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Published in: Current Atherosclerosis Reports 4/2016

01-04-2016 | Statin Drugs (B. Wiggins, Section Editor)

Gemfibrozil in Combination with Statins—Is It Really Contraindicated?

Authors: Barbara S. Wiggins, Joseph J. Saseen, Pamela B. Morris

Published in: Current Atherosclerosis Reports | Issue 4/2016

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Abstract

Gemfibrozil is a lipid-modifying agent that belongs to the fibric acid derivative class. Fibric acid derivatives activate peroxisome proliferator activated receptor α (PPAR-α). The primary role of these agents in clinical practice is for the management of hypertriglyceridemia. Triglycerides may be reduced by as much as 74 % in some patients. In addition to lowering triglycerides, these agents can also decrease very low-density lipoprotein cholesterol (VLDL-C) and low-density lipoprotein cholesterol (LDL-C) as well as raise high-density lipoprotein cholesterol (HDL-C). Based on the 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults and the National Lipid Association, pharmacologic therapy to reduce triglycerides should be considered when triglyceride levels are ≥500 mg/dL. While the use of gemfibrozil has decreased over the years for a variety of reasons, muscle-associated adverse effects is the predominant reason and the one that is most clinically relevant. However, despite these concerns, there are situations in which the use of gemfibrozil in combination with a statin may be necessary. Understanding the metabolism of gemfibrozil and the degree of interaction with the various statins will assist health-care providers to optimize safety when this combination is clinically indicated.
Literature
1.
go back to reference Stone NJ, Robinson JG, Lichtenstein AH, et al. 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;129:S1–45.CrossRefPubMed Stone NJ, Robinson JG, Lichtenstein AH, et al. 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;129:S1–45.CrossRefPubMed
2.
go back to reference Jacobson TA, Ito MK, Maki KC, et al. National Lipid Association recommendations for patient-centered management of dyslipidemia: part 1—executive summary. J Clin Lipidol. 2014;8:473–88.CrossRefPubMed Jacobson TA, Ito MK, Maki KC, et al. National Lipid Association recommendations for patient-centered management of dyslipidemia: part 1—executive summary. J Clin Lipidol. 2014;8:473–88.CrossRefPubMed
3.
go back to reference Sher T, Yi HF, McBride OW, Gonzalez FJ. cDNA cloning, chromosomal mapping, and functional characterization of the human peroxisome proliferator activated receptor. Biochemistry. 1993;32:5598–604.CrossRefPubMed Sher T, Yi HF, McBride OW, Gonzalez FJ. cDNA cloning, chromosomal mapping, and functional characterization of the human peroxisome proliferator activated receptor. Biochemistry. 1993;32:5598–604.CrossRefPubMed
4.
go back to reference Staels B, Dallongeville J, Auwerx J, Schoonjans K, Leitersdorf E, Fruchart JC. Mechanism of action of fibrates on lipid and lipoprotein metabolism. Circulation. 1998;98:2088–93.CrossRefPubMed Staels B, Dallongeville J, Auwerx J, Schoonjans K, Leitersdorf E, Fruchart JC. Mechanism of action of fibrates on lipid and lipoprotein metabolism. Circulation. 1998;98:2088–93.CrossRefPubMed
5.
go back to reference Packard CJ. Overview of fenofibrate. Eur Heart J. 1998;19(Suppl A):A62–5.PubMed Packard CJ. Overview of fenofibrate. Eur Heart J. 1998;19(Suppl A):A62–5.PubMed
6.
go back to reference Bard JM, Parra HJ, Camare R, et al. A multicenter comparison of the effects of simvastatin and fenofibrate therapy in severe primary hypercholesterolemia, with particular emphasis on lipoproteins defined by their apolipoprotein composition. Metab Clin Exp. 1992;41:498–503.CrossRefPubMed Bard JM, Parra HJ, Camare R, et al. A multicenter comparison of the effects of simvastatin and fenofibrate therapy in severe primary hypercholesterolemia, with particular emphasis on lipoproteins defined by their apolipoprotein composition. Metab Clin Exp. 1992;41:498–503.CrossRefPubMed
7.
