Received May 25, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA)) | MODERNA | UNK | — | — |
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
arm soreness/Pain in arm; This is a spontaneous report received from a Consumer or other non HCP. Other Case identifier(s): MOD-2026-796065 (Moderna). A patient (age and gender not provided) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunization; elasomeran (MODERNA COVID-19 VACCINE), as dose number unknown, single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm soreness/Pain in arm". Additional information: It was reported that, patient contacted Moderna customer service sought information on where could receive a Moderna COVID-19 vaccine. previous experience with both Moderna and Pfizer vaccines, expressed a preference for Moderna as it caused less arm soreness compared to Pfizer. It was unknown if the patient experienced any additional symptoms/events. Treatment medication was not reported The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received.