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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(781 ms)

#2890314Mar 23, 2026
Female·21 yrs·AL·HEPAB

Incomplete course of vaccination; late 2nd dose; This non-serious case was reported by a other health professional via call center representative and described the occurrence of drug dose administration interval too long in a 21-year-old female patient who rec…

Inappropriate schedule of product administrationIncomplete course of vaccination
#2890315Mar 23, 2026
Male·65 yrs·SC·HEP

inadvertently administered an expired dose of Engerix B; This non-serious case was reported by a nurse via call center representative and described the occurrence of expired vaccine used in a 65-year-old male patient who received HBV (Engerix B) (batch number…

Expired product administered
#2890318Mar 23, 2026
Female·66 yrs·PA·VARZOS

No adverse event indicated. Third dose given

Extra dose administeredNo adverse event
#2890319Mar 23, 2026
Female·9 yrs·COVID19

CMA administered the adult COVID vaccine to a 9 year old instead of the pediatric dose Spikevax 0.25 ml. The CMA noted the error immediately after injection was given and self-reported the error. The child was monitored for several minutes in the clinic and…

Incorrect dose administeredNo adverse event
#2890321Mar 23, 2026
Unknown·Age unknown·TN·TYP

Patient took Vivotif four doses correctly, but all stored at room temperature range from 71-75 F for more that 24 hours; Patient took Vivotif four doses correctly, but all stored at room temperature range from 71-75 F for more that 24 hours; Case reference num…

Product storage error
#2890322Mar 23, 2026
Female·Age unknown·MA·TYP

Patient took first dose of Vivotif and forgot to take second dose, its been about a week from the first dose; Case reference number US-BN-2024-002159 is a spontaneous case initially received from physician via agency (reference number: USBAV24-1588) on 08-Jul-…

Inappropriate schedule of product administration
#2890323Mar 23, 2026
Female·Age unknown·MD·TYP

The patient took first and second dose of Vivotif vaccine in two consecutive days instead of skipping day; Case reference number US-BN-2024-002164 is a spontaneous case initially received from a pharmacist via agency (reference number: USBAV24-1593) on 08-Jul-…

Inappropriate schedule of product administration
#2890324Mar 23, 2026
Female·Age unknown·ME·TYP

Patient took the first dose of Vivotif according to the schedule, but patient took a cup of coffee, ten minutes later after the dose; Case reference number US-BN-2024-002165 is a spontaneous case initially received from pharmacist via agency (reference number:…

Product administration error
#2890325Mar 23, 2026
Male·Age unknown·IN·TYP

The patient received fourth dose of Vivotif on day 12; Case reference number US-BN-2024-002175 is a spontaneous case initially received from a nurse via agency (reference number: USBAV24-1609) on 09-Jul-2024 and concerns a 57-year-old male patient. The patien…

Inappropriate schedule of product administrationNo adverse event
#2890326Mar 23, 2026
Unknown·Age unknown·TYP

Patient received last dose of Vivotif two weeks after the expiry date 30-Jun-2024; Case reference number US-BN-2024-002185 is a spontaneous case initially received from a pharmacist via agency (reference number: USBAV24-1634) on 12-Jul-2024 and concerns a pati…

Expired product administered
#2890327Mar 23, 2026
Female·Age unknown·TYP

The Vivotif vaccine was stored in the fridge, but the patient noticed uneven refrigeration, took two doses; The Vivotif vaccine was stored in the fridge, but the patient noticed uneven refrigeration, took two doses; Case reference number US-BN-2024-002292 is a…

Product storage error
#2890328Mar 23, 2026
Female·Age unknown·WA·TYP

Patient received first dose of Vivotif on 02-Aug-2024 and second dose on 03-Aug-2024, consecutively in two days; Case reference number US-BN-2024-002310 is a spontaneous case initially received from a pharmacist via agency (reference number: USBAV24-1871) on 0…

Inappropriate schedule of product administration
#2890329Mar 23, 2026
Unknown·Age unknown·TYP

The patient missed the fourth dose of Vivotif; Case reference number US-BN-2024-002311 is a spontaneous case initially received from nurse via agency (reference number: USBAV24-1882) on 05-Aug-2024 and concerns patient of unspecified age or gender. The patien…

Product dose omission issue
#2890330Mar 23, 2026
Female·Age unknown·WA·TYP

Diverticulosis; Infection; The patient took the first dose of Vivotif on 02-Aug-2024 and and then the doctor advised patient to stop Vivotif; Case reference number US-BN-2024-002354 is a spontaneous case initially received from a pharmacist via agency (referen…

Diverticulum intestinalInfection
#2890331Mar 23, 2026
Male·Age unknown·TYP

Patient received four doses of Vivotif in consecutive days, instead of every other day; Case reference number US-BN-2024-002380 is a spontaneous case initially received from physician via agency (reference number: USBAV24-2068) on 22-Aug-2024 and concerns a ma…

Inappropriate schedule of product administration
#2890332Mar 23, 2026
Unknown·Age unknown·TYP

The patient received two capsules of Vivotif during the first round, and had CBC abnormal; The patient received two capsules of Vivotif during the first round, then patient had CBC abnormal, all immunizations were stopped, subsequently, the patient began a sec…

Full blood count abnormal
#2890333Mar 23, 2026
Female·Age unknown·MT·TYP

Patient had severe stomach cramps; Patient felt very sick; Very nauseated; Case reference number US-BN-2024-002382 is a spontaneous case initially received from a nurse via agency (reference number: USBAV24-2087) on 22-Aug-2024 and concerns a 46-year-old femal…

Abdominal pain upperMalaiseNausea
#2890334Mar 23, 2026
Female·Age unknown·MN·TYP

The patient received four doses of Vivotif, three of those doses being taken were unrefrigerated; The patient received four doses of Vivotif, three of those doses being taken were unrefrigerated; Case reference number US-BN-2024-002391 is a spontaneous case in…

Product storage error
#2890335Mar 23, 2026
Unknown·Age unknown·NJ·TYP

The patient was feeling a little woozy; The patient took four Vivotif vaccine capsules, after meals, but Vivotif was not refrigerated.; The patient took four Vivotif vaccine capsules, after meals, but Vivotif was not refrigerated.; Case reference number US-BN-…

DizzinessProduct storage error
#2890336Mar 23, 2026
Female·Age unknown·TX·TYP

The patient received second dose of Vivotif on 25-Aug-2024 and third dose on 26-Aug-2024; Case reference number US-BN-2024-002401 is a spontaneous case initially received from a consumer via agency (reference number: USBAV24-2117) on 26-Aug-2024 and concerns a…

Inappropriate schedule of product administration
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