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  2. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    For example, steady-state concentrations of drugs eliminated mostly by the kidney are usually greater in patients with kidney failure than they are in patients with normal kidney function receiving the same drug dosage. Population pharmacokinetics seeks to identify the measurable pathophysiologic factors and explain sources of variability that ...

  3. Category:Pharmacology templates - Wikipedia

    en.wikipedia.org/.../Category:Pharmacology_templates

    [[Category:Pharmacology templates]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Pharmacology templates]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.

  4. Plateau principle - Wikipedia

    en.wikipedia.org/wiki/Plateau_Principle

    The plateau principle is a mathematical model or scientific law originally developed to explain the time course of drug action (pharmacokinetics). [1] The principle has wide applicability in pharmacology, physiology, nutrition, biochemistry, and system dynamics.

  5. Elimination rate constant - Wikipedia

    en.wikipedia.org/wiki/Elimination_rate_constant

    The elimination rate constant K or K e is a value used in pharmacokinetics to describe the rate at which a drug is removed from the human system. [1]It is often abbreviated K or K e.

  6. Drug metabolism - Wikipedia

    en.wikipedia.org/wiki/Drug_metabolism

    Drug metabolism is the metabolic breakdown of drugs by living organisms, usually through specialized enzymatic systems. More generally, xenobiotic metabolism (from the Greek xenos "stranger" and biotic "related to living beings") is the set of metabolic pathways that modify the chemical structure of xenobiotics, which are compounds foreign to an organism's normal biochemistry, such as any drug ...

  7. Absorption (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Absorption_(pharmacology)

    Zero-order absorption: rate of absorption is constant. A common example is continuous intravenous infusion. First-order absorption: rate of absorption is proportional to the amount of drug remaining to be absorbed. Representative examples include typical cases of oral administration, subcutaneous injection, and intramuscular injection.

  8. Biological half-life - Wikipedia

    en.wikipedia.org/wiki/Biological_half-life

    So, for example, digoxin has a half-life (or t ⁠ 1 / 2 ⁠) of 24–36 h; this means that a change in the dose will take the best part of a week to take full effect. For this reason, drugs with a long half-life (e.g., amiodarone , elimination t ⁠ 1 / 2 ⁠ of about 58 days) are usually started with a loading dose to achieve their desired ...

  9. Pharmaceutical manufacturing - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_manufacturing

    Pharmaceutical manufacturing is the process of industrial-scale synthesis of pharmaceutical drugs as part of the pharmaceutical industry. The process of drug manufacturing can be broken down into a series of unit operations, such as milling, granulation, coating, tablet pressing, and others.