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Report #2895889

Received May 8, 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
Unknown
Age
Age unknown
State
NM
Recovered
Unknown
Vaccinated
Onset
Days to onset
Hospital days

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
DTAPIPVHIBDTAP + IPV + HIB (PENTACEL)SANOFI PASTEURUNK
RV5ROTAVIRUS (ROTATEQ)MERCK & CO. INC.UNK2164395OT

Symptoms (2)

No adverse eventProduct storage issue

Symptom narrative

TE for ROTATEQ and Pentacel; No adverse effects reported; This spontaneous report was received from a pharmacy technician and refers to a patient of unknown gender and age. The patient's concurrent conditions, medical history and concomitant therapies were not provided. On an unknown date, the patient was vaccinated with rotavirus vaccine (ROTATEQ) orally lot # 2164395, expiration date 22-MAR-2027 (dose was not provided) and Diphtheria vaccine toxoid (+) HIB vaccine conj (tet tox) (+) Pertussis vaccine acellular 5-component (+) Polio vaccine inact 3v (MRC 5 (+) Tetanus vaccine toxoid (PENTACEL) (dose, route of administration, anatomical location, lot # and expiration date were not provided) for prophylaxis. Both suspect vaccines were improperly stored (Product storage issue). No details provided. No adverse effects were reported. This is one of 4 reports derived from the same reporter.