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dexmedetomidine 1 µg/kg IV

American University of Beirut Medical Center · FDA-approved active Small molecule

Dexmedetomidine is a selective alpha-2 adrenergic agonist that produces sedation, analgesia, and anxiolysis by activating alpha-2 receptors in the central nervous system.

Dexmedetomidine is a selective alpha-2 adrenergic agonist that produces sedation, analgesia, and anxiolysis by activating alpha-2 receptors in the central nervous system. Used for Sedation of intubated and mechanically ventilated patients in intensive care settings, Procedural sedation and analgesia, Perioperative anxiolysis and analgesia.

At a glance

Generic namedexmedetomidine 1 µg/kg IV
SponsorAmerican University of Beirut Medical Center
Drug classAlpha-2 adrenergic agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaAnesthesia/Sedation
PhaseFDA-approved

Mechanism of action

Dexmedetomidine binds with high selectivity to alpha-2 adrenergic receptors, particularly in the locus coeruleus and other brainstem regions, leading to decreased norepinephrine release and resulting in sedation and analgesia. Unlike general anesthetics, it preserves airway reflexes and allows patients to be aroused, making it useful for procedural sedation and ICU sedation. The drug also produces analgesic effects through spinal and supraspinal mechanisms.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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