Received Jan 8, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | — | — |
| TDAP | TDAP (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
Body aches; Weakness; Fever; This is a spontaneous report received from a Consumer or other non HCP. A 37-year-old male patient received BNT162b2 (COMIRNATY), on 02Jan2026 at 05:15 as dose number unknown, single (Batch/Lot number: unknown) at the age of 37 years for covid-19 immunisation; diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP), on 02Jan2026 as dose number unknown, single for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN (non-serious) with onset 02Jan2026 at 22:00, outcome "recovering", described as "Body aches"; PYREXIA (non-serious) with onset 02Jan2026 at 22:00, outcome "recovering", described as "Fever"; ASTHENIA (non-serious) with onset 02Jan2026 at 22:00, outcome "recovering", described as "Weakness". Therapeutic measures were taken as a result of pain, asthenia, pyrexia. Additional information: The adverse event was treated with Tylenol. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.