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Does additional monitoring status increase the reporting of adverse drug reactions? An interrupted time series analysis of EudraVigilance data

PURPOSE: To evaluate the impact of including a medicine in the list of medicinal products subject to additional monitoring (AM) on the reporting of adverse drug reactions (ADRs) in the european economic area (EEA). METHODS: Interrupted time series using the monthly number of EEA ADR reports in Eudra...

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Detalles Bibliográficos
Autores principales:	Segec, Andrej, Slattery, Jim, Morales, Daniel R., Januskiene, Justina, Kurz, Xavier, Arlett, Peter
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2020
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898803/ https://www.ncbi.nlm.nih.gov/pubmed/33197106 http://dx.doi.org/10.1002/pds.5174

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