INTRODUCTION
Remimazolam, an ultra-short-acting benzodiazepine, was developed as a new intravenous (IV) agent for general anesthesia and sedation. It is rapidly metabolized by carboxylesterases (CES) in the liver and other tissues including the lung. Combined with its rapid onset, remimazolam's unique metabolism facilitates easy and accurate titration, quick recovery, and few adverse events. 1 In recent clinical trials, the pharmacokinetics and pharmacodynamics, efficacy, and safety of remimazolam were evaluated in patients undergoing