A data science approach to drug safety: Semantic and visual mining of adverse drug events from clinical trials of pain treatments
Jean-Baptiste Lamy

TL;DR
This paper introduces a data science platform that uses semantic web technologies and visual analytics to analyze adverse drug events from clinical trials, aiming to improve safety monitoring and update processes.
Contribution
The paper presents a novel platform combining ontological modeling, semantic querying, and visual glyphs for analyzing trial data on drug safety, which was not previously applied in this context.
Findings
Platform successfully replicates meta-analysis conclusions.
Enables detailed analysis of adverse event rates.
Facilitates expert review and decision-making.
Abstract
Clinical trials are the basis of Evidence-Based Medicine. Trial results are reviewed by experts and consensus panels for producing meta-analyses and clinical practice guidelines. However, reviewing these results is a long and tedious task, hence the meta-analyses and guidelines are not updated each time a new trial is published. Moreover, the independence of experts may be difficult to appraise. On the contrary, in many other domains, including medical risk analysis, the advent of data science, big data and visual analytics allowed moving from expert-based to fact-based knowledge. Since 12 years, many trial results are publicly available online in trial registries. Nevertheless, data science methods have not yet been applied widely to trial data. In this paper, we present a platform for analyzing the safety events reported during clinical trials and published in trial registries. This…
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Taxonomy
TopicsPharmacovigilance and Adverse Drug Reactions · Biomedical Text Mining and Ontologies · Meta-analysis and systematic reviews
