Search and filter adverse-event reports.
1,929,324 reports(841 ms)
titer test showed zero immunity again; This non-serious case was reported by a consumer via call center representative and described the occurrence of therapy non-responder in a female patient who received MMR (Priorix) for prophylaxis. Previously administer…
Suspected vaccination failure; Enteric Shingles internal/ gut pain and stomach pain; rash was located on the Left side around the waist; the blisters never cracked; This serious case was reported by a consumer via call center representative and described the o…
Can not breath; my eyes are swollen and teary; my eyes are swollen and teary; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of difficulty breathing in a patient who received RSVPreF3 adjuvanted (Are…
Itching at injection site; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of injection site itching in a patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On an unknown date, the p…
Injection site pain; Injection site swelling; This non-serious case was reported by a consumer via call center representative and described the occurrence of injection site pain in a 78-year-old female patient who received Herpes zoster (Shingrix) (expiry date…
adjuvant was given without being mixed with the active ingredient; adjuvant was given without being mixed with the active ingredient; This non-serious case was reported by a other health professional and described the occurrence of inappropriate preparation of…
soreness; This non-serious case was reported by a consumer via call center representative and described the occurrence of pain in a patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received the 2nd dose of Shingr…
administration of Menveo diluent only to a patient; administration of Menveo diluent only to a patient; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of inappropriate preparation of medication in…
Hypersensitivity rxns; This spontaneous case was reported by a consumer and describes the occurrence of HYPERSENSITIVITY (Hypersensitivity rxns) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 prophylaxis.…
Resident passed away
Progressive ventricular heart arrhythmia with pre-syncope, chest pain and hardship breathing; followed by pericarditis, enlarged right ventricle; hospitalization after 4 weeks as symptoms progressed; scheduled for heart surgery (catheterization ablation) in Oc…
Patient passed out within seconds of the two shots. She woke up pale, clammy and nauseous. We waited at the office for another 30 minutes. She threw up on the way home and had chills, but no fever, when we arrived home.
Patient came in yesterday (7/9 at 12pm) to get a TDAP shot so that he could be vaccinated against whooping cough because he is expecting a new grandchild. Upon typing it up and putting through our DUR system, it went through fine without any DUR flag. Vaccine…
no known symptoms patient doing fine
The MMRV vaccine was administered to an adult aged 40. Recommendations state not to administer MMRV vaccine to anyone aged 12 and up. The patient experienced no adverse events and has been notified.
The 1st dose of the Pfizer Covid 19 vax (April 2021) caused an outbreak of the Shingle virus (Sep 2021). The 2nd dose of the Pfizer vax (Feb 2022, due to employer mandate) caused 3 separate trips to the ER. The symptoms were super high blood pressure (190/120…
Around 1:45 am on 7/9, my daughter started to develop what she described as a "scary headache". She couldn't move her head at her neck and felt like she couldn't move at all; she described it as if her neck/back was fused. She was scared to fall asleep because…
MEDICAL ASSISTANT ADMINISTERED ONLY THE DILUENT AND NOT THE ANTIGEN ON 2/4/2025. THIS WAS DISCOVERED RECENTLY, WHEN A SIMILIAR OCCURANCE WAS CAUGHT PRIOR TO ADMINISTRATION INVOLVING ANOTHER PATIENT. UPON FURTHER REVIEW, THE MEDICAL ASSISTANT INDICATED NOT BEI…
Patient was given Prevnar 20 vaccine on 7/10/2025. Patient had had already had the Prevnar 20 on 02/06/2024. Notified the patient's provider.
Beyfortus ordered by provider and administered by medical assistant in error. Patient should have received Abrysvo instead. No adverse reactions noted.