Search and filter adverse-event reports.
1,929,324 reports(821 ms)
no additional AE; " Consumer confirmed that they were not pregnant when they were administered their first dose of RECOMBIVAX HB; This spontaneous prospective pregnancy report was received from a Consumer or other non health professional (patient) and refers t…
No additional AE; The leaking product did not get on the patient. Leaking product did get on the gloved hand of the HCP, but did not get on the HCP's skin; reconstituted vaccine came out between the hub and the leur lock; This spontaneous report was received f…
The patient has not report any medical concerns or symptoms after being administered the dose of GARDASIL 9; A patient who was 8 months pregnant was administered their first dose of GARDASIL 9 on 9/15/2025; This spontaneous report was received from a nurse pre…
no adverse event; product storage error; patient received PROQUAD in April or May of 2025, VARIVAX on 22-May-2025; product storage error; This spontaneous report was received from a medical assistant and a clinic manager referring to a 1-year-old male patient.…
no patient symptoms have been reported; expired dose of PNEUMOVAX 23 was inadvertently administered; This spontaneous report was received from a Licensed Vocational Nurse and refers to a identified patient of unknown age and gender. The patient's medical his…
No adverse effects reported; patient received her 2nd dose of GARDASIL 9 too early; This spontaneous report was received from a Certified Medical Assistant (CMA) and refers to a 9-year-old female patient. The patient's medical history was not reported. The p…
No additional AE; temperature excursion and reports that a dose of PEDVAX HIB was administered; This spontaneous report was received from an Other health professional and refers to a patient of unknown age and gender. The patient's medical history was not re…
no adverse event; inappropriate schedule; This spontaneous report was received from an Other health professional and refers to a 31-year-old female patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported…
The patient received the Jynneos dose three weeks instead of four weeks apart; Case reference number US-BN-2025-000192 is a spontaneous case initially received from nurse via agency (reference number: USBAV25-0253) on 04-Feb-2025 and concerns a patient of unkn…
The first dose of Jynneos was administered intramuscularly rather than subcutaneously; The patient received the second dose of Jynneos four months and 10 days after the first dose; Case reference number US-BN-2025-000311 is a spontaneous case initially receive…
The patient received the first dose of Jynneos on 24-Nov-2024 and didn't receive the second dose still; Patient received Jynneos vaccine intramuscularly; Case reference number US-BN-2025-000353 is a spontaneous case initially received from pharmacist via agenc…
The patient received the first dose of Jynneos six months ago, and did not receive the second dose still; Case reference number US-BN-2025-000441 is a spontaneous case initially received from pharmacist via agency (reference number: USBAV25-0775) on 07-Apr-202…
The patient was given a seven-day expired m-pox vaccine; Case reference number US-BN-2025-000843 is a spontaneous case report initially received from an other health professional via Communication (reference number: USBAV25-0846) on 16-APR-2025 and concerns a…
The Jynneos vaccine was administered intramuscularly instead of subcutaneously; Patient received first dose (only one dose) of Jynneos vaccine on 08-Apr-2025; Case reference number US-BN-2025-000922 is a spontaneous case initially received from pharmacist via…
The patient developed induration at the injection site pretty big and 3-4 cm; The patient received Jynneos intramuscularly; Case reference number US-BN-2025-001182 is a spontaneous case report initially received from a physician via Communication (reference nu…
Had First Dose 22-Feb-2025, Second Dose Received 11-Sep-2025; Initial report received on 11-Sep-2025. A consumer reported that he, a 28-year-old male, received the second dose of HEPLISAV-B (hepatitis B vaccine) for hepatitis B immunization about six months…
HEPLISAV-B Exposed to a Temperature 32.8 C and Out of Range For 93 Hours, And It Was Administered to a Patient; Initial report received on 11-Sep-2025. A pharmacist reported that a 57-year-old male received HEPLISAV-B (hepatitis B vaccine) for hepatitis B imm…
Chills 24 Hours a Day; Initial report received on 12-Sep-2025. A consumer reported that a male patient received HEPLISAV-B (hepatitis B vaccine) for hepatitis B immunization and experienced chills 24 hours a day. No medical history or concomitant medicati…
Pain, swelling, redness at site; Pain, swelling, redness at site; Pain, swelling, redness at site; Muscle ache; This non-serious case was reported by a consumer and described the occurrence of injection site pain in a 54-year-old female patient who received He…
Large arm swelling; 101 fever; headache; extreme body aches; she cannot move her arm; This non-serious case was reported by a physician via sales rep and described the occurrence of large arm swelling in a female patient who received Men B NVS (Bexsero) for pr…