Antly h Higher percentage braf inhibitor of tolterodine ER M Men who tamsulosin reported treatment benefit by week 12 compared to placebo, tamsulosin or tolterodine ER alone, alone. Tolterodine ER tamsulosin also fell in Ma Of the symptoms of overactive bladder increased after 12 weeks compared to placebo, including normal variable log of the bladder and prostate symptom score and International total scores of storage and that the scores for each storage element IPSS. A significant h Herer proportion of M Nnern among tolterodine ER tamsulosin satisfied with the treatment were to continue to improve and patient perception of bladder condition, urgency perception scale, and the quality of t of Article I-PSS life to placebo at week 12 opposite. Improvements in symptoms questionnaire OAB Bother Me and health Lebensqualit t scales and took Anpassungsma, Anxiety and sleeping area at week 12 significantly gr It with tolterodine ER tamsulosin that with placebo. Many of these effects were already in week 1 Tolterodine ER alone significantly reduced urgency urinary incontinence compared with placebo at week 12, but no other results. Post-hoc analyzes showed that tolterodine ER tamsulosin was effective in patients independent Ngig whether their size E of the prostate or serum reference value of prostate-specific antigen was studied above or below the median are. Tolterodine ER significantly improved only diary variable bubble and the scores of several storage IPSS versus placebo in M Nnern with prostate size E or PSA levels below the median study, but no significant improvement was observed at any point on the end with a placebo in M nnern with prostate size e or PSA level Avasimibe CI-1011 compared to the median. In times AUR requiring catheterization in a nnern of 225 M With tolterodine ER and tamsulosin of 1217 M Nnern with tolterodine ER alone, two patients had a size E of the prostate and serum PSA level gr He than the treated, median study occurred. Changes in PVR and Qmax in the M Nnern with tamsulosin or tolterodine ER tolterodine ER alone were treated neither clinically nor statistically significantly different from placebo. There were no differences in Ver Changes in Qmax or PVR between subjects with a base size E of the prostate or upper or lower serum PSA in each treatment group. The double-blind Detrol LA on DD The study alpha blockers M Men, M Men aged 40 years with LUTS associated with overactive bladder were randomized to 12 weeks of treatment with tolterodine ER 4 mg or placebo. All subjects had again U-blocker A month before the study and continued to use this medication w Take during the study. The difference between the groups in the percentage of subjects reporting CBPP improvement at week 12 was not statistically significant. However, the decrease from baseline at Week 12 bubble in the number of cavities Rooms and the number of episodes of urgency and improvements on the subscale IPSS storage and symptoms of an overactive I st Ren scale and q range adjustment were significantly h Ago in the tolterodine ER group compared with placebo group blocking a blocker. The Aminopeptidase Signaling reduction in UUI episodes did not differ significantly between the groups, but only 16% of subjects initially reported UUI Highest. Similar to Times, showed a post-hoc analysis showed that tolterodine ER-blocker was more effective than placebo in a blocker of M Nnern with PSA values above and just fine.
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