ID

22131

Description

Study part: 60 Days Post- Treatment Concomitant medications. A phase III multinational, randomized, single-blind study of recombinant humanized anti-p185HER2 monoclonal antibody (rhuMAb HER2) in patients with HER2/neu overexpression who have not received prior cytotoxic chemotherapy for metastatic breast cancer. "Terms of use: You may not use this document or the information contained herein to a regulatory authority in connection with an application for a marketing authorization or any other regulatory submission without the express written consent of Roche"

Keywords

Versions (2)
  1. 5/20/17 5/20/17 -
  2. 3/15/21 3/15/21 - Dr. rer. medic Philipp Neuhaus
Copyright Holder

Roche

Uploaded on

May 20, 2017

DOI

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License

Creative Commons BY-NC 3.0
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60 DAYS POST-TREATMENT CONCOMITANT MEDICATIONS Roche H0650g Breast Cancer

English

60 DAYS POST-TREATMENT CONCOMITANT MEDICATIONS

1 forms  
CONCOMITANT MEDICATIONS
Description

CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C2347852
PATIENT INT.
Description

Patient initial

Data type

text

Alias
UMLS CUI [1]
C2986440
PATIENT NUMBER
Description

Patient id

Data type

integer

Alias
UMLS CUI [1]
C2348585
DRUG NAME
Description

concomitant medication

Data type

text

Alias
UMLS CUI [1]
C2347852
INDICATION- PROPHYLAXIS ?
Description

Prophylaxis Indication medication

Data type

boolean

Alias
UMLS CUI [1,1]
C0199176
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0013227
INDICATION
Description

Indication medication

Data type

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
TOTAL DAILY DOSE- PRN ?
Description

TOTAL DAILY DOSE

Data type

boolean

Alias
UMLS CUI [1]
C2348070
TOTAL DAILY DOSE (units)
Description

TOTAL DAILY DOSE

Data type

float

Alias
UMLS CUI [1]
C2348070
DATE OF FIRST DOSE
Description

therapy start date

Data type

date

Alias
UMLS CUI [1]
C1531783
FIRST DOSE- CONTINUING?
Description

CONCOMITANT MEDICATIONS

Data type

boolean

Alias
UMLS CUI [1]
C2347852
DATE OF FINAL DOSE
Description

therapy end date

Data type

date

Alias
UMLS CUI [1]
C1531784
FINAL DOSE- ONGOING?
Description

CONCOMITANT MEDICATIONS

Data type

boolean

Alias
UMLS CUI [1]
C2347852
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Similar models

60 DAYS POST-TREATMENT CONCOMITANT MEDICATIONS

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
CONCOMITANT MEDICATIONS
C2347852 (UMLS CUI-1)
Patient initial
Item
PATIENT INT.
text
C2986440 (UMLS CUI [1])
Patient id
Item
PATIENT NUMBER
integer
C2348585 (UMLS CUI [1])
concomitant medication
Item
DRUG NAME
text
C2347852 (UMLS CUI [1])
Prophylaxis Indication medication
Item
INDICATION- PROPHYLAXIS ?
boolean
C0199176 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
Indication medication
Item
INDICATION
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
TOTAL DAILY DOSE
Item
TOTAL DAILY DOSE- PRN ?
boolean
C2348070 (UMLS CUI [1])
TOTAL DAILY DOSE
Item
TOTAL DAILY DOSE (units)
float
C2348070 (UMLS CUI [1])
therapy start date
Item
DATE OF FIRST DOSE
date
C1531783 (UMLS CUI [1])
CONCOMITANT MEDICATIONS
Item
FIRST DOSE- CONTINUING?
boolean
C2347852 (UMLS CUI [1])
therapy end date
Item
DATE OF FINAL DOSE
date
C1531784 (UMLS CUI [1])
CONCOMITANT MEDICATIONS
Item
FINAL DOSE- ONGOING?
boolean
C2347852 (UMLS CUI [1])
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