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Report #2843168

Received May 29, 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 (2)

Lung hyperinflationPulmonary thrombosis

Symptom narrative

blood clot in both lungs; This serious case was reported by a consumer via interactive digital media and described the occurrence of pulmonary thrombosis in a patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On an unknown date, the patient received Arexvy. On an unknown date, less than a week after receiving Arexvy, the patient experienced pulmonary thrombosis (Verbatim: blood clot in both lungs) (serious criteria GSK medically significant). The outcome of the pulmonary thrombosis was not reported. It was unknown if the reporter considered the pulmonary thrombosis to be related to Arexvy. The company considered the pulmonary thrombosis to be unrelated to Arexvy. Additional Information: GSK Receipt Date: 26-MAY-2025 Patient took RSV shot and developed blood clots in both lungs and an unspecified enlargment within a week.; Sender's Comments: Pulmonary thrombosis is an unlisted event which is considered unrelated to GSK vaccine Arexvy