TEST BANK FOR Essentials of Pharmacology for Health Professions, 9th Edition by Bruce Colbert, Adam James, Elizabeth Katrancha.ISBN: 9780357618301 COMPLETE GUIDE All CHAPTERS COVERED 100% VERIFIED A+ GRADE ASSURED!!!!! NEW LATEST UPDATE!!!!!

,Chapter 1 Consumer Safety and Drug Regul
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,Chapter 1 Consumer Safety and Drug Regul
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atiA client calls her primary care provider requesting a prescription for an antidepressant medication. She tell s
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t he nurse that she is severely depressed and would like the prescription called in to her local pharmacy.
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How s hould the nurse respond?
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a. The nurse encourages the client to see a psychiatric professional for an evaluation to obtain t
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he prescription. d v




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 evalua
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b. Antidepressants are not sold as over-the- d v d v d v d v d v


counter medications; a prescription is required.Try again.d v d v dv d v d v d v




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 prac
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tition er. Tryagain. dv dv




POINTS: 1
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HAS VARIABLES: False dv




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2. A client visits her health care provider for her annual physical. She questions the nurse regarding the use
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of an herbal supplement that she saw advertised on television for weight loss. What information can the nur
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se s hare 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 responsibl
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e for 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 prescribe
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d medications. d v




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), t
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he di eta rymanufacturer is responsible for ensuring that a dietary supplement is
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safe be fore 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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be d medications. Try again.
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POINTS: 1
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HAS VARIABLES: False dv




DATE CREATED: 11/26/2017 8:22 PM
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DATE MODIFIED: 11/26/2017 8:32 PM
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, Chapter 1 Consumer Safety and Drug Regul
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ati
3. Upon leaving the exam room, a client tells the nurse that she is confused regarding her prescription. She a sk
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s the nurse if a cheaper, generic drug will be weaker than her current prescription. How should the nurse res pon
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d?
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 nam
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e prescriptions. d v




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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v str ength,quality, and purity.
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b. Generic and trade drugs are the same medication. Generic is the name that is
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assi gn edto a new drug. The trade name is the name the pharmaceutical company
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assi gns to that drug 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 pre
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para tio ns with the same name have the same uniform strength, quality, a
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nd purity. Try ag ain.
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POINTS: 1
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HAS VARIABLES: False
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DATE MODIFIED: 11/26/2017 8:31 PM
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4. The FDA, under the direction of the Department of Health and Human Services, mandates which of th
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e following?
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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 inactiv e
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i ngredients 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 a
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nd in acti ve ingredients. 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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. T ryagain.d v d v




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




HAS VARIABLES: False
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DATE CREATED: 11/26/2017 8:26 PM
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DATE MODIFIED: 11/26/2017 8:30 PM
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