首页> 外文期刊>Journal of pain & palliative care pharmacotherapy >Food and Drug Administration Requires Strong Warnings for Opioid Analgesics, Prescription Opioid Cough Products, and Benzodiazepine Labeling Related to Serious Risks and Death From Combined Use
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Food and Drug Administration Requires Strong Warnings for Opioid Analgesics, Prescription Opioid Cough Products, and Benzodiazepine Labeling Related to Serious Risks and Death From Combined Use

机译:食品和药物管理局需要强烈的阿片类镇痛药,处方阿片类药物咳嗽产品和苯二氮卓标签,与综合使用的严重风险和死亡有关

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摘要

After an extensive review of the latest scientific evidence, the U.S. Food and Drug Administration announced on August 31, 2016, that it is requiring class-wide changes to drug labeling, including patient information, to help inform health care providers and patients of the serious risks associated with the combined use of certain opioid medications and a class of central nervous system (CNS) depressant drugs called benzodiazepines.
机译:经过广泛审查最新的科学证据,美国食品和药物管理局于2016年8月31日宣布,这需要对药物标签的全类变化,包括患者信息,帮助通知医疗保健提供者和严重的患者 与某些阿片类药物和一类中枢神经系统(CNS)抑制药物相关的风险相关的风险,称为苯并二氮杂卓。

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