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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(851 ms)

#2829337Mar 4, 2025
Female·51 yrs·TX·FLU3

Patient received Flu vaccine on 2/8/25. Two days after vaccine, patient states she was experiencing neck, shoulder, trunk and left arm pain. She states it seems like it is "nerve pain." She visited her provider and they prescribed her 9 day steroid course.…

ArthralgiaNeck painNeuralgiaPainPain in extremity
#2829338Mar 4, 2025
Female·46 yrs·COVID19, FLU3, HEP, MMR, VARCEL

Patient received Covid, Flu, MMR, Varicella, and Hep B vaccines at facility for employment. She was due now (March 2025) for her second doses and mentioned to Employee Health (reporter of this VAERS submission) that she had a "bad reaction" and wanted to "opt…

Exercise tolerance decreasedMuscle fatigueRash
#2829339Mar 4, 2025
Female·32 yrs·IA·MMR

MMR vaccine was given and patient is pregnant. Did not share how many weeks as has not met with physician due to just finding out was pregnant.

Contraindication to vaccinationExposure during pregnancy
#2829340Mar 4, 2025
Male·17 yrs·NC·MENB

Severe right arm pain over deltoid. Waking him from sleep. Senior, baseball player - has not recovered and can not play.

Loss of personal independence in daily activitiesMyalgiaSleep disorderX-ray limb
#2829453Mar 4, 2025
Male·Age unknown·CA·TYP

The patient did not receive dose of Vivotif about 48 hours after the last dose; Case reference number US-BN-2024-000004 is a spontaneous case report initially received from pharmacist via Med Communications (reference number: USBAV24-0008) on 02-Jan-2024 and c…

Product dose omission issue
#2829454Mar 4, 2025
Unknown·Age unknown·NY·TYP

The patient missed the fourth dose of Vivotif.; Case reference number US-BN-2024-000013 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number: USBAV24-0020) on 04-Jan-2024 and concerns a 20-year-old patient…

Product dose omission issue
#2829455Mar 4, 2025
Female·Age unknown·KS·TYP

The patient took two doses of Vivotif on schedule and forgot next two doses due to busy schedule; Case reference number US-BN-2024-000014 is a spontaneous case report initially received from other health care professional via Med Communication (reference numbe…

Incomplete course of vaccination
#2829456Mar 4, 2025
Unknown·Age unknown·MT·TYP

The patient had cup of coffee about 15 minutes after administrating a dose of Vivotif on an empty stomach with cold water; Case reference number US-BN-2024-000016 is a spontaneous case report initially received from a nurse via Med Communications (reference nu…

Product administration error
#2829457Mar 4, 2025
Female·Age unknown·UT·TYP

The patient left Vivotif out of the refrigerator and took the second dose of Vivotif after the temperature excursion, maximum temperature was 70 degrees of Fahrenheit and it was left for two hours; The patient left Vivotif out of the refrigerator and took the…

Product storage error
#2829458Mar 4, 2025
Female·Age unknown·MN·TYP

The patient completed the whole series of Vivotif and then realized it should had been refrigerated after the patient left Vivotif capsules at room temperature for up to 48 hours; The patient completed the whole series of Vivotif and then realized it should ha…

Product storage error
#2829459Mar 4, 2025
Female·Age unknown·MO·TYP

The patient took the first and second doses of Vivotif vaccine at room temperature (reached 68 Fahrenheit) for three weeks; The patient took the first and second doses of Vivotif vaccine at room temperature (reached 68 Fahrenheit) for three weeks; The patient…

FatigueInappropriate schedule of product administrationNauseaProduct storage error
#2829460Mar 4, 2025
Male·Age unknown·MO·TYP

The patient took the first and second doses of Vivotif vaccine at room temperature (reached 68 Fahrenheit) for three weeks; The patient took the first and second doses of Vivotif vaccine at room temperature (reached 68 Fahrenheit) for three weeks; Anorrexia, a…

Decreased appetiteDiarrhoeaFatigueNauseaProduct storage error
#2829461Mar 4, 2025
Female·Age unknown·VI·TYP

The patient took the third dose of Vivotif three days after the first dose and the fourth dose of Vivotif six days after the first dose; Case reference number US-BN-2024-000051 is a spontaneous case report initially received from a nurse via Med Communication…

Inappropriate schedule of product administration
#2829462Mar 4, 2025
Male·Age unknown·AL·TYP

The patient took Vivotif capsules two days in a row instead of every other day.; Case reference number US-BN-2024-000052 is a spontaneous case report initially received from a pharmacist via Med Communication (reference number: USBAV24-0075) on 11-Jan-2024 and…

Inappropriate schedule of product administration
#2829463Mar 4, 2025
Female·Age unknown·WI·TYP

The patient took one capsule of Vivotif on Jan-2024, which was expired on Dec-2023; The patient took the second dose of Vivotif with the new lot dispensed after taking one capsule of Vivotif that was expired; Case reference number US-BN-2024-000056 is a sponta…

Expired product administeredExtra dose administered
#2829464Mar 4, 2025
Male·Age unknown·WI·TYP

The patient took four doses of Vivotif vaccine every day instead of every other day; Case reference number US-BN-2024-000057 is a spontaneous case report initially received from a pharmacist via Med Communications (reference number: USBAV24-0082) on 12-Jan-202…

Inappropriate schedule of product administrationNo adverse event
#2829465Mar 4, 2025
Female·Age unknown·CO·TYP

The patient took one capsule of Vivotif and the reporter was not sure if the product already suffered temperature excursion, which was two to ten days stood at max temperature of 20 degrees of Celsius; The patient took one capsule of Vivotif and the reporter w…

Product storage error
#2829466Mar 4, 2025
Female·Age unknown·NJ·TYP

The patient took the second and the third dose of Vivotif two days in a row; Case reference number US-BN-2024-000084 is a spontaneous case report initially received from nurse via Med Communications (reference number: USBAV24-0120) on 19-Jan-2024 and concerns…

Inappropriate schedule of product administration
#2829467Mar 4, 2025
Female·Age unknown·NY·TYP

Blisters on eyelids; The patient developed a rash eight-ten years ago on face after taking Vivotif; Case reference number US-BN-2024-000085 is a spontaneous case report initially received from a healthcare professional via Med Communications (reference number:…

BlisterRash
#2829468Mar 4, 2025
Male·Age unknown·CO·TYP

The patient forgot to take the fourth dose of Vivotif vaccine on day seven.; Case reference number US-BN-2024-000089 is a spontaneous case report initially received from other healthcare professional via Med Communication (reference number: USBAV24-0139) on 22…

Product dose omission issue
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