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Assessment of Adverse Events in Protocols, Clinical Study Reports, and Published Papers of Trials of Orlistat: A Document Analysis

BACKGROUND: Little is known about how adverse events are summarised and reported in trials, as detailed information is usually considered confidential. We have acquired clinical study reports (CSRs) from the European Medicines Agency through the Freedom of Information Act. The CSRs describe the resu...

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Detalles Bibliográficos
Autores principales: Schroll, Jeppe Bennekou, Penninga, Elisabeth I., Gøtzsche, Peter C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987052/
https://www.ncbi.nlm.nih.gov/pubmed/27529343
http://dx.doi.org/10.1371/journal.pmed.1002101