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Report #2851440

Received Jul 28, 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
WA
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
CHOLCHOLERA (VAXCHORA)PAXVAXUNKUnknown—

Symptoms (1)

Product administration error

Symptom narrative

The patient ate 15 minutes after taking a dose of Vaxchora vaccine; Case reference number US-BN-2024-002557 is a spontaneous case initially received from pharmacist via Communication (reference number USBAV24-2527) on 26-Sep-2024 and concerns a patient of unknown demographics. The patient's medical history and concomitant medication were not provided. On an unspecified date, the patient took a dose of Vaxchora (batch number: unknown), at an unknown dose, route, or site of administration, for an unknown indication. On the same day, reported as 15 minutes after taking Vaxchora vaccine, the patient ate (explicitly coded as 'product administration error'). At the time of the initial report, it was unknown if the patient experienced any adverse event due to Vaxchora vaccine. No further information was provided.; Reporter's Comments: A patient of unknown demographics ate 15 minutes after the patient took a dose of Vaxchora for an unknown indication, which is considered as product administration error. It was unknown if the patient experienced any adverse event due to Vaxchora vaccine. Product administration error is considered as listed per company convention. The patient's medical history and concomitant medication were not provided. Product administration error is not related to the suspect vaccine, but to a human factor. This case is considered as non-serious.; Sender's Comments: A patient of unknown demographics ate 15 minutes after the patient took a dose of Vaxchora for an unknown indication, which is considered as product administration error. It was unknown if the patient experienced any adverse event due to Vaxchora vaccine. Product administration error is considered as listed per company convention. The patient's medical history and concomitant medication were not provided. Product administration error is not related to the suspect vaccine, but to a human factor. This case is considered as non-serious.

Medical history

Comments: None