About: CDISC SDTM Common Terminology Criteria for Adverse Event Grade Terminology V3.0     Goto   Sponge   Distinct   Permalink

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  • CDISC SDTM Common Terminology Criteria for Adverse Event Grade Terminology V3.0
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  • Intellectual Product
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  • CDISC SDTM Common Terminology Criteria for Adverse Event Grade Terminology V3.0
UMLS_CUI
  • C1879929
Contributing_Source
  • CDISC
ALT_DEFINITION
  • A standard terminology developed to report adverse events occurring in cancer clinical trials. Common terminology criteria for adverse events (CTCAE) are used in study adverse event summaries and Investigational New Drug reports to the Food and Drug Administration. The CTCAE contain a grading scale for each adverse event term representing the severity of the event. (NCI)CDISC
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  • CDISC_SDTM_Common_Terminology_Criteria_for_Adverse_Event_Grade_Terminology
FULL_SYN
  • CDISC SDTM Common Terminology Criteria for Adverse Event Grade Terminology V3.0PTNCI
  • SDTM-TOXGRV3ABNCI
  • Common Terminology Criteria for Adverse Events V3.0SYCDISC
  • TOXGRV3PTCDISC
DEFINITION
  • Terminology codelist used with Common Criteria for Adverse Event Grade within the Clinical Data Interchange Standards Consortium Study Data Tabulation Model.NCI
code
  • C66784
is Concept_In_Subset of
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