Received May 6, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | — | — |
| FLUX | INFLUENZA (SEASONAL) (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
arm (biceps area) swelled, was slightly warm, very tender; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A patient (age and gender not provided) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 29Sep2025 as dose number unknown, single (Batch/Lot number: unknown), in arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 29Sep2025 as dose number unknown, single, in arm for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION SITE SWELLING (non-serious) with onset 30Sep2025, outcome "recovered" (02Oct2025), described as "arm (biceps area) swelled, was slightly warm, very tender". The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received. Additional information: last comirnaty was on 24Sep2025. On that day, patient received, same arm, the recommended Influenza shot for seniors at high risk. patient never have had local reaction to either covid or flu vaccines. patient arm (biceps area) swelled, was slightly warm, very tender, no pus, starting the next day. Everything resolved by day 3 after the injection.