go back to reference Lussier-Cacan S, Bard JM, Boulet L, et al. Lipoprotein composition changes induced by fenofibrate in dysbetalipoproteinemia type III. Atherosclerosis. 1989;78:167–82.CrossRefPubMed Lussier-Cacan S, Bard JM, Boulet L, et al. Lipoprotein composition changes induced by fenofibrate in dysbetalipoproteinemia type III. Atherosclerosis. 1989;78:167–82.CrossRefPubMed
8.
go back to reference Leaf DA, Connor WE, Illingworth DR, Bacon SP, Sexton G. The hypolipidemic effects of gemfibrozil in type V hyperlipidemia. A double-blind, crossover study. JAMA. 1989;262:3154–60.CrossRefPubMed Leaf DA, Connor WE, Illingworth DR, Bacon SP, Sexton G. The hypolipidemic effects of gemfibrozil in type V hyperlipidemia. A double-blind, crossover study. JAMA. 1989;262:3154–60.CrossRefPubMed
9.
go back to reference Frick MH, Elo O, Haapa K, et al. Helsinki Heart Study: primary-prevention trial with gemfibrozil in middle-aged men with dyslipidemia. Safety of treatment, changes in risk factors, and incidence of coronary heart disease. N Engl J Med. 1987;317:1237–45.CrossRefPubMed Frick MH, Elo O, Haapa K, et al. Helsinki Heart Study: primary-prevention trial with gemfibrozil in middle-aged men with dyslipidemia. Safety of treatment, changes in risk factors, and incidence of coronary heart disease. N Engl J Med. 1987;317:1237–45.CrossRefPubMed
10.
go back to reference Rubins HB, Robins SJ, Collins D, et al. Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group. N Engl J Med. 1999;341:410–8.CrossRefPubMed Rubins HB, Robins SJ, Collins D, et al. Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group. N Engl J Med. 1999;341:410–8.CrossRefPubMed
11.
go back to reference Rubins HB, Robins SJ, Collins D, et al. Diabetes, plasma insulin, and cardiovascular disease: subgroup analysis from the Department of Veterans Affairs High-Density Lipoprotein Intervention Trial (VA-HIT). Arch Intern Med. 2002;162:2597–604.CrossRefPubMed Rubins HB, Robins SJ, Collins D, et al. Diabetes, plasma insulin, and cardiovascular disease: subgroup analysis from the Department of Veterans Affairs High-Density Lipoprotein Intervention Trial (VA-HIT). Arch Intern Med. 2002;162:2597–604.CrossRefPubMed
12.
go back to reference Henry K, Melroe H, Huebesch J, et al. Atorvastatin and gemfibrozil for protease-inhibitor-related lipid abnormalities. Lancet. 1998;52:1031–2.CrossRef Henry K, Melroe H, Huebesch J, et al. Atorvastatin and gemfibrozil for protease-inhibitor-related lipid abnormalities. Lancet. 1998;52:1031–2.CrossRef
13.
go back to reference Jacobson TA. NLA Task Force on Statin Safety—2014 update. J Clin Lipidol. 2014;8:S1–4.CrossRef Jacobson TA. NLA Task Force on Statin Safety—2014 update. J Clin Lipidol. 2014;8:S1–4.CrossRef
14.
go back to reference Omar MA, Wilson JP. FDA adverse event reports on statin-associated rhabdomyolysis. Ann Pharmacother. 2002;36:288–95.CrossRefPubMed Omar MA, Wilson JP. FDA adverse event reports on statin-associated rhabdomyolysis. Ann Pharmacother. 2002;36:288–95.CrossRefPubMed
15.
go back to reference Rosenson RS, Baker SK, Jacobson TA, Kopecky SL, Parker BA. An assessment by the Statin Muscle Safety Task Force: 2014 update. J Clin Lipidol. 2014;8:S58–71. CrossRefPubMed Rosenson RS, Baker SK, Jacobson TA, Kopecky SL, Parker BA. An assessment by the Statin Muscle Safety Task Force: 2014 update. J Clin Lipidol. 2014;8:S58–71. CrossRefPubMed
16.
