Latanoprost-Induced Side Effects and Potential Mechanisms

X. Zhai, J. Samples
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Abstract

Latanoprost (13,16dihydro15R17-phenyl18,1 9,20-trinor-PGF2, isopropyl ester) is a synthetic analogue of prostaglandin Fza developed by Pharmacia and Upjohn as a glaucoma treatment. Since its approval by the Food and Drug Administration (FDA) in August, 1996, multiple published reports have linked a variety of side effects to the use of the drug, some of which are not listed in the original package insert. This review summarizes current understanding of latanoprost-induced side effects and explores potential mechanisms involved in causing these effects based on the available data on this class of medication from basic science and clinical re search.
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拉坦前列素诱导的副作用及其潜在机制
Latanoprost(13,16二氢15r17 -苯基18,1,20 -三- pgf2,异丙酯)是由Pharmacia和Upjohn开发的用于青光眼治疗的前列腺素Fza的合成类似物。自1996年8月获得美国食品和药物管理局(FDA)批准以来,已发表的多份报告已将各种副作用与该药物的使用联系起来,其中一些副作用未在原始包装说明书中列出。本文综述了目前对latanoprost诱导的副作用的认识,并基于基础科学和临床研究的这类药物的现有数据探讨了引起这些副作用的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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