspecified date.
The patient reported she had no physical health conditions that could have caused it.
She have had healthy pregnancies in the past.
This was the first ever miscarriage and the timing fit with when her family was vaccinated.
The event was considered serious, medically significant.
The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative covid-19 test on an unspecified date.
Patient has not tested positive for COVID-19 since having the vaccine.
The outcome of the event was reported as not recovered.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.
No further information is expected.