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Bioequivalence Study of Two Orodispersible Rizatriptan Formulations of 10 mg in Healthy Volunteers

The aim of the study was to assess the bioequivalence and tolerability of two different oral formulations of rizatriptan. A bioequivalence study was carried out in 40 healthy volunteers according to an open label, randomized, two-period, two-sequence, crossover, single dose, and fasting conditions d...

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Detalhes bibliográficos
Publicado no:Sci Pharm
Main Authors: Cánovas, Mercè, Polonio, Francisco, Cabré, Francesc
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5064242/
https://ncbi.nlm.nih.gov/pubmed/28117317
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/scipharm84030514
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