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Report #2844918

Received Jun 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
Female
Age
62 yrs
State
WV
Recovered
Unknown
Vaccinated
Jun 6, 2025
Onset
Jun 6, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALS2BL473—

Symptoms (1)

Extra dose administered

Symptom narrative

a patient was given another dose of AREXVY vaccine today; This non-serious case was reported by a nurse via call center representative and described the occurrence of extra dose administered in a 63-year-old female patient who received RSVPreF3 adjuvanted (Arexvy) (batch number BL473, expiry date 13-OCT-2026) for prophylaxis. Concomitant products included RSV VACCINE PROT. SUBUNIT PREF3 (AREXVY). On 06-JUN-2025, the patient received the 2nd dose of Arexvy. On 06-JUN-2025, an unknown time after receiving Arexvy, the patient experienced extra dose administered (Verbatim: a patient was given another dose of AREXVY vaccine today). The outcome of the extra dose administered was not applicable. Additional Information: GSK Receipt Date: 06-JUN-2025 Licensed Practical Nurse called to report a patient was given another dose of Arexvy vaccine today, which led to Extra dose administered. First dose was administered 21-03-2025. Licensed practical nurse wanted to know if there as any safety concern or guidance about this situation. No further information was obtained in this call. The reporter was consented to follow up.

Other medications

AREXVY