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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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Clin Interv Aging
Päätekijät: Yang, Pei-Shan, Chen, Chien-Lun, Hou, Chen-Pang, Lin, Yu-Hsiang, Tsui, Ke-Hung
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove Medical Press 2018
Aiheet:
Linkit: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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