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Report #2825485

Received Feb 10, 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
Male
Age
Age unknown
State
—
Recovered
Unknown
Vaccinated
Jan 1, 2025
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNKUNK—

Symptoms (2)

CoughDyspnoea

Symptom narrative

slight cough; breathing labored frequently; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of cough in a male patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. In JAN-2025, the patient received Arexvy. On an unknown date, less than a week after receiving Arexvy, the patient experienced cough (Verbatim: slight cough) and labored breathing (Verbatim: breathing labored frequently). The outcome of the cough and labored breathing were not reported. It was unknown if the reporter considered the cough and labored breathing to be related to Arexvy. It was unknown if the company considered the cough and labored breathing to be related to Arexvy. Additional Information: GSK Receipt Date: 01-FEB-2025 This case was reported by a patient via interactive digital media. The patient 's wife reported that her husband got Arexvy shot 6 days ago and had slight cough and breathing labored frequently. She enquired how long it would last. The follow-up could not be possible as no contact details were available