Adverse Event Reporting
| VAERS ID | 1938148 |
|---|---|
| Gender | Male |
| Age | 43 |
| StateCode | FR |
| Pharmaceutical Company | PFIZER\BIONTECH |
| Lot Number | |
| Number of vaccinations | |
| Vaccinated | |
| Onset | 2021-09-01 |
| Condition | Hospitalized |
Symptoms
- Cough
- Dyspnoea exertional
Current Illness
Preexisting Conditions
Other Medications
Previous Vaccinations
Allergies
Laboratory Data
Write-up
EXERTIONAL DYSPNEA; Cough; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from Regulatory Authority.
Regulatory number: PH-PHFDA-300120015 (PHFDA).
A 43 year-old male patient received bnt162b2 (COMIRNATY), intramuscular, administration date 2021 (Batch/Lot number: unknown) at the age of 43 years as dose number unknown, single for covid-19 immunisation.
The patient's relevant medical history and concomitant medications were not reported.
The following information was reported: COUGH (hospitalization) with onset Sep2021, outcome "recovering", described as "Cough"; DYSPNOEA EXERTIONAL (hospitalization) with onset Oct2021, outcome "recovering", described as "EXERTIONAL DYSPNEA".
No follow-up attempts are possible; information about lot/batch number cannot be obtained.
No further information is expected.