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Report #2845032

Received Jun 16, 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
IN
Recovered
Unknown
Vaccinated
—
Onset
Jun 10, 2025
Days to onset
—
Hospital days
—

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
HEPHEP B (RECOMBIVAX HB)MERCK & CO. INC.UNKX027728—
HPV9HPV (GARDASIL 9)MERCK & CO. INC.UNK——

Symptoms (1)

Wrong product administered

Symptom narrative

No additional AE; Caller confirmed that patient was not administered GARDASIL 9 same-day (missed dose); a patient who was inadvertently administered a pediatric dose of RECOMBIVAXHB instead of GARDASIL 9; This spontaneous report has been received from an other health professional, regarding to a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, concomitant medications, and previous drug reactions or allergies were not reported. On 10-JUN-2025, the patient who was inadvertently administered at a dose of Hepatitis B Vaccine (RECOMBIVAXHB) suspension for injection, at a dose of 0.5 milliliters (ml), lot number X027728, instead which has been verified to be valid, expiration date reported and established as 16-OCT-2026) route of administration, and anatomical site of injection were not provided) instead of Human Papillomavirus 9-valent (GARDASIL 9) (dose, route of administration, anatomical site of injection, lot number and expiration date were not reported), both vaccine administered as prophylaxis (Wrong product administered). Also, it was reported that the patient was not administered Human Papillomavirus 9-valent (GARDASIL 9) same-day (Product dose omission issue) and will come back a different day to continue vaccination with Human Papillomavirus 9-valent (GARDASIL 9). No additional adverse events were reported in the patient.