| Term 
 | Definition 
 
        | what happens to a drug from the time it is introduced into the body until it reaches the circulating fluids and tissues |  | 
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        | Term 
 | Definition 
 
        | the physiologic ability of the drug to reach its target cells and produce its effect |  | 
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        | Term 
 | Definition 
 
        | the enzymatic alteration of drug structure; often takes place in the liver; also called drug metabolism |  | 
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        | Term 
 | Definition 
 
        | movement of a drug to the body's tissues following absorption |  | 
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        | Term 
 | Definition 
 
        | the enzymatic alteration of drug structure; most drug metabolism takes place in the liver; also called biotransformation |  | 
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        | Term 
 | Definition 
 
        | many drugs bind reversibly to plasma proteins, particularly albumin; these complexes are too large to cross capillary membranes; thus, the drug is not available for distribution to body tissues; drugs bound to proteins circulate in the plasma until they are released or displaced from the protein to which they are bound |  | 
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        | Term 
 
        | Enterohepatic recirculation |  | Definition 
 
        | most bile is circulated back to the liver; may prolong the effects of a drug |  | 
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        | Term 
 | Definition 
 
        | an increased metabolic activity in the liver that is caused by a drug or other substance |  | 
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        | Term 
 
        | Enzyme induction [example] |  | Definition 
 
        | phenobarbital increases the rate of its own metabolism, as well as that of other drugs metabolized in the liver |  | 
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        | Term 
 | Definition 
 
        | removal of a drug from the body, such as via the skin, saliva, lungs, bile, kidneys, and feces |  | 
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        | Term 
 | Definition 
 
        | a phenomenon that occurs following ingestion of an oral drug, in which a large percentage of the drug is destroyed in the gastrointestinal system or liver and never reaches the tissues |  | 
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        | Term 
 | Definition 
 
        | the time it takes for the amount of drug in the body to decrease to one-half of the peak level it previously achieved |  | 
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        | Term 
 | Definition 
 
        | process of chemically converting a drug to a form that is usually more easily removed from the body |  | 
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        | Term 
 | Definition 
 
        | hepatic microsomal enzymes that inactivate drugs and either accelerate their excretion, or produce a chemical alteration that makes the resulting molecule more active than the original |  | 
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        | Term 
 | Definition 
 
        | the length of time required for the plasma concentration of a medication to decrease by one-half after administration |  | 
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        | Term 
 | Definition 
 
        | level of drug in the plasma is maintained continuously within the therapeutic range; the amount of drug administered has reached equilibrium with the amount of drug being eliminated, resulting in the distribution of a continuous therapeutic level of drug to body tissues |  | 
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        | Term 
 
        | Primary site of excretion of excretion of drugs |  | Definition 
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        | Term 
 
        | Primary site of metabolism of drugs |  | Definition 
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        | Term 
 | Definition 
 
        | drugs that have no pharmacologic activity unless they are first metabolized to their active form |  | 
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        | Term 
 | Definition 
 
        | after drug administration, the time when the plasma concentration of the medication falls below the minimum effective concentration |  | 
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