Adverse Events & Concomitant Medications Week 2 PK Through 2 (Visit 5)

ADVERSE EVENTS & CONCOMITANT MEDICATIONS
Description

ADVERSE EVENTS & CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C0877248
UMLS CUI-3
C2347852
Patient Number
Description

Patient Number

Type de données

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Description

Centre Number

Type de données

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Visit Date
Description

Visit Date

Type de données

date

Alias
UMLS CUI [1]
C1320303
Has the subject experienced any Adverse Events?
Description

Adverse Events

Type de données

boolean

Alias
UMLS CUI [1]
C0877248
Has the subject taken any Concomitant medications?
Description

Concomitant medications

Type de données

boolean

Alias
UMLS CUI [1]
C2347852

Similar models

Adverse Events & Concomitant Medications Week 2 PK Through 2 (Visit 5)

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
ADVERSE EVENTS & CONCOMITANT MEDICATIONS
C0877248 (UMLS CUI-1)
C2347852 (UMLS CUI-3)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Adverse Events
Item
Has the subject experienced any Adverse Events?
boolean
C0877248 (UMLS CUI [1])
Concomitant medications
Item
Has the subject taken any Concomitant medications?
boolean
C2347852 (UMLS CUI [1])