Received Mar 24, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| TYP | TYPHOID LIVE ORAL TY21A (VIVOTIF) | BERNA BIOTECH, LTD. | 1 | Unknown | — |
The patient took a dose of Vivotif vaccine which was left out of fridge on temperature more or less 70 degrees Fahrenheit for 20 to 23 hours; The patient took a dose of Vivotif vaccine which was left out of fridge on temperature more or less 70 degrees Fahrenheit for 20 to 23 hours; Case reference number US-BN-2024-002482 is a spontaneous case report initially received from a consumer via Med Communications (reference number USBAV24-2345) on 12-Sep-2024 and concerns a patient of unknown demographics. The patient's medical history and concomitant medication details were not provided. On an unspecified date, the doses of Vivotif were left out of the refrigerator for a temperature of more or less 70 degrees Fahrenheit for 20 to 23 hours (explicitly coded as 'product storage error'). On 11-Sep-2024, the patient took the affected first dose of Vivotif (batch number: unknown), at an unknown dose and route, for unknown indication (explicitly coded 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. 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-20240912-515723 to US-BAVARIAN NORDIC A/S-US-BN-2024-002482, in accordance with ICH guidance on WWID formatting.; Reporter's Comments: A patient of unknown demographics took the affected first dose of Vivotif for unknown indication, which was left out of the refrigerator for a temperature of more or less 70 degrees Fahrenheit for 20 to 23 hours, which is considered as product storage error and product administration error. It was unknown if the patient experienced any adverse events due to Vivotif vaccine. Product storage error and product administration error are considered as listed per company convention. The patient's medical history and concomitant medication details were not provided. 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-serous; Sender's Comments: A patient of unknown demographics took the affected first dose of Vivotif for unknown indication, which was left out of the refrigerator for a temperature of more or less 70 degrees Fahrenheit for 20 to 23 hours, which is considered as product storage error and product administration error. It was unknown if the patient experienced any adverse events due to Vivotif vaccine. Product storage error and product administration error are considered as listed per company convention. The patient's medical history and concomitant medication details were not provided. 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-serous
Comments: None.