Received May 4, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (NOVAVAX)) | NOVAVAX | UNK | — | — |
sore arm; Initial information received on 16-Apr-2026 (Live follow-up processed together) regarding an unsolicited valid non-serious case received from a patient. This case involves a 75-year-old female patient who experienced sore arm after receiving NVX-COV2373 (Original) Adjuvanted Vaccine [Novavax vaccine]. The patient's past medical history, past drugs, vaccination(s), family history, and concomitant medications were not provided. On an unknown date in 2025, the patient received an unknown dose of NVX-COV2373 (Original) Adjuvanted Vaccine, Dispersion for injection of unknown strength (batch/lot number: unknown) via unknown route in unknown administration site for prophylactic vaccination [Immunisation]. On an unknown date, The patient experienced sore arm (Pain in extremity) (latency: unknown). It was reported that, This spring, Patient was unable to get it in her area. She did get a booster, not novavax, but experienced side effects like those prior to using novavax. There will be no information on batch number and expiration date corresponding to the one at time of event occurrence. Action taken: not applicable. Corrective treatment: not reported. Event outcome: unknown for sore arm.