,Chapter 1 Consumer Safety and Drug Regulati
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ons
1. A client calls her primary care provider requesting a prescription for an antidepressant medication. Sh
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e tells the nurse that she is severely depressed and would like the prescription called in to her local pha
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rmacy. How should the nurse respond?
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a. The nurse encourages the client to see a psychiatric professional for an evaluation to obt
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ain the prescription.
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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 evaluati
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on to obtain the prescription.
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b. Antidepressants are not sold as over-the- z% z% z% z% z%
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 practit
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ioner. Try again. z% z%
POINTS: 1
QUESTION TYPE: z% Multiple Choice
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HAS VARIABLES:
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DATE CREATED: z% 11/26/2017 8:16 PM z% z%
DATE MODIFIED: z% z % 11/26/2017 8:32 PM z% z%
2. A client visits her health care provider for her annual physical. She questions the nurse regarding th
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e use of an herbal supplement that she saw advertised on television for weight loss. What information
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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 respo
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nsiblefor 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 pres
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cribed medications. z%
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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dietary manufacturer 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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cribed medications. Try again.
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POINTS: 1
QUESTION TYPE: z% Multiple Choice
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HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:22 PM z% z%
Copyrightz%Cengagez%Learning.z%Poweredz%byz%Cog Pagez%1
nero.
,Chapter 1 Consumer Safety and Drug Regulati
z% z% z% z% z% z%
DATE
ons MODIFIED:
z% 11/26/2017 8:32 PM
z % z% z%
Copyrightz%Cengagez%Learning.z%Poweredz%byz%Cog Pagez%2
nero.
, 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. S
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he asks the nurse if a cheaper, generic drug will be weaker than her current prescription. How should the
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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
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nameprescriptions. %
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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
z% z% z% z% z% z% z% z% z% z% z% z%
rm strength, 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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assigned to a new drug. The trade name is the name the pharmaceutical compa
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ny assigns 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 prep
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arations with the same name have the same uniform strength, quality, and pu
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rity. Try again. z% z%
POINTS: 1
QUESTION TYPE: z% Multiple Choice
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HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:23 PM z% z%
DATE MODIFIED: z% z % 11/26/2017 8:31 PM z% z%
4. The FDA, under the direction of the Department of Health and Human Services, mandates which
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%of the 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 in
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active ingredients 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
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inactive ingredients. Try again.
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c. The FDA must approve all new products before they are released to the p
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ublic. Try again. z% z%
d. Warning labels must be present on certain preparations. Try again.
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POINTS: 1
QUESTION TYPE: z% Multiple Choice
z % z%
HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:26 PM z% z%
DATE MODIFIED: z% z % 11/26/2017 8:30 PM z% z%
Copyrightz%Cengagez%Learning.z%Poweredz%byz%Cog Pagez%3
nero.
z% z% z% z% z% z%
ons
1. A client calls her primary care provider requesting a prescription for an antidepressant medication. Sh
z% z% z% z% z% z% z% z% z% z% z% z% z% z%
e tells the nurse that she is severely depressed and would like the prescription called in to her local pha
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rmacy. How should the nurse respond?
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a. The nurse encourages the client to see a psychiatric professional for an evaluation to obt
z% z% z% z% z% z% z% z% z% z% z% z% z% z%
ain the prescription.
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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.
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
ANSWER: a
FEEDBACK:
a. The client should be encouraged to seek a psychiatric professional evaluati
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on to obtain the prescription.
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b. Antidepressants are not sold as over-the- z% z% z% z% z%
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 practit
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
ioner. Try again. z% z%
POINTS: 1
QUESTION TYPE: z% Multiple Choice
z % z%
HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:16 PM z% z%
DATE MODIFIED: z% z % 11/26/2017 8:32 PM z% z%
2. A client visits her health care provider for her annual physical. She questions the nurse regarding th
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
e use of an herbal supplement that she saw advertised on television for weight loss. What information
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
can the nurse share with her client?
z% z% z% z% z% z%
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 respo
z% z% z% z% z% z% z% z% z% z% z% z% z% z%
nsiblefor 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 pres
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cribed medications. z%
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.
z% z% z% z% z% z% z% z% z% z% z%
b. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), the
z% z% z% z% z% z% z% z% z% z% z% z
dietary manufacturer 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
z% z% z% z% z% z% z% z% z%
cribed medications. Try again.
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POINTS: 1
QUESTION TYPE: z% Multiple Choice
z % z%
HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:22 PM z% z%
Copyrightz%Cengagez%Learning.z%Poweredz%byz%Cog Pagez%1
nero.
,Chapter 1 Consumer Safety and Drug Regulati
z% z% z% z% z% z%
DATE
ons MODIFIED:
z% 11/26/2017 8:32 PM
z % z% z%
Copyrightz%Cengagez%Learning.z%Poweredz%byz%Cog Pagez%2
nero.
, Chapter 1 Consumer Safety and Drug Regulati
z% z% z% z% z% z%
ons
3. Upon leaving the exam room, a client tells the nurse that she is confused regarding her prescription. S
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
he asks the nurse if a cheaper, generic drug will be weaker than her current prescription. How should the
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
nurse respond?
z% z%
a. Drug standards assure consumers that the same drug must be of uniform strength, quality, and purity.
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
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
z% z% z% z% z% z% z% z% z% z% z% z%
nameprescriptions. %
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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
z% z% z% z% z% z% z% z% z% z% z% z%
rm strength, 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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assigned to a new drug. The trade name is the name the pharmaceutical compa
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ny assigns 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 prep
z% z% z% z% z% z% z% z% z% z% z% z%
arations with the same name have the same uniform strength, quality, and pu
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rity. Try again. z% z%
POINTS: 1
QUESTION TYPE: z% Multiple Choice
z % z%
HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:23 PM z% z%
DATE MODIFIED: z% z % 11/26/2017 8:31 PM z% z%
4. The FDA, under the direction of the Department of Health and Human Services, mandates which
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z
%of the following?
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a. Prescription and nonprescription drugs must be shown to be effective as well as safe.
z% z% z% z% z% z% z% z% z% z% z% z% z%
b. All labels must include a listing of active ingredients; some labels require a listing of in
z% z% z% z% z% z% z% z% z% z% z% z% z% z% z%
active ingredients as well.
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c. All new products must be tested by the FDA before being released to the public.
z% z% z% z% z% z% z% z% z% z% z% z% z% z%
d. All drugs must have "warning" labels.
z% z% z% z% z%
ANSWER: a
FEEDBACK: a. Prescription and nonprescription drugs must be shown to be effective as well as safe.
z% z% z% z% z% z% z% z% z% z% z% z% z% z%
b. All labels must be accurate and must include a listing of all active and
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inactive ingredients. Try again.
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c. The FDA must approve all new products before they are released to the p
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ublic. Try again. z% z%
d. Warning labels must be present on certain preparations. Try again.
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POINTS: 1
QUESTION TYPE: z% Multiple Choice
z % z%
HAS VARIABLES:
z% z % False
DATE CREATED: z% 11/26/2017 8:26 PM z% z%
DATE MODIFIED: z% z % 11/26/2017 8:30 PM z% z%
Copyrightz%Cengagez%Learning.z%Poweredz%byz%Cog Pagez%3
nero.
