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Report #2830173

Received Mar 7, 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
—
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

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

Symptoms (2)

Inappropriate schedule of product administrationNo adverse event

Symptom narrative

Inappropriate schedule of product administration; No adverse event; Information has been received from Business Partner/CRO on 18-Feb-2025. This spontaneous report was received from a/an Consumer or other non health professional and refers to a(n) Child 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 an unknown date, the patient started therapy with Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), (indication, expiration date, and lot # were not reported). On an unknown date, the patient experienced Inappropriate schedule of product administration. On an unknown date, the patient experienced No adverse event. At the reporting time, the outcome of Inappropriate schedule of product administration and No adverse event was unknown.

Other medications

Sterile Diluent