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Report #2829527

Received Mar 4, 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
Male
Age
Age unknown
State
CA
Recovered
Unknown
Vaccinated
May 9, 2024
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
TYPTYPHOID LIVE ORAL TY21A (VIVOTIF)BERNA BIOTECH, LTD.1UnknownPO / MO

Symptoms (1)

Product administration error

Symptom narrative

The patient drank alcohol with dinner and after that took the first dose of Vivotif vaccine; Case reference number US-BN-2024-001905 is a spontaneous case initially received from a nurse via Med Communications (reference number: USBAV24-1008) on 10-May-2024 and concerns a male patient of unspecified age. The patient's medical history and concomitant medication details were not provided. On 09-May-2024, as reported, the patient drank alcohol with dinner and after dinner the patient took the first dose of Vivotif (batch number: unknown), at unknown dose, orally, for an unknown indication (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. No further information was provided.; Reporter's Comments: A male patient of unspecified age drank alcohol with dinner and after dinner the patient took the first dose of Vivotif, at unknown dose, orally, for an unknown indication which is considered as product administration error. Product administration error is considered listed per company convention. At this point, it was unknown if the patient experienced any adverse event due to Vivotif vaccine. The patient's medical history and concomitant medication details were not provided. Causality is assessed as not related to suspect product but to human factor. The case is non-serious.; Sender's Comments: A male patient of unspecified age drank alcohol with dinner and after dinner the patient took the first dose of Vivotif, at unknown dose, orally, for an unknown indication which is considered as product administration error. Product administration error is considered listed per company convention. At this point, it was unknown if the patient experienced any adverse event due to Vivotif vaccine. The patient's medical history and concomitant medication details were not provided. Causality is assessed as not related to suspect product but to human factor. The case is non-serious.

Medical history

Comments: None.