Core Concepts in Pharmacology 4th edition Holland, Adams, Brice Test Bank

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  • Published: 2014
  • ISBN-10: 0133449815
  • ISBN-13: 978-0133449815

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core concepts in pharmacology 4th edition test bank

Chapter 1-Introduction to Pharmacology: Drug Regulation and Approval

Holland/Adams/Brice, Core Concepts in Pharmacology 4th Edition Test Bank

Chapter 1

Question 1

Type: MCSA

A nurse educator wants to define the term pharmacology for the student. Which definition is most

appropriate?

The study of medicine.

The use of medicine to treat disease.

The branch of medicine concerned with the treatment of disease and suffering.

The use of herbs, natural extracts, vitamins, minerals, or dietary supplements to treat diseases.

Correct Answer: 1

Rationale 1: The study of medicine is the definition of pharmacology.

Rationale 2: The use of medicine to treat disease is incorrect because this is the definition for

pharmacotherapeutics.

Rationale 3: The branch of medicine concerned with the treatment of disease and suffering is incorrect because

this is the definition for therapeutics.

Rationale 4: The use of herbs, natural extracts, vitamins, minerals, or dietary supplements is incorrect because

this is the definition of natural alternative therapies.

Global Rationale: Pharmacology is the study of medicine. The use of medicine to treat disease is incorrect because

this is the definition for pharmacotherapeutics. The branch of medicine concerned with the treatment of disease

and suffering is incorrect because this is the definition for therapeutics. The use of herbs, natural extracts,

vitamins, minerals, or dietary supplements is incorrect because this is the definition of natural alternative

therapies.

Cognitive Level: Remembering

Client Need: Health Promotion and Maintenance

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-1 Explain the interdisciplinary nature of pharmacology and give examples of subject

area expertise needed to master the discipline.

Question 2

Type: MCMA

In addition to physicians, which health care providers are able to prescribe medications? (Select all that apply.)

Note: Credit will be given only if all correct choices and no incorrect choices are selected.

Physician’s assistants

.

Advanced nurse practitioners

.

Dentists

.

Medical assistants.

Registered nurses

Correct Answer: 1, 2, 3

Rationale 1: Physician’s assistants are able to prescribe medications.

Rationale 2: Advanced nurse practitioners are able to prescribe medications.

Rationale 3: Dentists are able to prescribe medications.

Rationale 4: Medical assistants is incorrect because medical assistants are unlicensed and unable to prescribe

medications.

Rationale 5: Registered nurses is incorrect because prescribing medications is not in their scope of practice.

Global Rationale: Physician assistants, advanced practice practitioners, and dentists are able to prescribe

medications. Medical assistants and registered nurses are able to dispense medications, but they are unable

to prescribe medication.

Cognitive Level: Remembering

Client Need: Health Promotion and Maintenance

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-2 Identify professions in which a knowledge of pharmacology is important.

Question 3

Type: MCSA

Which branch of medicine is concerned with the treatment of disease and suffering?

Pharmacology

Therapeutics.

Pathophysiology.

Pharmacotherapeutics.

Correct Answer: 2

Rationale 1: Pharmacology is the study of medicine.

Rationale 2: Therapeutics is the branch of medicine concerned with the treatment of disease and suffering.

Rationale 3: Pathophysiology is the study of the functional changes associated with or resulting from disease

or injury.

Rationale 4: Pharmacotherapeutics is the use of medicine to treat disease.

Global Rationale: Therapeutics is the branch of medicine concerned with the treatment of disease and suffering.

Pharmacology is the study of medicine. Pathophysiology is the study of the functional changes associated

with or resulting from disease or injury. Pharmacotherapeutics is the use of medicine to treat disease.

Cognitive Level: Remembering

Client Need: Health Promotion and Maintenance

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-3 Explain how the disciplines of therapeutics and pharmacology are interconnected.

Question 4

Type: MCSA

Which definition best describes the term pharmaceutics?

The science of preparing and dispensing drugs, and a very important part of pharmacotherapy

.

The use of medicine to treat disease

.

Agents naturally produced in animal cells, in microorganisms, or by the body itself.

Herbs, natural extracts, vitamins, minerals, and dietary supplements.

