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An open-label, prospective interventional study of the tolerability and efficacy of 0.4 mg oral tamsulosin oral controlled absorption system in men with lower urinary tract symptoms associated with benign prostatic hyperplasia who are unsatisfied with treatment with 0.2 mg tamsulosin

PURPOSE: The aim of this study was to investigate the efficacy and tolerability of switching from 0.2 mg tamsulosin to 0.4 mg tamsulosin oral controlled absorption system (OCAS) over a 12-week period in Taiwanese men with lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplas...

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Detalhes bibliográficos
Publicado no:Clin Interv Aging
Main Authors: Yang, Pei-Shan, Chen, Chien-Lun, Hou, Chen-Pang, Lin, Yu-Hsiang, Tsui, Ke-Hung
Formato: Artigo
Idioma:Inglês
Publicado em: Dove Medical Press 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5808696/
https://ncbi.nlm.nih.gov/pubmed/29445269
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CIA.S152701
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