Received Dec 18, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | — | OT |
| FLU3 | INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) | SANOFI PASTEUR | UNK | — | OT |
| RSV | RSV (AREXVY) | GLAXOSMITHKLINE BIOLOGICALS | UNK | — | OT |
Body pain and was just crummy; Really sick with flu-like symptoms; Arthralgia/didn't have the COVID arm but had the joint pain; Just crummy/not feeling well/really sick; Initial information received on 08-Dec-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 had body pain and was just crummy, really sick with flu-like symptoms, arthralgia/didn't have the covid arm but had the joint pain and just crummy/not feeling well/really sick after receiving Influenza Usp Trival A-B High Dose Subvirion Vaccine [Fluzone High Dose], Rsv Vaccine Prot. Subunit Pref3 [Arexvy] and Spikevax [Covid-19 Vaccine Mrna Omicron (Jn.1) Moderna]. The patient's past vaccination(s) included COVID-19 VACCINE with The patient had received every single dose of the Moderna COVID-19 vaccine since its initial circulation back in 2020. The patient's past medical history, medical treatment(s) and family history were not provided. At the time of the event, the patient had ongoing Rheumatoid arthritis and Immunodeficiency. On an unknown date In 2025, the patient received an unknown dose of suspect Influenza Usp Trival A-B High Dose Subvirion Vaccine, Suspension for injection in pre-filled syringe, (lot number, expiry date and strength not reported) via unknown route in unknown administration site for Prophylactic vaccination [Immunisation]. On an unknown date, the patient received an unknown dose of suspect Spikevax [Covid-19 Vaccine Mrna Omicron (Jn.1) Moderna] not produced by Sanofi Pasteur for COVID-19 Prophylaxis and received an unknown dose of suspect Rsv Vaccine Prot. Subunit Pref3 not produced by Sanofi Pasteur for Prophylactic vaccination [Immunisation], both with formulation: unknown (lot number, expiry date and strength not reported) via unknown route in unknown administration site. Information on the batch number cannot be requested corresponding to the one at time of event occurrence. On an unknown date In 2025 the patient had body pain and was just crummy (pain), really sick with flu-like symptoms (influenza like illness), arthralgia/didn't have the covid arm but had the joint pain (arthralgia) and just crummy/not feeling well/really sick (malaise) (latency: few days approximately). It was reported "The reporter could not remember when the Fluzone was administered but stated it was around 3 to 4 months ago. The patient was really sick with flu-like symptoms and arthralgia, but it was unknown if they had a fever because their body temperature was not monitored. The patient had completed all the recommended immunization courses and received the extra booster. The patient got lots of mRNA crawling". Action taken was not applicable. It was not reported if the patient received a corrective treatment for all the events. At time of reporting, the outcome was Unknown for the event Pain and Malaise and was Recovered / Resolved on an unknown date in 2025 for the event Influenza like illness and Arthralgia.
Immunodeficiency; Rheumatoid arthritis