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 | Definition 
 
        | Liquid dose form in an alcohol solution administered orally. |  | 
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        | Term 
 | Definition 
 
        | Drug suspended within an oil or liquid fat. |  | 
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 | Definition 
 
        | Topically applied dose form; drug is dissolved in alcohol. |  | 
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 | Definition 
 
        | Drug made from processed animal organs or plants. |  | 
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 | Definition 
 
        | Solid (powedered) dose form covered in gelatin. |  | 
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 | Definition 
 
        | Semisolid dose form that liquefies at body temperature. |  | 
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 | Definition 
 
        | Sucrose or other sugar-based liquid dose form administered orally. |  | 
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 | Definition 
 
        | Semisolid dose form that does not melt at body temperature. |  | 
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        | Term 
 
        | Sustained-release formulations |  | Definition 
 
        | Oral dosage form formulated to dissolve slowly as it moves through the GI tract. |  | 
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 | Definition 
 
        | Drug form formulated to be protected against stomach acid. |  | 
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 | Definition 
 
        | Drug produced by companies other than the original developer. |  | 
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 | Definition 
 
        | Small, airtight glass containers containing drug; meant to be broken open to extract the drug; used only one time. |  | 
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        | Term 
 | Definition 
 
        | Type of drug meant to be absorbed over a prolonged period of time after being injected. |  | 
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        | Term 
 | Definition 
 
        | The ingredient of the drug formulation that includes preservatives, stabilizers, and liquid media into which the drug is dissolved or suspended. |  | 
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        | Term 
 | Definition 
 
        | The reason or the condition for which the drug is to be used. |  | 
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        | Term 
 | Definition 
 
        | Any use of a drug in a manner other than that approved by the FDA. |  | 
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        | Term 
 | Definition 
 
        | Any effect of the drug other than the intended effect. |  | 
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        | Term 
 | Definition 
 
        | The chemical composition of a drug. |  | 
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        | Term 
 | Definition 
 
        | Generic name; a name given to the specific chemical compound. Usually listed as the active ingredient. |  | 
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        | Term 
 | Definition 
 
        | Trade name; the unique name a manufacturer gives its particular brand of drug. |  | 
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        | Term 
 | Definition 
 
        | The amount of drug administered at one time. |  | 
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        | Term 
 | Definition 
 
        | The general amount that any animal or patient should be given over time. |  | 
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 | Definition 
 
        | Circumstances in which the drug should not be used. |  | 
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        | Term 
 | Definition 
 
        | A drug that is considered toxic, potentially toxic if misused, or too readily misused. |  | 
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        | Term 
 | Definition 
 
        | Drugs considered safe for the animal, the person administering the medication, people coming into contact with the animal, the human food chain, and the environment. |  | 
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        | Term 
 | Definition 
 
        | A substance that has the potential for physical addiction, psychological addiction, and/or abuse. |  | 
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        | Term 
 | Definition 
 
        | Extreme potential for abuse and no approved medicinal purpose in the United States. |  | 
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        | Term 
 | Definition 
 
        | High potential for abuse and may lead to severe physical or psychological dependence. |  | 
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        | Term 
 | Definition 
 
        | Some potential for abuse; may lead to low to moderate physical dependence or high psychological dependence. |  | 
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        | Term 
 | Definition 
 
        | Low potential for abuse; limited physical or psychological dependence. |  | 
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        | Term 
 | Definition 
 
        | Subject to state and local regulations; low potential for abuse. |  | 
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        | Term 
 | Definition 
 
        | Occupational Safety and Health Administration. |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | Drugs used to treat cancer. |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | Induce cancer or preneoplastic changes. |  | 
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        | Term 
 | Definition 
 
        | Ideal range of drug concentrations within the body. |  | 
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        | Term 
 | Definition 
 
        | Larger than the drug's maintenance dose and is designed to raise the drug concentration to the theraputic range in a short time. |  | 
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        | Term 
 | Definition 
 
        | Smaller doses of drug administered to maintain the theraputic concentrations established by the loading dose. |  | 
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        | Term 
 | Definition 
 
        | The degree to which an administered drug is absorbed. |  | 
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        | Term 
 | Definition 
 
        | The liver removes so much of the drug that little reaches the systemic circulation. |  | 
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        | Term 
 | Definition 
 
        | The movement of drug from the blood, to the tissue, back to the blood, and to a second tissue. |  | 
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        | Term 
 
        | Volume of Distribution (Vd) |  | Definition 
 
        | A pharmacokinetic value that provides an approximation of the extent to which a drug is distributed throughout the body. |  | 
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        | Term 
 | Definition 
 
        | Types of compounds used as drugs that physically combine with ions or other specific compounds in the environment to produce their effects. |  | 
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        | Term 
 | Definition 
 
        | Drug metabolism; Drugs altered by the enzymes and chemical reactions in the body before they are eliminated. |  | 
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        | Term 
 | Definition 
 
        | Drugs that require biotransformation to become active. |  | 
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        | Term 
 | Definition 
 
        | The active form of the drug is more rapidly converted to a less-active form shortening the time in the body that the drug can be effective. |  | 
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        | Term 
 | Definition 
 
        | Elimination of drugs by the liver. |  | 
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        | Term 
 
        | Enterohepatic circulation |  | Definition 
 
        | Movement of drug from liver to intestinal tract and back to the liver. |  | 
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        | Term 
 | Definition 
 
        | The measure of how fast a volume of blood is cleared of the drug and is expressed as a volume of blood cleared over time. |  | 
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        | Term 
 | Definition 
 
        | A time value that describes how long the drug concentration, usually measured in the blood, takes to decrease by 50%. |  | 
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