TEST BANK FOR Essentials of Pharmacology for Health Professions (MindTap Course List) 9th Edition by Bruce Colbert, Adam 978-0357618301 GUIDE ALL CHAPTERS COVERED 100% VERIFIED A+ GRADE ASSURED!!!!! NEW LATEST UPDATE!!!!!

,Chapter 1 Consumer Safety and Drug Regulatio
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,Chapter 1 Consumer Safety and Drug Regulatio
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ns A client calls her primary care provider requesting a prescription for an antidepressant medication. She te
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llsthe nurse that she is severely depressed and would like the prescription called in to her local pharmacy.
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How should the nurse respond?
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a. The nurse encourages the client to see a psychiatric professional for an evaluation to obtain
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theprescription.
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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
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to obtainthe prescription.
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b. Antidepressants are not sold as over-the- 5% 5% 5% 5% 5%


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 practitione
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POINTS: 1
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HAS VARIABLES: 5% 5 % False
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DATE MODIFIED: 5% 5 % 11/26/2017 8:32 PM 5% 5%




2. A client visits her health care provider for her annual physical. She questions the nurse regarding the us
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e ofan herbal supplement that she saw advertised on television for weight loss. What information can the
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nurse share 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 responsi
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blefor 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 prescrib
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edmedications. 5%




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 di
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etarymanufacturer is responsible for ensuring that a dietary supplement is safe bef
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ore it is 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 prescri
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bedmedications. Try again.%
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POINTS: 1
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HAS VARIABLES: 5% 5 % False
DATE CREATED: 5% 11/26/2017 8:22 PM 5% 5%




DATE MODIFIED: 5% 5 % 11/26/2017 8:32 PM 5% 5%




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, Chapter 1 Consumer Safety and Drug Regulatio
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3. Upon leaving the exam room, a client tells the nurse that she is confused regarding her prescription. She a
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sks the nurse if a cheaper, generic drug will be weaker than her current prescription. How should the nurse r
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espond?
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 na
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meprescriptions. 5%




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
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% strength,quality, and purity. %
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b. Generic and trade drugs are the same medication. Generic is the name that is assi
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gnedto a new drug. The trade name is the name the pharmaceutical company assi
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gns to thatdrug 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 preparat
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ionswith the same name have the same uniform strength, quality, and purity. Tr
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y again.5%




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HAS VARIABLES:
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DATE CREATED:5% 11/26/2017 8:23 PM 5% 5%




DATE MODIFIED:
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4. The FDA, under the direction of the Department of Health and Human Services, mandates which of
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thefollowing?
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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 inacti
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veingredients as well.
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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 in
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activeingredients. Try again.
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c. The FDA must approve all new products before they are released to the public
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. Tryagain.
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d. Warning labels must be present on certain preparations. Try again.
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POINTS: 1
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HAS VARIABLES:
5% 5 % False
DATE CREATED:5% 11/26/2017 8:26 PM 5% 5%




DATE MODIFIED:
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