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Concomitant Medication

1 Formulär  
  1. StudyEvent: ODM
    1. Concomitant Medication
Administrative
Beskrivning

Administrative

Alias
UMLS CUI-1
C1320722
Subject Number
Beskrivning

Subject Number

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Concomitant Medication
Beskrivning

Concomitant Medication

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

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.

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0443172
Concomitant Medication
Beskrivning

Concomitant Medication

Alias
UMLS CUI-1
C2347852
Drug Name
Beskrivning

(Trade Name Preferred)

Datatyp

text

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

(eg.500mg)

Datatyp

text

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

(e.g.BID,PRN)

Datatyp

text

Alias
UMLS CUI [1]
C3476109
Concomitant Medication Route
Beskrivning

Concomitant Medication Route

Datatyp

text

Alias
UMLS CUI [1]
C2826730
Concomitant Medication Indication
Beskrivning

Concomitant Medication Indication

Datatyp

text

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

Concomitant Medication Start Date/Time

Datatyp

datetime

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

Concomitant Medication End Date/Time

Datatyp

datetime

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

Concomitant Medication continuing at end of Study?

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Concomitant Medication

1 Formulär
  1. StudyEvent: ODM
    1. Concomitant Medication
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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