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Test Bank for Understanding Pharmacology Essentials for Medication Safety, 3rd Edition by M. Linda Workman & LaCharity

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Test Bank for Understanding Pharmacology Essentials for Medication Safety, 3rd Edition by M. Linda Workman & LaCharity

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Pharmacology Essentials
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Pharmacology Essentials
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Subido en
22 de mayo de 2023
Número de páginas
419
Escrito en
2022/2023
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Med C Med C Test Bank For Understanding Pharmacology, Essentials for Medication Safety, 3rd Edition,Workman & LaCharity Chapter 01: Drug Regulation, Actions, and Responses MULTIPLE CHOICE BASIC CONCEPTS 1. Which health care professional has the major responsibility for dispensing prescribed drugs under the direction of a pharmacist? a. Physician b . Nurse practitioner c. Licensed nurse d . Pharmacy technician ANS: D The physician and nurse practitioner have the major responsibility for prescribing drugs, not dispensing them. The licensed nurse has the primary responsibility for administering drugs, although under some circumstances a licensed nurse may dispense prescribed drugs but this is not his or her major responsibility in drug therapy. The pharmacy techn ician has the major responsibility of dispensing prescribed drugs under the direction of a licensed pharmacist. DIF: Cognitive Level: Remembering REF: p. 3 2. Which term describes the effect of a drug that improves body function? a. Side effect b . Intended action c. Adverse reaction d . Idiosyncratic response ANS: B The purpose of drug therapy is to take a drug to prevent, reduce, or correct a health problem. This response is any drug’s intended action also known as a therapeutic response. DIF: Cognitive Level: Remembering REF: p. 3 3. Which type of drug name is “owned” by the company that manufactures it? a. Generic name b Chemical name Med C . c. Category name d . Trade name ANS: D The chemical name is a drug’s exact chemical composition. The generic name is the name assigned to the drug by the U.S. Adopted Names Council and is not owned by anyone. The category name refers to the type of drug (what it does or what it is used for) and is not an actual drug name. The trade name (brand name) is the name provided and owned by a specific drug’s manufacturer. DIF: Cognitive Level: Remembering REF: p. 4 4. Which drug or drug class is a “high alert” drug? a. Penicillin b . Insulin c. NSAIDs d . Calcium ANS: B A high alert drug is one in which harm is likely to result if given at the wrong dose, to the wrong patient, or not given to the correct patient. Drugs classified as high alert drugs include potassium, narcotics (opioids), insulin, cancer chemotherapy drugs, and heparin (or any drug that strongly affects blood clotting). Penicillin, NSAIDs, and calcium are not considered high alert drugs. DIF: Cognitive Level: Remembering REF: p. 4 5. What is the term for a drug that has the same action as a naturally occurring body hormone or enzyme? a. Agonist b . Blocking agent c. Chemical d . Duplicator ANS: A A drug agonist is an extrinsic drug that activates the receptor sites of a cell and mimics the actions of naturally occurring body substances (intrinsic drugs). A blocking agent is a drug Med C antagonist. A chemical would not necessarily be a drug at all. A duplicator is not a pharmacologic term. DIF: Cognitive Level: Remembering REF: pp. 6 -7 6. Which term describes how the body affects drug activity? a. Drug potency b . Pharmacodynamics c. Therapeutic effect d . Pharmacokinetics ANS: D The term pharmacokinetics refers to drug metabolism and how the body changes a drug. Pharmacodynamics refers to how a drug works to change body function. Drug potency refers to how strongly or to what degree a drug exerts its effects. The therapeutic effec t is closer to pharmacodynamics, meaning how a drug works to change body function. DIF: Cognitive Level: Remembering REF: p. 10 7. In the United States, which group is responsible for enforcing established standards for drug manufacturing? a. U.S. Pharmacopeia b . National Institutes of Health c. Food and Drug Administration d . Association of Pharmaceutical Manufacturers ANS: C The standards for drug manufacture are established by the U.S. Pharmacopeia. These standards are enforced by the Food and Drug Administration. Neither the National Institutes of Health nor the Association of Pharmaceutical Manufacturers has any authority to enforce drug standards. DIF: Cognitive Level: Remembering REF: p. 5 8. Which factor is a major disadvantage of the transdermal drug delivery route? a. Only a prescriber can administer drugs by the transdermal route. b . Transdermal drugs must be sterile rather than clean. c. First pass drug loss by this route is the most extensive. d Drug absorption is dependent on adequate circulation.
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