Concomitant Medication

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

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject number
Beschreibung

Subject number

Datentyp

integer

Alias
UMLS CUI [1]
C2348585
CONCOMITANT MEDICATION
Beschreibung

CONCOMITANT MEDICATION

Alias
UMLS CUI-1
C2347852
Are there any concomitant medication changes since the start of the study?
Beschreibung

If ‘Yes’, please record all medications below. When appropriate, medical conditions should be recorded on the Adverse Event form, utilising the same terminology. If a medication has had a dosage change it must be recorded with the start and stop date.

Datentyp

text

Alias
UMLS CUI [1]
C2347852
Drug Name
Beschreibung

(Trade name preferred)

Datentyp

text

Alias
UMLS CUI [1]
C0013227
Single dose/Unit
Beschreibung

Single dose/unit

Datentyp

text

Alias
UMLS CUI [1]
C1960417
Frequency of this dose
Beschreibung

dose frequency

Datentyp

text

Alias
UMLS CUI [1]
C2826654
Route
Beschreibung

Route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
Indication
Beschreibung

Indication

Datentyp

text

Alias
UMLS CUI [1]
C3146298
Start Date
Beschreibung

day month year

Datentyp

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0013227
Start Time
Beschreibung

00.00-23:59

Datentyp

time

Alias
UMLS CUI [1,1]
C1301880
UMLS CUI [1,2]
C0013227
End Date
Beschreibung

day month year

Datentyp

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
End Time
Beschreibung

00:00-23:59

Datentyp

time

Alias
UMLS CUI [1,1]
C1522314
UMLS CUI [1,2]
C0013227

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)
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Item Group
CONCOMITANT MEDICATION
C2347852 (UMLS CUI-1)
Item
Are there any concomitant medication changes since the start of the study?
text
C2347852 (UMLS CUI [1])
Code List
Are there any concomitant medication changes since the start of the study?
CL Item
Yes (Y)
CL Item
No (N)
Drug Name
Item
Drug Name
text
C0013227 (UMLS CUI [1])
Single dose/unit
Item
Single dose/Unit
text
C1960417 (UMLS CUI [1])
dose frequency
Item
Frequency of this dose
text
C2826654 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Indication
Item
Indication
text
C3146298 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Time
Item
Start Time
time
C1301880 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
End Date
Item
End Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
End Time
Item
End Time
time
C1522314 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])