Number
Item
Consecutive number
integer
C0750480 (UMLS CUI [1])
Indication
Item
Concomitant medication use indication
text
C2826696 (UMLS CUI [1])
Concomitant Agent
Item
Concomitant agent name or generic substance
text
C2347852 (UMLS CUI [1])
Concomitant Agent
Item
Please specify medication dose per day or Therapy
text
C2347852 (UMLS CUI [1])
Concomitant agent
Item
Frequency of intake
text
C2347852 (UMLS CUI [1,1])
C0439603 (UMLS CUI [1,2])
Item
Application route
integer
C0013153 (UMLS CUI [1])
Code List
Application route
CL Item
transdermally (5)
Concomitant Medication Start Date
Item
Concomitant Medication Start Date
date
C2826734 (UMLS CUI [1])
Concomitant medication end date
Item
Concomitant medication end date
date
C2826744 (UMLS CUI [1])
Item
Has concomitant medication been subject to change?
integer
C2347852 (UMLS CUI [1])
Code List
Has concomitant medication been subject to change?
CL Item
No change in medication dose (1)
CL Item
Dose reduction (2)
CL Item
Dose increased (3)
Concomitant Agent
Item
Please specify reason for changes of concomitant medication
text
C2347852 (UMLS CUI [1])
Concomitant Medication Ongoing
Item
Concomitant Medication ongoing after end of trial
boolean
C2826666 (UMLS CUI [1])