standards > terminology artifact > DOI:10.25504/FAIRsharing.36pf8q


ready RxNORM


General Information
RxNorm provides normalized names for clinical drugs and links its names to many of the drug vocabularies commonly used in pharmacy management and drug interaction software, including those of First Databank, Micromedex, MediSpan, Gold Standard Drug Database, and Multum. By providing links between these vocabularies, RxNorm can mediate messages between systems not using the same software and vocabulary. RxNorm now includes the National Drug File - Reference Terminology (NDF-RT) from the Veterans Health Administration. NDF-RT is a terminology used to code clinical drug properties, including mechanism of action, physiologic effect, and therapeutic category.



How to cite this record FAIRsharing.org: RxNORM; RxNORM; DOI: https://doi.org/10.25504/FAIRsharing.36pf8q; Last edited: Feb. 22, 2018, 2:05 p.m.; Last accessed: Oct 17 2018 4:36 a.m.


Record updated: Aug. 5, 2016, 4:13 p.m. by The FAIRsharing Team.



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Publications

RxTerms - a drug interface terminology derived from RxNorm.

Fung KW,McDonald C,Bray BE
AMIA Annu Symp Proc 2008

View Paper (PubMed)

Normalized names for clinical drugs: RxNorm at 6 years.

Nelson SJ,Zeng K,Kilbourne J,Powell T,Moore R
J Am Med Inform Assoc 2011

View Paper (PubMed) View Publication

RxNorm: prescription for electronic drug information exchange

S. Liu ; Wei Ma ; R. Moore ; V. Ganesan ; S. Nelson
IEEE Xplore Digital Library 2005

View Publication

RXNORM Ontology Display

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Implementing Databases (2)
Rhea
Rhea is a comprehensive and non-redundant resource of expert-curated biochemical reactions designed for the functional annotation of enzymes and the description of metabolic networks. Rhea describes enzyme-catalyzed reactions covering the IUBMB Enzyme Nomenclature list as well as additional reactions, including spontaneously occurring reactions, using entities from the ChEBI (Chemical Entities of Biological Interest) ontology of small molecules.

DrugCentral
DrugCentral is online drug information that provides information on active ingredients, chemical entities, pharmaceutical products, drug mode of action, indications, and pharmacologic mode of action. DrugCentral monitors FDA, EMA, and PMDA for new drug approval on regular basis to ensure currency of the resource. This resource was created and is maintained by the Division of Translational Informatics at the University of New Mexico School of Medicine.

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