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美国食品药品监督管理局(FDA)针对局部用钙调神经磷酸酶抑制剂的“黑框”警告:争议仍在继续。

The US FDA 'black box' warning for topical calcineurin inhibitors: an ongoing controversy.

作者信息

Ring Johannes, Möhrenschlager Matthias, Henkel Verena

机构信息

Department of Dermatology and Allergy Biederstein, Technical University of Munich, Munich, Germany.

出版信息

Drug Saf. 2008;31(3):185-98. doi: 10.2165/00002018-200831030-00001.

Abstract

Atopic dermatitis is a chronic inflammatory skin disease characterized by recurrent intense pruritus and a distinctive distribution of skin lesions. The topical calcineurin inhibitors tacrolimus and pimecrolimus were approved in the USA, as an ointment and a cream, respectively, for the treatment of atopic dermatitis in 2000 and 2001, respectively. In 2005, the Pediatric Advisory Committee of the US FDA implemented a 'black box' warning for tacrolimus ointment and pimecrolimus cream due to the lack of long-term safety data and the potential risk of the development of malignancies. This article focuses on the safety aspects of these agents by discussing the findings from preclinical and clinical studies and postmarketing reports with regard to malignancies occurring after the use of tacrolimus ointment and pimecrolimus cream.

摘要

特应性皮炎是一种慢性炎症性皮肤病,其特征为反复出现剧烈瘙痒和独特的皮损分布。局部用钙调神经磷酸酶抑制剂他克莫司和吡美莫司分别于2000年和2001年在美国被批准作为软膏和乳膏用于治疗特应性皮炎。2005年,由于缺乏长期安全性数据以及存在发生恶性肿瘤的潜在风险,美国食品药品监督管理局(FDA)的儿科咨询委员会对他克莫司软膏和吡美莫司乳膏实施了“黑框”警告。本文通过讨论临床前和临床研究结果以及上市后关于使用他克莫司软膏和吡美莫司乳膏后发生恶性肿瘤的报告,重点关注这些药物的安全性方面。

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