Darifenacin
File:Darifenacin.svg | |
Clinical data | |
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Pregnancy category | |
Routes of administration | Oral |
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Pharmacokinetic data | |
Bioavailability | 15 to 19% (dose-dependent) |
Protein binding | 98% |
Metabolism | Hepatic (CYP2D6- and CYP3A4-mediated) |
Elimination half-life | 13 to 19 hours |
Excretion | Renal (60%) and biliary (40%) |
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CAS Number | |
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DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C28H30N2O2 |
Molar mass | 426.55 g/mol |
WikiDoc Resources for Darifenacin |
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Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Darifenacin at Clinical Trials.gov Clinical Trials on Darifenacin at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Darifenacin
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Patient Resources / Community |
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Darifenacin (Enablex®, Novartis) is a medication used to treat urinary incontinence.
Darifenacin works by blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions. It thereby decreases the urgency to urinate. It should not be used in people with urinary retention.
It is not known whether this selectivity for the M3 receptor translates into any clinical advantage when treating symptoms of overactive bladder syndrome.(1)
Administration
Darifenacin is administered as a once-daily extended-release oral tablet.
References
(1) SPC for emselex-revised on 29/11/06 (available at www.medicines.org.uk)
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- Muscarinic antagonists