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Report #2876930

Received Dec 8, 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
60 yrs
State
IA
Recovered
Unknown
Vaccinated
Dec 1, 2025
Onset
Dec 1, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
FLU3INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE)SANOFI PASTEURUNKUT8781AAOT / RA

Symptoms (2)

No adverse eventProduct administered to patient of inappropriate age

Symptom narrative

inadvertently administered a dose of fluzone hd to a 60-year-old patient that had no underlying comorbidities, with no reported adverse event; Initial information received on 02-Dec-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 60 years old female patient who was inadvertently administered to Influenza Usp Trival A-B High Dose Subvirion Vaccine [Fluzone Hd], with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 01-Dec-2025, the patient received 0.5mL of suspect Influenza Usp Trival A-B High Dose Subvirion Vaccine, Suspension for injection in pre-filled syringe (lot UT8781AA, expiry date 30-Jun-2026, frequency once and strength Fluzone High Dose) via intramuscular route in the right deltoid for Influenza (Influenza Immunisation) and inadvertently administered, with no reported adverse event (off label use) (latency same day). It was reported 'that had no underlying comorbidities. She was asking if there was anything different they need to with the patient going forward'. Action taken was not applicable.