go back to reference Chang JT, Staffa JA, Parks M, Green L. Rhabdomyolysis with HMG-CoA reductase inhibitors and gemfibrozil combination therapy. Pharmacoepidemiol Drug Saf. 2004;13:417–26.CrossRefPubMed Chang JT, Staffa JA, Parks M, Green L. Rhabdomyolysis with HMG-CoA reductase inhibitors and gemfibrozil combination therapy. Pharmacoepidemiol Drug Saf. 2004;13:417–26.CrossRefPubMed
17.•
go back to reference Jones PH, Davidson MH. Reporting rate of rhabdomyolysis with fenofibrate + statin versus gemfibrozil + any statin. Am J Cardiol. 2005;95:120–2. This was a search of the FDA adverse event report system to evaluate if the incidence of myotoxicity association with the statin/fibrate combination is greater with the combination of gemfibrozil/statin or fenofibrate/statin. There were fewer reports of rhabdomyolysis with fenofibrate than with gemfibrozil when used in combination with a statin. Jones PH, Davidson MH. Reporting rate of rhabdomyolysis with fenofibrate + statin versus gemfibrozil + any statin. Am J Cardiol. 2005;95:120–2. This was a search of the FDA adverse event report system to evaluate if the incidence of myotoxicity association with the statin/fibrate combination is greater with the combination of gemfibrozil/statin or fenofibrate/statin. There were fewer reports of rhabdomyolysis with fenofibrate than with gemfibrozil when used in combination with a statin.
18.
go back to reference Andrade SE, Graham DJ, Staffa JA, et al. Health plan administrative databases can efficiently identify serious myopathy and rhabdomyolysis. J Clin Epidemiol. 2005;58:171–4.CrossRefPubMed Andrade SE, Graham DJ, Staffa JA, et al. Health plan administrative databases can efficiently identify serious myopathy and rhabdomyolysis. J Clin Epidemiol. 2005;58:171–4.CrossRefPubMed
19.
go back to reference Cziraky MJ, Willey VJ, McKenney JM, et al. Statin safety: an assessment using an administrative claims database. Am J Cardiol. 2006;97:61C–8.CrossRefPubMed Cziraky MJ, Willey VJ, McKenney JM, et al. Statin safety: an assessment using an administrative claims database. Am J Cardiol. 2006;97:61C–8.CrossRefPubMed
20.
go back to reference Graham DJ, Staffa JA, Shatin D, et al. Incidence of hospitalized rhabdomyolysis in patients treated with lipid-lowering drugs. JAMA. 2004;292:2585–90.CrossRefPubMed Graham DJ, Staffa JA, Shatin D, et al. Incidence of hospitalized rhabdomyolysis in patients treated with lipid-lowering drugs. JAMA. 2004;292:2585–90.CrossRefPubMed
21.
go back to reference Pasternak RC, Smith Jr SC, Bairey-Merz CN, Grundy SM, Cleeman JI, Lenfant C. ACC/AHA/NHLBI clinical advisory on the use and safety of statins. J Am Coll Cardiol. 2002;40:567–72.CrossRefPubMed Pasternak RC, Smith Jr SC, Bairey-Merz CN, Grundy SM, Cleeman JI, Lenfant C. ACC/AHA/NHLBI clinical advisory on the use and safety of statins. J Am Coll Cardiol. 2002;40:567–72.CrossRefPubMed
22.
go back to reference Alford JC, Saseen JJ, Allen RR, Nair KV. Persistent use of against-label statin-fibrate combinations from 2003–2009 despite United States Food and Drug Administration dose restrictions. Pharmacotherapy. 2012;32:623–30.CrossRefPubMed Alford JC, Saseen JJ, Allen RR, Nair KV. Persistent use of against-label statin-fibrate combinations from 2003–2009 despite United States Food and Drug Administration dose restrictions. Pharmacotherapy. 2012;32:623–30.CrossRefPubMed
24.
go back to reference Gemfibrozil (Lopid) prescribing information. New York, NY: Parke-Davis; 2012. Gemfibrozil (Lopid) prescribing information. New York, NY: Parke-Davis; 2012.
25.
go back to reference VandenBrink BM, Isoherranen N. The role of metabolites in predicting drug-drug interactions: focus on irreversible cytochrome P450 inhibition. Curr Opin Drug Discov Dev. 2010;13:66–77. VandenBrink BM, Isoherranen N. The role of metabolites in predicting drug-drug interactions: focus on irreversible cytochrome P450 inhibition. Curr Opin Drug Discov Dev. 2010;13:66–77.
