Pierce L R, Wysowski D K, Gross T P
Division of Metabolism and Endocrine Drug Products, Food and Drug Administration, Rockville, MD 20857.
JAMA. 1990 Jul 4;264(1):71-5.
The Food and Drug Administration documents the receipt of 12 case reports of severe myopathy or rhabdomyolysis associated with concomitant use of lovastatin and gemfibrozil, including 10 voluntary postmarketing, and 2 required, reports. All patients had serum creatine kinase levels of more than 10,000 U/L, 4 tested showed myoglobinuria, and 5 had acute renal failure. The patients' symptoms resolved when both drugs were discontinued. For the first year of marketing of lovastatin, spontaneous reports of myopathy with documentation of creatine kinase level were reviewed for the use of lovastatin, gemfibrozil, and combination therapy. The median creatine kinase level in reports involving concomitant lovastatin and gemfibrozil use was 15,250 U/L, 20 times that in reports with gemfibrozil use alone and 30 times that in reports with lovastatin use alone. Because of the potential for severe myopathy and life-threatening rhabdomyolysis, and given alternative drug combinations for treating hyperlipoproteinemia, the use of lovastatin in combination with gemfibrozil is to be discouraged.
美国食品药品监督管理局记录了12例与同时使用洛伐他汀和吉非贝齐相关的严重肌病或横纹肌溶解症的病例报告,其中包括10例上市后自愿报告病例和2例要求上报的病例。所有患者血清肌酸激酶水平均超过10,000 U/L,4例检测显示肌红蛋白尿,5例出现急性肾衰竭。停用两种药物后,患者症状缓解。在洛伐他汀上市的第一年,对洛伐他汀、吉非贝齐及联合治疗使用时伴有肌酸激酶水平记录的肌病自发报告进行了审查。同时使用洛伐他汀和吉非贝齐的报告中,肌酸激酶水平中位数为15,250 U/L,是单独使用吉非贝齐报告的20倍,是单独使用洛伐他汀报告的30倍。由于存在严重肌病和危及生命的横纹肌溶解症的可能性,且有治疗高脂蛋白血症的其他药物组合,不建议将洛伐他汀与吉非贝齐联合使用。