Search and filter adverse-event reports.
1,929,324 reports(848 ms)
Hives; Itching; This non-serious case was reported by a consumer via call center representative and described the occurrence of hives in a 68-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. The patient's past medical history in…
pentacel components were administered separately and that the hib was reconstituted with sterile water with no reported adverse event; Initial information received on 24-Jun-2025 regarding an unsolicited valid non-serious case received from a physician. This…
feeling badly; missed second dose of pre-exposure imovax therapy due to feeling badly; Initial information received on 24-Jun-2025 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age female patient wh…
Consumer called to report his father went in for his 3rd dose of TICE BCG today but was told they did not have a dose for him today due to the shortage of the product.; no AE; This spontaneous report was received from a consumer and refers to a male patient of…
No symptoms reported.; HCP calling to report inadvertently administering an expired dose of MMRII to a patient.; This spontaneous report was received from other health professional and refers to a patient of unknown age and gender. The patient's medical hist…
HCP stated female patient started her series at age 45 and has not received their 3rd dose within the guidelines of PI.; No additional AE reported; This spontaneous report was received from a Pharmacist and refers to a 45-year-old female patient. No informatio…
female patient last received 2 doses of GARDASIL-9 in 2021 but did not complete the series; No additional AE; This spontaneous report was received from a nurse referring to a 27-year-old female patient. No information regarding the patient's pertinent medical…
Patient was vaccinated with RabAvert and Immunoglobulin in the right shoulder; Case reference number US-BN-2024-002008 is a spontaneous case initially received from a pharmacist via Med Communication (reference number: USBAV24-1305) on 07-Jun-2024 and concerns…
Patient received first dose of Rabavert for pre-exposure and did not receive the second dose on day seven; Case reference number US-BN-2024-002069 is a spontaneous case initially received from a nurse via Med Communication (reference number: USBAV24-1402) on 1…
Patient received day zero dose of RabAvert and was supposed to receive the day seven dose but cant get it; Case reference number US-BN-2024-002110 is a spontaneous case initially received from a pharmacist via Med Communications (reference number: USBAV24-1497…
The patient received only diluent of RabAvert; The patient received only diluent of RabAvert; Case reference number US-BN-2024-002121 is a spontaneous case initially received from pharmacist via Med Communications (reference number USBAV24-1545) on 01-Jul-2024…
Patient received last dose of Rabavert, but it was administered in the buttock, instead of the deltoid; Case reference number US-BN-2024-002123 is a spontaneous case initially received from a pharmacist via Med Communication (reference number: USBAV24-1549) on…
The patient received the first dose of RabAvert on 05-Jul-2024, for pre-exposure, and missed the second dose; Case reference number US-BN-2024-002192 is a spontaneous case initially received from pharmacist via Med Communications (reference number USBAV24-1663…
The patient received two doses of RabAvert in May-2024, for pre-exposure prophylaxis, and did not receive the third dose; Case reference number US-BN-2024-002193 is a spontaneous case initially received from pharmacist via Med Communications (reference number…
The patient received the first and second RabAvert vaccine in thighs; The patient received the first dose of RabAvert two days after animal exposure and second dose five days after animal exposure; Case reference number US-BN-2024-002252 is a spontaneous case…
The second dose of RabAvert delayed one day; Case reference number US-BN-2024-002276 is a spontaneous case initially received from a nurse via Med Communication (reference number USBAV24-1827) on 31-Jul-2024 and concerns a *43-year-old female patient*. The pa…
Patient received second dose of preexposure prophylaxis with Rabavert on day 10, instead of day seven; Case reference number US-BN-2024-002289 is a spontaneous case initially received from a health care professional via Med Communications (reference number: US…
The patient only received the diluent and not the vial that contained the actual vaccine; The patient only received the diluent and not the vial that contained the actual vaccine; Case reference number US-BN-2024-002293 is a spontaneous case initially received…
The patient received RabAvert vaccine which expired in Apr-2024; Case reference number US-BN-2024-002315 is a spontaneous case initially received from physician via Med Communications (reference number: USBAV24-1894) on 07-Aug-2024 and concerns patient of unsp…
The patient received the first dose of RabAvert on day 0 and second dose on day 4; Case reference number US-BN-2024-002346 is a spontaneous case initially received from a pharmacist via Med Communications (reference number USBAV24-1967) on 14-Aug-2024 and conc…