Received May 6, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | — | — |
tinnitus; This is a spontaneous report received from a Consumer or other non HCP from a sales representative. An adult female patient (unknown if pregnant) received BNT162b2 (BNT162B2 NOS), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: TINNITUS (non-serious), outcome "unknown". The event "tinnitus" required physician office visit. It was unknown if therapeutic measures were taken as a result of tinnitus. Additional information: Unknown when or which vaccine was received. Patient went to ENT for evaluation. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.