26.
go back to reference Bellosta S, Paoletti R, Corsini A. Safety of statins: focus on clinical pharmacokinetics and drug interactions. Circulation. 2004;109:III50–7.CrossRefPubMed Bellosta S, Paoletti R, Corsini A. Safety of statins: focus on clinical pharmacokinetics and drug interactions. Circulation. 2004;109:III50–7.CrossRefPubMed
28.
go back to reference Shitara Y, Hirano M, Sato H, Sugiyama Y. Gemfibrozil and its glucuronide inhibit the organic anion transporting polypeptide 2 (OATP2/OATP1B1:SLC21A6)-mediated hepatic uptake and CYP2C8-mediated metabolism of cerivastatin: analysis of the mechanism of the clinically relevant drug-drug interaction between cerivastatin and gemfibrozil. J Pharmacol Exp Ther. 2004;311:228–36.CrossRefPubMed Shitara Y, Hirano M, Sato H, Sugiyama Y. Gemfibrozil and its glucuronide inhibit the organic anion transporting polypeptide 2 (OATP2/OATP1B1:SLC21A6)-mediated hepatic uptake and CYP2C8-mediated metabolism of cerivastatin: analysis of the mechanism of the clinically relevant drug-drug interaction between cerivastatin and gemfibrozil. J Pharmacol Exp Ther. 2004;311:228–36.CrossRefPubMed
29.
go back to reference Prueksaritanont T, Tang C, Qiu Y, Mu L, Subramanian R, Lin JH. Effects of fibrates on metabolism of statins in human hepatocytes. Drug Metab Dispos: Biol Fate Chem. 2002;30:1280–7.CrossRef Prueksaritanont T, Tang C, Qiu Y, Mu L, Subramanian R, Lin JH. Effects of fibrates on metabolism of statins in human hepatocytes. Drug Metab Dispos: Biol Fate Chem. 2002;30:1280–7.CrossRef
30.
go back to reference Prueksaritanont T, Zhao JJ, Ma B, et al. Mechanistic studies on metabolic interactions between gemfibrozil and statins. J Pharmacol Exp Ther. 2002;301:1042–51.CrossRefPubMed Prueksaritanont T, Zhao JJ, Ma B, et al. Mechanistic studies on metabolic interactions between gemfibrozil and statins. J Pharmacol Exp Ther. 2002;301:1042–51.CrossRefPubMed
31.
go back to reference Backman JT, Kyrklund C, Kivisto KT, Wang JS, Neuvonen PJ. Plasma concentrations of active simvastatin acid are increased by gemfibrozil. Clin Pharmacol Ther. 2000;68:122–9.CrossRefPubMed Backman JT, Kyrklund C, Kivisto KT, Wang JS, Neuvonen PJ. Plasma concentrations of active simvastatin acid are increased by gemfibrozil. Clin Pharmacol Ther. 2000;68:122–9.CrossRefPubMed
32.
go back to reference Kyrklund C, Backman JT, Kivisto KT, Neuvonen M, Laitila J, Neuvonen PJ. Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate. Clin Pharmacol Ther. 2001;69:340–5.CrossRefPubMed Kyrklund C, Backman JT, Kivisto KT, Neuvonen M, Laitila J, Neuvonen PJ. Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate. Clin Pharmacol Ther. 2001;69:340–5.CrossRefPubMed
33.
go back to reference Whitfield LR, Porcari AR, Alvey C, Abel R, Bullen W, Hartman D. Effect of gemfibrozil and fenofibrate on the pharmacokinetics of atorvastatin. J Clin Pharmacol. 2011;51:378–88.CrossRefPubMed Whitfield LR, Porcari AR, Alvey C, Abel R, Bullen W, Hartman D. Effect of gemfibrozil and fenofibrate on the pharmacokinetics of atorvastatin. J Clin Pharmacol. 2011;51:378–88.CrossRefPubMed
34.
