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Report #2842554

Received May 24, 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
Female
Age
Age unknown
State
NY
Recovered
Unknown
Vaccinated
—
Onset
May 5, 2025
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
MMRVMEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD)MERCK & CO. INC.UNKZ003308OT

Symptoms (4)

Circumstance or information capable of leading to medication errorExposure via eye contactNo adverse eventUnderdose

Symptom narrative

No additional AE/PQC.; HCP called and reported that during administration of PROQUAD to a child, the child moved their arm near the end of the dose which caused some of the residual liquid from the syringe to splash into the mother's eyes.; This spontaneous report was received from a Licensed Practical Nurse and refers to a female patient of unknown age. The patient's concurrent conditions, medical history, concomitant therapies, drug reactions or allergies were not reported. On 05-May-2025, the patient's child was receiving a dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) (lot #Z003308, expiration date: 21-Jul-2026) as Prophylaxis; but during administration, the child moved the arm near the end of the dose (child case # 2282979), which caused some of the residual liquid from the syringe to splash into the patient's eye (accidental exposure to product); therefore, she was treated with eye flush rinse in the office, as treatment for the event. No additional adverse event (AE) was reported. At the reporting time, the outcome of the event was unknown. This is one of two cases reported by the same reporter.

Other medications

Sterile diluent