Received Dec 16, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA MNEXSPIKE)) | MODERNA | UNK | — | IM |
"numbness and tingling" in their arms; "numbness and tingling" in their arms; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA ("numbness and tingling" in their arms) and PARAESTHESIA ("numbness and tingling" in their arms) in a female patient of an unknown age who received mRNA-1273.251 (Spikevax LP.8.1 PFS) for COVID-19 prophylaxis. The suspect product included Pre-filled Syringe injection for COVID-19 prophylaxis. No Medical History information was reported. In October 2025, the patient received dose of mRNA-1273.251 (Spikevax LP.8.1 PFS) (Intramuscular use) 1 dosage form. On an unknown date, the patient started Pre-filled Syringe (unknown route) at an unspecified dose. On an unknown date, the patient experienced HYPOAESTHESIA ("numbness and tingling" in their arms) and PARAESTHESIA ("numbness and tingling" in their arms). At the time of the report, HYPOAESTHESIA ("numbness and tingling" in their arms) and PARAESTHESIA ("numbness and tingling" in their arms) outcome was unknown. The action taken with mRNA-1273.251 (Spikevax LP.8.1 PFS) (Intramuscular use) was unknown. Concomitant medication was not provided. It was unknown if the patient experienced any additional symptoms or events. Treatment medication was not reported. Reporter did not allow further contact