Clinical data | |
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Pronunciation | /ælˈfjuːzoʊsɪn/ al-FEW-zoh-sin |
Trade names | Uroxatral, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a64002 |
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Routes of administration | By mouth |
Drug class | α1 blocker |
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Pharmacokinetic data | |
Bioavailability | 49% |
Protein binding | 82–90% |
Metabolism | Liver (CYP3A4-mediated) |
Elimination half-life | 10 hours |
Excretion | Feces (69%) and Urine (24%) |
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ECHA InfoCard | 100.108.671 |
Chemical and physical data | |
Formula | C19H27N5O4 |
Molar mass | 389.456 g·mol−1 |
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Alfuzosin, sold under the brand name Uroxatral among others, is a medication of the α1 blocker class. It is used to treat benign prostatic hyperplasia (BPH).[1]
As an antagonist of the α1-adrenergic receptor, it works by relaxing the muscles in the prostate and bladder neck, making urination easier.
Alfuzosin was patented in 1978 and approved for medical use in 1988.[2] It was approved in the US for benign prostatic hyperplasia in 2003. In 2020, it was the 336th-most commonly prescribed medication in the United States, with more than 700 thousand prescriptions.[3][4]