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Pharmacovigilance in Israel – tools, processes, and actions
BACKGROUND: Due to the limited safety data available at the time that a new medication is first marketed, it is essential to continue the collection and monitoring of safety data about adverse drug reactions (ADRs) during the medication’s life cycle. This activity, known as pharmacovigilance (PV), i...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537943/ https://www.ncbi.nlm.nih.gov/pubmed/28760141 http://dx.doi.org/10.1186/s13584-017-0154-3 |