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 2026-10-05. About this dataset
Newest records
- DRUG INEFFECTIVE1,299,281
- OFF LABEL USE856,381
- DEATH849,878
- NAUSEA778,547
- FATIGUE766,581
- DIARRHOEA634,725
- HEADACHE617,851
- PAIN607,165
- Drug interaction, Anxiety
Drugs: ARIPIPRAZOLE, TIRZEPATIDE
- Diarrhoea
Drugs: HUMIRA, AZATHIOPRINE, MERCAPTOPURINE +11
- Hospice care, Device use error
Drugs: VYALEV
- Drug dose omission by device, Device malfunction
Drugs: NEULASTA
- Breast cancer
Drugs: VYALEV
- Coronavirus infection
Drugs: ARNUITY ELLIPTA
- Gingival operation, Endodontic procedure
Drugs: SKYRIZI
- Cardiac flutter, Fall, Concussion +5
Drugs: RINVOQ, DUPIXENT
- Septic shock, Drug tolerance decreased, Anaemia +3
Drugs: VENETOCLAX
- Hysterectomy
Drugs: SKYRIZI
- Endoscopy small intestine, Weight fluctuation
Drugs: SKYRIZI
- Off label use
Drugs: SIMPONI ARIA
- Chronic obstructive pulmonary disease
Drugs: RINVOQ
- Death
Drugs: UPADACITINIB
- Ageusia, Taste disorder
Drugs: HERNEXEOS
- Drug interaction, Mood altered
Drugs: ARIPIPRAZOLE, WEGOVY
- Loss of consciousness, Fall, Hypotension +2
Drugs: VYALEV
- Brain injury, Drug ineffective, Treatment noncompliance
Drugs: ORENCIA
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.
