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Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

1 Formulaires  
Concomitant Medication
Description

Concomitant Medication

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C0244821
Are there any concomitant medication CHANGES since the start of the study?
Description

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.

Type de données

boolean

Alias
UMLS CUI [1]
C2347852
drug name
Description

Trade Name Preferred

Type de données

text

Alias
UMLS CUI [1,1]
C2360065
UMLS CUI [1,2]
C2347852
Single Dose/Unit
Description

dose per unit

Type de données

integer

Alias
UMLS CUI [1,1]
C3174092
UMLS CUI [1,2]
C2347852
Frequency of this Dose
Description

medication frequency

Type de données

text

Alias
UMLS CUI [1,1]
C3476109
UMLS CUI [1,2]
C2347852
Route
Description

drug application route

Type de données

text

Alias
UMLS CUI [1,1]
C0013153
UMLS CUI [1,2]
C2347852
Indication
Description

medication indication

Type de données

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C2347852
Duration
Description

duration of medication

Type de données

text

Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C2347852
End Date
Description

end date of medication

Type de données

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0806020
Continuing at end of study?
Description

continuing medication

Type de données

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
C0244821 (UMLS CUI-2)
concomitant medication
Item
Are there any concomitant medication CHANGES since the start of the study?
boolean
C2347852 (UMLS CUI [1])
drug name
Item
drug name
text
C2360065 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
dose per unit
Item
Single Dose/Unit
integer
C3174092 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
medication frequency
Item
Frequency of this Dose
text
C3476109 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
drug application route
Item
Route
text
C0013153 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
medication indication
Item
Indication
text
C3146298 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
duration of medication
Item
Duration
text
C0449238 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
end date of medication
Item
End Date
date
C2347852 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
continuing medication
Item
Continuing at end of study?
boolean
C2826666 (UMLS CUI [1])
Retour au début de la page