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Report #2881676

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

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALS1UNK—

Symptoms (1)

Hypoaesthesia

Symptom narrative

can't feel my arm; This serious case was reported by a consumer via interactive digital media and described the occurrence of numbness of upper arm in a patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On an unknown date, the patient received the 1st dose of Arexvy. On an unknown date, an unknown time after receiving Arexvy, the patient experienced numbness of upper arm (Verbatim: can't feel my arm) (serious criteria other: Serious as per reporter). The outcome of the numbness of upper arm was not reported. It was unknown if the reporter considered the numbness of upper arm to be related to Arexvy. The company considered the numbness of upper arm to be unrelated to Arexvy. Additional Information: GSK Receipt Date: 07-JAN-2026 This case was reported by a patient via interactive digital media. The patient got the first shot and couldn't feel the arm. The batch number was not provided, and we are unable to contact the reporter.; Sender's Comments: A case of Hypoaesthesia, unknown time after receiving 1st dose of Arexvy, in a patient. Based on the available information a?possible causality that the event was caused by the GSK product cannot be ascertained. Consent for further follow-up has not been received.