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    Bioavailability Protein Binding Metabolism Half-Life Excretion

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    ErwinRamadhani
    The document discusses the pharmacokinetic properties of three drugs: cimetidine, ranitidine, and clayden. It provides information on the bioavailability, protein binding, metabolism, half-life, and excretion of each drug. Cimetidine has a bioavailability of 60-70%, protein binding of 15-20%, is metabolized in the liver, has a half-life of 2 hours, and is excreted renally. Ranitidine has a bioavailability of 39-88%, protein binding of 15%, is metabolized in the liver, has a half-life of 2-3 hours, and is 30-70% renally excreted. The document also lists a source

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    Bioavailability Protein Binding Metabolism Half-Life Excretion

    Uploaded by

    ErwinRamadhani
    15 views1 page
    The document discusses the pharmacokinetic properties of three drugs: cimetidine, ranitidine, and clayden. It provides information on the bioavailability, protein binding, metabolism, half-life, and excretion of each drug. Cimetidine has a bioavailability of 60-70%, protein binding of 15-20%, is metabolized in the liver, has a half-life of 2 hours, and is excreted renally. Ranitidine has a bioavailability of 39-88%, protein binding of 15%, is metabolized in the liver, has a half-life of 2-3 hours, and is 30-70% renally excreted. The document also lists a source

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    yr

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    referat simetidin ranitidin

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    The document discusses the pharmacokinetic properties of three drugs: cimetidine, ranitidine, and clayden. It provides information on the bioavailability, protein binding, metabolism, half-life, and excretion of each drug. Cimetidine has a bioavailability of 60-70%, protein binding of 15-20%, is metabolized in the liver, has a half-life of 2 hours, and is excreted renally. Ranitidine has a bioavailability of 39-88%, protein binding of 15%, is metabolized in the liver, has a half-life of 2-3 hours, and is 30-70% renally excreted. The document also lists a source

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Flag for inappropriate content
    Download as docx, pdf, or txt
    15 views1 page

    Bioavailability Protein Binding Metabolism Half-Life Excretion

    Uploaded by

    ErwinRamadhani
    The document discusses the pharmacokinetic properties of three drugs: cimetidine, ranitidine, and clayden. It provides information on the bioavailability, protein binding, metabolism, half-life, and excretion of each drug. Cimetidine has a bioavailability of 60-70%, protein binding of 15-20%, is metabolized in the liver, has a half-life of 2 hours, and is excreted renally. Ranitidine has a bioavailability of 39-88%, protein binding of 15%, is metabolized in the liver, has a half-life of 2-3 hours, and is 30-70% renally excreted. The document also lists a source

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
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    Download as docx, pdf, or txt
    of 1

    Daftar pustaka

    Gambar cimetidine
    Clayden, Jonathan (2005). Organic chemistry (Reprinted (with corrections). ed.).
    Oxford [u.a.]: Oxford Univ. Press. p. 587. ISBN 0198503466.
    Ranitidin

    Pharmacokinetic data
    Bioavailability
    39 to 88%
    Protein binding
    15%
    Metabolism
    Hepatic
    Half-life
    23 hours
    Excretion
    3070% Renal
    Cimetidin

    Pharmacokinetic data
    Bioavailability
    6070%
    Protein binding
    1520%
    Metabolism
    Hepatic
    Half-life
    2 hours
    Excretion
    Renal

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