Date of assessment
Item
Date of assessment
date
C2985720 (UMLS CUI [1])
Subject Identification Number
Item
Subject Identification Number
text
C2348585 (UMLS CUI [1])
Item
Were any COPD medications taken by the subject during the study?
text
C0024117 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,4])
Code List
Were any COPD medications taken by the subject during the study?
Item
Were any concomitant medications taken by the subject during the study?
text
C2347852 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
Code List
Were any concomitant medications taken by the subject during the study?
Item
Did the subject experience a COPD exacerbation during the study?
text
C0740304 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
Code List
Did the subject experience a COPD exacerbation during the study?
Item
Did the subject experience a lower respiratory tract infection requiring treatment with antibiotics during the study?
text
C0149725 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0003232 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
C0347984 (UMLS CUI [1,5])
Code List
Did the subject experience a lower respiratory tract infection requiring treatment with antibiotics during the study?
Item
Did the subject experience any non-serious adverse-events during the study?
text
C1518404 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0347984 (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])
C0008976 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
Code List
Did the subject experience a serious adverse event during the study?