Series Page
Item
Series Page
text
C0205549 (UMLS CUI [1,1])
C1704732 (UMLS CUI [1,2])
Last Page
Item
Last Page
boolean
C1704732 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
Drug or Blood Product
Item
Drug or Blood Product
text
C0013227 (UMLS CUI [1])
C0456388 (UMLS CUI [2])
Drug or Blood Product Dose
Item
Drug or Blood Product Dose
text
C0013227 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
Drug or Blood Product Dose Unit
Item
Drug or Blood Product Dose Unit
text
C0013227 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,3])
C0456388 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0439148 (UMLS CUI [2,3])
Route of drug administration
Item
Route of drug administration
text
C0013153 (UMLS CUI [1])
Medication frequency | Transfusion (procedure); Frequencies (time pattern)
Item
Medication and Transfusion frequency
text
C3476109 (UMLS CUI [1])
C1879316 (UMLS CUI [2,1])
C0439603 (UMLS CUI [2,2])
Date treatment started
Item
Treatment Start Date (mm/dd/yy)
date
C3173309 (UMLS CUI [1])
Date treatment stopped
Item
Treatment Stop Date (mm/dd/yy)
date
C1531784 (UMLS CUI [1])
Item
If treatment is continuing, please check
text
C1553904 (UMLS CUI [1])
Code List
If treatment is continuing, please check
CL Item
continuing therapy (C)
Item
Check, if patient had no Adverse Experiences
text
C0877248 (UMLS CUI [1])
Code List
Check, if patient had no Adverse Experiences
adverse event; Numbers
Item
Number of Adverse Experience
integer
C0877248 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Adverse event
Item
Adverse Experience
text
C0877248 (UMLS CUI [1])
Adverse Event Grade Code
Item
Grade per CTC
text
C2985911 (UMLS CUI [1])
Serious Adverse Event
Item
Serious Adverse Experience?
boolean
C1519255 (UMLS CUI [1])
Adverse Event Onset Date
Item
Adverse Experience Onset Date (mm/dd/yy)
date
C2985916 (UMLS CUI [1])
Adverse event; End Date
Item
Adverse Experience Stop Date (mm/dd/yy)
date
C0877248 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
If Adverse Experience is continuig, please check
text
C0877248 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
Code List
If Adverse Experience is continuig, please check
CL Item
continuing AE (C)
Item
Adverse Experience Frequency
text
C0877248 (UMLS CUI [1,1])
C0439603 (UMLS CUI [1,2])
Code List
Adverse Experience Frequency
Item
Therapeutic measures drug
text
C0013227 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0079809 (UMLS CUI [1,3])
Code List
Therapeutic measures drug
CL Item
infusion rate slowed (2)
CL Item
infusion stopped permanently (3)
Item
Other therapeutic measures
text
C0087111 (UMLS CUI [1,1])
C0079809 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Code List
Other therapeutic measures
CL Item
Procedure or physical therapy (3)
CL Item
Blood or blood products (4)
CL Item
Withdrawn from study (5)
CL Item
Prescription drug therapy (6)
CL Item
Non- prescription drug therapy (7)
CL Item
Hospitalization (8)
Therapeutic procedure; Measures; Other; Specification
Item
If other therapeutic measures not listed, specify
text
C0087111 (UMLS CUI [1,1])
C0079809 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Item
Adverse Experience Outcome
text
C1705586 (UMLS CUI [1])
Code List
Adverse Experience Outcome
CL Item
Complete recovery (1)
CL Item
Unknown/ lost to follow-up (3)
CL Item
AE persisting (4)
Item
Relationship between Adverse Experience and Drug
text
C0877248 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
Code List
Relationship between Adverse Experience and Drug
Item
Relationship between Adverse Experience and Disease
text
C0877248 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
Code List
Relationship between Adverse Experience and Disease