Last reviewed · How we verify

dex

The Cleveland Clinic · FDA-approved active Small molecule

Dexmedetomidine is a selective alpha-2 adrenergic receptor agonist that induces sedation and reduces sympathetic nervous system activity.

Dexmedetomidine is a selective alpha-2 adrenergic receptor agonist that induces sedation and reduces sympathetic nervous system activity. Used for Sedation in intensive care unit (ICU) patients, Sedation in procedural sedation.

At a glance

Generic namedex
Also known asRopivacaine/dex, dexmedetomidine group
SponsorThe Cleveland Clinic
Drug classAlpha-2 adrenergic receptor agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaAnesthesiology
PhaseFDA-approved

Mechanism of action

Dexmedetomidine works by activating alpha-2 adrenergic receptors in the brain, which leads to a decrease in the activity of the sympathetic nervous system. This results in sedation, anxiolysis, and a decrease in blood pressure and heart rate. Additionally, dexmedetomidine has analgesic properties and can reduce the need for opioids in some patients.

Approved indications

Common side effects

Key clinical trials

Primary sources

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