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,Chapter 1 Consumer Safety and Drug Regulati
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,Chapter 1 Consumer Safety and Drug Regulati
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onsA client calls her primary care provider requesting a prescription for an antidepressant medication.
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She tellsthe nurse that she is severely depressed and would like the prescription called in to her loca
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l pharmacy. How should the nurse respond?
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a. The nurse encourages the client to see a psychiatric professional for an evaluation to o
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btain theprescription. XX X


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 evaluati
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on to obtainthe prescription.
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b. Antidepressants are not sold as over-the- XX XX XX XX XX

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 practiti
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oner. Tryagain. XX X



POINTS: 1
QUESTION TYPE: XX Multiple Choice
X X XX


HAS VARIABLES:
XX X X False
DATE CREATED: XX 11/26/2017 8:16 PM XX XX


DATE MODIFIED: XX X X11/26/2017 8:32 PM XX XX




2. A client visits her health care provider for her annual physical. She questions the nurse regarding
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the use ofan herbal supplement that she saw advertised on television for weight loss. What informati
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on can the 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 res
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ponsiblefor 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 pr
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escribedmedications. X



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
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dietarymanufacturer is responsible for ensuring that a dietary supplement is saf
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e before 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 pres
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cribedmedications. Try again.
X XX XX



POINTS: 1
QUESTION TYPE: XX Multiple Choice
X X XX


HAS VARIABLES:
XX X X False
DATE CREATED: XX 11/26/2017 8:22 PM XX XX


DATE MODIFIED: XX X X11/26/2017 8:32 PM XX XX



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, Chapter 1 Consumer Safety and Drug Regulati
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ons

3. Upon leaving the exam room, a client tells the nurse that she is confused regarding her prescription.
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X She asks the nurse if a cheaper, generic drug will be weaker than her current prescription. How should
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XX the nurse respond?
XX XX


a. Drug standards assure consumers that the same drug must be of uniform strength, quality, and puri
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ty.
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 bran
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d nameprescriptions.
XX X



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 unifo
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rm strength,quality, and purity.
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b. Generic and trade drugs are the same medication. Generic is the name that is a
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ssignedto a new drug. The trade name is the name the pharmaceutical company
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assigns 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 prep
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arationswith the same name have the same uniform strength, quality, and puri
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ty. Try again.
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POINTS: 1
QUESTION TYPE: XX X XMultiple Choice XX


HAS VARIABLES:
XX X XFalse
DATE CREATED: XX 11/26/2017 8:23 PM XX XX


DATE MODIFIED: XX X 11/26/2017 8:31 PM
X XX XX




4. The FDA, under the direction of the Department of Health and Human Services, mandates whi
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ch of 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
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inactiveingredients as well. X XX XX



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
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inactiveingredients. Try again.
X X XX XX


c. The FDA must approve all new products before they are released to the pu
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blic. Tryagain. XX X



d. Warning labels must be present on certain preparations. Try again.
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POINTS: 1
QUESTION TYPE: XX X XMultiple Choice XX


HAS VARIABLES:
XX X XFalse
DATE CREATED: XX 11/26/2017 8:26 PM XX XX


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