Empowering Pharmacovigilance: Unleashing the Potential of Generative AI in Drug Safety Monitoring

J. Praveen
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Abstract

Pharmacovigilance plays a crucial role in ensuring drug safety and promoting patient well-being throughout the life cycle of medicinal products. However, this field faces several challenges, including underreporting of adverse events, data quality issues, and the complexity of signal detection in large datasets. To address these challenges and enhance drug safety monitoring, there is a growing interest in harnessing the potential of generative artificial intelligence (AI) techniques. This article explores the applications and implications of generative AI in pharmacovigilance. It provides an overview of popular generative models and their working principles, highlighting their ability to analyse drug databases, medical literature, and real-world data sources to identify drug-drug interactions, adverse events, and potential safety signals. Moreover, it emphasizes the importance of human validation and expert oversight in interpreting and acting on the insights generated by generative AI algorithms. The integration of generative AI with traditional pharmacovigilance methods creates a synergistic approach, combining the computational power of AI with human expertise. This integration can lead to improved signal detection, efficient case report generation, proactive risk assessment, and optimized resource allocation. Additionally, the article addresses challenges related to data quality, interpretability, and model validation in generative AI applications, emphasizing the need for standardized protocols and collaborative efforts among stakeholders. Overall, the potential of generative AI in pharmacovigilance is vast. By leveraging its capabilities, we can enhance drug safety monitoring, facilitate early detection of adverse events, and improve patient outcomes. However, it is crucial to address ethical considerations, ensure data privacy, and maintain human oversight to foster responsible and effective implementation of generative AI in pharmacovigilance practices.
增强药物警戒能力:释放生成式人工智能在药物安全监测中的潜力
在药品的整个生命周期中,药物警戒在确保药品安全和促进患者健康方面发挥着至关重要的作用。然而,该领域面临着一些挑战,包括不良事件的少报、数据质量问题以及大数据集信号检测的复杂性。为了应对这些挑战并加强药物安全监测,人们对利用生成式人工智能(AI)技术的潜力越来越感兴趣。本文探讨了生成式人工智能在药物警戒中的应用和意义。它概述了流行的生成模型及其工作原理,强调了它们分析药物数据库、医学文献和现实世界数据源以识别药物-药物相互作用、不良事件和潜在安全信号的能力。此外,它强调了人类验证和专家监督在解释和采取由生成式人工智能算法产生的见解方面的重要性。生成式人工智能与传统药物警戒方法的整合创造了一种协同方法,将人工智能的计算能力与人类专业知识相结合。这种集成可以改进信号检测、高效生成病例报告、主动风险评估和优化资源分配。此外,本文还解决了生成式人工智能应用中与数据质量、可解释性和模型验证相关的挑战,强调了对标准化协议和利益相关者之间协作努力的需求。总的来说,生成人工智能在药物警戒方面的潜力是巨大的。通过利用其能力,我们可以加强药物安全监测,促进不良事件的早期发现,并改善患者的预后。然而,至关重要的是要解决伦理问题,确保数据隐私,并保持人类监督,以促进在药物警戒实践中负责任和有效地实施生成人工智能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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