Received Jun 29, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | — | — |
the 1st release of the emergency use COVID vaccine caused negative impacts to his kidney condition; This is a spontaneous report received from a Consumer or other non HCP from a sales representative. An adult male patient received BNT162b2 (BNT162B2), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "kidney condition" (ongoing). The patient's concomitant medications were not reported. The following information was reported: RENAL DISORDER (non-serious), outcome "recovered", described as "the 1st release of the emergency use COVID vaccine caused negative impacts to his kidney condition". It was unknown if therapeutic measures were taken as a result of renal disorder. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.
Renal disorder