ID
4772
Beschreibung
CDASH Adverse Event 2011-10-24
Stichworte
Versionen (4)
- 28.03.14 28.03.14 - Martin Dugas
- 29.03.14 29.03.14 - Martin Dugas
- 20.06.18 20.06.18 - Julian Varghese
- 09.03.20 09.03.20 - Sarah Riepenhausen
Hochgeladen am
28. März 2014
DOI
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Lizenz
Creative Commons BY-NC 3.0 Legacy
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CDASH Adverse Event
Adverse Event
- StudyEvent: Adverse Event
Beschreibung
Details
Alias
- UMLS CUI-1
- C1522508
Beschreibung
Verbatim (i.e., investigator-reported term) description of the adverse event.
Datentyp
text
Alias
- CDASH
- AETERM
- CDASH/SDTM
- AETERM
- UMLS CUI-1
- C2699044
Beschreibung
Date when the adverse event started.
Datentyp
partialDate
Alias
- CDASH
- AESTDAT
- UMLS CUI-1
- C2697888
Beschreibung
Indicates AE is ongoing when no End Date is provided.
Datentyp
text
Alias
- CDASH
- AEONGO
- UMLS CUI-1
- C2826663
Beschreibung
Date when the adverse event resolved.
Datentyp
partialDate
Alias
- CDASH
- AEENDAT
- UMLS CUI-1
- C2697886
Beschreibung
Description of the severity of the adverse event.
Datentyp
text
Alias
- CDASH
- AESEV
- CDASH/SDTM
- AESEV
- UMLS CUI-1
- C1710066
Beschreibung
Indicates whether or not the adverse event is determined to be “serious” based on what is defined in the protocol.
Datentyp
text
Alias
- CDASH
- AESER
- CDASH/SDTM
- AESER
- UMLS CUI-1
- C2985919
Beschreibung
Indicates if a “serious” adverse event was associated with a congenital anomaly or birth defect.
Datentyp
text
Alias
- CDASH
- AESCONG
- CDASH/SDTM
- AESCONG
- UMLS CUI-1
- C2826727
Beschreibung
Indicates if a “serious” adverse event was associated with a persistent or significant disability or incapacity.
Datentyp
text
Alias
- CDASH
- AESDISAB
- CDASH/SDTM
- AESDISAB
- UMLS CUI-1
- CL427997
Beschreibung
Indicates if a “serious” adverse event resulted in death.
Datentyp
text
Alias
- CDASH
- AESDTH
- CDASH/SDTM
- AESDTH
- UMLS CUI-1
- C1705232
Beschreibung
Indicates if a “serious” adverse event resulted in an initial or prolonged hospitalization for the subject.
Datentyp
text
Alias
- CDASH
- AESHOSP
- CDASH/SDTM
- AESHOSP
- UMLS CUI-1
- C2826664
Beschreibung
Indicates if a “serious” adverse event was life threatening.
Datentyp
text
Alias
- CDASH
- AESLIFE
- CDASH/SDTM
- AESLIFE
- UMLS CUI-1
- C1517874
Beschreibung
Indicates if a “serious” adverse event is associated with other serious or important medical events.
Datentyp
text
Alias
- CDASH
- AESMIE
- CDASH/SDTM
- AESMIE
- UMLS CUI-1
- C2826307
Beschreibung
Indication of whether the study treatment had a causal effect on the adverse event, as reported by the clinician/investigator.
Datentyp
text
Alias
- CDASH
- AEREL
- CDASH/SDTM
- AEREL
- UMLS CUI-1
- C1510821
Beschreibung
Changes made to the study treatment in response to the adverse event.
Datentyp
text
Alias
- CDASH
- AEACN
- CDASH/SDTM
- AEACN
- UMLS CUI-1
- C2826626
Beschreibung
Describes Other Action(s) taken in response to the adverse event that are unrelated to study treatment dose changes.
Datentyp
text
Alias
- CDASH
- AEACNOTH
- CDASH/SDTM
- AEACNOTH
- UMLS CUI-1
- C2826719
Beschreibung
Description of the subject’s status associated with an event.
Datentyp
text
Alias
- CDASH
- AEOUT
- CDASH/SDTM
- AEOUT
- UMLS CUI-1
- C1705586
Beschreibung
Indication of whether the adverse event caused the subject to discontinue from the study.
Datentyp
text
Alias
- CDASH
- AEDIS
- UMLS CUI-1
- C2826233
Ähnliche Modelle
Adverse Event
- StudyEvent: Adverse Event
AETERM (CDASH/SDTM)
C2699044 (UMLS CUI-1)
C2697888 (UMLS CUI-1)
C2697886 (UMLS CUI-1)
AESER (CDASH/SDTM)
C2985919 (UMLS CUI-1)
AESCONG (CDASH/SDTM)
C2826727 (UMLS CUI-1)
AESDISAB (CDASH/SDTM)
CL427997 (UMLS CUI-1)
AESDTH (CDASH/SDTM)
C1705232 (UMLS CUI-1)
AESHOSP (CDASH/SDTM)
C2826664 (UMLS CUI-1)
AESLIFE (CDASH/SDTM)
C1517874 (UMLS CUI-1)
AESMIE (CDASH/SDTM)
C2826307 (UMLS CUI-1)
AEREL (CDASH/SDTM)
C1510821 (UMLS CUI-1)
AEACN (CDASH/SDTM)
C2826626 (UMLS CUI-1)
AEACNOTH (CDASH/SDTM)
C2826719 (UMLS CUI-1)
C2826233 (UMLS CUI-1)