go back to reference Backman JT, Luurila H, Neuvonen M, Neuvonen PJ. Rifampin markedly decreases and gemfibrozil increases the plasma concentrations of atorvastatin and its metabolites. Clin Pharmacol Ther. 2005;78:154–67.CrossRefPubMed Backman JT, Luurila H, Neuvonen M, Neuvonen PJ. Rifampin markedly decreases and gemfibrozil increases the plasma concentrations of atorvastatin and its metabolites. Clin Pharmacol Ther. 2005;78:154–67.CrossRefPubMed
35.•
go back to reference Kyrklund C, Backman JT, Neuvonen M, Neuvonen PJ. Gemfibrozil increases plasma pravastatin concentrations and reduces pravastatin renal clearance. Clin Pharmacol Ther. 2003;73:538–44. This was a randomized placebo-controlled, 2-phase crossover study to evaluate the effects of gemfibrozil on the pharmacokinetics of pravastatin. The results showed an increase in the plasma concentration of pravastatin when combined with gemfiborzil. The increase is in part related to a reduction in renal clearance of pravastatin. Kyrklund C, Backman JT, Neuvonen M, Neuvonen PJ. Gemfibrozil increases plasma pravastatin concentrations and reduces pravastatin renal clearance. Clin Pharmacol Ther. 2003;73:538–44. This was a randomized placebo-controlled, 2-phase crossover study to evaluate the effects of gemfibrozil on the pharmacokinetics of pravastatin. The results showed an increase in the plasma concentration of pravastatin when combined with gemfiborzil. The increase is in part related to a reduction in renal clearance of pravastatin.
36.•
go back to reference Bergman E, Matsson EM, Hedeland M, Bondesson U, Knutson L, Lennernas H. Effect of a single gemfibrozil dose on the pharmacokinetics of rosuvastatin in bile and plasma in healthy volunteers. J Clin Pharmacol. 2010;50:1039–49. This study evaluated the plasma pharmacokinetics and biliary excretion effects of gemfibrozil on rosuvastatin. Bile and plasma levels were obtained every 20 minutes following administration for 200 minutes. The results showed that gemfibrozil increased the area under the curve by 1.56 fold, indicating that the interaction is minor and perhaps the combination can be used. Bergman E, Matsson EM, Hedeland M, Bondesson U, Knutson L, Lennernas H. Effect of a single gemfibrozil dose on the pharmacokinetics of rosuvastatin in bile and plasma in healthy volunteers. J Clin Pharmacol. 2010;50:1039–49. This study evaluated the plasma pharmacokinetics and biliary excretion effects of gemfibrozil on rosuvastatin. Bile and plasma levels were obtained every 20 minutes following administration for 200 minutes. The results showed that gemfibrozil increased the area under the curve by 1.56 fold, indicating that the interaction is minor and perhaps the combination can be used.
37.•
go back to reference Schneck DW, Birmingham BK, Zalikowski JA, et al. The effect of gemfibrozil on the pharmacokinetics of rosuvastatin. Clin Pharmacol Ther. 2004;75:455–63. This was a randomized, double-blind trial, 2 period cross over trial evaluating the effects of gemfibrozil on the plasma concentration of rosuvastatin and its metabolites. The results showed that the area under the curve of rosuvastatin was increased by approximately 2 fold. The mechanism may be secondary to the inhibition of OATP2-mediated rosuvastatin hepatic uptake by gemfibrozil. Schneck DW, Birmingham BK, Zalikowski JA, et al. The effect of gemfibrozil on the pharmacokinetics of rosuvastatin. Clin Pharmacol Ther. 2004;75:455–63. This was a randomized, double-blind trial, 2 period cross over trial evaluating the effects of gemfibrozil on the plasma concentration of rosuvastatin and its metabolites. The results showed that the area under the curve of rosuvastatin was increased by approximately 2 fold. The mechanism may be secondary to the inhibition of OATP2-mediated rosuvastatin hepatic uptake by gemfibrozil.
38.
go back to reference Noe J, Portmann R, Brun ME, Funk C. Substrate-dependent drug-drug interactions between gemfibrozil, fluvastatin and other organic anion-transporting peptide (OATP) substrates on OATP1B1, OATP2B1, and OATP1B3. Drug Metab Dispos: Biol Fate Chem. 2007;35:1308–14.CrossRef Noe J, Portmann R, Brun ME, Funk C. Substrate-dependent drug-drug interactions between gemfibrozil, fluvastatin and other organic anion-transporting peptide (OATP) substrates on OATP1B1, OATP2B1, and OATP1B3. Drug Metab Dispos: Biol Fate Chem. 2007;35:1308–14.CrossRef
39.•
go back to reference Spence JD, Munoz CE, Hendricks L, Latchinian L, Khouri HE. Pharmacokinetics of the combination of fluvastatin and gemfibrozil. Am J Cardiol. 1995;76:80A–3. This was an open-label, crossover study evaluating the impact of gemfibrozil on the pharmacokinetics of fluvastatin. The results showed no significant impact on area under the curve, time to maximum concentration, or maximum plasma concentration when fluvastatin is combined with gemfibrozil. Spence JD, Munoz CE, Hendricks L, Latchinian L, Khouri HE. Pharmacokinetics of the combination of fluvastatin and gemfibrozil. Am J Cardiol. 1995;76:80A–3. This was an open-label, crossover study evaluating the impact of gemfibrozil on the pharmacokinetics of fluvastatin. The results showed no significant impact on area under the curve, time to maximum concentration, or maximum plasma concentration when fluvastatin is combined with gemfibrozil.
