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Adverse Event Verbatim Description

Known as: AETERM, Adverse Event Reported Term 
The verbatim description of the adverse event.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
As discussed by one of the authors in 2013 (Wood. F, Considerations in Data Modeling when Creating Supplemental Qualifiers… 
Review
2015
Review
2015
Annotating a Blank Case Report Form -a collection of unique CRF pages stored in a file named BlankCRF.pdf is an important part in… 
2014
2014
Breaking long text strings into smaller strings can be tricky, if splitting the string needs to be based on something more than… 
Review
2012
Review
2012
Subject listings are a vital means for investigators to review clinical trial study data, although their usefulness often wanes… 
2012
2012
Everything that happens to a single subject in a clinical trial is interrelated. Most points of data can be reported and… 
2012
2012
A SAS programmer can have long text values in a character variable to wrap in multiple lines using the FLOW option and SPLIT… 
2012
2012
Typical clinical trial counts tables sometimes require listing specific terms and their respective groupings in the table… 
2010
2010
As our company‟s pipeline of drugs, which all utilize the same unique technology, continues to expand, access to an Integrated…