Febuxostat
| Clinical data | |
|---|---|
| Trade names | Uloric, Adenuric, others | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a609020 | 
| License data | 
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| Pregnancy category | 
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| Routes of administration | By mouth | 
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| Pharmacokinetic data | |
| Bioavailability | ≥84% absorbed | 
| Protein binding | 99.2% to albumin | 
| Metabolism | via CYP1A1, 1A2, 2C8, 2C9, UGT1A1, 1A8, 1A9 | 
| Elimination half-life | ~5–8 hours | 
| Excretion | Urine (~49%, mostly as metabolites, 3% as unchanged drug); feces (~45%, mostly as metabolites, 12% as unchanged drug) | 
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.207.329 | 
| Chemical and physical data | |
| Formula | C16H16N2O3S | 
| Molar mass | 316.38 g·mol−1 | 
| 3D model (JSmol) | |
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Febuxostat, sold under the brand name Uloric among others, is a medication used long-term to treat gout due to high uric acid levels. It is generally recommended only for people who cannot take allopurinol. It is taken by mouth.
Common side effects include liver problems, nausea, joint pain, and a rash. Serious side effects include an increased risk of death as compared with allopurinol, Stevens–Johnson syndrome, and anaphylaxis. Use is not recommended during pregnancy or breastfeeding. It inhibits xanthine oxidase, thus reducing production of uric acid in the body.
Febuxostat was approved for medical use in the European Union in 2008, and in the United States in 2009. A generic version was approved in 2019.