VAERS Explorer

Explore VAERS reports

Search and filter adverse-event reports.

View charts →
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(781 ms)

#2889054Mar 18, 2026
Female·68 yrs·MD·VARZOS

Nausea/s "still beyond nauseous; Fatigue/s severe fatigue; This non-serious case was reported by a consumer via call center representative and described the occurrence of nausea in a 68-year-old female patient who received Herpes zoster (Shingrix) for prophyla…

NauseaPeripheral swellingFatigue
#2889442Mar 18, 2026
Unknown·Age unknown·MD·VARCEL

No additional AE; Customer called to report TE. VARIVAX was administered to 3 patients.; This spontaneous report was received from a Nurse and refers to a 4-year-old patient of unknown gender. The patient's medical history, concurrent conditions, concomitant t…

No adverse eventProduct storage error
#2889444Mar 18, 2026
Unknown·Age unknown·VA·HEP, HEPA, MMR

Autistic; This spontaneous report was received from a Physician via vendor and refers to a Child patient of unknown gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not…

Autism spectrum disorder
#2889445Mar 18, 2026
Female·Age unknown·PA·TYP

A patient took the first two doses of Vivotif on two consecutive days; Case reference number US-BN-2025-000324 is a spontaneous case initially received from nurse via Communication (reference number: USBAV25-0506) on 06-Mar-2025 and concerns adult female patie…

Inappropriate schedule of product administration
#2889446Mar 18, 2026
Female·Age unknown·NC·TYP

Patient missed the third dose of Vivotif on Saturday; Case reference number US-BN-2025-000342 is a spontaneous case report initially received from a consumer via Communication (reference number: USBAV25-0516) on 07-Mar-2025 and concerns a female patient of uns…

Product dose omission issue
#2889447Mar 18, 2026
Male·Age unknown·VT·TYP

The patient left the Vivotif vaccine out at room temperature and then took one dose of vaccine; The patient left the Vivotif vaccine out at room temperature and then took one dose of vaccine; The patient left the Vivotif vaccine out at room temperature and the…

Product storage error
#2889448Mar 18, 2026
Female·Age unknown·ID·TYP

The patient took second dose of Vivotif and thrown up; The patient took first dose of Vivotif and thrown up; Case reference number US-BN-2025-000350 is a spontaneous case initially received from pharmacist via Communication (reference number: USBAV25-0561) on…

Vomiting
#2889450Mar 18, 2026
Female·Age unknown·TYP

The patient took all the treatment of Vivotif without being refrigerated; The patient picked up Vivotif vaccine but did not keep it refrigerated; The patient picked up Vivotif vaccine but did not keep it refrigerated; Case reference number US-BN-2025-000381 is…

Product storage error
#2889451Mar 18, 2026
Female·Age unknown·TYP

The patient took first dose of Vivotif with food; Case reference number US-BN-2025-000394 is a spontaneous case initially received from nurse via Communication (reference number: USBAV25-0642) on 20-Mar-2025 and concerns a 75-year-old, female patient. The pa…

Product administration error
#2889452Mar 18, 2026
Unknown·Age unknown·TYP

The patient took Vivotif capsules with small breakfast and supposed to be taken on an empty stomach; Case reference number US-BN-2025-000395 is a spontaneous case report initially received from a physician via Communication (reference number: USBAV25-0644) on…

Product administration error
#2889454Mar 18, 2026
Female·Age unknown·TYP

The patient took Vivotif vaccine which was left out looked like 14 hours, maximum temperature did not go above 77 degrees Fahrenheit; The patient took Vivotif vaccine which was left out looked like 14 hours, maximum temperature did not go above 77 degrees Fahr…

Product storage error
#2889455Mar 18, 2026
Male·Age unknown·TYP

The patient took first dose of VIVOTIF and had about 35 hours of fever; Case reference number US-BN-2025-000119 is a spontaneous case initially received from consumer via Communications (reference number: USBAV25-0094) on 13-Jan-2025 and concerns a male patien…

Pyrexia
#2889456Mar 18, 2026
Female·Age unknown·TYP

The patient took four doses of Vivotif vaccine every day instead of every other day; Case reference number US-BN-2025-000127 is a spontaneous case initially received from consumer via Communication (reference number: USBAV25-0121) on 15-Jan-2025 and concerns…

Inappropriate schedule of product administration
#2889458Mar 18, 2026
Female·Age unknown·IL·TYP

The patient missed a dose of VIVOTIF and took it a day later; Case reference number US-BN-2025-000030 is a spontaneous case report initially received from a nurse via Communication (reference number: USBAV25-0056) on 08-Jan-2025 and concerns a 70-years-old fem…

Inappropriate schedule of product administration
#2889459Mar 18, 2026
Male·Age unknown·TYP

The patient took fourth dose eight days after first dose of Vivotif; Case reference number US-BN-2025-000128 is a spontaneous case initially received from consumer via Emergent BioSolutions (reference number: EMG2025-032) on 14-Jan-2025 and concerns male patie…

Inappropriate schedule of product administration
#2889460Mar 18, 2026
Unknown·Age unknown·TYP

The patient received two doses of Vivotif which was stored at room temperature for 48 hours; The patient received two doses of Vivotif which was stored at room temperature for 48 hours; Case reference number US-BN-2025-000145 is a spontaneous case initially re…

Product storage error
#2889461Mar 18, 2026
Male·Age unknown·TYP

The patient took fourth dose of Vivotif eight days after first dose; Case reference number US-BN-2025-000148 is a spontaneous case initially received from consumer via Communication (reference number: USBAV25-0158) on 21-Jan-2025 and concern a *48-year-old* ma…

Inappropriate schedule of product administration
#2889462Mar 18, 2026
Female·Age unknown·CA·TYP

The patient supposed to took Vivotif last night, forgot and took it next morning; Case reference number US-BN-2025-000158 is a spontaneous case initially received from a nurse via Communications (reference number: USBAV25-0181) on 23-Jan-2025 and concerns a fe…

Inappropriate schedule of product administration
#2889463Mar 18, 2026
Female·Age unknown·TYP

Lethargic; Chills; Not feeling that great; The patient was not aware that Vivotif need to be refrigerated and took the first dose; The patient was not aware that Vivotif need to be refrigerated and took the first dose; The patient was not aware that Vivotif ne…

ChillsIncomplete course of vaccinationLethargyMalaiseProduct storage error
#2889464Mar 18, 2026
Female·Age unknown·NY·TYP

The patient missed third dose of Vivotif and took it one day later; Case reference number US-BN-2025-000165 is a spontaneous case initially received from pharmacist via Communication (reference number: USBAV25-0194) on 27-Jan-2025 and concerns a female patient…

Inappropriate schedule of product administration
Page 346 of 96,467