Adverse Event Reporting
| VAERS ID | 1834341 |
|---|---|
| Gender | Unknown |
| Age | |
| StateCode | FR |
| Pharmaceutical Company | PFIZER\BIONTECH |
| Lot Number | |
| Number of vaccinations | 2 |
| Vaccinated | 2021-08-11 |
| Onset | 2021-09-01 |
| Condition | Died |
Symptoms
- Maternal exposure during pregnancy
- Foetal growth restriction
Current Illness
Preexisting Conditions
Other Medications
Previous Vaccinations
Allergies
Laboratory Data
Write-up
Maternal exposure during pregnancy, first trimester; Growth of the embryo since the second vaccination dose (Biontech) is no longer sufficient; This is a spontaneous report from a non-contactable consumer.
This is the second of two reports.
The first report is a report downloaded from the regulatory authority number is DE-PEI-CADR2021174265, Safety Report Unique Identifier: DE-PEI-202100182650.
This consumer reported information for both mother and fetus.
This is a fetus report.
A fetus patient of an unspecified gender received BNT162B2 (COMIRNATY), dose 2 transplacental on 11Aug2021 (Batch/Lot Number: unknown) as dose 2, 0.
3 ml single for COVID-19 immunisation.
The patient's medical history and concomitant medications were not reported.
The patient's 31-year-old mother was on 2 months gestation period.
On 01Sep2021, the growth of the embryo since the second vaccination dose (Biontech) was no longer sufficient.
Hence, resulted to miscarriage/abortion by the patient's mother on the same day.
The patient died on 01Sep2021.
It was unknown if an autopsy was performed.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.
; Sender's Comments: Linked Report(s) : DE-PFIZER INC-202101435874 mother case; Reported Cause(s) of Death: Growth of the embryo since the second vaccination dose (Biontech) is no longer sufficient