INTERACTION BETWEEN FIBRATES AND STATINS - METABOLIC INTERACTIONS WITH GEMFIBROZIL
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Summary
It is proposed that the increase of plasma concentration caused by co-administration of gemfibrozil and statins is at least partially due to CYP-mediated inhibition.
- Type
- article
- Published
- 2003-03-01
- Cited by
- 21
- References
- 11
- OpenAlex
- https://openalex.org/W2028468709
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:43878643
Keywords
Gemfibrozil, Chemistry, Atorvastatin, CYP3A4, Pharmacology
References
- Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate
- Severe rhabdomyolysis associated with the cerivastin-gemfibrozil combination therapy: report of a case.
- A case with severe rhabdomyolysis and renal failure associated with cerivastatin-gemfibrozil combination therapy--a case report.
- Metabolism and drug interactions of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors in transplant patients: are the statins mechanistically similar?
- Withdrawal of cerivastatin from the world market
- A randomized, double-blind trial comparing the efficacy and safety of pitavastatin versus pravastatin in patients with primary hypercholesterolemia.
- NK-104: a novel synthetic HMG-CoA reductase inhibitor
- Application of radioluminography to off-line counting of radioactivity in high-performance liquid chromatographic eluates
- Hypolipidemic effect of NK-104, a potent HMG-CoA reductase inhibitor, in guinea pigs.
- Rifampin greatly reduces plasma simvastatin and simvastatin acid concentrations
- The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor fluvastatin: effect on human cytochrome P-450 and implications for metabolic drug interactions.
Cited by
- Pharmacokinetic interactions between statins and fibrates.
- Effect of Gemfibrozil on the Metabolism of Pitavastatin - Determining the Best Animal Model for Human CYP And UGT Activities
- Drug interactions with statins
- A phase I pharmacokinetic study of bexarotene with paclitaxel and carboplatin in patients with advanced non-small cell lung cancer (NSCLC)
- Pitavastatin: a New 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitor for the treatment of hyperlipidemia
- Chemical inhibitors of cytochrome P450 isoforms in human liver microsomes: a re-evaluation of P450 isoform selectivity
- Pitavastatin: efficacy and safety profiles of a novel synthetic HMG-CoA reductase inhibitor.
- Prediction of the metabolic interaction of nateglinide with other drugs based on in vitro studies.
- Statin/fibrate combination in patients with metabolic syndrome or diabetes: evaluating the risks of pharmacokinetic drug interactions
- GLUCURONIDATION CONVERTS GEMFIBROZIL TO A POTENT, METABOLISM-DEPENDENT INHIBITOR OF CYP2C8: IMPLICATIONS FOR DRUG-DRUG INTERACTIONS
- Inhibition of Hepatic Organic Anion-Transporting Polypeptide by RNA Interference in Sandwich-Cultured Human Hepatocytes: An In Vitro Model to Assess Transporter-Mediated Drug-Drug Interactions
- Mechanism-based inhibition of CYP2C8 by gemfibrozil in humans : characterisation of time and dose relationships
- Role of Cytochrome P450 2C8 in Drug Metabolism and Interactions
- Metabolic Stability and Uptake by Human Hepatocytes of Pitavastatin, a New Inhibitor of HMG-CoA Reductase
- Evaluation of Proposed In Vivo Probe Substrates and Inhibitors for Phenotyping Transporter Activity in Humans
- Role of CYP2C8 in the metabolism of montelukast and imatinib : Studies in vitro, in silico and in humans
- Quantitative Analysis of Complex Drug-Drug Interactions Between Repaglinide and Cyclosporin A/Gemfibrozil Using Physiologically Based Pharmacokinetic Models With In Vitro Transporter/Enzyme Inhibition Data.
- Pitavastatin: focus on safety and drug interactions
- Revisiting CYP2C9-Mediated drug-drug Interactions: A Review
- Role of CYP2C8 in the metabolism of montelukast and imatinib : Studies in vitro, in silico and in humans
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