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Study of serious adverse drug reactions using FDA-approved drug labeling and MedDRA
BACKGROUND: Adverse Drug Reactions (ADRs) are of great public health concern. FDA-approved drug labeling summarizes ADRs of a drug product mainly in three sections, i.e., Boxed Warning (BW), Warnings and Precautions (WP), and Adverse Reactions (AR), where the severity of ADRs are intended to decreas...
Tallennettuna:
| Julkaisussa: | BMC Bioinformatics |
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| Päätekijät: | , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6419320/ https://ncbi.nlm.nih.gov/pubmed/30871458 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-2628-5 |
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