The Importance of Direct Patient Reporting of Adverse Drug Reactions in the Safety Monitoring Process

All medicinal products authorized in the European Union are subjects of constant drug-safety monitoring processes. It is organized in a pharmacovigilance system that is designed to protect human health and life by the detection, analysis and prevention of adverse drug reactions (ADRs) and other drug...

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Detalles Bibliográficos
Autores principales: Sienkiewicz, Kamila, Burzyńska, Monika, Rydlewska-Liszkowska, Izabela, Sienkiewicz, Jacek, Gaszyńska, Ewelina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745009/
https://www.ncbi.nlm.nih.gov/pubmed/35010673
http://dx.doi.org/10.3390/ijerph19010413

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745009/
https://www.ncbi.nlm.nih.gov/pubmed/35010673
http://dx.doi.org/10.3390/ijerph19010413

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