Engels

WTZ-GIST-09-01 (Imatinib + LBH589) Dosage administration record 2009-011417-24

1 Formulieren  
Dosage administration - (V1+2)
Beschrijving

Dosage administration - (V1+2)

Alias
UMLS CUI-1
C0001555
Start Date
Beschrijving

Start Date

Datatype

date

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1]
C0808070
YYYY-MM-DD
OR Continuing
Beschrijving

Continuing therapy

Datatype

boolean

Alias
UMLS CUI [1]
C1553904
OR stop date
Beschrijving

Stop Date

Datatype

date

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1]
C0806020
YYYY-MM-DD
Time of administration
Beschrijving

Time of administration

Datatype

time

Maateenheden
  • HH:NN
Alias
UMLS CUI [1]
C1317775
HH:NN
Imatinib
Beschrijving

Imatinib high dosage

Datatype

integer

Maateenheden
  • tabs à 400mg for daily intake
Alias
UMLS CUI [1,1]
C0935989
UMLS CUI [1,2]
C0444956
tabs à 400mg for daily intake
Imatinib
Beschrijving

Imatinib low dosage

Datatype

integer

Maateenheden
  • tabs à 100mg for daily intake
Alias
UMLS CUI [1,1]
C0935989
UMLS CUI [1,2]
C0445550
tabs à 100mg for daily intake
Dose reduction to
Beschrijving

Dose reduction

Datatype

integer

Maateenheden
  • mg daily
Alias
UMLS CUI [1]
C1707814
mg daily
due to:
Beschrijving

Dose reduction cause

Datatype

text

Alias
UMLS CUI [1,1]
C0678226
UMLS CUI [1,2]
C1707814
Not taken due to:
Beschrijving

Compliance

Datatype

text

Alias
UMLS CUI [1]
C1321605
Contribution of study medication
Beschrijving

Contribution of study medication

Alias
UMLS CUI-1
C1880177
UMLS CUI-2
C0304229
Monday: date
Beschrijving

Monday: date

Datatype

date

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0585024
YYYY-MM-DD
Wednesday: date
Beschrijving

Wednesday: date

Datatype

date

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0585027
YYYY-MM-DD
Friday: date
Beschrijving

Friday: date

Datatype

date

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0585029
YYYY-MM-DD
Monday: cohort
Beschrijving

Monday: cohort

Datatype

integer

Alias
UMLS CUI [1,1]
C0599755
UMLS CUI [1,2]
C0585024
Wednesday: cohort
Beschrijving

Wednesday: cohort

Datatype

integer

Alias
UMLS CUI [1,1]
C0599755
UMLS CUI [1,2]
C0585027
Friday: cohort
Beschrijving

Friday: cohort

Datatype

integer

Alias
UMLS CUI [1,1]
C0599755
UMLS CUI [1,2]
C0585029
No. tabs 20 mg
Beschrijving

Number high dose

Datatype

integer

Alias
UMLS CUI [1,1]
C0449788
UMLS CUI [1,2]
C0444956
No. tabs 5 mg
Beschrijving

Number low dose

Datatype

integer

Alias
UMLS CUI [1,1]
C0449788
UMLS CUI [1,2]
C0445550
Dose reduction to:
Beschrijving

Contribution: Dose reduction

Datatype

integer

Maateenheden
  • mg daily
Alias
UMLS CUI [1,1]
C1707814
UMLS CUI [1,2]
C1880177
mg daily
due to:
Beschrijving

Contribution: Dose reduction cause

Datatype

text

Alias
UMLS CUI [1,1]
C1707814
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C1880177
Not taken due to:
Beschrijving

Contribution: compliance

Datatype

text

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C1880177
Terug naar het begin van de pagina

Similar models

WTZ-GIST-09-01 (Imatinib + LBH589) Dosage administration record 2009-011417-24

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Dosage administration - (V1+2)
C0001555 (UMLS CUI-1)
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Continuing therapy
Item
OR Continuing
boolean
C1553904 (UMLS CUI [1])
Stop Date
Item
OR stop date
date
C0806020 (UMLS CUI [1])
Time of administration
Item
Time of administration
time
C1317775 (UMLS CUI [1])
Imatinib high dosage
Item
Imatinib
integer
C0935989 (UMLS CUI [1,1])
C0444956 (UMLS CUI [1,2])
Imatinib low dosage
Item
Imatinib
integer
C0935989 (UMLS CUI [1,1])
C0445550 (UMLS CUI [1,2])
Dose reduction
Item
Dose reduction to
integer
C1707814 (UMLS CUI [1])
Dose reduction cause
Item
due to:
text
C0678226 (UMLS CUI [1,1])
C1707814 (UMLS CUI [1,2])
Compliance
Item
Not taken due to:
text
C1321605 (UMLS CUI [1])
Item Group
Contribution of study medication
C1880177 (UMLS CUI-1)
C0304229 (UMLS CUI-2)
Monday: date
Item
Monday: date
date
C0011008 (UMLS CUI [1,1])
C0585024 (UMLS CUI [1,2])
Wednesday: date
Item
Wednesday: date
date
C0011008 (UMLS CUI [1,1])
C0585027 (UMLS CUI [1,2])
Friday: date
Item
Friday: date
date
C0011008 (UMLS CUI [1,1])
C0585029 (UMLS CUI [1,2])
Item
Monday: cohort
integer
C0599755 (UMLS CUI [1,1])
C0585024 (UMLS CUI [1,2])
Monday: cohort
Code List
Monday: cohort
CL Item
10 mg LBH589 (-1)
CL Item
20 mg LBH589 (0)
CL Item
30 mg LBH589 (1)
CL Item
40 mg LBH589 (2)
Item
Wednesday: cohort
integer
C0599755 (UMLS CUI [1,1])
C0585027 (UMLS CUI [1,2])
Wednesday: cohort
Code List
Wednesday: cohort
CL Item
10 mg LBH589 (-1)
CL Item
20 mg LBH589 (0)
CL Item
30 mg LBH589 (1)
CL Item
40 mg LBH589 (2)
Item
Friday: cohort
integer
C0599755 (UMLS CUI [1,1])
C0585029 (UMLS CUI [1,2])
Friday: cohort
Code List
Friday: cohort
CL Item
10 mg LBH589 (-1)
CL Item
20 mg LBH589 (0)
CL Item
30 mg LBH589 (1)
CL Item
40 mg LBH589 (2)
Number high dose
Item
No. tabs 20 mg
integer
C0449788 (UMLS CUI [1,1])
C0444956 (UMLS CUI [1,2])
Number low dose
Item
No. tabs 5 mg
integer
C0449788 (UMLS CUI [1,1])
C0445550 (UMLS CUI [1,2])
Contribution: Dose reduction
Item
Dose reduction to:
integer
C1707814 (UMLS CUI [1,1])
C1880177 (UMLS CUI [1,2])
Contribution: Dose reduction cause
Item
due to:
text
C1707814 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C1880177 (UMLS CUI [1,3])
Contribution: compliance
Item
Not taken due to:
text
C1321605 (UMLS CUI [1,1])
C1880177 (UMLS CUI [1,2])
Terug naar het begin van de pagina