Droxicam:一种新的非甾体抗炎药的药理学和临床回顾。

F Jané, A Rodríguez de la Serna
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引用次数: 0

摘要

Droxicam通过抑制PGE2而起作用。虽然它属于奥昔康家族,但它的特点是作为吡罗西康的前药,分子一旦溶解在消化道中就会发生水解转化。这使我们原则上可以假设,由于活性药物(吡罗昔康)与胃粘膜的接触较少,因此对胃粘膜的副作用很小。已经在健康志愿者和患有骨关节炎和类风湿性关节炎的患者中进行了研究,以评估droxicam对患有这种明显炎症过程的患者的疗效和耐受性。研究表明,在治疗两周后,droxicam具有明显的镇痛和抗炎作用,并且该药耐受性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Droxicam: a pharmacological and clinical review of a new NSAID.

Droxicam acts by inhibition of PGE2 varies. Although it belongs to the oxicam family, it is characterised by being a pro-drug of piroxicam, the molecule undergoing conversion by hydrolysis once dissolved in the digestive tract. This allows us to suppose in principle that, there being less contact between the active drug (piroxicam) and the gastric mucosa, the side effects in the said mucosa would be slight. The studies which have already been performed in healthy volunteers and in patients with osteoarthritis and rheumatoid arthritis, to evaluate the efficacy and the tolerance of droxicam in patients suffering from such clearly inflammatory processes demonstrate an analgesic potential and anti-inflammatory effects which become noticeable after two weeks of treatment, and the drug is well-tolerated.

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