date of visit/assessment
Item
date of visit/assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
subject ID
Item
subject number
text
C2348585 (UMLS CUI [1])
Item
Were any concomitant medications taken by the subject prior to screening and/or during the study?
text
C2347852 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,3])
C2347852 (UMLS CUI [2,1])
C0347984 (UMLS CUI [2,2])
C2347804 (UMLS CUI [2,3])
Code List
Were any concomitant medications taken by the subject prior to screening and/or during the study?
Item
Did the subject experience any non-serious adverse events during the study?
text
C1518404 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
Code List
Did the subject experience any non-serious adverse events during the study?
Item
Did the subject experience a serious adverse event during the study?
text
C1519255 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
Code List
Did the subject experience a serious adverse event during the study?
Item
Were any blood products / blood supportive care products taken by the subject during the study?
text
C0456388 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0018938 (UMLS CUI [2,1])
C0347984 (UMLS CUI [2,2])
C2347804 (UMLS CUI [2,3])
Code List
Were any blood products / blood supportive care products taken by the subject during the study?
Item
Were any other/additional scans performed
text
C0205394 (UMLS CUI [1,1])
C0011923 (UMLS CUI [1,2])
C1524062 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
Code List
Were any other/additional scans performed