Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Liver, Chemistry, Clinical, Adverse Event
Item
Was there any protocol defined liver chemistry event for the lab samples collected at this visit?
boolean
C0023884 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
Item
If Yes, which type of liver chemistry event?
text
C0023884 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,4])
Code List
If Yes, which type of liver chemistry event?
CL Item
Liver Event Monitoring Criteria (subject has met protocol defined liver chemistry MONITORING criteria). (1)
CL Item
Liver Event Stopping Criteria (subject has met protocol defined liver chemistry STOPPING criteria or has been monitored for the protocol specific time period and continues to meet liver chemistry event criteria). (2)