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Pharmacokinetic drug–drug interactions between 14-dihydropyridine calcium channel blockers and statins: factors determining interaction strength and relevant clinical risk management

机译:14-二氢吡啶钙通道阻滞剂和他汀类药物之间的药代动力学药物相互作用:决定相互作用强度的因素和相关的临床风险管理

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摘要

BackgroundCoadministration of 1,4-dihydropyridine calcium channel blockers (DHP-CCBs) with statins (or 3-hydroxy-3-methylglutaryl-coenzyme A [HMG-CoA] reductase inhibitors) is common for patients with hypercholesterolemia and hypertension. To reduce the risk of myopathy, in 2011, the US Food and Drug Administration (FDA) Drug Safety Communication set a new dose limitation for simvastatin, for patients taking simvastatin concomitantly with amlodipine. However, there is no such dose limitation for atorvastatin for patients receiving amlodipine. The combination pill formulation of amlodipine/atorvastatin is available on the market. There been no systematic review of the pharmacokinetic drug–drug interaction (DDI) profile of DHP-CCBs with statins, the underlying mechanisms for DDIs of different degree, or the corresponding management of clinical risk.
机译:背景1,4-二氢吡啶钙通道阻滞剂(DHP-CCBs)与他汀类药物(或3-羟基-3-甲基戊二酰辅酶A [HMG-CoA]还原酶抑制剂)共同给药对于高胆固醇血症和高血压患者很常见。为了降低肌病的风险,2011年,美国食品药品监督管理局(FDA)药物安全通讯对辛伐他汀与氨氯地平同时服用的患者设定了辛伐他汀的新剂量限制。但是,接受氨氯地平的患者对阿托伐他汀的剂量没有限制。氨氯地平/阿托伐他汀的组合药丸制剂在市场上有售。 DHP-CCBs与他汀类药物的药代动力学药物相互作用(DDI),不同程度DDIs的潜在机制或临床风险的相应管理尚无系统评价。

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