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Report #2889929

Received Mar 19, 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
WI
Recovered
Unknown
Vaccinated
Onset
Days to onset
Hospital days

Vaccines (1)

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

Symptoms (1)

Product storage error

Symptom narrative

The patient left Vivotif out of the refrigerator on 72 degrees fahrenheit, and took unspecified number of doses of Vivotif; The patient left Vivotif out of the refrigerator on 72 degrees fahrenheit, and took unspecified number of doses of Vivotif; The patient left Vivotif out of the refrigerator on 72 degrees fahrenheit, and took unspecified number of doses of Vivotif; Case reference number US-BN-2025-000894 is a spontaneous case report initially received from a pharmacist via Communication (reference number: USBAV25-0992) on 01-May-2025 and concerns adult female patient of unspecified age. (DOB: XX-Sep-1961) The patient's relevant medical history and concomitant medications were not provided. On an unspecified date, the patient left Vivotif out of the refrigerator on 72 degrees Fahrenheit. On an unspecified date, reported as patient started taking the vaccine, the patient took unspecified number of doses of Vivotif vaccine (batch number: unknown) at unknown dose, or route for unknown indication (explicitly coded as 'product administration error', 'product storage error' and 'product temperature excursion issue'). At the time of the initial report, it was unknown if the patient experienced any adverse events due to Vivotif vaccine. No further information was provided.; Reporter's Comments: This case concerns an adult female patient of unspecified age. On unspecified date, patient left Vivotif out of the refrigerator which is considered as 'product temperature excursion issue', and 'product storage error'. As reported on an unspecified date, patient started taking the vaccine and took unspecified number of doses of Vivotif vaccine for unknown indication, which is considered as ‘product administration error'. At the time of the initial report, it was unknown if the patient experienced any adverse events due to Vivotif vaccine. Product temperature excursion issue, product storage error and product administration error are considered as listed as per company convention. The patients' medical history and concomitant medication details were not provided. Product temperature excursion issue, product storage error and product administration error are not related to the suspect vaccine, but to a human factor. This case is considered as non-serious.; Sender's Comments: This case concerns an adult female patient of unspecified age. On unspecified date, patient left Vivotif out of the refrigerator which is considered as 'product temperature excursion issue', and 'product storage error'. As reported on an unspecified date, patient started taking the vaccine and took unspecified number of doses of Vivotif vaccine for unknown indication, which is considered as ‘product administration error'. At the time of the initial report, it was unknown if the patient experienced any adverse events due to Vivotif vaccine. Product temperature excursion issue, product storage error and product administration error are considered as listed as per company convention. The patients' medical history and concomitant medication details were not provided. Product temperature excursion issue, product storage error and product administration error are not related to the suspect vaccine, but to a human factor. This case is considered as non-serious.

Medical history

Comments: None.

Lab data

Test Name: Temperature; Result Unstructured Data: 72ºF