Received Jan 16, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | LA |
| FLUX | INFLUENZA (SEASONAL) (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | LA |
Sore arm; This is a spontaneous report received from a Consumer or other non HCP. A 45-year-old female patient (not pregnant) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 12Jan2026 as dose 1, single (Batch/Lot number: unknown) at the age of 45 years, in left arm for covid-19 immunisation; influenza vaccine (FLU [INFLUENZA VACCINE]), on 12Jan2026 as dose number unknown, single, in left arm for immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 12Jan2026, outcome "recovering", described as "Sore arm". Therapeutic measures were not taken as a result of pain in extremity. Additional Information: The patient was not received any other vaccines within 4 weeks PRIOR to the vaccine. The patient was taking other medications within 2 weeks of the event starting. Patient had No known Allergies. The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received.