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Report #2842844

Received May 27, 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
11 yrs
State
NY
Recovered
Unknown
Vaccinated
Jan 1, 2024
Onset
May 1, 2025
Days to onset
486
Hospital days
—

Vaccines (3)

TypeNameManufacturerDoseLotRoute / Site
HPV4HPV (GARDASIL)MERCK & CO. INC.1——
HPV4HPV (GARDASIL)MERCK & CO. INC.2——
HPV4HPV (GARDASIL)MERCK & CO. INC.3——

Symptoms (2)

Extra dose administeredNo adverse event

Symptom narrative

no adverse event; HCP called to report that a 11 yr old patient received an extra 2nd dose of GARDASIL 9, 18 days after the actual 2nd dose had been administered. First dose of GARDASIL 9 was administered in January 2024, with the 2nd dose being administered on May 1; HCP called to report that a 11 yr old patient received an extra 2nd dose of GARDASIL 9, 18 days after the actual 2nd dose had been administered. First dose of GARDASIL 9 was administered in January 2024, with the 2nd dose being administered on May 1; This spontaneous report was received from a Physician and refers to a 11-year-old patient of unknown gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On Jan-2024, the patient started therapy with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL9), dose number 1, 0.5 mL (lot # and expiration date were not reported). On 01-May-2025, the patient received a second dose of with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL9), 0.5 mL (lot # and expiration date were not reported) which was a delayed 2nd dose not administered according to the schedule in the PI (inappropriate schedule of vaccine administered). On 19-May-2025, the patient received a third dose of with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL 9), 0.5 mL (lot # and expiration date were not reported) (inappropriate schedule of vaccine administered). No adverse event was reported.