Received Nov 13, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (UNKNOWN)) | UNKNOWN MANUFACTURER | UNK | — | OT |
had a sore arm; Initial information received on 07-Nov-2025 regarding an unsolicited valid non-serious case received from a consumer/non-hcp (non-healthcare professional). This case involves an unknown age female patient who had a sore arm after receiving NVX-COV2373 (Original) Adjuvanted Vaccine [Nuvaxovid PFS (Pre-filled syringe)]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date in 2024, the patient received an unknown dose of suspect NVX-COV2373 (Original) Adjuvanted Vaccine (Once), Injection (unknown strength and expiry date) lot number not reported via intramuscular route in the arm NOS (not otherwise specified) for Prevention of Covid-19 (Covid-19 immunisation). Information regarding batch number corresponding to the one at time of event occurrence is requested. On an unknown date in 2024, the patient had a sore arm (pain in extremity) (latency unknown). It was reported that, "patient received Novavax vaccine last year and felt it was administered a bit high in arm and had a sore arm afterwards" Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Recovered / Resolved on an unknown date for the event.