Date of Visit/Assessment
Item
Date of Visit/Assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
Study site
Item
Site
text
C2825164 (UMLS CUI [1])
Patient
Item
Patient
text
C1299487 (UMLS CUI [1])
Subject No.
Item
Patient No.
text
C2348585 (UMLS CUI [1])
Sequence Number
Item
Sequence Number
text
C2348184 (UMLS CUI [1])
Drug name
Item
Drug name
text
C2360065 (UMLS CUI [1])
Concomitant Medication Modified Reported Term
Item
Concomitant Medication Modified Reported Term
text
C2826819 (UMLS CUI [1])
Drug synonym
Item
GSK Drug synonym
text
C0013227 (UMLS CUI [1,1])
C0871468 (UMLS CUI [1,2])
Drug Collection code
Item
GSK Drug Collection code
text
C0013227 (UMLS CUI [1,1])
C1516698 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Failed coding
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Concomitant Medication Unit Dose
Item
Unit Dose
text
C2826811 (UMLS CUI [1])
Concomitant Medication Units
Item
Units
text
C2826646 (UMLS CUI [1])
Concomitant Medication Frequency
Item
Frequency
text
C2826654 (UMLS CUI [1])
Concomitant Medication Route
Item
Route
text
C2826730 (UMLS CUI [1])
Concomitant Medication reason
Item
Reason for Medication
text
C2826696 (UMLS CUI [1])
Concomitant Medication start date/time
Item
Start Date and Time
datetime
C2826825 (UMLS CUI [1])
Item
Taken Prior to Study?
text
C2826667 (UMLS CUI [1])
Code List
Taken Prior to Study?
Item
Ongoing?
text
C2826666 (UMLS CUI [1])
Concomitant Medication end date/time
Item
If no, specify End Date and Time
datetime
C2826815 (UMLS CUI [1])