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dexmedetomidine 0.25 µg/kg IV

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

dexmedetomidine 0.25 µg/kg IV is a Alpha-2 adrenergic receptor agonist Small molecule drug developed by American University of Beirut Medical Center. It is currently FDA-approved for Sedation of initially intubated and mechanically ventilated patients in intensive care settings, Procedural sedation in awake patients undergoing diagnostic or therapeutic procedures.

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 settings, Procedural sedation in awake patients undergoing diagnostic or therapeutic procedures.

At a glance

Generic namedexmedetomidine 0.25 µg/kg IV
SponsorAmerican University of Beirut Medical Center
Drug classAlpha-2 adrenergic receptor agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaAnesthesia and 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 reduced neuronal firing. This results in a unique sedative state characterized by maintained airway reflexes and the ability to be aroused, along with analgesic and anxiolytic effects. The drug is commonly used for procedural sedation and ICU sedation in mechanically ventilated patients.

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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Frequently asked questions about dexmedetomidine 0.25 µg/kg IV

What is dexmedetomidine 0.25 µg/kg IV?

dexmedetomidine 0.25 µg/kg IV is a Alpha-2 adrenergic receptor agonist drug developed by American University of Beirut Medical Center, indicated for Sedation of initially intubated and mechanically ventilated patients in intensive care settings, Procedural sedation in awake patients undergoing diagnostic or therapeutic procedures.

How does dexmedetomidine 0.25 µg/kg IV work?

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.

What is dexmedetomidine 0.25 µg/kg IV used for?

dexmedetomidine 0.25 µg/kg IV is indicated for Sedation of initially intubated and mechanically ventilated patients in intensive care settings, Procedural sedation in awake patients undergoing diagnostic or therapeutic procedures.

Who makes dexmedetomidine 0.25 µg/kg IV?

dexmedetomidine 0.25 µg/kg IV is developed and marketed by American University of Beirut Medical Center (see full American University of Beirut Medical Center pipeline at /company/american-university-of-beirut-medical-center).

What drug class is dexmedetomidine 0.25 µg/kg IV in?

dexmedetomidine 0.25 µg/kg IV belongs to the Alpha-2 adrenergic receptor agonist class. See all Alpha-2 adrenergic receptor agonist drugs at /class/alpha-2-adrenergic-receptor-agonist.

What development phase is dexmedetomidine 0.25 µg/kg IV in?

dexmedetomidine 0.25 µg/kg IV is FDA-approved (marketed).

What are the side effects of dexmedetomidine 0.25 µg/kg IV?

Common side effects of dexmedetomidine 0.25 µg/kg IV include Hypotension, Bradycardia, Hypertension (transient, initial), Dry mouth, Rebound hypertension on discontinuation.

What does dexmedetomidine 0.25 µg/kg IV target?

dexmedetomidine 0.25 µg/kg IV targets Alpha-2 adrenergic receptor and is a Alpha-2 adrenergic receptor agonist.

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