Search and filter adverse-event reports.
1,929,324 reports(787 ms)
The patient took first dose of Vivotif and was due to take second dose yesterday, but missed that dose; Case reference number US-BN-2024-002081 is a spontaneous case initially received from a pharmacist via Communication (reference number: USBAV24-1437) on 21-…
Cold sore activation on upper lip
The patient did not take fourth dose of Vivotif on scheduled date; The finale capsule of Vivotif was unrefrigerated for 16 hours at potentially room temperature; Case reference number US-BN-2024-002002 is a spontaneous case initially received from a pharmacist…
Patient took two doses of Vivotif consecutively, instead of taking the first two doses every other day; Case reference number US-BN-2024-002019 is a spontaneous case initially received from a pharmacist via Communication (reference number: USBAV24-1309) on 07-…
The patient had a local reaction of pain, redness, and swelling; The patient had a local reaction of pain, redness, and swelling; The patient had a local reaction of pain, redness, and swelling; The patient received one dose of Jynneos and decided not to get t…
The patient was late about 16 hours with fourth dose of Vivotif vaccine; The patient ate one half chocolate bar and fruit leather ten minutes prior to taking the fourth dose of Vivotif; Case reference number US-BN-2024-002087 is a spontaneous case initially re…
The patient took one dose of Vivotif vaccine which package was left out of the fridge for less than 12 hours; The patient took one dose of Vivotif vaccine which package was left out of the fridge for less than 12 hours; The patient took one dose of Vivotif vac…
clade II mpox, patient developed symptoms of tenesmus and pruritus ani; Literature citation. Case reference number US-BN-2026-000441 is a spontaneous literature case report, title as stated above, identified on 08-Jul-2025, and concerns a male patient of unkn…
Mild COVID-19 infections; Mild COVID-19 infections; This is a literature report for the following literature source(s). An elderly patient received BNT162b2 (BNT162B2), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknow…
patient reports arm hurts at the location site where shot was given since 10/2025
During vaccine administration, patient's arm tensed up. Immediately following this, looked pale, had nausea, dizziness, lightheadedness. BP 86/54, BG 113. Patient was sat down, given water, BP improved back to normal within 10 minutes. Patient had large BM aft…
There was no reaction, The TDAP should have been given
Patient took third dose of Vivotif 12 hours later (on day six instead on day five); Case reference number US-BN-2024-001980 is a spontaneous case initially received from a pharmacist via Communications (reference number: USBAV23-1229) on 03-Jun-2024 and concer…
The patient took first two doses of Vivotif, two days in row; Case reference number US-BN-2024-001982 is a spontaneous case initially received from pharmacist via Communications (reference number: USBAV23-1231) on 03-Jun-2024 and concerns female patient of uns…
The patient took the three doses of Vivotif, and missed the fourth dose; Case reference number US-BN-2024-001983 is a spontaneous case initially received from a pharmacist via Communications (reference number: USBAV23-1245) on 03-Jun-2024 and concerns a patien…
clade II mpox with a genital rash; Literature citation. Case reference number US-BN-2026-000442 is a spontaneous literature case report, title as stated above, identified on 08-Jul-2025, and concerns a male patient of unknown age (patient five). During the g…
suspected mpox, patient experienced fever, myalgia, general pain, tenesmus, and a rash on the trunk, extremities, and perianal area; Literature citation. Case reference number US-BN-2026-000443 is a spontaneous literature case report, title as stated above, i…
The morning after, my son woke up with a crossed eye. We took him to his pediatrician and were referred to [name withheld] Opthamology. Findings included Esotropia, Comitant. Control poor. Other fields of gaze were attempted but unable to be obtained. A sensor…
The patient is 36 weeks pregnant and requested an RSV vaccine. She was given Arexvy, which is not approved for maternal vaccination, instead of Abrysvo.
Due to a refrigerator malfunction the viability of the vaccines came into question. In speaking with both manufacturers, it was determined that the COVID vaccine was ok but the patient would need to be revaccinated for her flu shot. the patient has been contac…