Literature DB >> 6143766

Alprazolam pharmacokinetics in alcoholic liver disease.

R P Juhl, D H Van Thiel, L W Dittert, R B Smith.   

Abstract

Alprazolam, a triazolobenzodiazepine, was administered to 17 patients with alcoholic liver disease. The pharmacokinetic parameters derived from plasma alprazolam concentrations were compared with data obtained from 17 normal subjects who were matched for age and sex. The rate of absorption of alprazolam was slower in patients with alcoholic liver disease. The time of maximum serum concentration was 3.3 hours, compared with 1.5 hour in normals (P less than 0.02). The maximum concentrations, however, did not differ (18.4 vs. 17.2 micrograms/ml). The elimination half-life of drug was longer in the patients (19.7 hours) than in the normal subjects (11.4 hours), while the clearance of the drug was slower in the patients with alcoholic liver disease (0.6 vs 1.2 ml/min/kg). The volumes of distribution (area) did not differ between the two groups (1.1 vs. 1.2 liter/kg). The changes in elimination half-life and clearance indicate that the metabolism of the drug is slowed in patients with alcoholic liver disease.

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Year:  1984        PMID: 6143766     DOI: 10.1002/j.1552-4604.1984.tb02773.x

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  10 in total

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6.  Lack of interaction between disulfiram and alprazolam in alcoholic patients.

Authors:  B Diquet; L Gujadhur; D Lamiable; D Warot; H Hayoun; H Choisy
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8.  Effect of cirrhosis and renal failure on the kinetics of clotiazepam.

Authors:  H R Ochs; D J Greenblatt; M Knüchel
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Review 9.  Clinical pharmacokinetics of alprazolam. Therapeutic implications.

Authors:  D J Greenblatt; C E Wright
Journal:  Clin Pharmacokinet       Date:  1993-06       Impact factor: 6.447

10.  Physiologically Based Pharmacokinetic Modeling for Olaparib Dosing Recommendations: Bridging Formulations, Drug Interactions, and Patient Populations.

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  10 in total

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