Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item
Were any concomitant medications taken by the subject at screening or during the study?
text
C2347852 (UMLS CUI [1])
Code List
Were any concomitant medications taken by the subject at screening or during the study?
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Item
Taken Prior to Study?
text
C2826667 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Code List
Taken Prior to Study?
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Item
Ongoing Medication?
text
C2826666 (UMLS CUI [1])
Code List
Ongoing Medication?
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item
Is this subject receiving antiretroviral therapy (ART) other than the ABC-Containing product(s) during the study?
text
C1963724 (UMLS CUI [1])
Code List
Is this subject receiving antiretroviral therapy (ART) other than the ABC-Containing product(s) during the study?
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Unit Dose
Item
Unit Dose
text
C0869039 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Item
Unit
text
C1519795 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Item
Frequency
text
C3476109 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
CL Item
As required (PRN)
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Item
Ongoing Medication?
text
C2826666 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Code List
Ongoing Medication?