Received Oct 3, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA)) | MODERNA | UNK | — | IM |
she had COVID in early August; I got sick; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (she had COVID in early August) and ILLNESS (I got sick) in a 78-year-old female patient who received mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (in the past she always had Pfizer). Past adverse reactions to the above products included No adverse effect with Pfizer. On an unknown date, the patient received dose of mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) (Intramuscular use) 1 dosage form. In August 2025, the patient experienced COVID-19 (she had COVID in early August) and ILLNESS (I got sick). At the time of the report, COVID-19 (she had COVID in early August) and ILLNESS (I got sick) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In August 2025, SARS-CoV-2 test: Negative. Concomitant medications details were not reported by the reporter. Patient mentioned during a call that she had COVID in early August and that she had tested negative somewhere around the 18th. She added that "in August, both her husband and she got sick and neither one of us had had a second dose for 2024-2025. She asked if they'd had Moderna COVID vaccines in the past and she said "no, in the past they always had Pfizer. It was unknown if the patient experienced any additional symptoms/events. Treatment details were not reported by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2025-789716 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2025-789716:patient husband case
Test Date: 202508; Test Name: SARS-CoV-2 test; Test Result: Negative