Engelsk

Non-Serious Adverse Events (AE) Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

1 Formulär  
Non-Serious Adverse Event
Beskrivning

Non-Serious Adverse Event

Alias
UMLS CUI-1
C1518404
Did the subject experience any non-serious adverse events during the study? If YES, record details below.
Beskrivning

Non serious adverse event

Datatyp

boolean

Alias
UMLS CUI [1]
C1518404
Non-Serious Adverse Events (AE)
Beskrivning

Non-Serious Adverse Events (AE)

Alias
UMLS CUI-1
C1518404
Event Diagnosis Only (if known) Otherwise Sign/Symptoms e.g. Headache
Beskrivning

Non-Serious Adverse Event

Datatyp

text

Alias
UMLS CUI [1]
C1518404
Start Date (Day Month Year) (e.g. 25 JAN 03)
Beskrivning

Start Date

Datatyp

date

Måttenheter
  • dd/MMM/yy
Alias
UMLS CUI [1]
C0808070
dd/MMM/yy
Start time (e.g. 13:25)
Beskrivning

Start time

Datatyp

time

Måttenheter
  • hr:min
Alias
UMLS CUI [1]
C1301880
hr:min
Outcome
Beskrivning

Outcome

Datatyp

integer

Alias
UMLS CUI [1]
C1705586
End Date e.g. 27 Jan 03
Beskrivning

End Date

Datatyp

date

Alias
UMLS CUI [1]
C0806020
End Time e.g. 10:20
Beskrivning

End Time

Datatyp

time

Alias
UMLS CUI [1]
C1522314
Frequency
Beskrivning

Frequency

Datatyp

integer

Alias
UMLS CUI [1]
C3476109
Maximum Intensity
Beskrivning

Maximum Intensity

Datatyp

integer

Alias
UMLS CUI [1,1]
C0518690
UMLS CUI [1,2]
C0877248
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
Beskrivning

Action Taken with Investigational Product

Datatyp

integer

Alias
UMLS CUI [1]
C1704758
Withdrawal
Beskrivning

Withdrawal

Datatyp

boolean

Alias
UMLS CUI [1]
C2349954
Relationship to Investigational Product(s) Is there a reasonable possibility that the AE may have been caused by the investigational product?
Beskrivning

Relationship to Investigational Product

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0085978
UMLS CUI [1,2]
C0877248
Tillbaka till toppen

Similar models

Non-Serious Adverse Events (AE) Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Non-Serious Adverse Event
C1518404 (UMLS CUI-1)
Non serious adverse event
Item
Did the subject experience any non-serious adverse events during the study? If YES, record details below.
boolean
C1518404 (UMLS CUI [1])
Item Group
Non-Serious Adverse Events (AE)
C1518404 (UMLS CUI-1)
Non-Serious Adverse Event
Item
Event Diagnosis Only (if known) Otherwise Sign/Symptoms e.g. Headache
text
C1518404 (UMLS CUI [1])
Start Date
Item
Start Date (Day Month Year) (e.g. 25 JAN 03)
date
C0808070 (UMLS CUI [1])
Start time
Item
Start time (e.g. 13:25)
time
C1301880 (UMLS CUI [1])
Item
Outcome
integer
C1705586 (UMLS CUI [1])
Frequency
Code List
Outcome
CL Item
Single episode (1)
CL Item
Intermittent (2)
End Date
Item
End Date e.g. 27 Jan 03
date
C0806020 (UMLS CUI [1])
End Time
Item
End Time e.g. 10:20
time
C1522314 (UMLS CUI [1])
Item
Frequency
integer
C3476109 (UMLS CUI [1])
Frequency
Code List
Frequency
CL Item
Single episode (1)
CL Item
Intermittent (2)
Item
Maximum Intensity
integer
C0518690 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Frequency
Code List
Maximum Intensity
CL Item
Single episode (1)
CL Item
Intermittent (2)
Item
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
integer
C1704758 (UMLS CUI [1])
Frequency
Code List
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
CL Item
Single episode (1)
CL Item
Intermittent (2)
Withdrawal
Item
Withdrawal
boolean
C2349954 (UMLS CUI [1])
Relationship to Investigational Product
Item
Relationship to Investigational Product(s) Is there a reasonable possibility that the AE may have been caused by the investigational product?
boolean
C0085978 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Tillbaka till toppen