Inglés

Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

1 formularios  
Patient Information
Descripción

Patient Information

Alias
UMLS CUI-1
C1955348
Subject Identifier
Descripción

Subject Identifier

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Concomitant Medications
Descripción

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Were any concomitant medications taken by the subject during the study?
Descripción

If YES, record each medication on a seperate line using Trade Names where possible. If the medication is realted to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.

Tipo de datos

boolean

Drug Name (Trade name preferred) e.g. Aspirin
Descripción

Drug Name

Tipo de datos

text

Alias
UMLS CUI [1]
C0013227
Total Daily Dose e.g. 400
Descripción

Total Daily Dose

Tipo de datos

float

Alias
UMLS CUI [1]
C2348070
Unit (for Units and Route see facing page for examples of acceptable abbreviations) e.g. mg
Descripción

Unit

Tipo de datos

text

Alias
UMLS CUI [1]
C1519795
Route (For Units and Route see facing page for examples of acceptable abbreviations) e.g. PO
Descripción

Administration Route

Tipo de datos

text

Reason for Medication e.g. Headache
Descripción

Reason for Medication

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Start Date e.g. 31 MAY 02
Descripción

Start Date

Tipo de datos

date

Unidades de medida
  • dd-mmm-yy
dd-mmm-yy
Stop Date e.g. 31 MAY 02
Descripción

Stop Date

Tipo de datos

date

Unidades de medida
  • dd-mmm-yy
dd-mmm-yy
Ongoing Medication? e.g. N
Descripción

Ongoing

Tipo de datos

text

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Similar models

Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Patient Information
C1955348 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Concomitant Medications
Item
Were any concomitant medications taken by the subject during the study?
boolean
Drug Name
Item
Drug Name (Trade name preferred) e.g. Aspirin
text
C0013227 (UMLS CUI [1])
Total Daily Dose
Item
Total Daily Dose e.g. 400
float
C2348070 (UMLS CUI [1])
Unit
Item
Unit (for Units and Route see facing page for examples of acceptable abbreviations) e.g. mg
text
C1519795 (UMLS CUI [1])
Administration Route
Item
Route (For Units and Route see facing page for examples of acceptable abbreviations) e.g. PO
text
Reason for Medication
Item
Reason for Medication e.g. Headache
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Date
Item
Start Date e.g. 31 MAY 02
date
Stop Date
Item
Stop Date e.g. 31 MAY 02
date
Item
Ongoing Medication? e.g. N
text
Ongoing
Code List
Ongoing Medication? e.g. N
CL Item
Yes (Y)
CL Item
No (N)
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