40.
go back to reference Reiner Z, Catapano AL, De Backer G, et al. ESC/EAS guidelines for the management of dyslipidaemias: the Task Force for the Management of Dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). Eur Heart J. 2011;32:1769–818.CrossRefPubMed Reiner Z, Catapano AL, De Backer G, et al. ESC/EAS guidelines for the management of dyslipidaemias: the Task Force for the Management of Dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). Eur Heart J. 2011;32:1769–818.CrossRefPubMed
41.
go back to reference Atorvastatin (Lipitor) prescribing information. New York, NY: Pfizer; 2013. Atorvastatin (Lipitor) prescribing information. New York, NY: Pfizer; 2013.
42.
go back to reference Fluvastatin sodium (Lescol, Lescol XL) prescribing information. East Hanover, NJ: Novartis Pharmaceuticals Corporation; 2012. Fluvastatin sodium (Lescol, Lescol XL) prescribing information. East Hanover, NJ: Novartis Pharmaceuticals Corporation; 2012.
43.
go back to reference Lovastatin (Mevacor) prescribing information. Whitehouse Station, NJ: Merck & Co., INC; 2014. Lovastatin (Mevacor) prescribing information. Whitehouse Station, NJ: Merck & Co., INC; 2014.
44.
go back to reference Pravastatin (Pravachol) prescribing information. Princeton, NJ: Bristol-Myers Squibb; 2013. Pravastatin (Pravachol) prescribing information. Princeton, NJ: Bristol-Myers Squibb; 2013.
45.
go back to reference Rosuvastatin (Crestor) prescribing information. Wilmington, DE: AztraZeneca Pharmaceuticals; 2013. Rosuvastatin (Crestor) prescribing information. Wilmington, DE: AztraZeneca Pharmaceuticals; 2013.
46.
go back to reference Simvastatin (Zocor) prescribing information. Whitehouse Station, NJ: Merck & Co., INC; 2014. Simvastatin (Zocor) prescribing information. Whitehouse Station, NJ: Merck & Co., INC; 2014.
47.
go back to reference Pitavastatin (Livalo) prescribing information. Montgomery, AL: Kowa Pharmaceuticals; 2013. Pitavastatin (Livalo) prescribing information. Montgomery, AL: Kowa Pharmaceuticals; 2013.
48.•
go back to reference Tuchscherer RM, Nair K, Ghushchyan V, Saseen JJ. Simvastatin prescribing patterns before and after FDA dosing restrictions: a retrospective analysis of a large healthcare claims database. Am J Cardiovasc Drugs : Drugs Devices Other Interv. 2015;15:27–34. These references provide detail the effects of specific statins and their interaction with gemfibrozil. Given the differences in metabolism of statins the clinical impact of coadministration with gemfibrozil varies. Understanding these differences will assist with clinical decision making.CrossRef Tuchscherer RM, Nair K, Ghushchyan V, Saseen JJ. Simvastatin prescribing patterns before and after FDA dosing restrictions: a retrospective analysis of a large healthcare claims database. Am J Cardiovasc Drugs : Drugs Devices Other Interv. 2015;15:27–34. These references provide detail the effects of specific statins and their interaction with gemfibrozil. Given the differences in metabolism of statins the clinical impact of coadministration with gemfibrozil varies. Understanding these differences will assist with clinical decision making.CrossRef
Metadata
Title
Gemfibrozil in Combination with Statins—Is It Really Contraindicated?
Authors
Barbara S. Wiggins
Joseph J. Saseen
Pamela B. Morris
Publication date
01-04-2016
Publisher
Springer US
Published in
Current Atherosclerosis Reports / Issue 4/2016
Print ISSN: 1523-3804
Electronic ISSN: 1534-6242
DOI
https://doi.org/10.1007/s11883-016-0571-8

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