Target Adverse Event Profiles for Predictive Safety in the Postmarket Setting

We improved a previous pharmacological target adverse‐event (TAE) profile model to predict adverse events (AEs) on US Food and Drug Administration (FDA) drug labels at the time of approval. The new model uses more drugs and features for learning as well as a new algorithm. Comparator drugs sharing s...

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Bibliografiske detaljer
Udgivet i:Clin Pharmacol Ther
Main Authors: Schotland, Peter, Racz, Rebecca, Jackson, David B., Soldatos, Theodoros G., Levin, Robert, Strauss, David G., Burkhart, Keith
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2020
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8246740/
https://ncbi.nlm.nih.gov/pubmed/33090463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cpt.2074
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