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ID

42017

Description

Study part: Previous/ 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"

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Versions (2)
  1. 5/16/17 5/16/17 -
  2. 3/15/21 3/15/21 - Dr. rer. medic Philipp Neuhaus
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Roche

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March 15, 2021

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Creative Commons BY-NC 3.0
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    PREVIOUS/ CONCOMITANT MEDICATIONS Roche H0650g Breast Cancer

    English

    PREVIOUS/ CONCOMITANT MEDICATIONS

    1 forms  
    PREVIOUS/ CONCOMITANT MEDICATIONS
    Description

    PREVIOUS/ 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]
    C3173309
    DATE OF FINAL DOSE- ONGOING?
    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
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    Similar models

    PREVIOUS/ CONCOMITANT MEDICATIONS

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    PREVIOUS/ 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
    C3173309 (UMLS CUI [1])
    CONCOMITANT MEDICATIONS
    Item
    DATE OF FINAL DOSE- ONGOING?
    boolean
    C2347852 (UMLS CUI [1])
    therapy end date
    Item
    DATE OF FINAL DOSE
    date
    C1531784 (UMLS CUI [1])
    Back to the top of the page 

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