Correct Answer: 1

Rationale 1: Pharmaceutics is the science of preparing and dispensing drugs, and is a very important part of

pharmacotherapy.

Rationale 2: The use of medicine to treat disease is incorrect because this is the definition of

pharmacotherapeutics.

Rationale 3: Agents naturally produced in animal cells, microorganisms, or by the body itself is incorrect because

this is the definition of biologics.

Rationale 4: Herbs, natural extracts, vitamins, minerals, and dietary supplements is incorrect because this is

the definition of natural alternative therapies.

Global Rationale: Pharmaceutics is the science of preparing and dispensing drugs, and is a very important

part of pharmacotherapy. The use of medicine to treat disease is incorrect because this is the definition of pharmacotherapeutics.

Agents naturally produced in animal cells, microorganisms, or by the body itself is incorrect because

this is the definition of biologics. Herbs, natural extracts, vitamins, minerals, and dietary supplements is incorrect

because this is the definition of natural alternative therapies.

Cognitive Level: Remembering

Client Need: Health Promotion and Maintenance

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-3 Explain how the disciplines of therapeutics and pharmacology are interconnected.

Question 5

Type: MCMA

Which items are considered medically therapeutic? (Select all that apply.) Note: Credit will be given only if all

correct choices and no incorrect choices are selected.

Traditional drugs

.

Sunscreens.

Biologics.

Natural alternative therapies.

Antiperspirants.

Correct Answer: 1, 3, 4

Rationale 1: Traditional drugs are produced in a laboratory, and are routinely used by practitioners.

Rationale 2: Sunscreens can alter the body’s normal activities, but they are not considered to be medically

therapeutic.

Rationale 3: Biologics are routinely used by practitioners, and are naturally produced. Vaccines and hormones

are included in this type of medication.

Rationale 4: Natural alternative therapies include herbs, extracts, vitamins, minerals, and dietary supplements.

Rationale 5: Antiperspirants can alter the body’s normal activities, but they are not considered to be medically

therapeutic.

Global Rationale: Traditional drugs are produced in a laboratory, and are routinely used by practitioners. Biologics

are routinely used by practitioners, and are naturally produced. Vaccines and hormones are included in

this type of medication. Natural alternative therapies include herbs, extracts, vitamins, minerals, and dietary

supplements. Sunscreens and antiperspirants can alter the body’s normal activities, but they are not considered

to be medically therapeutic.

Cognitive Level: Analyzing

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-4 Distinguish between therapeutic drugs and agents such as foods, household products,

and cosmetics.

Question 6

Type: MCSA

Insulin would fall into which therapeutic drug category?

Biologics

Alternative therapies

Natural therapy

Traditional therapeutic drug

Correct Answer: 1

Rationale 1: Insulin is naturally produced by the body itself, in animal cells, and in microorganisms. Biologics

also include hormones and vaccines, and are routinely used by health care practitioners.

Rationale 2: Alternative therapies are produced naturally, and include herbs, extracts, vitamins, minerals, and

dietary supplements.

Rationale 3: Natural therapies are produced naturally, and include herbs, extracts, vitamins, minerals, and dietary

supplements.

Rationale 4: Traditional drug therapies are chemically produced in a lab.

Global Rationale: Insulin is naturally produced by the body itself, in animal cells, and in microorganisms. Biologics

also include hormones and vaccines, and are routinely used by health care practitioners. Natural and alternative

therapies are produced naturally, and include herbs, extracts, vitamins, minerals, and dietary supplements.

Traditional drug therapies are chemically produced in a lab.

Cognitive Level: Remembering

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-5 Compare and contrast traditional drugs, biologics, and natural alternative therapies.

Question 7

Type: MCSA

Which statement best describes how a traditional drug is different from a biologic agent?

Biologics and traditional drugs are identical chemically.

Traditional drugs are naturally produced by the body or in animal cells, whereas biologic agents are chemically

produced in a laboratory.

Traditional drugs are chemically produced in a laboratory, whereas biologic agents are naturally produced by

the body or in animal cells.

Biologics include herbs, natural extracts, vitamins, minerals, and dietary supplements.

