Search and filter adverse-event reports.
1,929,324 reports(922 ms)
they are now giving it to many adults; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of inappropriate age at vaccine administration in unspecified number of patients who received MMR (Priorix) fo…
Died; This spontaneous report received from a health care professional concerned an 82 year old female patient. The patient's height and weight were not reported. Age at time of vaccination 9 old. The patient's concurrent conditions included: carpal tunnel,…
the lymph nodes under the receiving arm (left) were killing her. Pain lasted for 2 days.; This is a spontaneous report received from a Consumer or other non HCP from a sales representative. A 72-year-old female patient (not pregnant) received BNT162b2 omicron…
covid; covid; This is a spontaneous report received from a Consumer or other non HCP. A female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's rel…
severe eczema flare ups all over my neck face back and arms; This is a spontaneous report received from a Consumer or other non HCP. A 33-year-old female patient received BNT162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), on 10Nov2023 as dose 1 (toppac); s…
Delayed reaction to pneumococcal - developed erythematous injection site reaction on 12/25/24, then redness spread to full circumference of arm (itchy, red), resolved after 4 days
swelling eye, face; swelling eye, face; Patient had rash toneck/face; This case has been migrated from the previous safety database to the current safety database and assigned new Case ID: 2227735. The previous case ID: 2501USA009410, and 2501USA009410. As a c…
No additional AE; Customer called and reported that an additional dose of MMR-II was administered to a 5-year-old consumer after the series was completed. The final dose of the series was administered on 2/15/2024. The additional dose was administered on 2/13/…
No additional AEs; expired dose of GARDASIL 9 was administered.; This spontaneous report was received from a medical assistant concerning to a patient of unspecified age and gender. The patient's medical history, concurrent conditions, concomitant therapies…
No adverse event reported; multiple patients may have received improperly stored PROQUAD since it "was stored in the refrigerator for months" instead of the freezer; This spontaneous report has been received from a nurse regarding an 8-year-old female patient…
innapropriate age of vaccine administered; HCP states she could not confirm if there were any symptomatic events that occurred; This spontaneous report has been received from a health care proffesional regarding a 11-months-old patient of unknown age and gende…
Improper storage of product in use; This spontaneous report was received from a nurse referring to a 6-year-old male patient. Information regarding the patient's concurrent conditions, historical conditions and concomitant or historical medications was not pro…
No additional AE/; Patient received a dose of PROQUAD in September and another dose in February. No reported signs or symptoms of adverse effects. Permission to contact HCP was given. No additional AE/no PQC; Patient received a dose of PROQUAD in September and…
No additional AE reported; products that experienced temperature excursion were administered to patient; This spontaneous report was received from a registered nurse and refers to a 12-month-old male patient. No information regarding the patient's medical hist…
No additional AE reported; products that experienced temperature excursion were administered to patient; This spontaneous report was received from a registered nurse and refers to a 12-month-old male patient. No information regarding the patient's medical hist…
Transient ischemic attack; Peripheral polyneuropathy; This serious case was reported by a consumer via other manufacturer and described the occurrence of transient ischemic attack in a 60-year-old female patient who received Herpes zoster (Shingrix) (batch num…
Skin Rash at injection site; This non-serious case was reported by a other health professional via sales rep and described the occurrence of injection site rash in a 50-year-old female patient who received Herpes zoster (Shingrix) (batch number KB2YT) for prop…
balance affected; walking affected; Sudden tingling in left foot and lower leg; Tingling and numbness in left foot; This non-serious case was reported by a consumer and described the occurrence of tingling of extremity in a 74-year-old female patient who recei…
Flu like symptoms; This non-serious case was reported by a consumer via sales rep and described the occurrence of influenza-like symptoms in a male patient who received Herpes zoster (Shingrix) for prophylaxis. On 08-JAN-2025, the patient received the 1st do…
my child was diagnosed with neutropenia 66 days after Pediarix3 (Hep b 4); This serious case was reported by a consumer via interactive digital media and described the occurrence of neutropenia in a child patient who received DTPa-HBV-IPV (Pediarix) for prophy…