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Report #2892656

Received Apr 14, 2026

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
Female
Age
Age unknown
State
VA
Recovered
Unknown
Vaccinated
Feb 24, 2026
Onset
Mar 18, 2026
Days to onset
22
Hospital days

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
MMRVMEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD)MERCK & CO. INC.UNK
MMRVMEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD)MERCK & CO. INC.UNKZ009075

Symptoms (3)

Extra dose administeredNo adverse eventWrong product administered

Symptom narrative

No side effects reported; came in to HCP office on 3/18/2026 and was supposed to receive Hep A or something, well she ended up getting another dose of PROQUAD; his is regarding a 12 month old baby girl who received PROQUAD twice; This spontaneous report was received from a nurse and refers to a 12-month-old female patient. The patient's medical history and concurrent conditions were not reported. Concomitant medications included Pneumococcal vaccine conj 20v (CRM197) (PREVENAR 20). On 24-FEB-2026, the patient was vaccinated with a dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), powder for solution for injection, 1 dosage form administered for prophylaxis (strength, lot # and expiration date, route and anatomical site were not reported). The vaccine was reconstituted with sterile diluent (Hollister-Stier STERILE DILUENT) (lot # and expiration date were not reported). On 18-MAR-2026 at 10 am (also reported as yesterday), the patient was accidentally vaccinated with another dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), powder for solution for injection, lot #Z009075 [which has been verified to be a valid lot number for Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live], expiration date reported and upon internal validation establish as 15-NOV-2026, 1 dosage form administered for prophylaxis (strength, route and anatomical site were not reported). The vaccine was reconstituted with sterile diluent (Hollister-Stier STERILE DILUENT) (lot # and expiration date were not reported); although was supposed to receive hepatitis a vaccine, inactivated suspension for injection (reported as Hep A or something). Provider and nurse neither checked and did not realize until it was flagged in the system (wrong product administered; accidental overdose). No side effects reported (No adverse event).

Other medications

PREVENAR 20; MERCK STERILE DILUENT