Received Sep 19, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA)) | MODERNA | UNK | 3046714 | OT |
| FLU3 | INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) | SANOFI PASTEUR | UNK | — | OT |
sometimes feel had a sore throat/oropharyngeal pain (sore throat); Initial information received on 11-Sep-2025 regarding an unsolicited valid non-serious courtesy case received from a consumer/non-health care professional. This case involves an unknown age and unknown gender patient who sometimes feel had a sore throat/oropharyngeal pain (sore throat) after receiving Influenza Usp Trival A-B High Dose Subvirion Vaccine [Fluzone High Dose] and Spikevax 2024-2025 Formula [Covid-19 Vaccine Mrna Omicron (Jn.1) Moderna]. The patient's past medical treatment(s), and family history were not provided. Patient(s) Medical History information was not reported. Concomitant medications were not reported. On 22-Aug-2025, the patient received 1 DF (dosage form) of suspect Influenza Usp Trival A-B High Dose Subvirion Vaccine, Suspension for injection in pre-filled syringe, lot number and expiry date not reported via unknown route for prophylactic vaccination and received 0.5 ml dose of suspect Spikevax 2024-2025 Formula [Covid-19 Vaccine Mrna Omicron (Jn.1) Moderna] not produced by Sanofi Pasteur, unknown formulation, lot 3046714, expiry date:-06-Sep-2025, via intramuscular route for Covid-19 prophylaxis and product used for unknown indication (both withstrength not reported) in unknown administration site. Information on the batch number was requested corresponding to the one at time of event occurrence. On an unknown date In 2025 the patient sometimes feel had a sore throat/oropharyngeal pain (sore throat) (oropharyngeal pain) (latency: few days approximately). Reportedly, It was reported that patient's all previous vaccines shots were Moderna. Patient did not had effect like this. It was the first time. Patient had a negative effect to where patient was in bed all day the following day, and don't know if it was the flu shot, or the extra COVID shot. Regarding whether patient was still experiencing symptoms it was reported that it was probably a phantom thing. Patient was so upset about it. Patient sometimes feel had a sore throat, when it's probably just normal. It was unknown if the patient experienced any additional symptoms/events Action was not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Not Recovered / Not Resolved for the event.