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莫西普利在原发性高血压中的应用 被引量:3

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摘要 莫西普利 (moexipril)是一种不含巯基的前体药物 ,po给药后水解成具有活性的代谢物moex iprilat———一种血管紧张素转化酶抑制剂 po生物利用度 2 2 % ,用药后 2h达到峰浓度 ,消除半衰期为 1 0h。莫西普利每日每次po 7.5mg或 1 5mg能有效地降低原发性高血压病人的血压 (包括老人和绝经后妇女 )。其与卡托普利、氢氧噻嗪、阿替洛尔、美托洛尔、维拉帕米缓释剂和尼群地平等的降压效果相近 ,与氢氯噻嗪联用的降压作用显著强于各自单用时的效果。莫西普利具有良好的耐受性 ,通常对糖、脂及电解质代谢和血流动力学参数没有显著影响。临床尤适用于绝经后妇女。
出处 《药学实践杂志》 CAS 1999年第5期267-270,共4页 Journal of Pharmaceutical Practice
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  • 1符蓉,祝世法,陈宜方,陈新宇,江缨,杨俊.洛沙坦对老年高血压病多种血管活性物质的影响[J].浙江临床医学,1999,1(5):290-291. 被引量:1
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  • 8AGABITII ROSEI E, AMBROSIONI E, PIRELLI A, et al. Efficacy and tolerability of moexipril and nitrendipine in postmenopausal women with hypertension, MADAM. study group moexipril as antihypertensine drug after menopause [J]. Eur J Clin Pharmacol, 1999, 55 (3) - 185.
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