Concomitant Medications Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941

Concomitant Medication
Beschrijving

Concomitant Medication

Alias
UMLS CUI-1
C2347852
Were any concomitant medications taken by the subject during the study? if YES record each medication on a separate line using Trade Names where possible. If yes, record each medication on a separate line using Trade Names where possible.
Beschrijving

Concomitant Medication

Datatype

boolean

Alias
UMLS CUI [1]
C2347852
Medication
Beschrijving

Medication

Alias
UMLS CUI-1
C0013227
Drug name (Trade Name preferred) e.g. Aspirin
Beschrijving

Drug name

Datatype

text

Alias
UMLS CUI [1]
C0013227
Unit Dose e.g. 200
Beschrijving

Unit Dose

Datatype

float

Alias
UMLS CUI [1]
C0869039
Units* (eg. mg)
Beschrijving

Units

Datatype

text

Alias
UMLS CUI [1]
C1519795
Frequency* (e.g. BID)
Beschrijving

Frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
Route* (e.g. PO)
Beschrijving

Route

Datatype

text

Alias
UMLS CUI [1]
C0013153
Reason for Medication (e.g. Headache)
Beschrijving

Reason for Medication

Datatype

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Start Date (e.g. 31 May 03)
Beschrijving

Start Date

Datatype

date

Alias
UMLS CUI [1]
C0808070
Start time (e.g. 14:10)
Beschrijving

Start time

Datatype

time

Maateenheden
  • hh:min
Alias
UMLS CUI [1]
C1301880
hh:min
Taken Prior to Study? (e.g. N)
Beschrijving

Taken Prior to Study

Datatype

boolean

Alias
UMLS CUI [1]
C2826667
Stop Date (e.g. 31 May 03)
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI [1]
C0806020
Stop Time (e.g. 23:00)
Beschrijving

Stop Time

Datatype

time

Alias
UMLS CUI [1]
C1522314
Ongoing Medication? (e.g. N)
Beschrijving

Ongoing Medication

Datatype

boolean

Alias
UMLS CUI [1]
C2826666

Similar models

Concomitant Medications Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
Concomitant Medication
Item
Were any concomitant medications taken by the subject during the study? if YES record each medication on a separate line using Trade Names where possible. If yes, record each medication on a separate line using Trade Names where possible.
boolean
C2347852 (UMLS CUI [1])
Item Group
Medication
C0013227 (UMLS CUI-1)
Drug name
Item
Drug name (Trade Name preferred) e.g. Aspirin
text
C0013227 (UMLS CUI [1])
Unit Dose
Item
Unit Dose e.g. 200
float
C0869039 (UMLS CUI [1])
Units
Item
Units* (eg. mg)
text
C1519795 (UMLS CUI [1])
Frequency
Item
Frequency* (e.g. BID)
text
C3476109 (UMLS CUI [1])
Route
Item
Route* (e.g. PO)
text
C0013153 (UMLS CUI [1])
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 03)
date
C0808070 (UMLS CUI [1])
Start time
Item
Start time (e.g. 14:10)
time
C1301880 (UMLS CUI [1])
Taken Prior to Study
Item
Taken Prior to Study? (e.g. N)
boolean
C2826667 (UMLS CUI [1])
Stop Date
Item
Stop Date (e.g. 31 May 03)
date
C0806020 (UMLS CUI [1])
Stop Time
Item
Stop Time (e.g. 23:00)
time
C1522314 (UMLS CUI [1])
Ongoing Medication
Item
Ongoing Medication? (e.g. N)
boolean
C2826666 (UMLS CUI [1])