Steady-state pharmacokinetics of nefazodone in subjects with normal and impaired renal function
β Scribed by R. H. Barbhaiya; M. E. Brady; U. A. Shukla; D. S. Greene
- Publisher
- Springer
- Year
- 1995
- Tongue
- English
- Weight
- 604 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0031-6970
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β¦ Synopsis
The steady-state pharmacokinetics of nefazodone (NEF) and its metabolites hydroxynefazodone (HO-NEF) and m-chlorophenylpiperazine (mCPP) were compared in subjects with normal and impaired renal function. Patients: The Study was of parallel group design which included 7 subjects with normal (NOR) renal function, CLcR > 72 ml'min -1' 1.73 m -2, 6 with moderate (MOD) renal impairment, CLcR 31-60 ml'min 1.1.73 m -2 and 9 with severe (SEV) renal impairment, CLcR < 30 ml. min -1' 1.73 m 2. Subjects in each renal function group received a 100-mg oral dose of nefazodone hydrochloride BID for 7 days and a single morning dose on day 8. Starting 48 h after the last 100-mg dose, 200-mg doses were administered on a similar schedule to 3, 4 and 3 subjects from each renal function group (NOR, MOD and SEV, respectively). Single trough blood samples just prior to each
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The pharmacokinetics of oral nicorandil 20 mg 12 hourly for 9 doses was evaluated in 21 hospitalized patients with angina pectoris due to coronary heart disease and with normal and impaired renal function. Patients were divided into 3 groups based on creatinine clearance (CLCr): GROUP I (n = 6) grea
The single-dose pharmacokinetics of nefazodone (NEF) and its metabolites hydroxynefazodone (HO-NEF) and m-chlorophenylpiperazine (mCPP) were examined in 12 healthy younger subjects < 55 years of age (YNG), 12 elderly subjects > 65 years of age (ELD), 12 patients with biopsy proven hepatic cirrhosis