VAERS Explorer
Back to explore

Report #2881153

Received Jan 8, 2026

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
FL
Recovered
Not recovered
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
FLU3INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE)SANOFI PASTEURUNKU8875AAOT

Symptoms (2)

Mobility decreasedMyalgia

Symptom narrative

unable to lift her arm; severe muscular pain in the hand and upper arm; Initial information received on 05-Jan-2026 regarding an unsolicited valid non-serious case received from a consumer/non-hcp (Healthcare professional). This case involves an unknown age female patient who was unable to lift her arm and severe muscular pain in the hand and upper arm after receiving INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE [FLUZONE HD]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect Influenza USP Trival A-B High Dose Subvirion Vaccine Suspension for injection in pre-filled syringe of lot U8875AA and expiry date: 30-Jun-2026 (strength: not reported) via unknown route in unknown administration site for prophylactic vaccination. On an unknown date the patient developed unable to lift her arm (movement disorder) and severe muscular pain in the hand and upper arm (myalgia) (unknown latency). Action taken was not applicable. Corrective treatment: She used anti-inflammatory agents. At time of reporting, the outcome was Not Recovered / Not Resolved for the events.