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Dexmedetomidine load

University of Pennsylvania · 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 in perioperative and diagnostic settings.

At a glance

Generic nameDexmedetomidine load
Also known asPrecedex, Dexmedetomidine Hydrochloride
SponsorUniversity of Pennsylvania
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, resulting in decreased norepinephrine release and subsequent sedation. This mechanism also provides analgesic and anxiolytic effects while maintaining a unique 'cooperative sedation' profile where patients remain arousable. The drug is the active d-enantiomer of medetomidine and has a rapid onset and short duration of action.

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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