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Dexmedetomidine Hydrochloride (dexmedetomidine-hydrochloride)

Pfizer · FDA-approved approved Verified Quality 80/100

Dexmedetomidine Hydrochloride is a relatively selective centrally acting alpha 2 -adrenergic agonist with sedative properties.

Dexmedetomidine Hydrochloride is a marketed drug by Pfizer Inc. It is a relatively selective centrally acting alpha 2 -adrenergic agonist with sedative properties. The key indications include sedation of non-intubated patients in the ICU or in a hospital setting receiving mechanical ventilation. Dexmedetomidine Hydrochloride has clinical differentiation due to its sedative properties and alpha 2 selectivity. The commercial significance is evident with revenue of 63.6B. There are 100 trials and 103 publications associated with the drug. Pipeline developments are not mentioned.

At a glance

Generic namedexmedetomidine-hydrochloride
SponsorPfizer
Drug classdexmedetomidine
TargetAlpha-1A adrenergic receptor
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1999

Mechanism of action

Dexmedetomidine Hydrochloride is a medication used for sedation in various settings. It works by activating alpha 2-adrenergic receptors in the brain, which leads to sedative effects. This mechanism of action is unique compared to other sedatives, making it a valuable option for certain patients.

Approved indications

Common side effects

Drug interactions

Key clinical trials

Patents

PatentExpiryType

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

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