Other medical information

Administrative Documentation
Descrição

Administrative Documentation

Alias
UMLS CUI-1
C1320722
Subject Number
Descrição

Subject Number

Tipo de dados

integer

Alias
UMLS CUI [1]
C2348585
Concomitant Vaccination
Descrição

Concomitant Vaccination

Alias
UMLS CUI-1
C0042196
UMLS CUI-2
C2347852
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol ?
Descrição

Concomitant vaccination

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0042196
UMLS CUI [1,2]
C2347852
Concomitant Vaccination
Descrição

Concomitant Vaccination

Alias
UMLS CUI-1
C0042196
UMLS CUI-2
C2347852
Trade / (Generic) Name
Descrição

Trade name

Tipo de dados

text

Alias
UMLS CUI [1]
C0013227
Route
Descrição

Route

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0013153
UMLS CUI [1,2]
C0042210
Administration date
Descrição

Administration date

Tipo de dados

date

Alias
UMLS CUI [1,1]
C1533734
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0042210
For GSK
Descrição

Investigator Use

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C0457083
Medication
Descrição

Medication

Alias
UMLS CUI-1
C0013227
Have any medications/treatments been administered during study period?
Descrição

Concomitant Medication

Tipo de dados

text

Alias
UMLS CUI [1]
C2347852
Medication
Descrição

Medication

Alias
UMLS CUI-1
C0013227
Trade/Generic Name
Descrição

Trade/Generic Name

Tipo de dados

text

Alias
UMLS CUI [1]
C0013227
Medical indication
Descrição

Indication

Tipo de dados

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
Total daily dose
Descrição

Daily dose

Tipo de dados

text

Alias
UMLS CUI [1]
C2348070
Route
Descrição

Route

Tipo de dados

text

Alias
UMLS CUI [1]
C0013153
Start date
Descrição

Start date

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0013227
End date
Descrição

End date

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0013227
tick box if continuing at end of study
Descrição

Continuing

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2826666
For GSK
Descrição

Investigator Use

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C0457083

Similar models

Other medical information

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Administrative Documentation
C1320722 (UMLS CUI-1)
Subject Number
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
Item Group
Concomitant Vaccination
C0042196 (UMLS CUI-1)
C2347852 (UMLS CUI-2)
Item
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol ?
text
C0042196 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Code List
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol ?
CL Item
No (No)
CL Item
Yes, please record concomitant vaccination with trade name and / or generic name, route and vaccine (Yes, please record concomitant vaccination with trade name and / or generic name, route and vaccine)
CL Item
administration date. (administration date.)
Item Group
Concomitant Vaccination
C0042196 (UMLS CUI-1)
C2347852 (UMLS CUI-2)
Trade name
Item
Trade / (Generic) Name
text
C0013227 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1,1])
C0042210 (UMLS CUI [1,2])
Administration date
Item
Administration date
date
C1533734 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0042210 (UMLS CUI [1,3])
Investigator Use
Item
For GSK
text
C0008961 (UMLS CUI [1,1])
C0457083 (UMLS CUI [1,2])
Item Group
Medication
C0013227 (UMLS CUI-1)
Item
Have any medications/treatments been administered during study period?
text
C2347852 (UMLS CUI [1])
Code List
Have any medications/treatments been administered during study period?
CL Item
No (No)
CL Item
Yes, please complete the following table. (Yes, please complete the following table.)
Item Group
Medication
C0013227 (UMLS CUI-1)
Trade/Generic Name
Item
Trade/Generic Name
text
C0013227 (UMLS CUI [1])
Item
Medical indication
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Code List
Medical indication
CL Item
Specify (Specify)
CL Item
Prophylactic (Prophylactic)
Daily dose
Item
Total daily dose
text
C2348070 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Start date
Item
Start date
date
C0808070 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
End date
Item
End date
date
C0806020 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Continuing
Item
tick box if continuing at end of study
boolean
C2826666 (UMLS CUI [1])
Investigator Use
Item
For GSK
text
C0008961 (UMLS CUI [1,1])
C0457083 (UMLS CUI [1,2])