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Report #2879268

Received Dec 23, 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
NM
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RV5ROTAVIRUS (ROTATEQ)MERCK & CO. INC.UNK2142137—

Symptoms (2)

No adverse eventProduct storage error

Symptom narrative

Temperature excursion where one patient received ROTATEQ after stored improperly; No side effects or symptoms reported. No Additional AE; This spontaneous report was received from an other non-health professional and referred to a 4 months patient of unknown gender. The patient's medical history, past medications, and concomitant medications were not reported. On an unknown date, the patient was vaccinated with Rotavirus Vaccine, Live, Oral, Pentavalent (ROTATEQ) vial, 2 mL (batch/lot number 2142137 has been verified to be a valid batch/lot number for Rotavirus Vaccine, Live, Oral, Pentavalent, expiration date reported and confirmed as 27-Jun-2026); administered as prophylaxis (route and strength were not reported). The vaccine administered underwent a temperature excursion (46.7F for 0 hours 6 minutes 0 seconds); no previous temperature excursion (Product storage error). No side effects, symptoms nor additional AE (adverse event) were reported.