Adverse Events Week 1 PK Visit (Visit 3)

ADVERSE EVENTS +4.5 HOURS
Descrição

ADVERSE EVENTS +4.5 HOURS

Alias
UMLS CUI-1
C0877248
Patient Number
Descrição

Patient Number

Tipo de dados

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Descrição

Centre Number

Tipo de dados

integer

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

Visit Date

Tipo de dados

date

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

Adverse Events

Tipo de dados

boolean

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

Concomitant medications

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2347852
ADVERSE EVENTS +12.5 HOURS
Descrição

ADVERSE EVENTS +12.5 HOURS

Alias
UMLS CUI-1
C0877248
Has the subject experienced any Adverse Events?
Descrição

Adverse Events

Tipo de dados

boolean

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

Concomitant medications

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2347852
ADVERSE EVENTS +24.5 HOURS
Descrição

ADVERSE EVENTS +24.5 HOURS

Alias
UMLS CUI-1
C0877248
Has the subject experienced any Adverse Events?
Descrição

Adverse Events

Tipo de dados

boolean

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

Concomitant medications

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2347852

Similar models

Adverse Events Week 1 PK Visit (Visit 3)

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
ADVERSE EVENTS +4.5 HOURS
C0877248 (UMLS CUI-1)
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])
Item Group
ADVERSE EVENTS +12.5 HOURS
C0877248 (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])
Item Group
ADVERSE EVENTS +24.5 HOURS
C0877248 (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])