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Adverse drug event reporting systems: a systematic review
AIM: Adverse drug events (ADEs) are harmful and unintended consequences of medications. Their reporting is essential for drug safety monitoring and research, but it has not been standardized internationally. Our aim was to synthesize information about the type and variety of data collected within AD...
Gorde:
| Argitaratua izan da: | Br J Clin Pharmacol |
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| Egile Nagusiak: | , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley and Sons Inc.
2016
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4917803/ https://ncbi.nlm.nih.gov/pubmed/27016266 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.12944 |
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