Correct Answer: 3

Rationale 1: Biologic agents are naturally produced by the body or in animal cells, and traditional drugs are

chemically produced in a laboratory.

Rationale 2: Biologic agents are naturally produced by the body or in animal cells, and traditional drugs are

chemically produced in a laboratory.

Rationale 3: Biologic agents are naturally produced by the body or in animal cells, and traditional drugs are

chemically produced in a laboratory.

Rationale 4: This is the definition of natural alternative therapies.

Global Rationale: Biologic agents are naturally produced by the body or in animal cells, and traditional drugs

are chemically produced in a laboratory. Biologics that include herbs, natural extracts, vitamins, minerals, and

dietary supplements is the definition of natural alternative therapies.

Cognitive Level: Analyzing

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-5 Compare and contrast traditional drugs, biologics, and natural alternative therapies.

Question 8

Type: MCSA

Which medication change often occurs when a drug demonstrates a wide margin of safety and is used over

long periods of time?

Prescription-only to over-the-counter (OTC) drug.

One classification to a lower, less restrictive one.

Traditional drug therapy classification to biologics classification.

Therapeutic to effective.

Correct Answer: 1

Rationale 1: Medications with wide margins of safety that are used over long periods of time are often

changed to over-the-counter medications.

Rationale 2: A wide margin of safety does not change the classification of the drug.

Rationale 3: Biologics are produced by the body itself, in animal cells, or in microorganisms. Traditional drug

therapies are chemically produced in the laboratory.

Rationale 4: The safety of a drug is related to the effectiveness of the medication without producing serious

side effects.

Global Rationale: Medications with wide margins of safety that are used over long periods of time are often

changed to over-the-counter medications. A wide margin of safety does not change the classification of the

drug. Biologics are produced by the body itself, in animal cells, or in microorganisms. Traditional drug therapies

are chemically produced in the laboratory. The safety of a drug is related to the effectiveness of the medication

without producing serious side effects.

Cognitive Level: Analyzing

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-6 Identify the advantages and disadvantages of prescription and OTC drugs.

Question 9

Type: MCMA

Which statement best describes the advantages of prescription drugs versus over-the-counter (OTC) drugs?

(Select all that apply.) Note: Credit will be given only if all correct choices and no incorrect choices are selected.

The cost of the drug is always less than the cost of an OTC drug.

The practitioner can maximize therapy by ordering the proper medication for the client’s condition.

There are fewer side effects of prescription drugs than of OTC drugs.

The practitioner is able to control the dose and frequency of dosing of the drug.

Prescription drugs do not require a practitioner order.

Correct Answer: 2, 4

Rationale 1: There are a variety of prices for prescription and OTC drugs.

Rationale 2: The practitioner can maximize therapy by ordering the proper medication for the client’s condition,

and can control the dose and frequency of dosing.

Rationale 3: There are many possible side effects for prescription or OTC drugs, but with prescription drugs,

the practitioner is able to inform the client of potential side effects.

Rationale 4: The practitioner can maximize therapy by ordering the proper medication for the client’s condition,

and can control the dose and frequency of dosing.

Rationale 5: To obtain prescription drugs, patients must get a physician’s order authorizing them to receive

the drugs.

Global Rationale: The practitioner can maximize therapy by ordering the proper medication for the client’s

condition, and can control the dose and frequency of dosing. There are a variety of prices for prescription and

OTC drugs. There are many possible side effects for prescription or OTC drugs, but with prescription drugs, the

practitioner is able to inform the client of potential side effects. To obtain prescription drugs, patients must get

a physician’s order authorizing them to receive the drugs.

Cognitive Level: Analyzing

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-6 Identify the advantages and disadvantages of prescription and OTC drugs.

Question 10

Type: MCMA

The nurse is discussing the advantages over-the-counter (OTC) medications with a client. Which statements are

disadvantages of OTC drugs versus prescription drugs?(Select all that apply.) Note: Credit will be given only if all

correct choices and no incorrect choices are selected.

OTC drugs can react with foods, herbal products, and prescriptions, or with other OTC drugs.

A client can obtain OTC drugs more easily than prescription drugs.

Self-treatment is sometimes ineffective.

Choosing the proper medication for a specific problem can be challenging.

