Inglese

Concomitant Medication

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

Administrative

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?
Descrizione

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.

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
Descrizione

(Trade Name Preferred)

Tipo di dati

text

Alias
UMLS CUI [1]
C2360065
SINGLE Dose/Unit
Descrizione

(eg.500mg)

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1960417
UMLS CUI [1,2]
C0869039
Frequency of this Dose
Descrizione

(e.g.BID,PRN)

Tipo di dati

text

Alias
UMLS CUI [1]
C3476109
Concomitant Medication Route
Descrizione

Concomitant Medication Route

Tipo di dati

text

Alias
UMLS CUI [1]
C2826730
Concomitant Medication Indication
Descrizione

Concomitant Medication Indication

Tipo di dati

text

Alias
UMLS CUI [1]
C2826696
Concomitant Medication Start Date/Time
Descrizione

Concomitant Medication Start Date/Time

Tipo di dati

datetime

Alias
UMLS CUI [1]
C2826825
Concomitant Medication End Date/Time
Descrizione

Concomitant Medication End Date/Time

Tipo di dati

datetime

Alias
UMLS CUI [1]
C2826815
Concomitant Medication continuing at end of Study?
Descrizione

Concomitant Medication continuing at end of Study?

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Concomitant Medication

1 moduli
  1. StudyEvent: ODM
    1. Concomitant Medication
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
Are there any concomitant medication CHANGES since the start of the study?
Item
Are there any concomitant medication CHANGES since the start of the study?
boolean
C2347852 (UMLS CUI [1,1])
C0443172 (UMLS CUI [1,2])
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
SINGLE Dose/Unit
Item
SINGLE Dose/Unit
text
C1960417 (UMLS CUI [1,1])
C0869039 (UMLS CUI [1,2])
Frequency of this Dose
Item
Frequency of this Dose
text
C3476109 (UMLS CUI [1])
Concomitant Medication Route
Item
Concomitant Medication Route
text
C2826730 (UMLS CUI [1])
Concomitant Medication Indication
Item
Concomitant Medication Indication
text
C2826696 (UMLS CUI [1])
Concomitant Medication Start Date/Time
Item
Concomitant Medication Start Date/Time
datetime
C2826825 (UMLS CUI [1])
Concomitant Medication End Date/Time
Item
Concomitant Medication End Date/Time
datetime
C2826815 (UMLS CUI [1])
Concomitant Medication continuing at end of Study?
Item
Concomitant Medication continuing at end of Study?
boolean
C2826666 (UMLS CUI [1])
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