Item
Cycle Number
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C2045829 (UMLS CUI [1,3])
Item
Day
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
Experimental drug, Dosage, Start Date
Item
Infusion Start Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Experimental drug, Dosage, Start Time
Item
Infusion Start Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
Experimental drug, Dosage, End Date
Item
Infusion Stop Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Experimental drug, Dosage, End Time
Item
Infusion Stop Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
Experimental drug, Dosage
Item
Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Experimental drug, Dosage, Actual
Item
Actual Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0237400 (UMLS CUI [1,3])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 1, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 1, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 2, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 2, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 2, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 2, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 3, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 3, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 3, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 3, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 4, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 4, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 4, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 4, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 6, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 6, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 6, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 6, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Item
Cycle Number
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C2045829 (UMLS CUI [1,3])
Item
Day
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
Experimental drug, Dosage, Start Date
Item
Infusion Start Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Experimental drug, Dosage, Start Time
Item
Infusion Start Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
Experimental drug, Dosage, End Date
Item
Infusion Stop Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Experimental drug, Dosage, End Time
Item
Infusion Stop Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
Experimental drug, Dosage
Item
Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Experimental drug, Dosage, Actual
Item
Actual Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0237400 (UMLS CUI [1,3])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 2 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 2 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 3 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 3 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 4 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 4 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])