OTC drugs are more expensive than prescription drugs.

Correct Answer: 1, 3, 4

Rationale 1: This is a disadvantage of OTC drugs.

Rationale 2: An advantage of OTC drug is that the client can obtain these drugs more easily than prescription

drugs.

Rationale 3: This is a disadvantage of OTC drugs.

Rationale 4: This is a disadvantage of OTC drugs.

Rationale 5: Not all OTC drugs are more expensive than prescription drugs.

Global Rationale: Drug interactions, ineffective self-treatment, and choosing the proper medication for specific

problems are all disadvantages of OTC drugs. Not all OTC drugs are more expensive than prescription drugs.

An advantage of OTC drugs is that the client can obtain them more easily than prescription drugs.

Cognitive Level: Analyzing

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-6 Identify the advantages and disadvantages of prescription and OTC drugs.

Question 11

Type: MCSA

Which science is known for preparing and dispensing drugs?

Pharmacology

Pharmaceutics

Traditional drug therapy

Therapeutics

Correct Answer: 2

Rationale 1: Pharmacology is incorrect because pharmacology is the study of medicine and of how drugs improve

the health of the human body.

Rationale 2: Pharmaceutics is the science of preparing and dispensing drugs.

Rationale 3: Traditional drug therapy is incorrect because traditional drug therapy refers to medications that

are chemically produced in a laboratory.

Rationale 4: Therapeutics is incorrect because therapeutics is the branch of medicine concerned with the

treatment of disease and suffering.

Global Rationale: Pharmaceutics is the science of preparing and dispensing drugs. Pharmacology is incorrect

because pharmacology is the study of medicine and of how drugs improve the health of the human body. Traditional

drug therapy is incorrect because traditional drug therapy refers to medications that are chemically produced

in a laboratory. Therapeutics is incorrect because therapeutics is the branch of medicine concerned with

the treatment of disease and suffering.

Cognitive Level: Remembering

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-7 Distinguish between pharmaceutics and pharmacology.

Question 12

Type: MCSA

A client expresses concerns about a newly prescribed medication. The nurse explains that the safety and effectiveness

of the medication have been proven, according to the statutes of which law?

Public Health Service Act

FDA Modernization Act

Food, Drug, and Cosmetic Act

Pure Food and Drug Act

Correct Answer: 3

Rationale 1: The Public Health Service Act of 1944 covers many health issues, including biological products

and the control of communicable diseases.

Rationale 2: The FDA Modernization Act is the largest reform effort of the drug review process since 1938.

Rationale 3: The Food, Drug, and Cosmetic Act, passed in 1938, prevents the marketing of drugs that have not

been thoroughly tested prior to marketing. Drug companies are required to prove the safety and efficacy of

any drug before it can be sold in the United States.

Rationale 4: The Pure Food and Drug Act gives the government power to control the labeling of medicine.

Global Rationale: The Food, Drug, and Cosmetic Act, passed in 1938, prevents the marketing of drugs that

have not been thoroughly tested prior to marketing. Drug companies are required to prove the safety and efficacy

of any drug before it can be sold in the United States. The Public Health Service Act of 1944 covers many

health issues, including biological products and the control of communicable diseases. The FDA Modernization

Act is the largest reform effort of the drug review process since 1938. The Pure Food and Drug Act gives the

government power to control the labeling of medicine.

Cognitive Level: Analyzing

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-8 Discuss the history of U.S. standards, acts, and organizations leading to the requirement

that drug safety must be proven before marketing.

Question 13

Type: MCSA

A client asks the nurse whether the claims made regarding a new medication are true. The nurse responds

based on which act or amendment passed in 1912 that prevents the sale of drugs with false therapeutic claims

intended to cheat the consumer?

Food, Drug, and Cosmetic Act

FDA Modernization Act

The Sherley Amendment

Pure Food and Drug Act

Correct Answer: 3

Rationale 1: The Food, Drug, and Cosmetic Act prevents the marketing of drugs that have not been thoroughly

tested prior to marketing. Drug companies are required to prove the safety and efficacy of any drug before it

can be sold in the United States.

Rationale 2: The FDA Modernization Act is the largest reform effort of the drug review process since 1938.

