Test Bank for Essentials of Pharmacology for Health Professions 9th Edition (Cengage, 2022) by Bruce Colbert, Adam James and Elizabeth Katrancha, Isbn no; 9780357618301, all 27 Chapters Covered

,Chapter 1 Consumer Safety and Drug Regulations
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,Chapter 1 Consumer Safety and Drug Regulations
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1. A client calls her primary care provider requesting a prescription for an antidepressant medication. She tellst
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he nurse that she is severely depressed and would like the prescription called in to her local pharmacy. How s
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hould the nurse respond?
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a. The nurse encourages the client to see a psychiatric professional for an evaluation to obtain the
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prescription.
b. The nurse tells the client to ask the pharmacist to recommend an over-the-counter antidepressant.
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c. The nurse can offer to write the client a prescription if it is a refill.
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d. The nurse offers to give the client a few samples to use until her next appointment.
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ANSWER: a
FEEDBACK:
a. The client should be encouraged to seek a psychiatric professional evaluation to
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obtainthe prescription. sf sf


b. Antidepressants are not sold as over-the- sf sf sf sf sf

counter medications; a prescription is required.Try again.
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c. The nurse cannot write a prescription without evaluating the client. Try again.
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d. Samples are not given out to a client who has not been evaluated by a practitioner. Tr
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yagain.
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POINTS: 1
QUESTION TYPE: sf s f Multiple Choice sf


HAS VARIABLES: sf s f False
DATE CREATED: sf 11/26/2017 8:16 PM sf sf


DATE MODIFIED: sf s f 11/26/2017 8:32 PM sf sf




2. A client visits her health care provider for her annual physical. She questions the nurse regarding the use of
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an herbal supplement that she saw advertised on television for weight loss. What information can the nurse sh
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are with her client?
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a. The production of herbal medicines is not regulated by the FDA.
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b. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), the FDA is responsiblef
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or ensuring that a dietary supplement is safe before it is marketed.
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c. Herbal medicines are tested by the FDA to determine if they have interactions with prescribed
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medications.
d. Herbal medicines, while not approved by the FDA, are considered harmless.
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ANSWER: a
FEEDBACK: a. The production of herbal medicines is not regulated by the FDA.
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b. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), the dietar
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ymanufacturer is responsible for ensuring that a dietary supplement is safe before it i
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s marketed. Try again.
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c. The FDA does not test supplements. Try again.
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d. There are documented interactions with specific herbal supplements and prescribe
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dmedications. Try again.
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POINTS: 1
QUESTION TYPE: sf s f Multiple Choice sf


HAS VARIABLES: sf s f False
DATE CREATED: sf 11/26/2017 8:22 PM sf sf


DATE MODIFIED: sf s f 11/26/2017 8:32 PM sf sf



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, Chapter 1 Consumer Safety and Drug Regulations
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3. Upon leaving the exam room, a client tells the nurse that she is confused regarding her prescription. She asks t
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he nurse if a cheaper, generic drug will be weaker than her current prescription. How should the nurse respond?
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a. Drug standards assure consumers that the same drug must be of uniform strength, quality, and purity.
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b. The prescribed medication is of better quality but will cost more.
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c. The insurance companies mandate there are different strengths between generic and brand name
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prescriptions.
d. Every drug has a different chemical composition that cannot be duplicated.
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ANSWER: a
FEEDBACK:
a. Drug standards assure consumers that the same drug must be of uniform str
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ength,quality, and purity. sf sf sf


b. Generic and trade drugs are the same medication. Generic is the name that is assigne
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dto a new drug. The trade name is the name the pharmaceutical company assigns to t
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hatdrug to have exclusive rights to market it. Try again.
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c. Insurance companies have no control over the production of medication. Try again.
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d. The laws regulating drugs state that consumers can be assured that all preparation
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swith the same name have the same uniform strength, quality, and purity. Try again
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.
POINTS: 1
QUESTION TYPE: sf s f Multiple Choice sf


HAS VARIABLES:
sf s f False
DATE CREATED:sf 11/26/2017 8:23 PM sf sf



DATE MODIFIED:
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4. The FDA, under the direction of the Department of Health and Human Services, mandates which of thef
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ollowing?
a. Prescription and nonprescription drugs must be shown to be effective as well as safe.
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b. All labels must include a listing of active ingredients; some labels require a listing of inactivei
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ngredients as well. sf sf


c. All new products must be tested by the FDA before being released to the public.
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d. All drugs must have "warning" labels.
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ANSWER: a
FEEDBACK: a. Prescription and nonprescription drugs must be shown to be effective as well as safe.
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b. All labels must be accurate and must include a listing of all active and inactiv
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eingredients. Try again.
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c. The FDA must approve all new products before they are released to the public. Tr
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yagain. sf


d. Warning labels must be present on certain preparations. Try again.
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POINTS: 1
QUESTION TYPE: sf s f Multiple Choice sf


HAS VARIABLES:
sf s f False
DATE CREATED:sf 11/26/2017 8:26 PM sf sf


DATE MODIFIED:
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