Clinical Trial Subject Unique Identifier
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Experimental drug, Discontinued
Item
Was the investigational product stopped permanently before the end of the scheduled dosing period?
boolean
C0304229 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
Item
If YES, check the primary reason the investigational product was stopped, check one
text
C0304229 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Code List
If YES, check the primary reason the investigational product was stopped, check one
CL Item
Adverse event (1)
CL Item
Consent withdrawn (2)
CL Item
Lost to follow up (3)
CL Item
Protocol violation (4)
Experimental drug, Discontinued, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])