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Dexmedetomidine 0.5μg/kg

Eye & ENT Hospital of Fudan University · FDA-approved active Small molecule

Dexmedetomidine 0.5μg/kg is a Alpha-2 adrenergic receptor agonist Small molecule drug developed by Eye & ENT Hospital of Fudan University. It is currently FDA-approved for Sedation in perioperative and intensive care unit settings, Analgesia and anxiolysis in procedural sedation. Also known as: Dexmedetomidine Hydrochloride Injection.

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 in perioperative and intensive care unit settings, Analgesia and anxiolysis in procedural sedation.

At a glance

Generic nameDexmedetomidine 0.5μg/kg
Also known asDexmedetomidine Hydrochloride Injection
SponsorEye & ENT Hospital of Fudan University
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 sedation in perioperative and intensive care settings.

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 0.5μg/kg

What is Dexmedetomidine 0.5μg/kg?

Dexmedetomidine 0.5μg/kg is a Alpha-2 adrenergic receptor agonist drug developed by Eye & ENT Hospital of Fudan University, indicated for Sedation in perioperative and intensive care unit settings, Analgesia and anxiolysis in procedural sedation.

How does Dexmedetomidine 0.5μg/kg 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 0.5μg/kg used for?

Dexmedetomidine 0.5μg/kg is indicated for Sedation in perioperative and intensive care unit settings, Analgesia and anxiolysis in procedural sedation.

Who makes Dexmedetomidine 0.5μg/kg?

Dexmedetomidine 0.5μg/kg is developed and marketed by Eye & ENT Hospital of Fudan University (see full Eye & ENT Hospital of Fudan University pipeline at /company/eye-ent-hospital-of-fudan-university).

Is Dexmedetomidine 0.5μg/kg also known as anything else?

Dexmedetomidine 0.5μg/kg is also known as Dexmedetomidine Hydrochloride Injection.

What drug class is Dexmedetomidine 0.5μg/kg in?

Dexmedetomidine 0.5μg/kg 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 0.5μg/kg in?

Dexmedetomidine 0.5μg/kg is FDA-approved (marketed).

What are the side effects of Dexmedetomidine 0.5μg/kg?

Common side effects of Dexmedetomidine 0.5μg/kg include Hypotension, Bradycardia, Dry mouth, Hypertension (transient, initial), Dizziness.

What does Dexmedetomidine 0.5μg/kg target?

Dexmedetomidine 0.5μg/kg targets Alpha-2 adrenergic receptor and is a Alpha-2 adrenergic receptor agonist.

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