Rationale 3: The Sherley Amendment was passed in 1912 to prohibit the sale of drugs labeled with false therapeutic

claims intended to cheat the consumer.

Rationale 4: The Pure Food and Drug Act gives the government power to control the labeling of medicine.

Global Rationale: The Sherley Amendment was passed in 1912 to prohibit the sale of drugs labeled with false

therapeutic claims intended to cheat the consumer. The Food, Drug, and Cosmetic Act prevents the marketing

of drugs that have not been thoroughly tested prior to marketing. Drug companies are required to prove the

safety and efficacy of any drug before it can be sold in the United States. The FDA Modernization Act is the

largest reform effort of the drug review process since 1938. The Pure Food and Drug Act gives the government

power to control the labeling of medicine.

Cognitive Level: Analyzing

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-8 Discuss the history of U.S. standards, acts, and organizations leading to the requirement

that drug safety must be proven before marketing.

Question 14

Type: MCSA

The nurse is discussing a medication with a patient. This approved medication is discovered to have serious

problems. Which FDA response does the nurse expect?

Require the medication to have additional clinical trials conducted.

Issue a warning to practitioners to watch for side effects in clients taking the drug.

Continue to monitor the medication in post-marketing studies.

Require that the drug be withdrawn from the market and its use discontinued.

Correct Answer: 4

Rationale 1: Require the medication to have additional clinical trials conducted is incorrect because the drug

will be withdrawn from the market and its use discontinued.

Rationale 2: Issue a warning to practitioners to watch for side effects in clients taking the drug is incorrect because

the drug will be withdrawn and its use discontinued.

Rationale 3: Continue to monitor the medication in post-marketing studies is incorrect because the drug will

be withdrawn from the market and its use discontinued.

Rationale 4: The FDA requires that the drug be withdrawn from the market and its use discontinued.

Global Rationale: The FDA requires that the drug be withdrawn from the market and its use discontinued. Require

the medication to have additional clinical trials conducted is incorrect because the drug will be withdrawn

from the market and its use discontinued. Issue a warning to practitioners to watch for side effects in clients taking

the drug is incorrect because the drug will be withdrawn and its use discontinued. Continue to monitor the medication

in post-marketing studies is incorrect because the drug will be withdrawn from the market and its use

discontinued.

Cognitive Level: Applying

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-8 Discuss the history of U.S. standards, acts, and organizations leading to the requirement

that drug safety must be proven before marketing.

Question 15

Type: MCSA

The nurse is caring for a client with migraine headaches. The client asks why she has been prescribed a medication

for seizures. Which legislation allows drug companies to share off-label drug use information with

health care practitioners to allow such a prescription to occur?

Therapeutic Products Programme

Food and Drugs Act

Prescription Drug User Fee Act

Health Products and Food Branch

Correct Answer: 3

Rationale 1: The Therapeutic Products Programme is a piece of Canadian legislation to ensure safety of that

country’s medications and drugs.

Rationale 2: The Food and Drugs Act is a piece of Canadian legislation to ensure safety of that country’s medications

and drugs.

Rationale 3: The FDA Modernization Act reauthorized the Prescription Drug User Fee Act, which allows drug

companies to give health care practitioners information about non-FDA-approved tests of certain drugs. When

a drug provides benefits for treatment of a different problem than that for which it was originally prescribed,

the drug company is allowed to share accurate information with other physicians about the drug’s “unapproved”

but effective use in treating that other condition.

Rationale 4: The Health Products and Food Branch is a piece of Canadian legislation to ensure safety of that

country’s medications and drugs.

Global Rationale: The FDA Modernization Act reauthorized the Prescription Drug User Fee Act, which allows

drug companies to give health care practitioners information about non—FDA-approved tests of certain drugs.

When a drug provides benefits for treatment of a different problem than that for which it was originally prescribed,

the drug company is allowed to share accurate information with other physicians about the drug’s “unapproved”

but effective use in treating that other condition. The Therapeutic Products Programme is a piece of

Canadian legislation to ensure safety of that country’s medications and drugs. The Food and Drugs Act is a

piece of Canadian legislation to ensure safety of that country’s medications and drugs. The Health Products

and Food Branch is a piece of Canadian legislation to ensure safety of that country’s medications and drugs.

