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Dexmetomidine intravenously

KAT General Hospital · FDA-approved active Small molecule

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

Dexmedetomidine is a selective alpha-2 adrenergic receptor agonist that produces sedation, analgesia, and anxiolysis by activating presynaptic and postsynaptic alpha-2 receptors in the central nervous system. Used for Sedation of initially intubated and mechanically ventilated patients in intensive care units, Sedation and analgesia for procedural sedation in awake, non-intubated patients.

At a glance

Generic nameDexmetomidine intravenously
Also known asDEX
SponsorKAT General Hospital
Drug classAlpha-2 adrenergic receptor agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaAnesthesia and Critical Care
PhaseFDA-approved

Mechanism of action

By binding to alpha-2 adrenergic receptors, dexmedetomidine reduces norepinephrine release and enhances inhibitory neurotransmission, resulting in sedation without respiratory depression. It also provides analgesic and anxiolytic effects, making it useful for procedural sedation and ICU sedation. The drug maintains airway reflexes better than many other sedatives, which is a key clinical advantage.

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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