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Report #2830923

Received Mar 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
Male
Age
16 yrs
State
TX
Recovered
Unknown
Vaccinated
Feb 28, 2025
Onset
Feb 28, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HPV9HPV (GARDASIL 9)MERCK & CO. INC.3Y018389—

Symptoms (2)

Extra dose administeredNo adverse event

Symptom narrative

No additional AE; HCP called to report a patient received a third dose of GARDASIL 9 after competition of the two-dose series on February 19, 2019. No side effects or symptoms reported. No additional information provided. No Additional AE/ No PQC.; This spontaneous report was received from medical assistant and refers to 16-year-old male patient. The patient's medical history was not reported. His drug history included Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL 9). The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 28-FEB-2025, the patient started therapy with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL 9), (valid lot #Y018389, expiration date: 04-NOV-2026) 0.5 mL. On 28-FEB-2025, the patient received a third dose of Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL9) after competition of the two-dose series on 19-FEB-2019. No side effects or symptoms reported. No additional information provided. No Additional AE/ No PQC.. On an unknown date, the patient experienced No additional AE. At the reporting time, the outcome of HCP called to report a patient received a third dose of GARDASIL 9 after competition of the two-dose series on February 19, 2019. No side effects or symptoms reported. No additional information provided. No Additional AE/ No PQC. and No additional AE was unknown. The action taken with Human Papillomavirus 9-valent Vaccine, Recombinant was reported as not applicable.