Adverse Event Reporting
| VAERS ID | 1493065 |
|---|---|
| Gender | Female |
| Age | 32 |
| StateCode | GA |
| Pharmaceutical Company | PFIZER\BIONTECH |
| Lot Number | |
| Number of vaccinations | |
| Vaccinated | |
| Onset | 2021-03-03 |
| Condition |
Symptoms
- Pregnancy test
- Menstruation delayed
Current Illness
Preexisting Conditions
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Other Medications
Previous Vaccinations
Allergies
Laboratory Data
Test Name: Pregnancy test; Test Result: Negative
Write-up
Have not have a period since February and I am late.
; This is a spontaneous report received from a contactable nurse, the patient.
A 32-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNOWN), via an unspecified route of administration on 25Feb2021 (at the age of 32-years-old), as a single dose for COVID-19 immunisation.
Medical history was reported as none.
The patient had no known allergies to medications, food or other products.
The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNOWN), via an unspecified route of administration in the right arm on 04Feb2021 (at the age of 32-years-old), as a single dose for COVID-19 immunisation.
The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.
The patient did not receive any other medications within 2 weeks of vaccination.
Prior to vaccination, the patient was not diagnosed with COVID-19.
Since the vaccination, the patient had not tested for COVID-19.
On 03Mar2021, the patient experienced late and did not had a period since February.
The patient never been late on period in the life.
Negative pregnancy tests.
The adverse events result in a visit to the doctors or other healthcare professional office/clinic visit.
The patient did not receive any treatment for late period.
The clinical outcome of the event late period was not resolved at the time of the report.
No follow-up attempts are needed; Information about lot/batch number cannot be obtained.