Adverse Event
Item
No adverse event within the whole study?
boolean
C0877248 (UMLS CUI [1])
Adverse Event Number
Item
Adverse Event Number
integer
C0877248 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Adverse Event Description
Item
Adverse Event Description
text
C0877248 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Adverse Event Onset Date
Item
Adverse Event Onset
date
C2985916 (UMLS CUI [1])
Adverse Event Ongoing
Item
Adverse Event Ongoing?
boolean
C2826663 (UMLS CUI [1])
Adverse Event End Date
Item
Stop Date
date
C2697886 (UMLS CUI [1])
CTC grade
Item
CTC grade
text
C2985911 (UMLS CUI [1])
Adverse Event Severity
Item
Adverse Event Severity
text
C1710066 (UMLS CUI [1])
Relationship
Item
Relationship
text
C0015608 (UMLS CUI [1])
Imatinib
Item
Action Imatinib
text
C0935989 (UMLS CUI [1])
LBH
Item
Action LBH
text
C1566164 (UMLS CUI [1])
Action
Item
Further action
text
C0441472 (UMLS CUI [1])
Adverse Event Outcome
Item
Outcome?
text
C1705586 (UMLS CUI [1])
Seriousness of Adverse Event
Item
Serious
boolean
C1710056 (UMLS CUI [1])