Adverse Event Reporting
| VAERS ID | 925730 |
|---|---|
| Gender | Unknown |
| Age | |
| StateCode | FR |
| Pharmaceutical Company | PFIZER\BIONTECH |
| Lot Number | |
| Number of vaccinations | |
| Vaccinated | |
| Onset | |
| Condition | Permanent Disability Recovered |
Symptoms
- Rash
- SARS-CoV-2 test
Current Illness
Preexisting Conditions
Other Medications
Previous Vaccinations
Allergies
Laboratory Data
Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
Write-up
Rash; This is a spontaneous report from a contactable other hcp downloaded from the Medicines Agency (EMA) EudraVigilance-WEB, Regulatory Authority number: GB-MHRA-ADR 24545560, Safety Report Unique Identifier [GB-MHRA-WEBCOVID- 20201221122717].
A 22-year-old patient of an unspecified gender received bnt162b2 (COMIRNATY, Lot/batch number and Expiration date were not provided), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization.
The patient medical history and concomitant medications were not reported.
The patient experienced rash on an unspecified date.
The event resulted disability.
Patient has not had symptoms associated with COVID-19.
Patient is not enrolled in clinical trial.
The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test on an unspecified date.
The outcome of the event was recovered on unspecified date.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.