Cognitive Level: Analyzing

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-9 Discuss the role of the United States Food and Drug Administration (FDA) in determining

the safety of drugs and whether they may be used for therapy.

Question 16

Type: MCSA

A client asks the nurse if all herbal supplements undergo the same testing that prescription drugs undergo.

Which statement is the best response by the nurse?

“Herbal and dietary supplements may not be marketed without prior approval from the FDA.”

“The Center for Food Safety and Applied Nutrition (CFSAN) regulates use of herbal supplements, which means

the medication must be safe.”

“Herbal products and dietary supplements are regulated by the Dietary Supplement Health and Education Act

of 1994. This act does not require the same research for herbal or dietary supplements.”

“All medications and herbal supplements undergo the same testing before being made available for purchase.”

Correct Answer: 3

Rationale 1: Herbal and dietary supplements may be marketed without prior approval from the FDA.

Rationale 2: Herbal and dietary supplements do not undergo the same testing that prescription or OTC medications

do.

Rationale 3: Herbal products and dietary supplements are regulated by the Dietary Supplement Health and

Education Act of 1994. This act does not require the same research for herbal and dietary supplements.

Rationale 4: Herbal supplements may be marketed without prior approval from the FDA, and are not required

to be tested in clinical trials.

Global Rationale: Herbal products and dietary supplements are regulated by the Dietary Supplement Health

and Education Act of 1994. This act does not require the same research for herbal and dietary supplements.

Herbal and dietary supplements may be marketed without prior approval from the FDA. Herbal and dietary

supplements do not undergo the same testing that prescription or OTC medications do. Herbal supplements

may be marketed without prior approval from the FDA, and are not required to be tested in clinical trials.

Cognitive Level: Evaluating

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-9 Discuss the role of the United States Food and Drug Administration (FDA) in determining

the safety of drugs and whether they may be used for therapy.

Question 17

Type: MCSA

Which government agency has control over which prescription or OTC drugs may be used for therapy?

The Center for Biologics Evaluation and Research (CBER)

The Center for Food Safety and Applied Nutrition (CFSAN)

The Center for Drug Evaluation and Research (CDER)

The National Institutes of Health (NIH)

Correct Answer: 3

Rationale 1: The Center for Biologics Evaluation and Research (CBER) regulates the use of biologics, including

serums, vaccines, and products found in the bloodstream.

Rationale 2: The Center for Food Safety and Applied Nutrition (CFSAN) regulates use of herbal products and

dietary supplements.

Rationale 3: The Center for Drug Evaluation and Research (CDER) has powerful control over whether prescription

drugs and OTC drugs may be used for therapy.

Rationale 4: The National Institutes of Health (NIH) do not have control over prescription or OTC drugs.

Global Rationale: The Center for Drug Evaluation and Research (CDER) has powerful control over whether

prescription drugs and OTC drugs may be used for therapy. The Center for Biologics Evaluation and Research

(CBER) regulates the use of biologics, including serums, vaccines, and products found in the bloodstream. The

Center for Food Safety and Applied Nutrition (CFSAN) regulates use of herbal products and dietary supplements.

The National Institutes of Health (NIH) do not have control over prescription or OTC drugs.

Cognitive Level: Remembering

Client Need: Health Promotion and Maintenance

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-10 Discuss the roles and responsibilities of branches within the FDA in overseeing traditional

therapeutic drugs, biologics, and natural alternative therapies.

Question 18

Type: MCMA

Which branch of the FDA is responsible for the use of biologics, including serums, vaccines, and products

found in the bloodstream?

The Center for Biologics Evaluation and Research (CBER)

The Center for Drug Evaluation and Research (CDER)

The Center for Food Safety and Applied Nutrition (CFSAN)

The FDA does not have a branch responsible for the use of biologics.

Correct Answer: 1

Rationale 1: The Center for Biologics Evaluation and Research (CBER) is responsible for the use of biologics, including

serums, vaccines, and products found in the bloodstream.

Rationale 2: The Center for Drug Evaluation and Research (CDER) has control over whether medications may

be used for therapy.

