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Define pharmacodynamics.
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The study of drug interactions including the drug receptors and the series of events that culminates the pharmacologic response.
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Define receptors.
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The sites on the cells where chemical bonding of drugs occurs.
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Define agonists.
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Drugs that STIMULATE a response at a receptor site.
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Define antagonists.
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Drugs that attach to receptor sites but do NOT stimulate a response.
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Define partial agonists.
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Drugs that interact with a receptor to stimulate a response and concurrently inhibit other responses are partial agonists.
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Define ADME.
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The four stages of drug processing: absorption, distribution, metabolism, and exretion.
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Define pharmacokinetics.
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The study of the mathematical relationship among the ADME of medicines.
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Define absorption.
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The process by which the drug is made available to the body fluids for distribution.
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Define enteral.
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The enteral route of drug administration is placing the drug directly into the gastrointestinal tract by ORAL, RECTAL, or NASOGASTRIC routes.
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Define parenteral.
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Routes of administration are SUBCUTANEOUS, INTRAMUSCULAR (IM), or INTRAVENOUS (IV) INJECTION
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Define percutaneous.
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Routes of administration are done via INHALATION, SUBLINGUAL, or TOPICAL.
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Define distribution.
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The ways in which the drug is transported via the body fluids to the sites of action for metabolism and excretion.
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Drug blood level.
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Measures the amount of drug present in the blood to determine if it is within, below (subtherapeutic), or above (toxic) the therapeutic range.
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Drugs that interact with a receptor to stimulate a response are known as _____________.
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Agonists
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The study of the mathematical relationships among the absorption, distribution, metabolism, and excretion of individual medicines over time is called ______________.
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Pharmacokinetics
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