Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.
Description

If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.

1. Start Date Investigational Product [-99]
Description

Start Date Investigational Product treatment period

Data type

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
1. Start Date Investigational Product not applicable [-98]
Description

Start Date Investigational Product treatment period not applicable

Data type

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1272460
2. End Date Investigational Product [-99]
Description

End Date Investigational Product treatment period

Data type

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
2. End Date Investigational Product not applicable [-98]
Description

End Date Investigational Product treatment period not applicable

Data type

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
UMLS CUI [1,3]
C1272460
If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.
Description

If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.

3. Start Date Investigational Product [-99]
Description

Start Date Investigational Product

Data type

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
3. Start Date Investigational Product not applicable [-98]
Description

Start Date Investigational Product not applicable

Data type

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1272460
4. End Date Investigational Product [-99]
Description

End Date Investigational Product

Data type

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
4. End Date Investigational Product not applicable [-98]
Description

End Date Investigational Product not applicable

Data type

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
UMLS CUI [1,3]
C1272460

Similar models

Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.
Start Date Investigational Product treatment period
Item
1. Start Date Investigational Product [-99]
date
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date Investigational Product treatment period not applicable
Item
1. Start Date Investigational Product not applicable [-98]
boolean
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
End Date Investigational Product treatment period
Item
2. End Date Investigational Product [-99]
date
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
End Date Investigational Product treatment period not applicable
Item
2. End Date Investigational Product not applicable [-98]
boolean
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
Item Group
If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.
Start Date Investigational Product
Item
3. Start Date Investigational Product [-99]
date
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date Investigational Product not applicable
Item
3. Start Date Investigational Product not applicable [-98]
boolean
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
End Date Investigational Product
Item
4. End Date Investigational Product [-99]
date
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
End Date Investigational Product not applicable
Item
4. End Date Investigational Product not applicable [-98]
boolean
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])