Fentanyl
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Revision as of 18:31, 1 February 2023 by Jashvin Patel (talk | contribs)
Fentanyl
Trade names |
Actiq, Duragesic, Sublimaze |
---|---|
Clinical data | |
Drug class |
Opioid |
Uses |
Analgesia |
Routes of administration |
Buccal, Epidural, Intrathecal, Intravenous, Transdermal |
Dosage | |
Pharmacodynamics | |
Mechanism of action |
μ-opioid agonism |
Pharmacokinetics | |
Onset of action |
5 minutes |
Duration of action |
30-60 minutes |
Metabolism |
Hepatic (CYP3A4) |
Redistribution half-life |
6 minutes (initial) 1 hour (slow) |
Elimination half-life |
16 hours |
Protein binding |
80-85% |
Physical and chemical data | |
Formula |
5 minutes |
Molar mass |
336.479 g/mol |
Article quality | |
Editor rating | |
User likes | 0 |
Fentanyl is a synthetic, lipophilic phenylpiperidine opioid agonist used for analgesia. It is highly lipophilic leading to fast passage across the blood-brain barrier with a 6.8 minute onset time. Fentanyl will also rapidly redistribute to adipose and fatty tissue leading to a short duration of action.
Uses
- Administration
- IV, IM, transdermal, intranasal, intrathecal, epidural, buccal.
Contraindications
Absolute contraindications
Precautions
Pharmacology
Pharmacodynamics
Mechanism of action
- µ-selective opioid receptor
- Low affinity: delta & kappa opioid receptors
Adverse effects
Pharmacokinetics
- Context Sensitive Half Time
- Infusion or repeated doses lead to prolong duration of action as drug redistributes back from tissue to plasma.
Chemistry and formulation
History
References
- Comer SD, Cahill CM. Fentanyl: Receptor pharmacology, abuse potential, and implications for treatment. Neurosci Biobehav Rev. 2019 Nov;106:49-57.
Top contributors: Chris Rishel and Jashvin Patel