Information:
Error:
Concomitant medication
- StudyEvent: ODM-Test
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
CL Item
NO (N)
CL Item
YES (Y)
Concomitant Agent
Item
Medication or Therapy
text
CMTRT (CDASH)
CMTRT (CDASH/SDTM)
C2347852 (UMLS CUI-1)
CMTRT (CDASH/SDTM)
C2347852 (UMLS CUI-1)
Item
Taken Prior to Study?
text
CMPRIOR (CDASH)
C2826667 (UMLS CUI-1)
C2826667 (UMLS CUI-1)
CL Item
NO (N)
CL Item
YES (Y)
Concomitant Medication Start Date
Item
Start Date
partialDate
CMSTDAT (CDASH)
C2826734 (UMLS CUI-1)
C2826734 (UMLS CUI-1)
CL Item
NO (N)
CL Item
YES (Y)
Concomitant Medication End Date
Item
End Date
partialDate
CMENDAT (CDASH)
C2826744 (UMLS CUI-1)
C2826744 (UMLS CUI-1)
Concomitant Medication Dose
Item
Dose
float
CMDOSE (CDASH)
CMDOSE+CMDOSU (CDASH/SDTM)
C2826811 (UMLS CUI-1)
CMDOSE+CMDOSU (CDASH/SDTM)
C2826811 (UMLS CUI-1)
Item
Frequency
text
CMDOSFRQ (CDASH)
CMDOSFRQ (CDASH/SDTM)
C2826654 (UMLS CUI-1)
CMDOSFRQ (CDASH/SDTM)
C2826654 (UMLS CUI-1)
CL Item
BID (BID)
CL Item
TID (TID)
CL Item
QID (QID)
CL Item
QOD (QOD)
CL Item
QM (QM)
CL Item
PRN (PRN)
CL Item
UNKNOWN (UNKNOWN)
Item
Route
text
CMROUTE (CDASH)
CMROUTE (CDASH/SDTM)
C2826730 (UMLS CUI-1)
CMROUTE (CDASH/SDTM)
C2826730 (UMLS CUI-1)
CL Item
ORAL (ORAL)
CL Item
TOPICAL (TOPICAL)
CL Item
SUBCUTANEOUS (SUBCUTANEOUS)
CL Item
TRANSDERMAL (TRANSDERMAL)
CL Item
INTRAOCULAR (INTRAOCULAR)
CL Item
INTRAMUSCULAR (INTRAMUSCULAR)
CL Item
RESPIRATORY (INHALATION) (RESPIRATORY (INHALATION))
CL Item
INTRALESIONAL (INTRALESIONAL)
CL Item
INTRAPERITONEAL (INTRAPERITONEAL)
CL Item
NASAL (NASAL)
CL Item
VAGINAL (VAGINAL)
CL Item
RECTAL (RECTAL)