Info
Item
Treatments given for an adverse event should be recorded on the appropriate “Adverse event” page. Treatments given for prophylaxis or treatment of abnormal laboratory values (e.g. blood cells, potassium supplements, etc.) should be recorded on this page. List any treatments continuing at screen or that have begun since screen (or medical procedures performed) that are not recorded on Adverse event pages.
text
Name of treatment
Item
Name of concomitant treatment
text
C1707479 (UMLS CUI [1])
Concomitant Medication Daily Dose
Item
Total Daily Dose of Agent (or Drug)
float
C2826638 (UMLS CUI [1])
Concomitant Medication Start Date
Item
Start date
date
C2826734 (UMLS CUI [1])
Concomitant Medication End Date
Item
End Date
date
C2826744 (UMLS CUI [1])
Concomitant Medication Ongoing
Item
Ongoing
boolean
C2826666 (UMLS CUI [1])
Concomitant Medication Use Reason
Item
Reason
text
C0450442 (UMLS CUI [1,1])
C0521115 (UMLS CUI [1,2])