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Lpn fall 2008

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Question
Answer
Pharmacology   the study of drugs & their action on living organisms.  
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Orphan drug program act   passed in 1983 to encourage the development & marketing of products used to treat rare diseases.  
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Trade name (brand name)   name that is registered by the manufacturer & is followed by the trademark symbol; the name can be used only by the manufacturer; a drug may have several trade names depending on the # of manufacturers; 1st letter is capitalized. Official name  
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Generic name (nonproprietary)   Name given to a drug before it becomes official; may be used in all countries; by all manufacturers, the generic name is not capitalized.  
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Chemical name (scientific name)   Gives the exact chemical makeup of the drug & placing of the atoms or molecular structure; the chemical name is not capitalized.  
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Prescription drugs   designated by the federal government as potentially harmful unless their use is supervised by a licensed health care provider, such as a nurse practitioner, physician, or dentist.  
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Nonprescription drugs   designated by the FDA as safe when taken as directed & can be obtained w/out a prescription.  
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Controlled substances   most carefully monitored of all drugs, have high potential for abuse & may cause physical or psychological dependency.  
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Controlled substances Act   passed in 1970 regulates the manufacture, distribution, & dispensing of drugs that have abuse potential.  
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Drugs under the controlled substances Act   are divided into five schedules, based on their potential for abuse & physical & psychological dependence.  
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Physical dependency   a compulsive need to use a substance repeatedly to avoid mild to severe withdrawal symptoms; it is the body’s dependence on repeated administration of a drug.  
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Psychological dependency   a compulsion to use a substance to obtain a pleasurable experience; it is the minds’ dependence on the repeated administration of a drug.  
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Teratogen   any substance that causes abnormal development of the fetus, often leading to severe deformation.  
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Pharmaceutics phase   dissolution of the drug occurs, drugs must be soluble to be absorbed. Drugs that are liquid or drugs given by injection (parenteral drugs) are already dissolved & are absorbed quickly. Tablets that are enteric coating do not disintegrate until they reach  
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Enteric coated tablets   can not be crushed.  
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Pharmacokinetics   refers to activities w/in the body after a drug is administered which include: absorption, distribution, metabolism, & excretion.  
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Half   life is a measure of the rate @ which drugs are removed from the body. Refers to the time required for the body to eliminate 50% of the drug.  
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Absorption   follows administration & is the process by which a drug is made available for use in the body.  
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Distribution   systemic circulation distributes drugs to various body tissues or target sites. Drugs interact w/ specific receptors during distribution.  
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Active transport   cellular energy is used to move the drug from an area of low concentration to one of high concentration.  
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Passive transport   no cellular energy is used as the drug moves from an area of high concentration to an area of low concentration (small molecules diffuse across cell membrane).  
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Pincytosis   cells engulf the drug particle (the cell forms a vesicle to transport the drug into the inner cell).  
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1st pass effect   may also affect absorption. When a drug is absorbed by the small intestine it travels to the liver before being released to circulate to the rest of the body. Liver may metabolize a significant amt of the drug before releasing it again into the body.  
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Metabolism (biotransformation)   process by which the body changes a drug to a more or less active form that can be excreted. Usually resulting form is metabolite.  
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Metabolite   an inactive form of the original drug, may undergo further metabolism r may be excreted from the body unchanged. Most drugs are metabolized by the liver, although the kidneys, lungs, plasma, & intestinal mucosa also aid in the metabolism of drugs.  
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Excretion   elimination of drugs from the body. After the liver renders drugs inactive, the kidney excretes the inactive compounds from the body. Some drugs are excreted unchanged by the kidney w/out liver involvement.  
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Onset of action   time between administration of the drug & onset of its therapeutic effect.  
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Peak concentration   when absorption rate equals the elimination rate (not always the time of peak response).  
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Duration of action   length of time the drug produces a therapeutic effect.  
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Pharmacodynamics   the study of the drug mechanisms that produce biochemical or physiologic changes in the body. Drug exerts it action by; alteration in cellular function & alteration in cellular environment.  
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Receptor   reactive site on the surface of a cell; when a drug binds to & interacts w/ the receptor, a pharmacologic response occurs.  
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Agonist   a drug that binds w/ a receptor & stimulates the receptor to produce a therapeutic response.  
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Antagonist   a drug that joins w/ receptors but does not stimulate the receptors.  
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Adverse reactions   undesirable drug effects; may be common or may occur infrequently. Maybe mild, severe, or life threatening.  
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Allergic reaction (hypersensitivity)   allergy to a drug usually begins to occur after more than one dose of the drug is given.  
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Antigen   a drug allergy occurs b/c the individual’s immune system views the drug as foreign substance. Antibodies  
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Examples of some allergic symptoms   include itching, various types of skin rashes, & hives (urticaria), other symptoms include difficulty breathing, wheezing, cyanosis, a sudden loss of consciousness, & swelling of the eyes, lips, or tongue.  
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Anaphylactic shock   an extremely serious allergic drug reaction that usually occurs shortly after the administration of a drug to which the individual is sensitive.  
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Angioedema (angioneurotic edema)   another type of allergic drug reaction. It is manifested by the collection of fluid in subcutaneous tissues. Areas that are most commonly affected are the eyelids, lips, mouth, & throat, although other areas also may be affected.  
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Drug idiosyncrasy   any unusual or abnormal reaction to a drug. Ex; pt maybe given a drug to help him or her sleep instead of falling asleep, the pt remains wide awake & shows signs of nervousness or excitement.  
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Drug tolerance   decreased response to a drug, requiring an increase in dosage to achieve the desired effect. Drug tolerance may develop when a pt takes certain drugs, such as narcotics & tranquilizers, for a long time.  
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Cumulative drug effect   may be seen in those w/ liver or kidney disease b/c these organs are the major sites for the breakdown & excretion of most drugs. This occurs when the body is unable to metabolize & excrete 1 normal dose of a drug before the next dose is given.  
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Toxic reactions   most drugs can produce toxic or harmful reactions if administered in large dosages or when blood concentration levels exceed the therapeutic level.  
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Pharmacogenetic disorder   a genetically determined abnormal response to normal doses of a drug.  
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Drug/drug interactions   occurs when one drug interacts w/ or interferes w/ the action of another drug. Ex: taking an antacid w/ oral tetracycline causes decrease in effectiveness of the tetracycline. The antacid chemically interact w/ the tetracycline & impairs its absorption i  
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Additive drug reaction   occurs when the combined effect of two drugs is equal to the sum of each drug given alone. Ex: taking the drug heparin w/ alcohol will increase bleeding.  
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Synergism   occurs when drugs interact w/ each other & produce an effect that is greater than the sum of their separate actions.  
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Antagonistic drug reaction   occurs when one drug interferes w/ the action of another, causing neutralization or a decrease in the effect of one drug. Ex: protamine sulfate is heparin antagonist, meaning that the administration of protamine sulfate completely neutralizes the effects  
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Drug food interactions   When drugs are given orally food may impair or enhances its absorption. A drug taken on an empty stomach is absorbed into the bloodstream more quickly than when the drug is taken w/ food in the stomach.  
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Polypharmacy   the taking of numerous drugs that can potentially react w/ 1 another.  
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