Item
Point in time
integer
C1442880 (UMLS CUI-1)
CL Item
Induction II (optional) (2)
CL Item
Consolid. III (5)
Item
If Maintenance: Month
integer
C0481504 (UMLS CUI-1)
C0439231 (UMLS CUI-2)
Code List
If Maintenance: Month
CL Item
after 1 Month (1)
CL Item
after 2 Months (2)
CL Item
after 3 Months (3)
CL Item
after 4 Months (4)
CL Item
after 5 Months (5)
CL Item
after 6 Months (6)
CL Item
after 7 Months (7)
CL Item
after 8 Months (8)
CL Item
after 9Months (9)
CL Item
after 10 Months (10)
CL Item
after 11 Months (11)
CL Item
after 12 Months (12)
Desciption of Adverse Event
Item
Desciption of Adverse Event
text
C0877248 (UMLS CUI-1)
Adverse Event Term
Item
Adverse Event Term
text
C2826934 (UMLS CUI-1)
Serious Adverse Event
Item
Serious Adverse Event
boolean
C1519255 (UMLS CUI-1)
Item
Grade of Adverse Event
integer
C2985911 (UMLS CUI-1)
Code List
Grade of Adverse Event
CL Item
Life-Threatening (4)
CL Item
Death related to AE (5)
Item
Outcome
integer
C1705586 (UMLS CUI-1)
CL Item
not yet recovered (2)
CL Item
recovered with sequelae (3)
Treatment/Action taken
Item
Treatment/Action taken
text
C0087111 (UMLS CUI-1)
C0877248 (UMLS CUI-2)
Adverse Event Start Date
Item
Adverse Event Start Date
date
C2697888 (UMLS CUI-1)
Adverse Event End Date
Item
Adverse Event End Date
date
C2697886 (UMLS CUI-1)
Item
Cytarabine
integer
C0877248 (UMLS CUI-1)
C0010711 (UMLS CUI-2)
CL Item
Medication not administered (6)
Item
Daunorubicin
integer
C0877248 (UMLS CUI-1)
C0011015 (UMLS CUI-2)
CL Item
Medication not administered (6)
Item
Dasatinib
integer
C0877248 (UMLS CUI-1)
C1455147 (UMLS CUI-2)
CL Item
Medication not administered (6)
Item
Underlying Disease
text
C0877248 (UMLS CUI-1)
C0277554 (UMLS CUI-2)
Code List
Underlying Disease
CL Item
Medication not administered (6)
Item
Concomitant medication
text
C0877248 (UMLS CUI-1)
C2347852 (UMLS CUI-2)
Code List
Concomitant medication
CL Item
Medication not administered (6)
Item
Other
integer
C0877248 (UMLS CUI-1)
(UMLS CUI-2)
C0205394 (UMLS CUI-3)
CL Item
Medication not administered (6)
Date
Item
Date
date
C2346576 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
Name of Investigator
Item
Name of Investigator
text
C0008961 (UMLS CUI-1)
Signature of investigator
Item
Signature of investigator
text
C2346576 (UMLS CUI-1)