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5-hydroxymethyl tolterodine

National Institutes of Health

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Related topics

3 relations

Broader (2)

Benzhydryl CompoundsCresols

Narrower (1)

PNU 200577

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Selective inhibitory effect of imidafenacin and 5-hydroxymethyl tolterodine on capsaicin sensitive C fibers of the primary bladder mechanosensitive afferent nerves in the rat.
2014
2014
Population pharmacokinetics of the 5‐hydroxymethyl metabolite of tolterodine after administration of fesoterodine sustained release tablet in western and east Asian populations
This analysis was conducted to investigate factors that affect 5‐hydroxymethyl tolterodine (5‐HMT) pharmacokinetics after… 
2013
2013
Fesoterodine, its active metabolite, and tolterodine bind selectively to muscarinic receptors in human bladder mucosa and detrusor muscle.
2011
2011
Fesoterodine: Individualised Treatment of Urgency Urinary Incontinence Across Patient Groups
2010
2010
Spinal effects of the fesoterodine metabolite 5-hydroxymethyl tolterodine and/or doxazosin in rats with or without partial urethral obstruction.
2010
2010
The pharmacokinetic profile of fesoterodine 8 mg with daytime or nighttime dosing
PurposeDiurnal variation can affect drug pharmacokinetics. Fesoterodine is a new antimuscarinic drug for the treatment of… 
2010
2010
Fesoterodine fumarate.
Overactive bladder (OAB) is a common condition that causes a profound impact on an individual's overall health and quality of… 
2009
2009
Urodynamic evaluation of fesoterodine metabolite, doxazosin and their combination in a rat model of partial urethral obstruction
To evaluate the urodynamic effects of fesoterodine, a new antimuscarinic agent, alone and combined with doxazosin, in a rat model… 
2009
2009
Influence of food on the pharmacokinetic profile of fesoterodine.
OBJECTIVE Fesoterodine is a new, once-daily, oral, antimuscarinic agent indicated for the treatment of overactive bladder. It… 
2008
2008
Lipophilicity of 5-Hydroxymethyl Tolterodine, the Active Metabolite of Fesoterodine
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