Search and filter adverse-event reports.
1,929,324 reports(821 ms)
Patient reported no symptoms of pain or concern the day of vaccine. Patient reported symptoms of burning to feet, groin area and fingertips to bilateral upper and lower extremities within two days after receiving vaccine.
Patient received an extra Pedvaxhib at 6 month well check. Patient had already received a Pedvaxhib dose at 2 month and 4 month well check. Patient was not due for booster until 12 month of age. Parent reported redness and swelling at the injection site.…
Pain that lasted 6 days. Lump, swollen
Developed discomfort over LT arm and fingers. Blisters over fingers, LT 5th finger and middle fingers- developed 7/22/2025. No fever, vomiting or diarrhea.
There is no adverse event, this is just report that pharmacist only administered diluent to patient, pharmacist did not mix vaccine prior to administration.
Mother mentioned when bringing in the daughter in at 1:00 pm this afternoon, that she wanted to mention that the Patient upon getting in the car was complaining of rash on chest and pain in chest, this was around 10:30 this morning, after mom told MA the MA we…
n/a
Arexvy administered to pregnant women; healthcare system decided to switch from Arexvy to Abrysvo due to some instances where Arexvy was administered to pregnant women; This non-serious prospective pregnancy case was reported by a other health professional via…
Inappropriate schedule of vaccine administered; This non-serious case was reported by a consumer via call center representative and described the occurrence of incomplete course of vaccination in a 61-year-old female patient who received Herpes zoster (Shingri…
patient received Bexsero inadvertently, the patient was supposed to receive Menveo; This non-serious case was reported by a nurse and described the occurrence of wrong vaccine administered in a 11-year-old male patient who received Men B NVS (Bexsero) (batch n…
vaccine not administered within time frame specified in PI; This non-serious case was reported by a consumer via call center representative and described the occurrence of incomplete course of vaccination in a female patient who did not receive Herpes zoster (…
Suspected vaccination failure; Patient got shingles after receiving immunization; This serious case was reported by a other health professional via sales rep and described the occurrence of vaccination failure in a female patient who received Herpes zoster (Sh…
fainted seconds after receiving the vaccines; very limp; This serious case was reported by a pharmacist via other manufacturer and described the occurrence of fainting in a patient who received DTPa (Reduced antigen) (Boostrix) (batch number H4279, expiry date…
Suspected vaccination failure; got shingles anyway; 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…
had like a type of palsy after vaccinations; This serious case was reported by a consumer via other manufacturer and described the occurrence of paralysis in a 15-month-old female patient who received DTPa (DTPa vaccine) for prophylaxis. Co-suspect products…
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 (Shingrix) for prophylaxis. On an unknown date, th…
Suspected Vaccination failure; got it 3 months after my 2nd shot; 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 prop…
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. Co-suspect pro…
localized reaction of redness; localized reaction of pain; gave a patient a Kinrix and a Pediarix at the same time; were the 3rd dose of Kinrix and 4th dose of Pediarix of the patient in the DTap series; This non-serious case was reported by a other health pro…
Twinrix subcutaneous administration; This non-serious case was reported by a other health professional via call center representative and described the occurrence of intramuscular formulation administered by other route in a 66-year-old male patient who recei…