What is the black box warning on droperidol?
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3 min read
In December 2001, the U.S. Food and Drug Administration (FDA) mandated a **black box warning on droperidol** due to reported risks of serious cardiac arrhythmias, including torsades de pointes. This significant regulatory action dramatically curtailed the use of droperidol, a potent antiemetic and sedative that was once a staple in many clinical settings. The warning prompted extensive debate within the medical community and led to revised guidelines for patient screening and monitoring.