{"title":"A systematic mapping review on the capability of large language models in drug-drug interaction analysis.","authors":"Himel Mondal, Ipsita Dash, Shaikat Mondal, Seshadri Reddy Varikasuvu, Rintu Kumar Gayen, Shreya Sharma, Sairavi Kiran Biri","doi":"10.1080/17512433.2025.2568090","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Drug-drug interaction (DDI) is a global health concern affecting patient safety and treatment outcomes. Large language models (LLMs), such as ChatGPT, offer accessible alternatives; however, their effectiveness in DDI analysis remains unclear. This review evaluates the current evidence on the performance of LLM-based chatbots in identifying DDIs.</p><p><strong>Methods: </strong>A PRISMA-compliant systematic review (PROSPERO: CRD420251020360) was conducted using PubMed, Scopus, and Web of Science (studies published between 1 January 2015, and 31 March 2025). Eligible studies included those using publicly accessible LLM chatbots for DDI detection.</p><p><strong>Results: </strong>Nine studies (2023-2025) evaluated publicly accessible LLM chatbots, including ChatGPT, Bing AI, and Google Bard, for DDI identification. Methods varied from patient-level polypharmacy screening to single-drug checks and case vignettes. Chatbot performance was inconsistent: ChatGPT identified many potential DDIs, with ChatGPT-4.0 generally identifying more potential DDIs, but with variable accuracy, while Bing AI and Google Bard were less reliable.</p><p><strong>Conclusion: </strong>Publicly accessible LLM chatbots demonstrate variable and partial effectiveness in detecting DDIs. There is a clear need to develop dedicated, freely available chatbots designed specifically for DDI identification. Future research should focus on standardizing evaluation methods and expanding access to improve medication safety in clinical practice.</p><p><strong>Prospero: </strong>CRD420251020360.</p>","PeriodicalId":12207,"journal":{"name":"Expert Review of Clinical Pharmacology","volume":" ","pages":"1-8"},"PeriodicalIF":3.0000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert Review of Clinical Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17512433.2025.2568090","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Drug-drug interaction (DDI) is a global health concern affecting patient safety and treatment outcomes. Large language models (LLMs), such as ChatGPT, offer accessible alternatives; however, their effectiveness in DDI analysis remains unclear. This review evaluates the current evidence on the performance of LLM-based chatbots in identifying DDIs.
Methods: A PRISMA-compliant systematic review (PROSPERO: CRD420251020360) was conducted using PubMed, Scopus, and Web of Science (studies published between 1 January 2015, and 31 March 2025). Eligible studies included those using publicly accessible LLM chatbots for DDI detection.
Results: Nine studies (2023-2025) evaluated publicly accessible LLM chatbots, including ChatGPT, Bing AI, and Google Bard, for DDI identification. Methods varied from patient-level polypharmacy screening to single-drug checks and case vignettes. Chatbot performance was inconsistent: ChatGPT identified many potential DDIs, with ChatGPT-4.0 generally identifying more potential DDIs, but with variable accuracy, while Bing AI and Google Bard were less reliable.
Conclusion: Publicly accessible LLM chatbots demonstrate variable and partial effectiveness in detecting DDIs. There is a clear need to develop dedicated, freely available chatbots designed specifically for DDI identification. Future research should focus on standardizing evaluation methods and expanding access to improve medication safety in clinical practice.
期刊介绍:
Advances in drug development technologies are yielding innovative new therapies, from potentially lifesaving medicines to lifestyle products. In recent years, however, the cost of developing new drugs has soared, and concerns over drug resistance and pharmacoeconomics have come to the fore. Adverse reactions experienced at the clinical trial level serve as a constant reminder of the importance of rigorous safety and toxicity testing. Furthermore the advent of pharmacogenomics and ‘individualized’ approaches to therapy will demand a fresh approach to drug evaluation and healthcare delivery.
Clinical Pharmacology provides an essential role in integrating the expertise of all of the specialists and players who are active in meeting such challenges in modern biomedical practice.