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Report #2872373

Received Nov 12, 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
Unknown
Age
Age unknown
State
—
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNKUNK—

Symptoms (3)

DyspnoeaNasal congestionRhinorrhoea

Symptom narrative

Runny nose; could not breath; Nose Blockage; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of runny nose in a patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On an unknown date, the patient received Arexvy. On an unknown date, an unknown time after receiving Arexvy, the patient experienced runny nose (Verbatim: Runny nose), difficulty breathing (Verbatim: could not breath) and nasal congestion (Verbatim: Nose Blockage). The outcome of the runny nose, difficulty breathing and nasal congestion were not reported. It was unknown if the reporter considered the runny nose, difficulty breathing and nasal congestion to be related to Arexvy. It was unknown if the company considered the runny nose, difficulty breathing and nasal congestion to be related to Arexvy. Additional Information: GSK receipt date: 27-OCT-2025 The reporter was the patient. The patient had runny nose for quite a while and had nose blocked. The patient could not breath through nose. The batch number was not provided, and we are unable to contact the reporter.