INCREASING THE DOSE OF A SELECTIVE ANTIMUSCARINIC MEDICATION HELPS IMPROVE THE KEY SYMPTOMS OF OVERACTIVE BLADDER

dc.contributor.authorKasimov S. S.
dc.contributor.authorRahmonberdiyev Kh. K.
dc.date.accessioned2025-12-28T10:43:57Z
dc.date.issued2025-12-11
dc.description.abstractOveractive bladder (OAB) is a serious urinary disorder affecting at least 17% of individuals over the age of 40. In most cases, treatment for OAB begins with pharmacological therapy. Currently, medications that block muscarinic receptors in the bladder are most commonly used. Among these medications, solifenacin stands out due to its high selectivity for the bladder compared to other muscarinic antagonists. The studies presented in this article demonstrate that a flexible dosing approach with solifenacin can effectively improve OAB symptoms with minimal impact on tolerability. Based on numerous studies, both the positive effect of increasing the solifenacin (Vesicare) dose on the key symptoms of OAB and the relevance of starting therapy with a 10 mg dose are confirmed. Unlike oxybutynin, this medication does not significantly affect cognitive function in elderly patients. Thus, solifenacin 10 mg, with its optimal balance of efficacy and safety, provides better treatment adherence compared to other muscarinic antagonists.
dc.formatapplication/pdf
dc.identifier.urihttps://usajournals.org/index.php/1/article/view/1560
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/4175
dc.language.isoeng
dc.publisherModern American Journals
dc.relationhttps://usajournals.org/index.php/1/article/view/1560/1638
dc.rightshttps://creativecommons.org/licenses/by/4.0
dc.sourceModern American Journal of Medical and Health Sciences; Vol. 1 No. 9 (2025); 108-119
dc.source3067-803X
dc.subjectOveractive bladder, muscarinic antagonists, solifenacin 5/10 mg.
dc.titleINCREASING THE DOSE OF A SELECTIVE ANTIMUSCARINIC MEDICATION HELPS IMPROVE THE KEY SYMPTOMS OF OVERACTIVE BLADDER
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

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