Concomitant Medication

  1. StudyEvent: ODM
    1. Concomitant Medication
Administrative data
Beschreibung

Administrative data

Alias
UMLS CUI-1
C1320722
Centre Number
Beschreibung

Centre Number

Datentyp

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Patient Initials
Beschreibung

Patient Initials

Datentyp

text

Alias
UMLS CUI [1]
C2986440
Concomitant Medication
Beschreibung

Concomitant Medication

Alias
UMLS CUI-1
C2347852
No new/change in concomitant medication
Beschreibung

Please mark if no new or change in concomitant medication during the module

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C1298908
UMLS CUI [1,3]
C0580105
Drug Name
Beschreibung

Drug Name

Datentyp

text

Alias
UMLS CUI [1]
C0013227
Total Daily Dose
Beschreibung

Total Daily Dose

Datentyp

integer

Alias
UMLS CUI [1]
C2348070
Medical illness/ Diagnosis
Beschreibung

(or symptom in absence of diagnosis)

Datentyp

text

Alias
UMLS CUI [1]
C0011900
Start Date
Beschreibung

Start Date

Datentyp

date

Alias
UMLS CUI [1]
C0808070
End Date
Beschreibung

End Date

Datentyp

date

Alias
UMLS CUI [1]
C0806020

Ähnliche Modelle

Concomitant Medication

  1. StudyEvent: ODM
    1. Concomitant Medication
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
No new/change in concomitant medication
Item
No new/change in concomitant medication
boolean
C2347852 (UMLS CUI [1,1])
C1298908 (UMLS CUI [1,2])
C0580105 (UMLS CUI [1,3])
Drug Name
Item
Drug Name
text
C0013227 (UMLS CUI [1])
Total Daily Dose
Item
Total Daily Dose
integer
C2348070 (UMLS CUI [1])
Diagnosis
Item
Medical illness/ Diagnosis
text
C0011900 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date
date
C0806020 (UMLS CUI [1])