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Dexmedetomidine 0.5 microgram/kg

Sindh Institute of Urology and Transplantation · FDA-approved active Small molecule

Dexmedetomidine 0.5 microgram/kg is a Alpha-2 adrenergic receptor agonist Small molecule drug developed by Sindh Institute of Urology and Transplantation. It is currently FDA-approved for Sedation of intubated and mechanically ventilated patients in intensive care units, Sedation and analgesia for procedural sedation, Perioperative anxiolysis and analgesia.

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, Sedation and analgesia for procedural sedation, Perioperative anxiolysis and analgesia.

At a glance

Generic nameDexmedetomidine 0.5 microgram/kg
SponsorSindh Institute of Urology and Transplantation
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 intensive care and procedural settings.

Approved indications

Common side effects

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Frequently asked questions about Dexmedetomidine 0.5 microgram/kg

What is Dexmedetomidine 0.5 microgram/kg?

Dexmedetomidine 0.5 microgram/kg is a Alpha-2 adrenergic receptor agonist drug developed by Sindh Institute of Urology and Transplantation, indicated for Sedation of intubated and mechanically ventilated patients in intensive care units, Sedation and analgesia for procedural sedation, Perioperative anxiolysis and analgesia.

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

Dexmedetomidine 0.5 microgram/kg is indicated for Sedation of intubated and mechanically ventilated patients in intensive care units, Sedation and analgesia for procedural sedation, Perioperative anxiolysis and analgesia.

Who makes Dexmedetomidine 0.5 microgram/kg?

Dexmedetomidine 0.5 microgram/kg is developed and marketed by Sindh Institute of Urology and Transplantation (see full Sindh Institute of Urology and Transplantation pipeline at /company/sindh-institute-of-urology-and-transplantation).

What drug class is Dexmedetomidine 0.5 microgram/kg in?

Dexmedetomidine 0.5 microgram/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 0.5 microgram/kg in?

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

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

Common side effects of Dexmedetomidine 0.5 microgram/kg include Hypotension, Bradycardia, Hypertension (transient, initial), Dry mouth, Rebound hypertension on withdrawal.

What does Dexmedetomidine 0.5 microgram/kg target?

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

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