Detect adverse drug reactions for drug Atorvastatin
Yihui Liu, Uwe Aickelin

TL;DR
This paper introduces a feature selection method to detect adverse drug reactions for Atorvastatin by analyzing patient medical event data before and after drug intake, addressing limitations of existing detection methods.
Contribution
The study proposes a novel feature selection approach using the THIN database to improve ADR detection accuracy for Atorvastatin.
Findings
Effective detection of ADRs from medical event data
Addresses underreporting issues in spontaneous reporting systems
Achieves good performance in experiments
Abstract
Adverse drug reactions (ADRs) are big concern for public health. ADRs are one of most common causes to withdraw some drugs from markets. Now two major methods for detecting ADRs are spontaneous reporting system (SRS), and prescription event monitoring (PEM). The World Health Organization (WHO) defines a signal in pharmacovigilance as "any reported information on a possible causal relationship between an adverse event and a drug, the relationship being unknown or incompletely documented previously". For spontaneous reporting systems, many machine learning methods are used to detect ADRs, such as Bayesian confidence propagation neural network (BCPNN), decision support methods, genetic algorithms, knowledge based approaches, etc. One limitation is the reporting mechanism to submit ADR reports, which has serious underreporting and is not able to accurately quantify the corresponding risk.…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsComputational Drug Discovery Methods · Pharmacovigilance and Adverse Drug Reactions · Biosimilars and Bioanalytical Methods
