Literature DB >> 10471983

Rabeprazole: pharmacokinetics and tolerability in patients with stable, end-stage renal failure.

W F Keane1, S K Swan, I Grimes, T J Humphries.   

Abstract

The authors compare the pharmacokinetic profiles, safety, and tolerability of rabeprazole, a new proton pump inhibitor (PPI), in healthy volunteers and in subjects with stable, end-stage renal failure. This single-center, open-label trial included two groups of subjects: 10 healthy males with 24-hour creatinine clearance > or = 90 mL/min/m2 and 10 males with renal failure (24-hour creatinine clearance < or = 5 mL/min/m2) receiving hemodialytic therapy. Normal subjects received a single, oral 20 mg rabeprazole dose. Those with renal failure received a 20 mg dose of rabeprazole on the day after hemodialysis and a second dose after a 2-week washout period during dialysis. Blood samples were drawn before and up to 24 hours after rabeprazole administration for determination of plasma rabeprazole concentrations by high-performance liquid chromatography. Safety and tolerability of rabeprazole were determined by reporting adverse events and comparing vital signs, ECG, physical examinations, and clinical laboratory tests before and during treatment. Comparison of pharmacokinetic results from healthy volunteers with those from subjects with renal failure indicated no clinically significant differences between groups. In addition, there were no statistically significant differences between any pharmacokinetic parameters recorded during or after hemodialysis. Rabeprazole was well tolerated by both groups. Only two drug-related adverse events were reported, and there were no significant treatment-emergent changes in vital signs or ECG. Treatment-emergent changes in hematologic and clinical chemistry parameters were observed for a few subjects in each group and generally represented only slight deviations from the normal range. These results indicate that no dosage adjustment of rabeprazole is required in patients with renal dysfunction. These findings and the well-documented clinical efficacy of this new PPI in patients with gastric ulcers, duodenal ulcers, or gastroesophageal reflux disease support rabeprazole's use in the treatment of patients with acid peptic disorders.

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Year:  1999        PMID: 10471983     DOI: 10.1177/00912709922008542

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


  9 in total

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Review 4.  Rabeprazole: an update of its use in acid-related disorders.

Authors:  C I Carswell; K L Goa
Journal:  Drugs       Date:  2001       Impact factor: 9.546

Review 5.  Pharmacokinetics of proton pump inhibitors in children.

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6.  Effect of gastric acid suppressants and prokinetics on peritoneal dialysis-related peritonitis.

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Review 7.  Proton pump inhibitors in cirrhosis: tradition or evidence based practice?

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Journal:  World J Gastroenterol       Date:  2008-05-21       Impact factor: 5.742

8.  Development and validation of a high throughput UPLC-MS/MS method for simultaneous quantification of esomeprazole, rabeprazole and levosulpiride in human plasma.

Authors:  Raja Haranadha Babu Chunduri; Gowri Sankar Dannana
Journal:  J Pharm Anal       Date:  2016-01-08

9.  Proton pump inhibitor use increases the risk of peritonitis in peritoneal dialysis patients.

Authors:  Sayaka Maeda; Makoto Yamaguchi; Kunihiro Maeda; Naoto Kobayashi; Naoki Izumi; Masaaki Nagai; Takaaki Obayashi; Wataru Ohashi; Takayuki Katsuno; Hironobu Nobata; Yasuhiko Ito
Journal:  PLoS One       Date:  2019-11-07       Impact factor: 3.240

  9 in total

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