Drug adverse event reports (FAERS)
Reports of adverse events and medication errors sent to FDA for drugs and therapeutic biologics. 21,054,159 records; openFDA updated it 2026-11-09. About this dataset
86,061 records match “semaglutide”
- NAUSEA12,276
- OFF LABEL USE8,375
- VOMITING8,326
- DIARRHOEA7,496
- DECREASED APPETITE5,378
- CONSTIPATION5,295
- WEIGHT DECREASED5,210
- IMPAIRED GASTRIC EMPTYING4,272
- Impaired gastric emptying, Emotional distress
Drugs: OZEMPIC
- Impaired gastric emptying, Emotional distress
Drugs: OZEMPIC
- Impaired gastric emptying, Emotional distress
Drugs: OZEMPIC
- Impaired gastric emptying, Emotional distress
Drugs: OZEMPIC
- Psoriatic arthropathy, Depression, Arthropathy +2
Drugs: OZEMPIC
- Impaired gastric emptying, Emotional distress
Drugs: OZEMPIC
- Death
Drugs: OZEMPIC
- Impaired gastric emptying
Drugs: OZEMPIC, MOUNJARO
- Depressed mood, Fatigue, Depression
Drugs: OZEMPIC
- Chromaturia, Dark circles under eyes, Swelling of eyelid +4
Drugs: TREMFYA, OZEMPIC
- Impaired gastric emptying, Emotional distress
Drugs: OZEMPIC
- Cardioversion
Drugs: OZEMPIC
- Fall, Off label use, Weight decreased
Drugs: OZEMPIC
- Syncope, Asthenia, Urine output decreased +11
Drugs: OZEMPIC, Lantus (insulina glargine), LOSARTAN +3
- Neuropathy peripheral, Heart valve incompetence, Arthropathy +1
Drugs: CAMZYOS, CYCLOBENZAPRINE, ZETIA +28
- Corrective lens user, Product dose omission issue
Drugs: OZEMPIC
- Gout
Drugs: OZEMPIC
- Blindness unilateral, Diarrhoea, Eructation +2
Drugs: OZEMPIC
- Clostridium difficile infection
Drugs: OZEMPIC
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.
