Transdermal drug delivery treatment for overactive bladder

Overactive bladder is commonly treated with oral anticholinergic drugs such as oxybutynin chloride. Although oral anticholinergic agents have been effective in controlling urinary urgency and incontinence, adverse events, particularly dry mouth, often cause patients to discontinue oral therapy and to endure incontinence. Oxybutynin can be delivered transcutaneously, maintaining the efficacy of oral oxybutynin while significantly minimizing side effects (e.g., dry mouth) that may complicate therapy. By avoiding hepatic and gastrointestinal metabolism of oxybutynin, less N-desethyloxybutynin (N-DEO) is produced and this compound is deemed to be responsible for anticholinergic side effects such as dry mouth. This novel oxybutynin formulation offers patients with OAB and urge urinary incontinence a well-tolerated option for managing the symptoms of overactive bladder.

Saved in:
Bibliographic Details
Main Authors: Dmochowski,Roger R., Starkman,Jonathan S., Davila,G. Willy
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Urologia 2006
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382006000500003
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S1677-55382006000500003
record_format ojs
spelling oai:scielo:S1677-553820060005000032006-12-13Transdermal drug delivery treatment for overactive bladderDmochowski,Roger R.Starkman,Jonathan S.Davila,G. Willy overactive bladder oxybutynin administration cutaneous urinary incontinence Overactive bladder is commonly treated with oral anticholinergic drugs such as oxybutynin chloride. Although oral anticholinergic agents have been effective in controlling urinary urgency and incontinence, adverse events, particularly dry mouth, often cause patients to discontinue oral therapy and to endure incontinence. Oxybutynin can be delivered transcutaneously, maintaining the efficacy of oral oxybutynin while significantly minimizing side effects (e.g., dry mouth) that may complicate therapy. By avoiding hepatic and gastrointestinal metabolism of oxybutynin, less N-desethyloxybutynin (N-DEO) is produced and this compound is deemed to be responsible for anticholinergic side effects such as dry mouth. This novel oxybutynin formulation offers patients with OAB and urge urinary incontinence a well-tolerated option for managing the symptoms of overactive bladder.info:eu-repo/semantics/openAccessSociedade Brasileira de UrologiaInternational braz j urol v.32 n.5 20062006-10-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382006000500003en10.1590/S1677-55382006000500003
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Dmochowski,Roger R.
Starkman,Jonathan S.
Davila,G. Willy
spellingShingle Dmochowski,Roger R.
Starkman,Jonathan S.
Davila,G. Willy
Transdermal drug delivery treatment for overactive bladder
author_facet Dmochowski,Roger R.
Starkman,Jonathan S.
Davila,G. Willy
author_sort Dmochowski,Roger R.
title Transdermal drug delivery treatment for overactive bladder
title_short Transdermal drug delivery treatment for overactive bladder
title_full Transdermal drug delivery treatment for overactive bladder
title_fullStr Transdermal drug delivery treatment for overactive bladder
title_full_unstemmed Transdermal drug delivery treatment for overactive bladder
title_sort transdermal drug delivery treatment for overactive bladder
description Overactive bladder is commonly treated with oral anticholinergic drugs such as oxybutynin chloride. Although oral anticholinergic agents have been effective in controlling urinary urgency and incontinence, adverse events, particularly dry mouth, often cause patients to discontinue oral therapy and to endure incontinence. Oxybutynin can be delivered transcutaneously, maintaining the efficacy of oral oxybutynin while significantly minimizing side effects (e.g., dry mouth) that may complicate therapy. By avoiding hepatic and gastrointestinal metabolism of oxybutynin, less N-desethyloxybutynin (N-DEO) is produced and this compound is deemed to be responsible for anticholinergic side effects such as dry mouth. This novel oxybutynin formulation offers patients with OAB and urge urinary incontinence a well-tolerated option for managing the symptoms of overactive bladder.
publisher Sociedade Brasileira de Urologia
publishDate 2006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382006000500003
work_keys_str_mv AT dmochowskirogerr transdermaldrugdeliverytreatmentforoveractivebladder
AT starkmanjonathans transdermaldrugdeliverytreatmentforoveractivebladder
AT davilagwilly transdermaldrugdeliverytreatmentforoveractivebladder
_version_ 1756427985996480512