Meloxicam.

Q1 Pharmacology, Toxicology and Pharmaceutics
Nasr Y Khalil, Khalid F Aldosari
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引用次数: 4

Abstract

Meloxicam, an oxicam derivative: 4-Hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2- benzothiazine-3-carboxamide 1,1-dioxide, is a nonsteroidal anti-inflammatory drug (NSAID). It is a selective inhibitor of cyclooxygenase-2 (COX-2). It is used in the management of rheumatoid arthritis, acute exacerbations of osteoarthritis, ankylosing spondylitis and juvenile idiopathic arthritis. It is given in a single oral dose of 7.5mg, increased if necessary to a maximum of 15mg daily (7.5mg in the elderly). It may also be given by rectal suppository in doses similar to those used orally. The reported side effects of meloxicam are similar to those of nonsteroidal anti-inflammatory drugs (NSAIDs), such as abdominal pain, anemia, and edema. There is also an increased risk of serious gastrointestinal (GI) adverse events, including ulceration and bleeding. This profile is prepared to discuss and explain physical characteristics, Proprietary and nonproprietary names of meloxicam. It also includes methods of preparation, thermal and spectral behavior, methods of analysis, pharmacokinetics, metabolism, excretion and pharmacology.

Meloxicam。
美洛昔康是一种非甾体抗炎药(NSAID),是一种奥昔康衍生物:4-羟基-2-甲基- n -(5-甲基-2-噻唑基)- 2h -1,2-苯并噻唑-3-羧酰胺1,1-二氧化。它是环氧化酶-2 (COX-2)的选择性抑制剂。它用于类风湿关节炎,骨关节炎急性加重,强直性脊柱炎和青少年特发性关节炎的管理。单次口服剂量为7.5mg,必要时增加至每日最大15mg(老年人7.5mg)。它也可以通过直肠栓剂给予,剂量与口服剂量相似。据报道,美洛昔康的副作用与非甾体类抗炎药(NSAIDs)相似,如腹痛、贫血和水肿。严重胃肠道(GI)不良事件的风险也增加,包括溃疡和出血。本简介旨在讨论和解释美洛昔康的物理特性、专有和非专有名称。它还包括制备方法,热学和光谱行为,分析方法,药代动力学,代谢,排泄和药理学。
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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来源期刊
Profiles of drug substances, excipients, and related methodology
Profiles of drug substances, excipients, and related methodology Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
13.10
自引率
0.00%
发文量
4
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