Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
study subject participation status
Item
Did the subject complete the study as planned?
boolean
C2348568 (UMLS CUI [1])
Item
If ‘No’, mark one most appropriate category:
integer
C0392360 (UMLS CUI [1])
Code List
If ‘No’, mark one most appropriate category:
CL Item
Adverse event (complete adverse event form) (1)
CL Item
Insufficient therapeutic effect (2)
CL Item
Deviation from protocol (including non-compliance) (3)
CL Item
Lost to Follow-Up (4)
Other
Item
Other, please specify
text
C0205394 (UMLS CUI [1])
reason for withdrawal
Item
Comments on reason for withdrawal:
text
C2349954 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Date of withdrawal
Item
Date of withdrawal:
date
C0011008 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
Time of withdrawal
Item
Time of withdrawal:
time
C0040223 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
Date of final dose
Item
Date of final dose:
date
C1531784 (UMLS CUI [1])
Time of final dose
Item
Time of final dose:
time
C1522314 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])