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Report #2856480

Received Sep 2, 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
Aug 1, 2025
Onset
Aug 1, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
MNQMENINGOCOCCAL CONJUGATE (MENVEO)NOVARTIS VACCINES AND DIAGNOSTICS2AMVB030A—

Symptoms (1)

Inappropriate schedule of product administration

Symptom narrative

2nd dose received late; This non-serious case was reported by a nurse via call center representative and described the occurrence of drug dose administration interval too long in a female patient who received Men ACWY-CRM NVS (Menveo) (batch number AMVB030A, expiry date 30-APR-2025) for prophylaxis. Previously administered products included Menveo (1st dose received in JUL-2024 with batch number AMVA994Z and expiry date 30-APR-2025) and Menactra (received in 2019). In AUG-2025, the patient received the 2nd dose of Menveo. In AUG-2025, an unknown time after receiving Menveo, the patient experienced drug dose administration interval too long (Verbatim: 2nd dose received late). The outcome of the drug dose administration interval too long was not applicable. Additional Information: GSK Receipt Date: 04-AUG-2025 The nurse called to inform that a patient that had already completed the Menactra. The patient received two doses of Menveo and the second dose was late which led lengthening of vaccination schedule.