Información:
Error:
ID
13979
Descripción
Study part: Adverse Events.Observational study on CML patients in any phase treated with ponatinib (Iclusig®) at any dose. Principal Investigator Prof. Dr. A. Hochhaus.
Palabras clave
Versiones (1)
- 20/3/16 20/3/16 -
Subido en
20 de marzo de 2016
DOI
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Licencia
Creative Commons BY-NC 3.0
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Adverse Events Ponderosa CML ZKSJ0083
Similar models
Adverse Events
- StudyEvent: ODM
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Adverse Event
Item
Did Adverse Events occur?
boolean
C0877248 (UMLS CUI [1])
Adverse Event
Item
Adverse Event:
text
C0877248 (UMLS CUI [1])
Adverse Event Start Date Time
Item
Adverse Event Start Date Time
datetime
C2826806 (UMLS CUI [1])
Adverse Event End Date Time
Item
Adverse Event End Date Time
datetime
C2826793 (UMLS CUI [1])
Serious adverse event
Item
Serious adverse event, SAE
text
C1519255 (UMLS CUI [1])
CL Item
no connection (1)
CL Item
connection exists (2)
CL Item
unknown (3)
CL Item
mild (1 )
CL Item
moderate (2 )
CL Item
severe (3 )
CL Item
life-threatening (4 )
CL Item
fatal (death) (5 )
Item
Measures taken regarding adverse event
text
C1608430 (UMLS CUI [1])
C0677850 (UMLS CUI [2])
C0677850 (UMLS CUI [2])
CL Item
no (1 )
CL Item
dose reduction (2 )
CL Item
dose increase (3 )
CL Item
drug interrupted (4 )
CL Item
drug discontinued (5 )
CL Item
adjunctive therapy (6 )
CL Item
unknown (9 )
CL Item
recovered (1 )
CL Item
recovered with consequential damages (2 )
CL Item
unchanged (3 )
CL Item
fatal (4 )
CL Item
unknown (9 )