Rhabdomyolysis with HMG-CoA reductase inhibitors and gemfibrozil combination therapy

被引:117
作者
Chang, JT
Staffa, JA
Parks, M
Green, L
机构
[1] US FDA, Div Drug Risk Evaluat, Off Drug Safety, Rockville, MD 20857 USA
[2] US FDA, Div Metab & Endocrine Drug Prod, Rockville, MD 20857 USA
关键词
rhabdomyolysis; statins; fibrates; HMG-CoA reductase inhibitors; adverse reactions; renal failure;
D O I
10.1002/pds.977
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Context Elevated total cholesterol (total-C) and low-density lipoprotein cholesterol (LDL-C) levels are established risk factors for cardiovascular disease (CVD). HMG-CoA reductase inhibitors (statins) are effective cholesterol-lowering drugs that are commonly prescribed to treat this condition. These drugs are often combined with another class of drugs, fibric acid derivatives, to lower both cholesterol and triglyceride levels. Rhabdomyolysis is a known, rare serious side effect of statin monotherapy and of statin-fibrate combination therapy. Objective To examine Food and Drug Administration's (FDA:s) postmarketing database for cases of rhabdomyolysis in relation to monotherapy and combination use and calculate reporting rates for this event. Design Domestic cases of statin- and statin/gemfibrozil-associated rhabdomyolysis were culled from FDAs database and reviewed. Rhabdomyolysis was defined by CPK greater than or equal to 10 000 IU/L, myopathic signs and symptoms and clinical diagnosis of rhabdomyolysis. Reporting rates, consisting of number of reported cases/number of prescriptions for each drug, were then calculated to determine whether the reporting of rhabdomyolysis cases was commensurate with extent of use of each statin in the population. Setting Cases were obtained from the FDA adverse event reporting system (AERS) database. Patients NA. Main Outcome Measures Number of rhabdomyolysis cases were evaluated, along with outcomes, such as renal failure, dialysis and death. Results Of 866 total reported cases, 482 (56%) were associated with monotherapy and 384 (44%) related to combination therapy. More than 80% of reported cases for each drug resulted in hospitalization for renal failure and dialysis. 80 patients expired from events related directly to rhabdomyolysis. Reporting rates for all statins, except for cerivastatin, were similar and much lower than I per 100000 prescriptions. The cerivastatin-reporting rate was much higher at 4.24/100000 prescriptions. Conclusions Rhabdomyolysis is a rare, serious side effect of statin monotherapy and of statin-fibrate combination therapy. Clinicians need to remain cognizant of this potential adverse event and discuss signs and symptoms of muscle toxicity with patients in order improve the benefits-to-risks of treating dyslipidemia with statins. Published in 2004 by John Wiley Sons, Ltd.
引用
收藏
页码:417 / 426
页数:10
相关论文
共 17 条
[1]  
*AM HEART ASS, 1999, 2000 HEART STROK STA
[2]   Drug interactions of lipid-altering drugs [J].
Bays, HE ;
Dujovne, CA .
DRUG SAFETY, 1998, 19 (05) :355-371
[3]   Etiology and frequency of rhabdomyolysis [J].
Black, C ;
Jick, H .
PHARMACOTHERAPY, 2002, 22 (12) :1524-1526
[4]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[5]   Lipid-lowering drugs and mitochondrial function: Effects of HMG-CoA reductase inhibitors on serum ubiquinone and blood lactate/pyruvate ratio [J].
DePinieux, G ;
Chariot, P ;
AmmiSaid, M ;
Louarn, F ;
Lejonc, JL ;
Astier, A ;
Jacotot, B ;
Gherardi, R .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 42 (03) :333-337
[6]   Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels - Results of AFCAPS/TexCAPS [J].
Downs, JR ;
Clearfield, M ;
Weis, S ;
Whitney, E ;
Shapiro, DR ;
Beere, PA ;
Langendorfer, A ;
Stein, EA ;
Kruyer, W ;
Gotto, AM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (20) :1615-1622
[7]  
*FDA, ADV EV REP SYST 2000
[8]   Statins and chronic heart failure: Do we need a large-scale outcome trial? [J].
Krum, H ;
McMurray, JJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (10) :1567-1573
[9]   DECREASES IN SERUM UBIQUINONE CONCENTRATIONS DO NOT RESULT IN REDUCED LEVELS IN MUSCLE-TISSUE DURING SHORT-TERM SIMVASTATIN TREATMENT IN HUMANS [J].
LAAKSONEN, R ;
JOKELAINEN, K ;
SAHI, T ;
TIKKANEN, MJ ;
HIMBERG, JJ .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1995, 57 (01) :62-66
[10]   MYOPATHY AND RHABDOMYOLYSIS ASSOCIATED WITH LOVASTATIN-GEMFIBROZIL COMBINATION THERAPY [J].
PIERCE, LR ;
WYSOWSKI, DK ;
GROSS, TP .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 264 (01) :71-75