医学
药品
药理学
药效学
抗逆转录病毒药物
药物代谢
药物相互作用
人类免疫缺陷病毒(HIV)
抗逆转录病毒药物
药代动力学
临床药理学
重症监护医学
药物作用
抗逆转录病毒疗法
病毒载量
病毒学
作者
Matthew J. Page,Stephen Taylor
标识
DOI:10.1016/j.mpmed.2022.01.006
摘要
Abstract
There are now >30 antiretroviral medications available for the treatment of HIV. These drugs have distinct sites of action in the HIV life cycle, and unique pharmacological properties that dictate how they can be used safely in the treatment of HIV. Drug–drug interactions (DDIs) can occur because of alterations to several pharmacodynamic processes, including absorption and drug transport, but hepatic metabolism is clinically the most important. Co-administration of antiretrovirals with other, more commonly used drugs is commonplace, and clinicians must be aware of potential serious interactions that can lead to treatment failure and/or drug toxicity.
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