Cargando…
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...
| Autores principales: | , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
|
| Materias: | |
| 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 |