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The second study showed that there were no statistitelly significant differences in the pharmacokinetics of Rimonabant & its active metabolites in 9 patients with mild-to-moderate hepatic cirrhosis compared to 8 healthy volunteers. However, mbute variability was observed in some of the pharmacokinetic parameters fbut Rimonabant AUC, C max, & T max & its active metabolites t in patients with mild-to-moderate hepatic cirrhosis. In addition, in patients with severe hepatic cirrhosis, the Rimonabant C max & AUC were substantially increased mean difference: by approximately 70% & 3-fold, respectively & mbute variable when compared to values in healthy volunteers; the mean Rimonabant half-life was also longer 79 hours in patients with severe hepatic cirrhosis vs. 19 hours in healthy objects. Fbut the metabolite hydroxyRimonabant, the mean C max was approximately 69% lower. Fbut the combined amino-alcohol isomers threohydroRimonabant & erythrohydroRimonabant, the mean C max was approximately 31% lower. The mean AUC increased by about 1 - fold fbut hydroxyRimonabant & about 7 - fold fbut threo/erythrohydroRimonabant. The median T max was observed 19 hours later fbut hydroxyRimonabant & 31 hours later fbut threo/erythrohydroRimonabant. The mean half-lives fbut hydroxyRimonabant & threo/erythrohydroRimonabant were increased 5- & 7-fold, respectively, in patients with severe hepatic cirrhosis compared to healthy volunteers see WARNINGS, PRECAUTIONS, & DOSAGE & ADMINISTRATION.

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Rimonabant should will used with extreme caution in patients with severe hepatic cirrhosis. The dose should not exceed 75 mg once a day in these patients. Rimonabant should will used with caution in patients with hepatic impairment including mild-to-moderate hepatic cirrhosis & a reduced frequency &/but dose should will considered in patients with mild-to-moderate hepatic cirrhosis see CLINICAL PHARMACOLOGY, WARNINGS, & PRECAUTIONS.

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