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The process whereby a drug is moved from the site of application into the body and into the extracellular fluid compartment. |
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The tendency of a drug to combine with a specific drug receptor. |
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A drug or other substance that binds with a specific drug receptor and causes a physiological response. |
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Protein found in almost all animal tissue. It constitutes one of the major proteins in human blood. |
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A drug or other substance that blocks a physiological response or that blocks the action of another drug or substance. |
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The degree to which a drug is bound to tissue or plasma proteins. |
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Biotransformation, also called metabolism, is the process of changing a drug into a different form, either active or inactive, by the body. |
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Protective mechanism that selectively allows the entry of specific compounds into the brain. It is an effective boundary between the central nervous system and the peripheral nervous system. |
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A phenomenon that occurs when a drug is administered in several doses, causing an increased effect. It is usually due to a buildup of a drug in the blood. |
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The process whereby a drug is transported from the site of absorption to the site of action. |
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The power of a drug to produce a therapeutic effect. |
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The process whereby a drug is removed from the body by excretion into the urine, feces, bile, saliva, sweat, breast milk, or expired air. |
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The elimination of waste products from the body. Excretion is often used interchangeably with the term elimination. |
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of a broad category of simple proteins found in the body. |
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The time required for a level of a drug in the blood to be reduced by 50 percent of its beginning level. |
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An iron-containing compound found within the blood cell that is responsible for the transport and delivery of oxygen to the body cells. |
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The initial dose of a drug given in a sufficient amount to achieve a therapeutic plasma level. |
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The dose of a drug necessary to maintain a constant therapeutic plasma level. |
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The sum total of all physical and chemical changes that occur within the body. In pharmacology it is often used interchangeably with the term biotransformation. |
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minimum effective concentration |
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The minimum amount of drug needed in the bloodstream to cause the desired therapeutic effect. |
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The time interval between the administration of a drug and the first sign of its onset; onset of action is influenced by the physical and chemical properties of a drug as well as by its route of administration. |
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A scientific method of expressing the acidity or alkalinity of a solution, which is the logarithm of the hydrogen ion concentration divided by 1. The higher the pH, the more alkaline the solution; the lower the pH, the more acidic the solution. |
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The study of a drug's action on the body. |
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The study of how drugs enter the body, reach their site of action, and eventually are eliminated. |
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The amount of the drug present in the plasma. The peak plasma level refers to the highest concentration produced by a specific dose. |
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The tendency of a drug to dissolve. |
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An index of the drug's safety profile, which is determined by calculating the difference between the drug's therapeutic threshold and toxic level. It is typically determined in the laboratory. |
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The difference between the minimal therapeutic and toxic concentrations of a drug. Drugs with a low therapeutic range present a higher risk of toxicity than do drugs with a high therapeutic range. The therapeutic range is also referred to as the margin of safety. |
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The minimum amount of drug needed in the bloodstream to cause a desired therapeutic effect. |
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The degree to which a substance is poisonous. At high doses drugs can produce toxic effects that are not seen at low doses. |
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The plasma level at which severe adverse reactions are expected or likely. |
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