Video Experimental Relacionado
Updated: Jan 15, 2026

Evidence-based Knowledge Synthesis and Hypothesis Validation: Navigating Biomedical Knowledge Bases via Explainable AI and Agentic Systems
Published on: June 13, 2025
Sistema de modelo de lenguaje grande aumentado por recuperación para contraindicaciones farmacológicas integrales
Byeonghun Bang1, Jongsuk Yoon1, Dong-Jin Chang2
1Department of Computer Engineering, Hongik University, Seoul, 04066 South Korea.
Abstract:
The versatility of large language models (LLMs) has been explored across various sectors, but their application in healthcare poses challenges, particularly in the domain of pharmaceutical contraindications where accurate and reliable information is required. This study enhances the capability of LLMs to address contraindications effectively by implementing a Retrieval Augmented Generation (RAG) pipeline. Utilizing OpenAI's GPT-4o-mini as the base model, and the text-embedding-3-small model for embeddings, our approach integrates LangChain to orchestrate a hybrid retrieval system with re-ranking. This system leverages Drug Utilization Review (DUR) data from public databases, focusing on contraindications for specific age groups, pregnancy, and concomitant drug use. The dataset includes 300 question-answer pairs across three categories, with baseline model accuracy ranging from 0.49 to 0.57. Post-integration of the RAG pipeline, we observed a significant improvement in model accuracy, achieving rates of 0.94, 0.87, and 0.89 for contraindications related to age groups, pregnancy, and concomitant drug use, respectively. The results indicate that augmenting LLMs with a RAG framework can substantially reduce uncertainty in prescription and drug intake decisions by providing more precise and reliable drug contraindication information.
Videos de Conceptos Relacionados
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Drug Nomenclature
Drug Dosage Regimen: Overview
Typically, the starting dose and dosing interval are guided by the manufacturer's recommendations based on clinical trials conducted during and after drug...
Therapeutic Drug Monitoring: Overview and Classification
Bioequivalence of Drugs: Drugs with Multiple Indications
Drug-Receptor Interactions
Several parameters, such as the drug's affinity for its receptor and its efficacy, which is its ability to activate the receptor, determine the drug's effect on the tissue....

