Cimetidine inhibits renal procainamide clearance
- 1 August 1984
- journal article
- research article
- Published by Wiley in Clinical Pharmacology & Therapeutics
- Vol. 36 (2) , 221-227
- https://doi.org/10.1038/clpt.1984.166
Abstract
Procainamide and cimetidine [a histamine H2-receptor antagonist used in peptic ulcer disease] are eliminated in large part by the kidneys. Both are secreted by an active transport mechanism in the proximal tubule and each inhibits secretion of the other in the isolated, perfused rabbit tubule. In this study in man, cimetidine inhibited renal clearance of oral procainamide by 36%. This was associated with a 28% decrease in the ratio of systemic clearance of procainamide to bioavailability, an 18% decrease in the elimination rate constant and a 24% prolongation of elimination t1/2 [half-life]. Cimetidine apparently increased plasma t1/2 and decreased systemic clearance of procainamide in part by inhibiting its active secretion by the kidneys.This publication has 18 references indexed in Scilit:
- Increased Toxicity and Reduced Clearance of Lidocaine by CimetidineAnnals of Internal Medicine, 1982
- Cimetidine Impairs Elimination of Chlordiazepoxide (Librium) in ManAnnals of Internal Medicine, 1980
- CIMETIDINE: INTERACTION WITH ORAL ANTICOAGULANTS IN MANThe Lancet, 1979
- Digoxin-Quinidine InteractionNew England Journal of Medicine, 1979
- The Effect of Cimetidine, a New Histamine H2‐Receptor Antagonist, on Renal FunctionActa Medica Scandinavica, 1979
- Effect of cimetidine on renal function in normal manClinical Pharmacology & Therapeutics, 1978
- Kinetics of procainamide and N-acetylprocainamide in renal failureKidney International, 1977
- Influence of probenecid and spironolactone on furosemide kinetics and dynamics in manClinical Pharmacology & Therapeutics, 1977
- Procainamide and N‐acetylprocainamide kinetics investigated simultaneously with stable isotope methodologyClinical Pharmacology & Therapeutics, 1977
- Absorption Kinetics of Procainamide in HumansJournal of Pharmaceutical Sciences, 1977