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Unrestricted Fentanyl
Fentanyl is a synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation.
Fentanyl is a synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation. Used for Moderate to severe acute and chronic pain, Cancer pain, Perioperative anesthesia and analgesia.
At a glance
| Generic name | Unrestricted Fentanyl |
|---|---|
| Also known as | Unlimited intraoperative opiates |
| Sponsor | Virginia Commonwealth University |
| Drug class | Synthetic opioid agonist |
| Target | Mu-opioid receptor (OPRM1) |
| Modality | Small molecule |
| Therapeutic area | Pain management |
| Phase | FDA-approved |
Mechanism of action
Fentanyl activates mu-opioid receptors throughout the brain and spinal cord, inhibiting pain signal transmission and modulating emotional responses to pain. It is approximately 50-100 times more potent than morphine. The term 'Unrestricted Fentanyl' likely refers to a formulation or research context without standard regulatory restrictions, though the underlying mechanism remains opioid receptor agonism.
Approved indications
- Moderate to severe acute and chronic pain
- Cancer pain
- Perioperative anesthesia and analgesia
Common side effects
- Respiratory depression
- Sedation
- Nausea and vomiting
- Constipation
- Dizziness
- Pruritus
Key clinical trials
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 |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Unrestricted Fentanyl CI brief — competitive landscape report
- Unrestricted Fentanyl updates RSS · CI watch RSS
- Virginia Commonwealth University portfolio CI