Saito M, Hirata-Koizumi M, Urano T, Miyake S, Hasegawa R
Division of Medicinal Safety Science, National Institute of Health Sciences, Kamiyoga, Setagaya-ku, Tokyo, Japan.
J Clin Pharm Ther. 2005 Feb;30(1):21-37. doi: 10.1111/j.1365-2710.2004.00605.x.
Statins (HMG-CoA reductase inhibitors) are one of the most widely prescribed classes of drugs throughout the world, because of their excellent cholesterol-lowering effect and overall safety profile except for rare but fatal rhabdomyolysis arising either directly or indirectly by pharmacokinetic interactions with certain other drugs. As package inserts in pharmaceuticals are the primary source of information for health care providers, we carried out a literature search to examine how crucial information was provided in package inserts of five statins approved in Japan (simvastatin, atorvastatin, fluvastatin, pravastatin and pitavastatin).
A MEDLINE search from 1996 to June 2004 was carried out to identify studies on clinical pharmacokinetic drug interactions for the five statins. We mainly collected information on area under plasma concentration (AUC) following co-administration of statins with other drugs. The current package inserts used in Japan were obtained from the website of the Pharmaceutical and Medical Device Agency whereas USA package inserts were obtained from the Food and Drug Administration website.
The majority of package inserts listed the drugs that interacted with statins with most describing the risk of rhabdomyolysis because of the possibility of increases in blood concentration. However, quantitative information such as change in AUC was provided in only a few cases. Instructions for dosage adjustment are seldom provided in the Japanese package inserts. USA package inserts list almost identical drug interactions as the Japanese package inserts, although they contain more quantitative data, especially for typical cytochrome P450 (CYP) inhibitors.
All pharmacokinetic drug interactions including relevant quantitative data for potential effectors and details on mechanisms of interaction need to be given in package inserts as soon as the information becomes available, to ensure safe and proper use of the drugs concerned. Including such information in the package insert will be an extremely valuable aid for health care providers.
他汀类药物(HMG-CoA还原酶抑制剂)是全球处方量最大的药物类别之一,因其出色的降胆固醇效果和总体安全性,不过与某些其他药物存在药代动力学相互作用,可能直接或间接引发罕见但致命的横纹肌溶解症。由于药品说明书是医疗保健人员的主要信息来源,我们进行了文献检索,以研究在日本获批的五种他汀类药物(辛伐他汀、阿托伐他汀、氟伐他汀、普伐他汀和匹伐他汀)的说明书中,关键信息是如何呈现的。
对1996年至2004年6月期间的MEDLINE进行检索,以确定关于这五种他汀类药物临床药代动力学药物相互作用的研究。我们主要收集了他汀类药物与其他药物联合使用后血浆浓度曲线下面积(AUC)的信息。日本目前使用的药品说明书从药品和医疗器械局网站获取,而美国的药品说明书则从食品药品监督管理局网站获取。
大多数药品说明书列出了与他汀类药物相互作用的药物,大多数都描述了因血药浓度升高而导致横纹肌溶解症的风险。然而,只有少数情况提供了诸如AUC变化等定量信息。日本的药品说明书很少提供剂量调整说明。美国的药品说明书列出的药物相互作用与日本的药品说明书几乎相同,尽管它们包含更多的定量数据,尤其是对于典型的细胞色素P450(CYP)抑制剂。
一旦有相关信息,药品说明书应尽快给出所有药代动力学药物相互作用,包括潜在效应物的相关定量数据和相互作用机制的详细信息,以确保相关药物的安全合理使用。在药品说明书中纳入此类信息将对医疗保健人员提供极有价值的帮助。