Received Sep 26, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA)) | MODERNA | 1 | 3051995 | IM / LA |
| FLU3 | INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) | SANOFI PASTEUR | 1 | U8855AA | IM / LA |
Fluzone HD and MNexspike vaccines were administered to patient at the pharmacy at approximately 10:00 AM on 9/25/25. The patient left the pharmacy without incident. The patient contacted the pharmacy via phone at approximately 4:00 PM on 9/25/25 stating they were having trouble swallowing with no other symptoms of anaphylaxis (no hives, rash, trouble breathing). The patient denied any other cause of allergic reaction other than the vaccines. Patient was instructed to seek medical attention by the pharmacist. The patient returned to the pharmacy on 9/26/25 and informed pharmacy staff that they did have an episode of anaphylaxis.