Received Sep 26, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA)) | MODERNA | UNK | — | IM |
| FLUX | INFLUENZA (SEASONAL) (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
I don't feel well. As to COVID disease; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (I don't feel well. As to COVID disease) in a 76-year-old female patient who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. Co-suspect product included non-company product Influenza vaccine for an unknown indication. No Medical History information was reported. In 2024, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. On 22-Sep-2025, the patient received dose of Influenza vaccine (unknown route) 1 dosage form. On 22-Sep-2025, the patient experienced COVID-19 (I don't feel well. As to COVID disease). At the time of the report, COVID-19 (I don't feel well. As to COVID disease) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 22-Sep-2025, SARS-CoV-2 test: Positive. No concomitant medication was reported. She received all the Moderna vaccines available in last year and everything but nothing this year. The patient had Covid, and she took a test on 22-Sep-2025. She was a senior and curious if she needed vaccine after that even though she had tested it. She did not feel well. Regarding the Covid illness she took a test at home and did 2 of them and it was confirmed. It was unknown if the patient experienced any additional symptoms or events. No treatment medication was reported. Reporter causality was not reported. Reporter did not allow further contact
Test Date: 20250922; Test Name: Covid test; Test Result: Positive