Knowledge of Adverse Drug Reaction Reporting and the Pharmacovigilance of Biological Medicines: A Survey of Healthcare Professionals in Ireland

BACKGROUND: In Europe, changes to pharmacovigilance legislation, which include additional monitoring of medicines, aim to optimise adverse drug reaction (ADR) reporting systems. The legislation also makes provisions related to the traceability of biological medicines. OBJECTIVE: The objective of thi...

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Detalles Bibliográficos
Autores principales: O’Callaghan, J., Griffin, B. T., Morris, J. M., Bermingham, Margaret
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990561/
https://www.ncbi.nlm.nih.gov/pubmed/29721705
http://dx.doi.org/10.1007/s40259-018-0281-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990561/
https://www.ncbi.nlm.nih.gov/pubmed/29721705
http://dx.doi.org/10.1007/s40259-018-0281-6

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