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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(827 ms)

#2829549Mar 4, 2025
Unknown·Age unknown·IL·TYP

The patient received one dose of Vivotif, which was left out of the refrigerator for two hours, reached a maximum temperature of 70 degrees Fahrenheit; The patient received one dose of Vivotif, which was left out of the refrigerator for two hours, reached a ma…

No adverse eventProduct storage error
#2829550Mar 4, 2025
Female·Age unknown·TYP

The patient took the first, second and third dose of Vivotif vaccine and realized that did not refrigerated vaccines; The patient took the first, second and third dose of Vivotif vaccine and realized that did not refrigerated vaccines; Case reference number US…

Product storage error
#2829551Mar 4, 2025
Unknown·Age unknown·IN·TYP

The patients took Vivotif every other day with food instead of taking it on empty stomach; Case reference number US-BN-2024-002412 is a spontaneous case report initially received from a consumer via Emergent BioSolutions (reference number: EMG2024-928) on 29-A…

Product administration error
#2829552Mar 4, 2025
Unknown·Age unknown·TYP

Clay colored stools; Discomfort from stomach; Abdominal pain; Case reference number US-BN-2024-002542 is a spontaneous case initially received from a consumer via Bavarian Nordic (reference number: BN_2024_02980) on 24-Sep-2024 and concerns a patient of unknow…

Abdominal discomfortAbdominal painFaeces discoloured
#2829553Mar 4, 2025
Unknown·Age unknown·TYP

The patient missed a day to take a dose of Vivotif; Case reference number US-BN-2024-002636 is a spontaneous case initially received from pharmacist via Med Communications (reference number: USBAV24-2672) on 10-Oct-2024 and concerns a patient of unknown age or…

Product dose omission issue
#2829554Mar 4, 2025
Unknown·Age unknown·IL·TYP

Patient had nausea after receiving fist dose of Vivotif; The patient had one or two bouts of diarrhea after second dose of Vivotif; Patient experienced diarrhea after third dose of Vivotif; Patient had never taken the fourth dose of Vivotif; The patient took t…

DiarrhoeaIncomplete course of vaccinationInterchange of vaccine productsNausea
#2829555Mar 4, 2025
Male·Age unknown·CA·TYP

The patient with lactose intolerance received dose of Vivotif; The patient with lactose intolerance received dose of Vivotif; Case reference number US-BN-2024-002698 is a spontaneous case initially received from a nurse via Med Communication (reference number:…

Contraindication to vaccinationLabelled drug-disease interaction medication errorNo adverse event
#2829556Mar 4, 2025
Female·Age unknown·FL·TYP

The patient had rash on the neck and trunk; Case reference number US-BN-2024-002739 is a spontaneous case initially received from other health care professional via Bavarian Nordic (reference number: BN_2024_03049) on 04-Nov-2024 and concerns a female patient…

Rash
#2829557Mar 4, 2025
Female·Age unknown·CO·TYP

Increased heart rate (could feel heartbeat in her teeth); Itching on the roof of mouth; Itching on the top of head; Case reference number US-BN-2024-002771 is a spontaneous case initially received from other health care professional via Bavarian Nordic (refere…

Heart rate increasedOral pruritusPruritus
#2829558Mar 4, 2025
Male·Age unknown·NY·TYP

The patient received first dose of Vivotif on Friday and second dose on Saturday instead of Sunday, the third dose on day four, the forth dose on day six, and fifth dose on day eight; The patient took five doses of Vivotif vaccine as it was suggested to the p…

Extra dose administeredInappropriate schedule of product administration
#2829559Mar 4, 2025
Male·Age unknown·SMALLMNK

Jynneos vaccines were administered at dose of 0.1 ml intradermally; Jynneos vaccines were administered at dose of 0.1 ml intradermally; Case reference number US-BN-2024-002867 is a spontaneous case initially received from other health care professional via Med…

Incorrect route of product administrationUnderdose
#2829560Mar 4, 2025
Female·Age unknown·CO·TYP

The patient took the pills last minute and the box obtained from vendor had a short date on it and expired on 30-Nov-2024; The patient received only one dose of Vivotif, then realised that box expired; Case reference number US-BN-2024-002886 is a spontaneous c…

Expired product administeredIncomplete course of vaccinationNo adverse event
#2829561Mar 4, 2025
Female·Age unknown·TYP

The patient did not notice and took all four Vivotif capsules instead of one capsule every other day; The patient did not notice and took all four Vivotif capsules instead of one capsule every other day; Case reference number US-BN-2024-002905 is a spontaneous…

Inappropriate schedule of product administrationIncorrect dose administered
#2829562Mar 4, 2025
Female·Age unknown·TYP

The patient received first dose of Vivotif capsule when it had been in the counter for about a week and a half and then skipped a day and took second dose without being refrigerated; The patient received first dose of Vivotif capsule when it had been in the co…

Product storage error
#2829563Mar 4, 2025
Female·78 yrs·NY·COVID19, RSV

Bone pain, Balance issues. weakness, dizziness, burning sensation throughout body, severe temperature fluctuations (freezing then sweating),

AstheniaBalance disorderBone painBurning sensationDizzinessFeeling cold+1 more
#2829564Mar 4, 2025
Male·34 yrs·SC·HPV9

The patient developed a localized lump (knot) on the left arm where the Gardasil injection was administered.

Injection site nodule
#2829565Mar 4, 2025
Female·69 yrs·FL·COVID19, PNC20

Pt requested to receive the Prevnar 20 shot. State Shots system wasn't checked but pt had received a dose of the Prevnar 20 back in November of 2022. There are currently no treatments or symptoms the pt has reported to us.

Extra dose administeredNo adverse event
#2829566Mar 4, 2025
Female·7 yrs·WA·IPV

No adverse reaction in patient. This was a vaccine error or suspected error. The IPOL is a 10 dose vial and 11 doses were pulled from vial. According to system, the 11th dose is invalid. We had siblings vaccinated together and we are unsure of who actually…

Circumstance or information capable of leading to medication errorNo adverse event
#2829567Mar 4, 2025
Male·12 yrs·WA·IPV

No adverse reaction in patient. This was a vaccine error or suspected error. The IPOL is a 10 dose vial and 11 doses were pulled from vial. According to system, the 11th dose is invalid. We had siblings vaccinated together and we are unsure of who actually…

Circumstance or information capable of leading to medication errorNo adverse event
#2829568Mar 4, 2025
Female·47 yrs·CT·COVID19

Itching all over that started within 1 hour of vaccination. Then for that day and the next I had very low blood pressure and a feeling like I was going to pass out. The same thing happened with my Pfizer booster one month later. The itching and low blood pr…

DizzinessHypotensionPruritus
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