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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

1,929,324 reports(903 ms)

#2829469Mar 4, 2025
Male·Age unknown·OH·TYP

The patient took second dose of Vivotif, five days after the first dose; Case reference number US-BN-2024-00092 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number: USBAV24-0141) on 22-Jan-2024 and concern…

Inappropriate schedule of product administration
#2829470Mar 4, 2025
Female·Age unknown·ID·TYP

Patient took three doses of Vivotif vaccine that was exposed to minimum temperature of 65 degrees Fahrenheit and maximum temperature of 72 degrees Fahrenheit for seven days; Patient took three doses of Vivotif vaccine that was exposed to minimum temperature of…

Product storage error
#2829471Mar 4, 2025
Male·Age unknown·KS·TYP

The patient took Vivotif day one dose and day three dose two days in a row, as reported the first dose was yesterday and the second dose as today; Case reference number US-BN-2024-000100 is a spontaneous case report initially received from a nurse via Med Comm…

Inappropriate schedule of product administration
#2829472Mar 4, 2025
Female·Age unknown·IL·TYP

Patient took a dose of Vivotif stored for 12 hours at maximum temperature of 55 degrees Fahrenheit; Patient took a dose of Vivotif stored for 12 hours at maximum temperature of 55 degrees Fahrenheit; Case reference number US-BN-2024-000144 is a spontaneous cas…

No adverse eventProduct storage error
#2829473Mar 4, 2025
Unknown·Age unknown·UT·TYP

Patient took the first dose of Vivotif with a full breakfast; Case reference number US-BN-2024-000158 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number: USBAV24-0283) on 07-Feb-2024 and concerns a patien…

Product administration error
#2829474Mar 4, 2025
Unknown·Age unknown·UT·TYP

The patient administrated a dose of Vivotif vaccine with food instead of one-hour prior meal; Case reference number US-BN-2024-000160 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number: USBAV24-0284) on 0…

Product administration error
#2829475Mar 4, 2025
Unknown·Age unknown·TYP

Patient took Vivotif capsules stored at room temperature with maximum temperature reached for 67 degree farhenheit and the time out of range was one month; Patient took Vivotif capsules stored at room temperature with maximum temperature reached for 67 degree…

Product storage error
#2829476Mar 4, 2025
Male·Age unknown·OH·TYP

The patient forgot to take final dose of Vivotif and could not take additionally because of traveling out of country; Case reference number US-BN-2024-000162 is a spontaneous case report initially received from other health care professional via Med Communicat…

Incomplete course of vaccination
#2829477Mar 4, 2025
Unknown·Age unknown·CA·TYP

The patient took one capsule of Vivotif vaccine once daily for four days instead of every other day; Case reference number US-BN-2024-000174, initially received from Med Communications on 09-Feb-2024 (reference number USBAV24-0291), is a spontaneous case recei…

Inappropriate schedule of product administration
#2829478Mar 4, 2025
Male·Age unknown·UT·TYP

The patient took four capsules of Vivotif every day rather than every other day.; Case reference number US-BN-2024-000175 is a spontaneous case report initially received from other health care professional via Med Communications (reference number: USBAV24-0292…

No adverse eventProduct administered to patient of inappropriate age
#2829479Mar 4, 2025
Male·Age unknown·GA·TYP

The patient took first dose of Vivotif vaccine with food; The patient received five doses of Vivotif; Patient experienced nausea after first dose of Vivotif; Case reference number US-BN-2024-000178 is a spontaneous case report initially received from a nurse v…

NauseaProduct administration error
#2829480Mar 4, 2025
Female·Age unknown·MI·TYP

The patient received third Vivotif capsule on day 7 and fourth capsule on day 12; Case reference number US-BN-2024-000194 is a spontaneous case report initially received from a nurse via Med Communication on 19-Feb-2024 and concerns a *17-years-old* female pat…

Inappropriate schedule of product administrationNo adverse event
#2829481Mar 4, 2025
Male·Age unknown·UT·TYP

The patient took Vivotif every day, instead of every other day; Case reference number US-BN-2024-000198 is a spontaneous case report initially received from a healthcare professional via Med Communications (reference number: USBAV24-0348) on 20-Feb-2024 and co…

Inappropriate schedule of product administration
#2829482Mar 4, 2025
Male·Age unknown·CA·TYP

Patient ate 15 minutes after taking the first dose of Vivoitf; Case reference number US-BN-2024-000199 is a spontaneous case report initially received from a pharmacist via Med Communication (reference number: USBAV24-0346) on 20-Feb-2024 and concerns a 64-yea…

Product administration error
#2829483Mar 4, 2025
Female·Age unknown·TN·TYP

Patient was due to take second dose of Vivotif at 2PM, patient was approximately 3 hours overdue, second dose not yet taken; Patient had gastrointestinal (GI) side effects; Vomited; Case reference number US-BN-2024-000200 is a spontaneous case report initially…

Gastrointestinal disorderInappropriate schedule of product administrationVomiting
#2829484Mar 4, 2025
Unknown·Age unknown·CA·TYP

Patient took Vivotif once a day, instead of every other day; Case reference number US-BN-2024-000221 is a spontaneous case report initially received from a health care professional via Med Communications (reference number: USBAV24-0378) on 23-Feb-2024 and conc…

Inappropriate schedule of product administration
#2829485Mar 4, 2025
Male·Age unknown·MA·TYP

The patient received three doses of Vivotif vaccine instead of four; The patient vomited the full capsule three hours after the ingestion of the first dose; Case reference number US-BN-2024-000566 is a spontaneous case report initially received from a pharmaci…

Incomplete course of vaccinationVomiting
#2829486Mar 4, 2025
Male·Age unknown·MT·TYP

The patient took a partial dosage of Vivotif; took one or two pills of Vivotif which were prescribed three weeks ago; Case reference number US-BN-2024-000606 is a spontaneous case report initially received from a nurse via Med Communications (reference number:…

Inappropriate schedule of product administration
#2829487Mar 4, 2025
Unknown·Age unknown·NC·TYP

Vivotif vaccine was stored at 72 Fahrenheit degrees for one week; The patients did the entire course of vaccination after temperature excursion; Vivotif vaccine was stored at 72 Fahrenheit degrees for one week; The patients did the entire course of vaccination…

Product storage error
#2829488Mar 4, 2025
SeriousHospitalized
Female·Age unknown·TYP

The patient develop rash after receiving two of four doses of the Vivotif vaccine; The patient received two of the four doses of the Vivotif vaccine; Case reference number US-BN-2024-000625 is a spontaneous case initially received from other health professiona…

Incomplete course of vaccinationRash
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