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Erschienen in: Drugs & Aging 2/2000

01.02.2000 | New Drug Profile

Extended-Release Oxybutynin

verfasst von: Alison M. Comer, Karen L. Goa

Erschienen in: Drugs & Aging | Ausgabe 2/2000

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Abstract

  • ▲ Extended-release oxybutynin (Ditropan XL®1) uses an osmotic system (OROS®) to deliver a controlled amount of oxybutynin chloride into the gastrointestinal tract over a 24-hour period when taken once daily.
  • ▲ Oxybutynin binds to M3 muscarinic receptors on the detrusor muscle of the bladder, preventing acetylcholinergic activation and relaxing the muscle.
  • ▲ Mean peak plasma concentrations are lower with extended-release oxybutynin 15mg once daily than with conventional immediate-release oxybutynin 5mg taken 3 times daily. Relative bioavailabilities of parent drug and metabolite N-desethoxybutynin are 153 and 69%, respectively, for extended-release oxybutynin when compared with immediate-release oxybutynin.
  • ▲ In short (≤6 weeks) randomised, double-blind clinical trials of patients with detrusor instability, extended-release oxybutynin 5 to 30mg once daily significantly reduced the mean weekly number of urge incontinence episodes by 84 to 90%. Extended-release oxybutynin had similar efficacy to immediate-release oxybutynin.
  • ▲ Adverse events reported by patients taking extended-release oxybutynin were dose-related anticholinergic effects, most frequently dry mouth, somnolence, constipation, blurred vision and dizziness.
  • ▲ A large noncomparative study demonstrated that approximately two thirds of the patients prescribed extended-release oxybutynin for detrusor instability were still taking the medication 6 months later.
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Metadaten
Titel
Extended-Release Oxybutynin
verfasst von
Alison M. Comer
Karen L. Goa
Publikationsdatum
01.02.2000
Verlag
Springer International Publishing
Erschienen in
Drugs & Aging / Ausgabe 2/2000
Print ISSN: 1170-229X
Elektronische ISSN: 1179-1969
DOI
https://doi.org/10.2165/00002512-200016020-00008

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