常用药物和遗传对奈比洛尔药代动力学的影响:药物-药物相互作用研究。

IF 2.9 4区 医学 Journal of Clinical Pharmacology Pub Date : 2011-04-01 Epub Date: 2010-05-20 DOI:10.1177/0091270010370846
Charles Lindamood, Stephan Ortiz, Andrew Shaw, Russ Rackley, J Christopher Gorski
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引用次数: 30

摘要

药物相互作用是一个重要的临床问题,特别是在患有心脏病和高血压等疾病的患者中,多种药物共同给药是很常见的。Nebivolol是一种选择性β(1)受体阻滞剂,具有血管舒张特性,被批准用于治疗高血压。当奈比洛尔同时给那些被归类为CYP2D6代谢不良者和广泛的CYP2D6代谢者时,研究了药物与药物的相互作用,这些患者正在接受其他常用的高血压患者药物或由细胞色素P450 (CYP) 2D6代谢的化合物。当奈比洛尔与氢氯噻嗪、呋塞米、雷米普利、氯沙坦、地高辛或华法林共给药时,没有药物-药物相互作用。与氟西汀(也由CYP2D6代谢)在广泛的CYP2D6代谢物中共给药阻碍了奈比洛尔的明显清除。作者得出结论,无论基因型和联合用药类型如何,奈比洛尔都是安全且耐受性良好的。
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Effects of commonly administered agents and genetics on nebivolol pharmacokinetics: drug-drug interaction studies.

Drug interactions are a significant clinical concern, particularly in patients with conditions such as heart disease and hypertension, in whom coadministration of multiple drugs is common. Nebivolol is a selective β(1)-blocker with vasodilatory properties approved for the treatment of hypertension. Drug-drug interactions were investigated when nebivolol was coadministered to subjects classified as poor CYP2D6 metabolizers and extensive CYP2D6 metabolizers who were receiving other drugs commonly administered to patients with hypertension or compounds metabolized by cytochrome P450 (CYP) 2D6. There were no drug-drug interactions when nebivolol was coadministered with hydrochlorothiazide, furosemide, ramipril, losartan, digoxin, or warfarin. Coadministration with fluoxetine (also metabolized by CYP2D6) in extensive CYP2D6 metabolizers impeded the apparent clearance of nebivolol. The authors conclude that nebivolol is safe and well tolerated regardless of genotype and type of medication coadministered.

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来源期刊
Journal of Clinical Pharmacology
Journal of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
自引率
3.40%
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期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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