Dedicated mobile application for drug adverse reaction reporting by patients with relapsing remitting multiple sclerosis (Vigip-SEP study): study protocol for a randomized controlled trial

BACKGROUND: The reporting of adverse drug reactions (ADR) by patients represents an interesting challenge in the field of pharmacovigilance, but the reporting system is not adequately implemented in France. In 2015, only 20 MS patients in France reported ADR due to first-line disease-modifying drugs...

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Detalles Bibliográficos
Autores principales: Defer, Gilles, Le Caignec, Florian, Fedrizzi, Sophie, Montastruc, François, Chevanne, Damien, Parienti, Jean-Jacques, Peyro-Saint-Paul, Laure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845183/
https://www.ncbi.nlm.nih.gov/pubmed/29523169
http://dx.doi.org/10.1186/s13063-018-2560-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845183/
https://www.ncbi.nlm.nih.gov/pubmed/29523169
http://dx.doi.org/10.1186/s13063-018-2560-4

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