Rationale 3: The Center for Food Safety and Applied Nutrition (CFSAN) regulates herbal and dietary

supplements.

Rationale 4: The Center for Biologics Evaluation and Research (CBER) is responsible for the use of biologics, including

serums, vaccines, and products found in the bloodstream.

Global Rationale: The Center for Biologics Evaluation and Research (CBER) is responsible for the use of biologics,

including serums, vaccines, and products found in the bloodstream. The Center for Drug Evaluation and

Research (CDER) has control over whether medications may be used for therapy. The Center for Food Safety

and Applied Nutrition (CFSAN) regulates herbal and dietary supplements. The Center for Biologics Evaluation

and Research (CBER) is responsible for the use of biologics, including serums, vaccines, and products found in

the bloodstream.

Cognitive Level: Analyzing

Client Need: Health Promotion and Maintenance

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Assessment

Learning Outcome: 1-10 Discuss the roles and responsibilities of branches within the FDA in overseeing traditional

therapeutic drugs, biologics, and natural alternative therapies.

Question 19

Type: MCSA

A client has been selected as a participant in the approval process of a particular drug. The client’s dose and

any effects from the medication are being monitored. Which phase of drug approval is this client participating

in?

Post-marketing study

Clinical phase trial

Postclinical investigation

Preclinical investigation

Correct Answer: 4

Rationale 1: Post-marketing studies take place after clinical trials to check for any new harmful effects in a

larger and more diverse population.

Rationale 2: Clinical investigation is the second and longest part of the drug approval process, and takes place

in three different phases, termed clinical phase trials. During this phase, clinical investigators address concerns

such as whether the drug worsens other medical conditions; establish drug doses; and try to identify adverse

effects.

Rationale 3: Postclinical investigation is not a phase of the approval process.

Rationale 4: Preclinical investigation involves basic science research.

Global Rationale: Preclinical investigation involves basic science research. Post-marketing studies take place

after clinical trials to check for any new harmful effects in a larger and more diverse population. Clinical investigation

is the second and longest part of the drug approval process, and takes place in three different phases,

termed clinical phase trials. During this phase, clinical investigators address concerns such as whether the drug

worsens other medical conditions; establish drug doses; and try to identify adverse effects. Postclinical investigation

is not a phase of the approval process.

Cognitive Level: Understanding

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-11 Identify four stages of approval for therapeutic and biologic drugs.

Question 20

Type: MCSA

Which phase of clinical research involves basic science research?

Submission of NDA

Clinical phase trials

Post-marketing study

Preclinical investigation

Correct Answer: 4

Rationale 1: A review of the NDA is the third stage of drug approval. During this stage, clinical phase III trials

and animal testing may continue, depending on the results obtained from preclinical testing. If the NDA is approved,

the process continues to the final stage. If the NDA is rejected, the process stops until concerns are

addressed.

Rationale 2: During these phases, clinical pharmacologists, researchers, and health care providers examine

data from volunteers and large groups of selected patients with certain diseases.

Rationale 3: Post-marketing surveillance is the fourth stage of the drug approval process. It takes place after

clinical trials and the NDA review process have been completed. Testing in humans is continued to check for

any new harmful effects in larger and more diverse populations.

Rationale 4: Preclinical investigation involves basic science research.

Global Rationale: Preclinical investigation involves basic science research. A review of the NDA is the third

stage of drug approval. During this stage, clinical phase III trials and animal testing may continue, depending

on the results obtained from preclinical testing. If the NDA is approved, the process continues to the final

stage. If the NDA is rejected, the process stops until concerns are addressed. During these phases, clinical

pharmacologists, researchers, and health care providers examine data from volunteers and large groups of selected

patients with certain diseases.

Cognitive Level: Remembering

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-11 Identify four stages of approval for therapeutic and biologic drugs.

Question 21

Type: MCSA

The nurse is providing care to a client who is taking several different medications, both prescribed and overthe-

counter (OTC). The nurse is consulting with the charge nurse about possible interactions. Which statement

by the nurse explains the increased potential for adverse drug–drug and drug–herbal interactions?

“The restrictions placed by the FDA are stricter.”

“People are using more herbs, so the risk for interaction is greater.”

