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Related Concept Videos

Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
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...
Dosage Regimens: Designs and Approaches01:28

Dosage Regimens: Designs and Approaches

Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...
Pharmaceutical Poisoning: Potential Scenarios01:26

Pharmaceutical Poisoning: Potential Scenarios

Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
Drug Dosing: Geriatric Patients01:15

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Elderly individuals encompass a diverse population with varying degrees of age-related physiological changes. Defining the elderly presents challenges, as the geriatric population is often arbitrarily categorized as individuals older than 65. However, many individuals in this group lead active and healthy lives, with an increasing number surpassing 85 years and falling into the older elderly category. Physiological changes associated with aging impact performance capacity and homeostatic...
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
Dosage Regimen: Individualization01:24

Dosage Regimen: Individualization

Individualization in dosing regimens is the customization of medication doses for individual patients. Its necessity arises from the goal of maximizing therapeutic benefits while minimizing risks. This approach is pivotal because human responses to drugs can vary widely; what is effective for one person may be inadequate or excessive for another. Interpatient (intersubject) variability refers to differences in drug responses between individuals, while intrapatient (intrasubject) variability...

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Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
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Published on: December 11, 2016

Retrieval-augmented generation for medication safety: A case study using drug package inserts.

Yuanyuan Sun1, Wei Wang2, Wanqiu Cheng3

  • 1Center for Clinical Pharmacology, The Third Xiangya Hospital, Central South University, Changsha 410013, China.

International Journal of Medical Informatics
|July 11, 2026
PubMed
Summary

Clinical experts excel at medication safety education, but GPT-4o shows promise. LLM evaluations need expert oversight due to limited agreement with human judgments.

Keywords:
LLM-as-a-judgeLarge language modelsMedication safetyPatient education as topicRetrieval-augmented generation

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Last Updated: Jul 13, 2026

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Published on: December 11, 2016

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07:50

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Area of Science:

  • Artificial Intelligence in Healthcare
  • Medical Education Technology
  • Natural Language Processing

Background:

  • Retrieval-augmented generation (RAG) shows potential for reducing large language model (LLM) hallucinations.
  • The application of RAG in medication safety education is not well-studied.
  • This study evaluates RAG-based LLMs for generating patient medication safety education materials.

Purpose of the Study:

  • To assess the performance of RAG-based LLMs in creating patient medication safety education.
  • To compare LLM-generated content with materials created by clinical experts.
  • To evaluate the agreement between LLM-as-a-judge assessments and clinical expert judgments.

Main Methods:

  • Clinical pharmacists developed an ontology for medication safety information.
  • GPT-4o, OAGLLM, and human experts generated educational materials.
  • Seven pharmacists conducted blinded evaluations using a 5-point Likert scale across six dimensions.

Main Results:

  • Human experts achieved the highest overall score (0.89 ± 0.16), followed by GPT-4o (0.86 ± 0.20) and OAGLLM (0.84 ± 0.17).
  • Human-generated materials excelled in Coverage, Relevance, and Accuracy.
  • LLM evaluations showed fair agreement (κ = 0.21-0.24) and low-to-moderate alignment (ρ = 0.40-0.53) with human experts.

Conclusions:

  • Clinical experts remain superior in generating medication safety education materials.
  • GPT-4o demonstrates significant potential for medication safety education.
  • Expert oversight is crucial due to limited agreement between LLM evaluations and human judgments.