Related Experiment Video
Updated: May 3, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
Published on: December 11, 2016
An informatics framework for the standardized collection and analysis of medication data in networked research
1Duke University School of Nursing, 2007 Pearson Bldg, 307 Trent Drive, Durham, NC 27710, United States.
Abstract:
Medication exposure is an important variable in virtually all clinical research, yet there is great variation in how the data are collected, coded, and analyzed. Coding and classification systems for medication data are heterogeneous in structure, and there is little guidance for implementing them, especially in large research networks and multi-site trials. Current practices for handling medication data in clinical trials have emerged from the requirements and limitations of paper-based data collection, but there are now many electronic tools to enable the collection and analysis of medication data. This paper reviews approaches to coding medication data in multi-site research contexts, and proposes a framework for the classification, reporting, and analysis of medication data. The framework can be used to develop tools for classifying medications in coded data sets to support context appropriate, explicit, and reproducible data analyses by researchers and secondary users in virtually all clinical research domains.
Related Concept Videos
Nursing Clinical Information System
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include:
Model Approaches for Pharmacokinetic Data: Distributed Parameter Models
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
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...
Dosage Regimens: Partial Pharmacokinetic Parameters
Dosage Regimens: Designs and Approaches
Analysis of Population Pharmacokinetic Data

