2007
DOI: 10.1016/j.juro.2007.08.033
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Efficacy, Safety and Tolerability of Fesoterodine for Overactive Bladder Syndrome

Abstract: The 2 doses of fesoterodine were well tolerated and they statistically significantly improved overactive bladder symptoms.

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Cited by 177 publications
(174 citation statements)
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“…The majority of adverse events were mild or moderate (fesoterodine, 94%; placebo, 98%). No meaningful mean change from baseline (fesoterodine, n = 374; placebo, n = 382) to week 12 (fesoterodine, n = 341; placebo, n = 356) in MMSE score was observed in the fesoterodine (0.24 AE 1.76) or placebo [19][20][21][22][23][24][25][26][27][28][29][30] in the placebo group. No clinically relevant changes from baseline were observed in vital sign measurements in either group.…”
Section: Safetymentioning
confidence: 99%
“…The majority of adverse events were mild or moderate (fesoterodine, 94%; placebo, 98%). No meaningful mean change from baseline (fesoterodine, n = 374; placebo, n = 382) to week 12 (fesoterodine, n = 341; placebo, n = 356) in MMSE score was observed in the fesoterodine (0.24 AE 1.76) or placebo [19][20][21][22][23][24][25][26][27][28][29][30] in the placebo group. No clinically relevant changes from baseline were observed in vital sign measurements in either group.…”
Section: Safetymentioning
confidence: 99%
“…Both formulations of fesoterodine significantly improved urgency and UUI episodes, mean voided volume [37]. Nitti et al [38] recorded similar results in a subsequent phase 3 trial with 832 participants randomly assigned to placebo, fesoterodine (4 mg), or fesoterodine (8 mg). A pooled subanalysis from the two latter trials evaluated outcomes in 358 men [15].…”
Section: Efficacymentioning
confidence: 75%
“…Phase 3 trials show an incidence of 16% to 22% of dry mouth for the 4-mg dose and 34% to 36% for the 8-mg dose [37,38]. Older patients appear to be more susceptible to AEs, especially with the 8-mg dose.…”
Section: Adverse Eventsmentioning
confidence: 99%
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“…Patients receiving 8 mg/day of fesoterodine reported a greater side effect profile compared with placebo and fesoterodine, 4 mg/day [16,66,67]. The most common AEs were dry mouth in 37.7% and 12.5% and constipation in 8.8% and 2.5% with 8 mg and 4 mg, respectively.…”
Section: Safety Of Anticholinergic Pharmacotherapymentioning
confidence: 98%