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Precedex Injectable Product
Precedex Injectable Product is an alpha-2 adrenergic agonist that induces sedation and hypnosis.
Precedex Injectable Product is an alpha-2 adrenergic agonist that induces sedation and hypnosis. Used for Sedation of intubated and mechanically ventilated patients, Sedation of patients in intensive care units.
At a glance
| Generic name | Precedex Injectable Product |
|---|---|
| Also known as | dexmedetomidine |
| Sponsor | Children's Cancer Hospital Egypt 57357 |
| Drug class | alpha-2 adrenergic agonist |
| Target | alpha-2 adrenergic receptor |
| Modality | Small molecule |
| Therapeutic area | Anesthesiology |
| Phase | Phase 3 |
Mechanism of action
It works by stimulating alpha-2 adrenergic receptors in the brain, leading to a decrease in the activity of neurons and a subsequent sedative effect. This results in a decrease in the amount of neurotransmitters such as norepinephrine and serotonin, which are involved in arousal and wakefulness.
Approved indications
- Sedation of intubated and mechanically ventilated patients
- Sedation of patients in intensive care units
Common side effects
- Respiratory depression
- Hypotension
- Bradycardia
Key clinical trials
- Using Lidocaine or Dexmedetomidine to Help Control Blood Pressure Spikes From a Tourniquet During Knee Surgery (PHASE2)
- PENG Block With Dexmedetomidine in Older Adults (NA)
- Effect of Tegileridine on Postoperative Bowel Function Recovery in Abdominal Surgery (PHASE4)
- Opioid Sparing Analgesia Continuous Intraoperative Infusion of Dexmedetomidine Versus Lidocaine for Laparoscopic Cholecystectomy (PHASE4)
- Sedation Efficacy and Safety of Remazolam Besylate in Ventilated Surgical Critically Ill Patients (PHASE4)
- Effect of Intravenous or Intrathecal Dexmedetomidine on Bupivacaine Spinal Block in Lower Abdominal Surgery (PHASE2, PHASE3)
- Investigation of Sleep in the Intensive Care Unit (PHASE2)
- Dexmedetomidine and Long-term Outcomes in Elderly Patients After Cardiac Surgery (NA)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |