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Post‐marketing dosing changes in the label of biologicals
AIM: The aim of this study was to evaluate post‐marketing label changes in dosing information of biologicals. METHODS: Biologicals authorized between 2007 and 2014 by the European Medicines Agency (EMA) were included and followed up from marketing authorization until 31 December 2016 or date of with...
Autores principales: | Minnema, Lotte A., Giezen, Thijs J., Gardarsdottir, Helga, Egberts, Toine C. G., Leufkens, Hubert G. M., Mantel‐Teeuwisse, Aukje K. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422665/ https://www.ncbi.nlm.nih.gov/pubmed/30593087 http://dx.doi.org/10.1111/bcp.13843 |
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