Received Sep 11, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
dizzy; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), in 2024 as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Comirnaty (2023-2024 formula) (DOSE NUMBER UNKNOWN, SINGLE), administration date: 2023, for COVID-19 immunization, reaction(s): "dizzy". The following information was reported: DIZZINESS (hospitalization), outcome "unknown", described as "dizzy". The event "dizzy" required emergency room visit. Clinical course: Patient got the Pfizer covid vaccine in 2023 and 2024 and got dizzy and had dizzy ever since. Patient had to the hospital, emergency rooms and her doctor and no one knows why patient was dizzy. Patient would like to see the recall letter. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.