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A 6-month, randomized, double-blind, placebo-controlled pilot discontinuation trial following response to haloperidol treatment of psychosis and agitation in Alzheimer’s disease

OBJECTIVE: In patients with Alzheimer’s disease (AD) with psychosis or agitation that respond to haloperidol treatment, to evaluate the risk of relapse following discontinuation. METHODS: In outpatients with AD with symptoms of psychosis or agitation, responders to 20 weeks of haloperidol (0.5 to 5...

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Detalhes bibliográficos
Main Authors: Devanand, D. P., Pelton, Gregory H., Cunqueiro, Karine, Sackeim, Harold A., Marder, Karen
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3685500/
https://ncbi.nlm.nih.gov/pubmed/21845596
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gps.2630
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