Received Oct 16, 2025
| 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 | — | RA |
sore arm; general body aches; headache; This is a spontaneous report received from a Consumer or other non HCP. A 37-year-old female patient (not pregnant) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 14Oct2025 at 10:45 as dose 1, single (Batch/Lot number: unknown) at the age of 37 years, in left arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 14Oct2025 as dose number unknown, single, in right arm. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: PAIN (non-serious) with onset 14Oct2025, outcome "not recovered", described as "general body aches"; HEADACHE (non-serious) with onset 14Oct2025, outcome "not recovered"; PAIN IN EXTREMITY (non-serious) with onset 14Oct2025, outcome "not recovered", described as "sore arm". Therapeutic measures were not taken as a result of pain in extremity, pain, headache. Additional information: Patient did not receive any other vaccines within 4 weeks PRIOR to the vaccine(s). Patient reported taking other medications within 2 weeks of the event starting. Patient has no allergy. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.