Received Sep 15, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | N/A | my9550 | IM / LA |
| FLU3 | INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) | SANOFI PASTEUR | N/A | u8764bb | IM / LA |
| RSV | RSV (AREXVY) | GLAXOSMITHKLINE BIOLOGICALS | 2 | 52z52 | IM / RA |
Reporting due to second Arexvy vaccine not recommended. First dose was not reported to agency and patient had no recollection of getting before, but patient had dose 8/2023. No signs or symptoms reported by patient