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Report #2865542

Received Oct 13, 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
Male
Age
Age unknown
State
—
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
COVID19COVID19 (COVID19 (MODERNA))MODERNA1——

Symptoms (2)

PainPyrexia

Symptom narrative

Achy type of reaction; A fever; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Achy type of reaction) and PYREXIA (A fever) in an elderly male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Flu vaccine. Past adverse reactions to the above products included Vaccination adverse reaction with Flu vaccine. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN (Achy type of reaction) and PYREXIA (A fever). At the time of the report, PAIN (Achy type of reaction) and PYREXIA (A fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not reported. Patient had received the first shot back in 2021 or whenever it first came out. It was reported that patient does a lot, it was just the usual things, patient would get maybe a little bit of a fever something like that. After the first one patient had a reaction, a fever, achy type of reaction, and now it was much less. For the first shot patient had most reacted. It was just that patient reacted to the flu shot the same way. It was reported that years ago, for the shingles shot patient had a shot reaction to it. It was nothing alarming, so it was not any big deal. It was unknown if the patient experienced any additional symptoms/events. Treatment information was not reported. This case was linked to MOD-2025-790050 (Patient Link).