Martin Caren McHenry, Borgelt Laura
Consult Pharm. 2012 Jul;27(7):482-92. doi: 10.4140/TCP.n.2012.482.
The Food and Drug Administration (FDA), which oversees and regulates prescription and over-the-counter medications, issues several types of advisories about medication safety. Pharmacists and other practitioners are responsible for carefully evaluating these communications and assessing the potential risk for their individual patients. Focusing on black box warnings-the most serious type of warning from FDA-this article discusses a strategy for evaluating and implementing FDA's safety warnings to provide optimal patient care.
负责监督和管理处方药及非处方药的美国食品药品监督管理局（FDA）发布了几种关于药物安全的公告。药剂师和其他从业者有责任仔细评估这些信息，并评估其个体患者的潜在风险。本文聚焦于黑框警告（FDA最严重的一种警告），讨论了一种评估和实施FDA安全警告以提供最佳患者护理的策略。
