start of the study for subject
Item
date of visit/assessment
date
C2348568 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
subject ID
Item
subject ID
text
C2348585 (UMLS CUI [1])
concomitant medications taken during study
Item
were any concomitant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
adverse events during study
Item
Did the subject experience any adverse events during the study?
boolean
C0877248 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
repeat lab samples
Item
Were any repeat lab samples taken?
boolean
C0200345 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])
repeat ECGs
Item
Were any repeat ECGs performed?
boolean
C1623258 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])
repeat vital signs
Item
Were any repeat vital signs recorded?
boolean
C0518766 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])