Zolpidem prescribing practices before and after Food and Drug Administration required product labeling changes

BACKGROUND: Women have higher morning serum zolpidem concentrations than men after taking an evening dose, potentially leading to increased risk of harm. On 19 April 2013, the United States Food and Drug Administration required labeling changes for zolpidem, recommending an initial dose of no greate...

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Detalles Bibliográficos
Autores principales: Norman, Jessica L, Fixen, Danielle R, Saseen, Joseph J, Saba, Laura M, Linnebur, Sunny A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423710/
https://www.ncbi.nlm.nih.gov/pubmed/28515934
http://dx.doi.org/10.1177/2050312117707687

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423710/
https://www.ncbi.nlm.nih.gov/pubmed/28515934
http://dx.doi.org/10.1177/2050312117707687

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