| Absorption | Rapidly absorbed into the systemic cirulation following oral administration. Peak plasma concentrations are usually attained within 2 hours under fasting conditions, with steady-state plasma concentrations attained in approximately 7 days. |
| Volume of distribution | Not Available |
| Protein binding | 40% |
| Metabolism | Hepatic. Metabolized mainly by N-dealkylation, hydroxylation, and glucuronidation to inactive metabolites. Primary metabolite is an inactive triazole. |
| Route of elimination | Hepatic metabolism accounts for approximately 85% of anastrozole elimination. Renal elimination accounts for approximately 10% of total clearance. |
| Half life | 50 hours |
| Clearance | Not Available |
| Toxicity | In rats, lethality is greater than 100 mg/kg. |
| Affected organisms |
|
Anastrozole
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