Adverse effects of biologics used to treat asthma.

IF 3.3 3区 医学 Q2 RESPIRATORY SYSTEM
Andrea Sitek, Sergio E Chiarella, Thanai Pongdee
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引用次数: 0

Abstract

In this review, we discuss the risks and adverse effects reported for the current Food and Drug Association (FDA)-approved biologics used in the management of asthma, including omalizumab, benralizumab, dupilumab, mepolizumab, reslizumab, and tezepelumab. Our review focuses on the risk of hypersensitivity reactions, infection, and malignancy. Where relevant, we have included information regarding the risk of cardiovascular disease and eosinophilia, and we have included specific information regarding vaccine use among patients receiving the above biologics. We also review currently available data regarding the use of biologics in the context of pregnancy. Our goal is to provide a comprehensive resource for providers utilizing these agents, so that they may adequately counsel patients about the risks of therapy and identify adverse events if they occur.

用于治疗哮喘的生物制剂的不良反应。
在这篇综述中,我们讨论了目前FDA批准的用于哮喘治疗的生物制剂的风险和不良反应,包括omalizumab、benralizumab、dupilumab、mepolizumab、reslizumab和tezepelumab。我们的综述集中在过敏反应、感染和恶性肿瘤的风险上。在相关的情况下,我们纳入了有关心血管疾病和嗜酸性粒细胞增多的风险的信息,并纳入了有关接受上述生物制剂的患者使用疫苗的具体信息。我们还回顾了目前关于在妊娠期间使用生物制剂的可用数据。我们的目标是为使用这些药物的提供者提供一个全面的资源,这样他们就可以充分地向患者咨询治疗的风险,并在发生不良事件时识别它们。
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
CiteScore
6.90
自引率
0.00%
发文量
57
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Respiratory Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of respiratory disease.
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