Document Detail


The use of a medical dictionary for regulatory activities terminology (MedDRA) in prescription-event monitoring in Japan (J-PEM).
MedLine Citation:
PMID:  10961570     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Medical Dictionary for Regulatory Activities Terminology (MedDRA) version 2.1 (V2.1) was released in March 1999 accompanied by the MedDRA/J V2.1J specifically for Japanese users. In prescription-event monitoring in Japan (J-PEM), we have employed the MedDRA/J for data entry, signal generation and event listing. In J-PEM, the lowest level terms (LLTs) in the MedDRA/J are used in data entry because the richness of LLTs is judged to be advantageous. A signal is generated normally at the preferred term (PT) level, but it has been found that various reporters describe the same event using descriptions that are potentially encoded by LLTs under different PTs. In addition, some PTs are considered too specific to generate the proper signal. In the system used in J-PEM, when an LLT is selected as a candidate to encode an event, another LLT under a different PT, if any, is displayed on the computer screen so that it may be coded instead of, or in addition to, the candidate LLT. The five-level structure of the MedDRA is used when listing events but some modification is required to generate a functional event list.
Authors:
M Yokotsuka; M Aoyama; K Kubota
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  International journal of medical informatics     Volume:  57     ISSN:  1386-5056     ISO Abbreviation:  Int J Med Inform     Publication Date:  2000 Jul 
Date Detail:
Created Date:  2000-12-29     Completed Date:  2000-12-29     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  9711057     Medline TA:  Int J Med Inform     Country:  IRELAND    
Other Details:
Languages:  eng     Pagination:  139-53     Citation Subset:  IM    
Affiliation:
Department of Pharmacoepidemiology, Faculty of Medicine, University of Tokyo, Japan.
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MeSH Terms
Descriptor/Qualifier:
Adverse Drug Reaction Reporting Systems*
Dictionaries, Medical*
Humans
Japan
Pilot Projects
Product Surveillance, Postmarketing
Terminology as Topic

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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