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Report #2851703

Received Jul 29, 2025

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex
Female
Age
Age unknown
State
—
Recovered
Recovered
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
COVID19COVID19 (COVID19 (MODERNA))MODERNAUNK——

Symptoms (2)

MyalgiaPain in extremity

Symptom narrative

so her arm would be pretty sore; she'd have muscle aches, particularly around her thumbs, the wrist muscles; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (so her arm would be pretty sore) and MYALGIA (she'd have muscle aches, particularly around her thumbs, the wrist muscles) in a female patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (so her arm would be pretty sore) and MYALGIA (she'd have muscle aches, particularly around her thumbs, the wrist muscles). At the time of the report, PAIN IN EXTREMITY (so her arm would be pretty sore) and MYALGIA (she'd have muscle aches, particularly around her thumbs, the wrist muscles) had resolved. Concomitant medication was not reported. The caller described that with previous vaccinations, after about 48 hours or so her arm would be pretty sore, and she had muscle aches, particularly around her thumbs, the wrist muscles, but she did not have that now. All her vaccines have been Moderna so far. Started in 2021 and has had a total of 9 vaccines including the dose on 22-Jul-2025. It was unknown if the patient experienced any additional symptoms/events. Treatment medication was not reported. This case was linked to MOD-2025-788313 (Patient Link). Reporter did not allow further contact