2025· Proceedings of the 1st International Conference on Interdisciplinary Technology & Science Convergence (FusionX Global)· pp. 226-232· 0 citations· 16 references
TL;DR
This work proposes an AI-driven system that consolidates disparate information sources, including patient demographics, medical history, and pharmacological properties of drugs, to enable early and accurate prediction of ADRs, and uses machine learning models to model complex relationships and generate predictive insights.
Abstract
: Adverse Drug Reactions (ADRs) are one of the main reasons for the increased rate of disease worldwide. Most of the conventional medication surveillance systems often identify ADRs only after their occurrences and hence cannot prevent patient harm. These approaches also continue to suffer from a variety of issues, including underreporting, biased reporting, and inability to record the complexity of drug-drug and drug-patient interactions. To overcome these limitations, this work proposes an AI-driven system that consolidates disparate information sources, including patient demographics, medical history, and pharmacological properties of drugs, to enable early and accurate prediction of ADRs. The proposed framework uses machine learning models to model complex relationships and generate predictive insights. Explainable AI (XAI) techniques such as SHAP are used to interpret model predictions. A dashboard displays the risk severity, assessment results, and suggested alternative drugs, offering useful and actionable insights. The system has been assessed using standard datasets such as FAERS, DrugBank, and SIDER, showing notable improvements in F1-score and ROC-AUC over their baselines. The integration of biomedical data with personalized patient information, this study, is supposed to revolutionize pharmacovigilance in the future by facilitating safer prescribing practices, improving patient safety, and encouraging the adoption of AI-powered decision support technologies in healthcare industry.
Background: Adverse drug reactions (ADRs) continue to be a leading source of morbidity, hospitalization, hospital stay, and avoidable health expenditure. The conventional pharmacovigilance process has relied heavily upon spontaneous, manual reporting, prone to the following limitations: under-reporting, delayed reporti...
The systematic monitoring of post-marketing drug safety is paramount to ensuring patient
welfare and population-level health, requiring the timely detection and prevention of adverse
drug events. Traditional pharmacovigilance schemes, which largely rely on spontaneous
reporting, have weaknesses, including underrepo...
C. R. Darwin, Meruva Sathish Kumar, S. Marakatham et al.· Current Drug Safety· 0 citations
Background/Objectives: Adverse drug reactions (ADRs) caused by drug–drug interactions (DDIs) represent an important problem in pharmacotherapy, especially in patients receiving multiple medications. Most computational approaches to DDI-associated ADR prediction formulate the task as a binary classification, but they do...
V. S. Sukhachev, S. M. Ivanov, D. Filimonov et al.· Pharmaceuticals· 0 citations
AI's ability to alter AD care opens the door to precision medicine paradigms that use repurposed medications, digital tools and intelligent decision-making to improve patient outcomes.
Bhagawati Saxena, Neha Sisodiya, R. Khabiya et al.· Current pharmaceutical desig...· 0 citations
Adverse drug reaction (ADR) signal detection is the process of identifying new or previously unclear associations between a medicine and an unwanted effect, using data collected after the medicine has been approved for use. Because clinical trials involve limited numbers of patients over a short period, many uncommon o...
Mohamed Arshak, Mohamed Shafeek A, A. A· International journal of all...· 0 citations
Background Adverse drug reactions (ADRs) are a leading cause of preventable hospitalization, yet the dominant pharmacovigilance paradigm remains reactive. Machine learning (ML) offers a data-driven alternative, but the evidence base has not been formally meta-analyzed under clinically realistic inclusion criteria and a...
G. Cappello, C. Oster, T. Schmidt et al.· Frontiers in Pharmacology· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.