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Intravenous dexmedetomidine

University of Jordan · 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 intubated and mechanically ventilated patients in intensive care units, Procedural sedation for awake fiberoptic intubation, Sedation during regional anesthesia procedures.

At a glance

Generic nameIntravenous dexmedetomidine
Also known asprecedex, Propofol 2 mg/kg,, fentanyl 1 µg/kg , Cis-atracurium 0.15mg / kg and Isoflurane 1-1.5% in 50% oxygen, Precedex, Intravenous Precedex
SponsorUniversity of Jordan
Drug classAlpha-2 adrenergic receptor agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaAnesthesia and Critical Care
PhaseFDA-approved

Mechanism of action

Dexmedetomidine binds with high selectivity to alpha-2 adrenergic receptors, which are G-protein coupled receptors found throughout the brain and spinal cord. This activation leads to decreased norepinephrine release and reduced neuronal firing, resulting in sedation and analgesia without respiratory depression. The drug produces a unique 'cooperative sedation' where patients can be easily aroused, making it useful for procedural sedation and ICU sedation.

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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