The Hepatic and Renal Mechanisms of Drug Interactions with Cimetidine
- 1 May 1986
- journal article
- review article
- Published by SAGE Publications in Drug Intelligence & Clinical Pharmacy
- Vol. 20 (5) , 342-348
- https://doi.org/10.1177/106002808602000502
Abstract
Cimetidine is one of the most frequently prescribed drugs with a known potential to interfere with the metabolic disposition of numerous other medications. Some of these drug interactions may be hazardous to patients. The hepatic and renal mechanisms of drug interactions with cimetidine are discussed in this article. The interactive processes include inhibition of hepatic microsomal enzyme activity, reduction of liver blood flow, and competition for renal tubular secretory sites. The clinical significance and proposed mechanisms of interaction for individual drugs are also presented.Keywords
This publication has 75 references indexed in Scilit:
- Lack of Effect of Histamine H2‐Receptor Antagonists on Indocyanine Green Disposition Measured by Two MethodsThe Journal of Clinical Pharmacology, 1984
- Effect of cimetidine on the hepatic extraction of indocyanine green, the portal pressure and the systemic circulation in patients with cirrhosis of the liverJournal of Molecular Medicine, 1984
- Interaction between Cimetidine and MetronidazoleNew England Journal of Medicine, 1983
- Cimetidine-procainamide pharmacokinetic interaction in man: Evidence of competition for tubular secretion of basic drugsEuropean Journal of Clinical Pharmacology, 1983
- Drug Interactions with CimetidineClinical Pharmacokinetics, 1982
- Reduction of Liver Blood Flow and Propranolol Metabolism by CimetidineNew England Journal of Medicine, 1981
- Clinical Implications of Enzyme Induction and Enzyme InhibitionClinical Pharmacokinetics, 1981
- Delayed Clearance of Diazepam Due to CimetidineNew England Journal of Medicine, 1980
- Effect of Cimetidine and other antihistaminics on the elimination of aminopyrine, phenacetin and caffeinLife Sciences, 1980
- Drug Kinetics and Hepatic Blood FlowClinical Pharmacokinetics, 1979