| Absorption | Absorption is 50% lower under fasting conditions |
| Volume of distribution |
|
| Protein binding | 82%-90% |
| Metabolism | Hepatic. Alfuzosin undergoes extensive metabolism by the liver, with only 11% of the administered dose excreted unchanged in the urine. Alfuzosin is metabolized by three metabolic pathways: oxidation, O-demethylations, and N-dealkylation. The metabolites are not pharmacologically active. CYP3A4 is the principal hepatic enzyme isoform involved in its metabolism. |
| Route of elimination | Following oral administration of 14C-labeled alfuzosin solution, the recovery of radioactivity after 7 days (expressed as a percentage of the administered dose) was 69% in feces and 24% in urine. |
| Half life | 10 hours |
| Clearance | Not Available |
| Toxicity | Side effects are dizziness (due to postural hypotension), upper respiratory tract infection, headache, and fatigue. |
| Affected organisms |
|
| Pathways | Not Available |
Alfuzosin
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