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Report #2841863

Received May 20, 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
GA
Recovered
Unknown
Vaccinated
Oct 24, 2024
Onset
Nov 21, 2024
Days to onset
28
Hospital days
—

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
HPV9HPV (GARDASIL 9)MERCK & CO. INC.1Y012864—
HPV9HPV (GARDASIL 9)MERCK & CO. INC.21965045—

Symptoms (2)

Inappropriate schedule of product administrationNo adverse event

Symptom narrative

Nurse does not report any side effects/symptoms.; patient received GARDASIL 9 outside of the recommended dosing schedule/first dose 24OCT2024/second dose 21NOV2024. Patient has returned for dose 3 today but has not yet received it.; This spontaneous report was received from a nurse referring a 33-year-old male patient. His medical history, concurrent conditions, concomitant therapies and drug reactions/allergies were not reported. On 24-Oct-2024, the patient was vaccinated with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL 9) injection pre-filled syringe (batch/lot number Y012864 has been verified to be a valid batch lot number for Human Papillomavirus 9-valent Vaccine, Recombinant, expiration reported as 19-Jan-2026 but upon internal validation established as 29-May-2026), dose number 1, 0.5 mL (anatomical location and route of administration were not reported). On 21-Nov-2024, he was vaccinated with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL 9) injection pre-filled syringe (batch/lot number 1965045 has been verified to be a valid batch lot number for Human Papillomavirus 9-valent Vaccine, Recombinant, expiration reported and upon internal validation established as 19-Jan-2026), dose number 2, 0.5 mL (anatomical location and route of administration were not reported) (inappropriate schedule of product administration.) Both vaccine doses were administered as prophylaxis. Patient returned for dose 3 on 01-May-2025 (reported as "today"), but he had not yet received it. Nurse did not report any side effects/symptoms (no adverse event). No additional details were provided.