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WHODrug: A Global, Validated and Updated Dictionary for Medicinal Information
Olof Lagerlund1, Sara Strese2, Malin Fladvad2
1Uppsala Monitoring Centre, Box 1051, 751 40, Uppsala, Sweden. Olof.lagerlund@who-umc.org.
The WHODrug dictionary provides global medicinal information to standardize medication coding in clinical trials and monitor patient safety. This ensures the development and use of effective, safe medications worldwide.
Area of Science:
- Pharmacovigilance
- Clinical Pharmacology
- Drug Information Systems
Background:
- The World Health Organization Collaborating Centre for International Drug Monitoring (WHO-UMC) developed the WHODrug dictionary.
- Accurate medication information is crucial for clinical trials and patient safety.
- Existing systems may lack comprehensive global medication data.
Purpose of the Study:
- To describe the structure and utility of the WHODrug medicinal information dictionary.
- To highlight its role in standardizing medication data for clinical trials and pharmacovigilance.
- To emphasize the importance of maintaining a comprehensive, validated, and updated global drug dictionary.
Main Methods:
- The WHODrug dictionary systematically collects and structures medicinal information, including trade names, active ingredients, and pharmaceutical details.
- Medications are linked via a structured alphanumeric code to their active moiety.
- Classification systems like the Anatomical Therapeutic Chemical (ATC) system and Standardised Drug Groupings are employed.
Main Results:
- WHODrug facilitates the coding of medications in clinical trials and the identification of medication-related problems.
- Its structured data enables the aggregation of medications for analyzing adverse drug reactions.
- It supports the exploration of relationships between medications and adverse events.
Conclusions:
- The WHODrug dictionary is an essential global resource for accurate and standardized medication information.
- Its use in clinical trials and post-marketing safety improves data exchange and drug safety monitoring.
- Continuous updates and validation are necessary to meet the evolving needs of pharmaceutical industries, academia, and regulatory bodies.
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