Drug adverse event reports (FAERS)
Reports of adverse events and medication errors sent to FDA for drugs and therapeutic biologics. 20,692,690 records; openFDA updated it 2026-09-23. About this dataset
Newest records
- DRUG INEFFECTIVE1,299,282
- OFF LABEL USE856,387
- DEATH849,919
- NAUSEA778,535
- FATIGUE766,575
- DIARRHOEA634,732
- HEADACHE617,855
- PAIN607,148
- Incorrect dose administered
Drugs: TREMFYA
- Brain natriuretic peptide increased, Cardiac failure
Drugs: SKYCLARYS
- Blood potassium increased, Glaucoma, Blood creatinine abnormal +1
Drugs: RAVULIZUMAB
- Movement disorder, Myopathy, Myalgia
Drugs: PITAVASTATIN, ASPIRIN\CLOPIDOGREL, EPLERIUM +3
- Warm autoimmune haemolytic anaemia
Drugs: TACROLIMUS, ALLOPURINOL, BISOPROLOL
- Pulmonary valve incompetence
Drugs: FINTEPLA
- Seizure, Aspiration, Acute kidney injury +3
Drugs: METHOTREXATE, AZATHIOPRINE
- Injury
Drugs: SPRAVATO
- Cardiotoxicity
Drugs: HERCEPTIN
- Dyspnoea, Hernia
Drugs: AMJEVITA
- Cardiotoxicity
Drugs: HERCEPTIN
- Somnolence, Cardiac disorder
Drugs: THALOMID
- Death, Product use issue
Drugs: TECVAYLI, DARZALEX
- Death
Drugs: OLAPARIB
- Muscular weakness
Drugs: CAMZYOS, BISOPROLOL, FUROSEMIDE +5
- Condition aggravated
Drugs: OMVOH
- Abdominal pain upper
Drugs: ZEPBOUND
- Drug ineffective
Drugs: ZEPBOUND
- Hypersensitivity
Drugs: HUMALOG, INSULIN LISPRO
- Extra dose administered
Drugs: MOUNJARO
Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.
How to read this: Each report says someone told FDA an event happened while a product was used. A report does not show the product caused it, and counts rise and fall with how many people report. Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.
