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Report #2890356

Received Mar 23, 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
Female
Age
Age unknown
State
CA
Recovered
Unknown
Vaccinated
Onset
Days to onset
Hospital days

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
TYPTYPHOID LIVE ORAL TY21A (VIVOTIF)BERNA BIOTECH, LTD.UNKUnknownPO / MO

Symptoms (1)

Product administration error

Symptom narrative

Patient took Vivotif vaccine with alcohol; Case reference number US-BN-2024-002339 is a spontaneous case initially received from nurse via agency (reference number USBAV24-1955) on 13-Aug-2024 and concerns a female patient of unspecified age. The patient's medical history and concomitant medication details were not provided. On an unspecified date, the patient took a dose of Vivotif (batch number: unknown), the dose, and site of administration were unknown, orally, for unknown indication. As reported, the patient took a dose with alcohol (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 Vivotif vaccine. Non-significant follow-up was downloaded from VAERS on 09-May-2025 included new reference number. Administrative update performed within the case: Worldwide Unique Case Identification Number (WWID) updated from US-20240813-63cc3a to US-BAVARIAN NORDIC A/S-US-BN-2024-002339, in accordance with ICH guidance on WWID formatting.; Reporter's Comments: A female patient consumed alcohol while taking Vivotif, which is considered a product administration error. No associated adverse events were reported. Product administration error is listed per company convention. The patient's medical history and concomitant medication details were not provided. Product administration error is not related to Vivotif, but to a human error. The case is non-serious.; Sender's Comments: A female patient consumed alcohol while taking Vivotif, which is considered a product administration error. No associated adverse events were reported. Product administration error is listed per company convention. The patient's medical history and concomitant medication details were not provided. Product administration error is not related to Vivotif, but to a human error. The case is non-serious. USBAV24-1955:

Medical history

Comments: None