Concomitant Medication

  1. StudyEvent: ODM
    1. Concomitant Medication
Administrative Documentation
Descrizione

Administrative Documentation

Alias
UMLS CUI-1
C1320722
Subject Number
Descrizione

Subject Number

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Concomitant Medication
Descrizione

Concomitant Medication

Alias
UMLS CUI-1
C2347852
Are there any concomitant medication CHANGES since the start of the study? If 'YES', please record all medications used below. Where appropriate, medical conditions should be recorded on the Adverse Events Form, utilizing the same terminology. If a medication has had a dosage change it must be recorded with the start and stop date.
Descrizione

Concomitant Medication Changes

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0443172
CONCOMITANT MEDICATION
Descrizione

CONCOMITANT MEDICATION

Alias
UMLS CUI-1
C2347852
Drug Name (Trade Name Preferred)
Descrizione

Drug Name

Tipo di dati

text

Alias
UMLS CUI [1]
C0013227
SINGLE Dose/Unit
Descrizione

Drug Dosage

Tipo di dati

text

Alias
UMLS CUI [1]
C0870450
Frequency of this Dose (e.g. BID, PRN)
Descrizione

Frequency

Tipo di dati

text

Alias
UMLS CUI [1]
C3476109
Route
Descrizione

Administration Route

Tipo di dati

text

Alias
UMLS CUI [1]
C0013153
Indication
Descrizione

Indication

Tipo di dati

text

Alias
UMLS CUI [1]
C3146298
Start Date / Time
Descrizione

Start Date and Time

Tipo di dati

datetime

Alias
UMLS CUI [1,1]
C3897500
UMLS CUI [1,2]
C2347852
End Date /Time
Descrizione

End Date and Time

Tipo di dati

datetime

Alias
UMLS CUI [1,1]
C3899266
UMLS CUI [1,2]
C2347852
Continuing at end of Study?
Descrizione

Continuing at end of Study

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1553904

Similar models

Concomitant Medication

  1. StudyEvent: ODM
    1. Concomitant Medication
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1320722 (UMLS CUI-1)
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Item Group
C2347852 (UMLS CUI-1)
Concomitant Medication Changes
Item
Are there any concomitant medication CHANGES since the start of the study? If 'YES', please record all medications used below. Where appropriate, medical conditions should be recorded on the Adverse Events Form, utilizing the same terminology. If a medication has had a dosage change it must be recorded with the start and stop date.
boolean
C2347852 (UMLS CUI [1,1])
C0443172 (UMLS CUI [1,2])
Item Group
C2347852 (UMLS CUI-1)
Drug Name
Item
Drug Name (Trade Name Preferred)
text
C0013227 (UMLS CUI [1])
Drug Dosage
Item
SINGLE Dose/Unit
text
C0870450 (UMLS CUI [1])
Frequency
Item
Frequency of this Dose (e.g. BID, PRN)
text
C3476109 (UMLS CUI [1])
Administration Route
Item
Route
text
C0013153 (UMLS CUI [1])
Indication
Item
Indication
text
C3146298 (UMLS CUI [1])
Start Date and Time
Item
Start Date / Time
datetime
C3897500 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
End Date and Time
Item
End Date /Time
datetime
C3899266 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Continuing at end of Study
Item
Continuing at end of Study?
boolean
C1553904 (UMLS CUI [1])