Search and filter adverse-event reports.
1,929,324 reports(726 ms)
Patient left Vivotif capsules out the refrigerator for 48 hours at home, and took one dose after excursion; Patient left Vivotif capsules out the refrigerator for 48 hours at home, and took one dose after excursion; Patient left Vivotif capsules out the refrig…
Patient ate food half an hour after taking his third dose of the Vivotif; Case reference number US-BN-2025-001801 is a spontaneous case initially received from a nurse via Bavarian Nordic (reference number: CASE-000745) on 14-Nov-2025 and concerns a 19-years-o…
The patient took the Vivotif vaccine on days 1,3,6 and 8 instead of on days 1,3,5, and 7; Case reference number US-BN-2025-001814 is a spontaneous case initially received from a pharmacist via Bavarian Nordic (reference number: CASE-000808) on 18-Nov-2025 and…
Cramping; Nausea; Vomiting; Diarrhea; Headache; patient inadvertently taking Vivotif, took all four tablets at once; patient inadvertently taking Vivotif, took all four tablets at once; Case reference number US-BN-2025-001835 is a spontaneous case initially re…
Patient stored Vivotif at home at 65 to 68 degrees and Vivotif was out of the fridge for 5 days and patient took two doses; Patient stored Vivotif at home at 65 to 68 degrees and Vivotif was out of the fridge for 5 days and patient took two doses; Patient stor…
The whole family (3 males and 1 female) took the first dose of Vivotif which was left at room temperature probably 68-70 F.; The whole family (3 males and 1 female) took the first dose of Vivotif which was left at room temperature probably 68-70 F.; The whole…
The patient took two doses of Vivotif in a row instead of every other day; Case reference number US-BN-2025-001896 is a spontaneous case initially received from a pharmacist via Bavarian Nordic (reference number: CASE-000994) on 02-Dec-2025 and concerns an adu…
The patient took first two doses of Vivotif in the week of 24-Nov-2025 and last two doses in the week of 01-Dec-2025; Case reference number US-BN-2025-001897 is a spontaneous case initially received from other health professional via Bavarian Nordic (reference…
The patient took Vivotif every day; Vivotif was never kept in refrigerator; Vivotif was never kept in refrigerator; Vivotif was never kept in refrigerator; Case reference number US-BN-2025-001901 is a spontaneous case initially received from consumer via Bavar…
The patient took three doses of Vivotif on consecutive days instead of every other day; Case reference number US-BN-2025-001902 is a spontaneous case initially received from other health professional via Bavarian Nordic (reference number: CASE-001022) on 03-De…
The patient took the first dose of Vivotif on 06-Dec-2025, which was not refrigerate since 03-Dec-2025; The patient took the first dose of Vivotif on 06-Dec-2025, which was not refrigerate since 03-Dec-2025; The patient took the first dose of Vivotif on 06-Dec…
The patient took a dose of Vivotif that was out of refrigerator for three days; The patient took a dose of Vivotif that was out of refrigerator for three days; The patient took a dose of Vivotif that was out of refrigerator for three days; Case reference numbe…
Greater than 48 interval between third and fourth dose. Patient did not complete one week prior to exposure to S. Typhi.; he lost the last pill and wants another one; Case reference number US-BN-2025-001927 is a spontaneous case initially received from other h…
The patient took all 4 doses of Vivotif but did not refrigerate it; The patient took all 4 doses of Vivotif but did not refrigerate it; The patient took all 4 doses of Vivotif but did not refrigerate it; Case reference number US-BN-2025-001929 is a spontaneous…
some sort of heart issues that landed the patient in the hospital; This serious case was reported by a other health professional via sales rep and described the occurrence of heart disorder in a patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis…
suspected vaccination failure; shingles; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown…
design/colorway is very similar to the peds Hep A carton; design/colorway is very similar to the peds Hep A carton which could increase the risk of vaccine administration errors; This non-serious case was reported by a non-health professional and described the…
I have shingles and had both shots; I have shingles and had both shots; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) f…
arm is a little sore; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of pain in arm in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On 11-MAR-2026, the patient received…
patients have received only the diluent portion of Shingrix; Inappropriate dose of vaccine administered; This non-serious case was reported by a nurse via call center representative and described the occurrence of inappropriate preparation of medication in a 5…