Success rate, efficacy, and safety/tolerability of overnight switching from immediate‐ to extended‐release pramipexole in advanced Parkinson's disease
Identifieur interne : 000E25 ( Main/Exploration ); précédent : 000E24; suivant : 000E26Success rate, efficacy, and safety/tolerability of overnight switching from immediate‐ to extended‐release pramipexole in advanced Parkinson's disease
Auteurs : A. H. V. Schapira [Royaume-Uni] ; P. Barone [Italie] ; R. A. Hauser [États-Unis] ; Y. Mizuno [Japon] ; O. Rascol [France] ; M. Busse [Allemagne] ; C. Debieuvre [France] ; M. Fraessdorf [Allemagne] ; Werner Poewe [Autriche]Source :
- European Journal of Neurology [ 1351-5101 ] ; 2013-01.
Abstract
For Parkinson's disease (PD), an extended‐release (ER) pramipexole formulation taken once daily, has shown efficacy, safety, and tolerability resembling those of immediate‐release (IR) pramipexole taken three times daily. The present study assessed, in advanced PD, the success of an overnight switch from adjunctive IR to ER.
Url:
DOI: 10.1111/j.1468-1331.2012.03822.x
Affiliations:
- Allemagne, Autriche, France, Italie, Japon, Royaume-Uni, États-Unis
- Angleterre, Champagne-Ardenne, Grand Est, Grand Londres, Midi-Pyrénées, Occitanie (région administrative), Tyrol (Land)
- Innsbruck, Londres, Reims, Toulouse
- Université de médecine d'Innsbruck
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Le document en format XML
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<front><div type="abstract">For Parkinson's disease (PD), an extended‐release (ER) pramipexole formulation taken once daily, has shown efficacy, safety, and tolerability resembling those of immediate‐release (IR) pramipexole taken three times daily. The present study assessed, in advanced PD, the success of an overnight switch from adjunctive IR to ER.</div>
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