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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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Dettagli Bibliografici
Pubblicato in:Clin Pharmacol Ther
Autori principali: Schotland, Peter, Racz, Rebecca, Jackson, David B., Soldatos, Theodoros G., Levin, Robert, Strauss, David G., Burkhart, Keith
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2020
Soggetti:
Accesso online: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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