“Drugs are being developed at a faster rate than their risk can be assessed.”

“Managed care has made a greater number of drugs available to consumers.”

Correct Answer: 3

Rationale 1: “The restrictions placed by the FDA are stricter” is incorrect because FDA restrictions are broader,

and cover information about non-FDA-approved uses of certain drugs.

Rationale 2: “People are using more herbs, so the risk for interaction is greater” is incorrect. While the use of

herbal products has increased, this is not the underlying reason for increased adverse potential.

Rationale 3: “Drugs are being developed at a faster rate than their risk can be assessed” is correct. Because of

the higher number of drugs being approved for therapy, the potential for adverse drug-drug and drug-herbal

interactions is greater than ever before.

Rationale 4: “Managed care has made a greater number of drugs available to consumers” is incorrect because

managed care involvement does not come into play with higher number of interactions.

Global Rationale: “Drugs are being developed at a faster rate than their risk can be assessed” is correct. Because

of the higher number of drugs being approved for therapy, the potential for adverse drug—drug and

drug—herbal interactions is greater than ever before. “The restrictions placed by the FDA are stricter” is incorrect

because FDA restrictions are broader, and cover information about non—FDA-approved uses of certain

drugs. “People are using more herbs, so the risk for interaction is greater” is incorrect. While the use of herbal

products has increased, this is not the underlying reason for increased adverse potential. “Managed care has

made a greater number of drugs available to consumers” is incorrect because managed care involvement does

not come into play with higher number of interactions.

Cognitive Level: Analyzing

Client Need: Physiological Integrity

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-12 Discuss current challenges facing the FDA in approving new drugs for market.

Question 22

Type: MCSA

A public health nurse is seeking information on bioterrorist agents to present education regarding security and

defense in case of attack. Which resource is the most appropriate?

U.S. Department of Homeland Security

FEMA

U.S. Armed Forces

U.S. National Guard

Correct Answer: 1

Rationale 1: The U.S. Department of Homeland Security was organized to provide additional security and defense

for the United States in a terrorist attack.

Rationale 2: FEMA would be activated or utilized in cases of bioterrorist attack, if necessary, but does not have

the bulk of information that the Department of Homeland Security has gathered for this need.

Rationale 3: The U.S. Armed Forces would be activated or utilized in cases of bioterrorist attack, if necessary,

but do not have the bulk of information that the Department of Homeland Security has gathered for this need.

Rationale 4: The U.S. National Guard would be activated or utilized in cases of bioterrorist attack, if necessary,

but does not have the bulk of information that the Department of Homeland Security has gathered for this

need.

Global Rationale: The U.S. Department of Homeland Security was organized to provide additional security and

defense for the United States in a terrorist attack. FEMA would be activated or utilized in cases of bioterrorist

attack, if necessary, but does not have the bulk of information that the Department of Homeland Security has

gathered for this need. The U.S. Armed Forces would be activated or utilized in cases of bioterrorist attack, if

necessary, but do not have the bulk of information that the Department of Homeland Security has gathered

for this need. The U.S. National Guard would be activated or utilized in cases of bioterrorist attack, if necessary,

but does not have the bulk of information that the Department of Homeland Security has gathered for this

need.

Cognitive Level: Analyzing

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-13 Discuss the challenges facing healthcare providers in view of modern-day bioterrorist

threats.

Question 23

Type: SEQ

A nurse is discussing how drugs are approved with a health care provider. Place the stages of approval for

therapeutic and biological drugs in the appropriate sequence.

NDA submission with review

Preclinical investigation

Clinical investigation

Post-marketing studies

Correct Answer: 2, 3, 1, 4

Global Rationale: The correct order of drug review is preclinical investigation, clinical investigation, NDA submission

with review followed by post-marketing studies.

Cognitive Level: Understanding

Client Need: Safe Effective Care Environment

Client Need Sub:

Nursing/Integrated Concepts: Nursing Process: Implementation

Learning Outcome: 1-11 Identify four stages of approval for therapeutic and biologic drugs.

Holland/Adams/Brice, Core Concepts in Pharmacology, 4th edition

 

core concepts in pharmacology 4th edition test bank

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