Deck 2: Medication Development,regulation,and Resources

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Question
Who assigns a brand name to a new medication?

A)The FDA
B)Manufacturer
C)Pharmacist
D)Drug reference publishers
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Question
The full quantity contained in a medication bottle is its

A)control number.
B)administration route.
C)total volume.
D)supply dosage.
Question
Nonprescription medications are also known as which one of the following?

A)Addictive medications
B)Over-the-counter medications
C)Controlled substances
D)Schedule C-II medications
Question
Which federal action sets the standards for quality and requires proper medication labeling for preparations containing morphine?

A)Durham-Humphrey Amendments
B)Food, Drug, and Cosmetic Act
C)Pure Food and Drug Act
D)Controlled Substances Act
Question
Which government agency was established to enforce the Controlled Substances Act?

A)Occupational Safety and Health Administration (OSHA)
B)The U.S. Food and Drug Administration (FDA)
C)The Drug Enforcement Agency (DEA)
D)The Joint Commission
Question
On some medication labels,the generic name is

A)placed inside parentheses.
B)capitalized.
C)not required.
D)most prominent.
Question
Coordination of research about drug abuse in another country is regulated by the

A)CDC
B)WHO
C)FDA
D)DEA
Question
Drugs that are listed with a C-I are considered to

A)have a high-abuse potential with no medical use.
B)be appropriate for postoperative pain control.
C)have a low-abuse potential (e.g., steroids).
D)be available over the counter.
Question
All of the following are on the "Do Not Use" list of abbreviations except

A)U for unit.
B)the trailing zero.
C)QD for once daily.
D)zero before the decimal point.
Question
The organization that internationally regulates medications is

A)The Joint Commission.
B)FDA.
C)OSHA.
D)The World Health Organization.
Question
Which drug law established classifications,known as schedules,of medications that had potential for abuse?

A)Controlled Substances Act
B)Pure Food and Drug Act
C)Federal Food, Drug, and Cosmetic Act
D)Drug Enforcement Administration
Question
Which of the following is an advantage of pharmacogenomics?

A)Complexity of the genetic research
B)Cost of the genetic research
C)Education in the use of this technology
D)Facilitate the medication approval process
Question
Drugs from which controlled substance schedule have an accepted use in the surgical setting?

A)C-I
B)C-II
C)C-III
D)C-IV
Question
A medication's generic name is

A)never capitalized on the label.
B)followed by the registered trademark (®) symbol.
C)its formula.
D)its proprietary name.
Question
All are found on medication labels,except

A)supply dosage.
B)control number.
C)label alert.
D)PDR number.
Question
What should be done to an otic suspension medication to dilute the particles before it is administered to the patient?

A)It must be liquefied.
B)It must be concentrated.
C)It must be shaken.
D)It must be sterilized.
Question
All of the following are disadvantages to pharmacogenetics except

A)its use to target specific diseases.
B)the complexity of its development.
C)the cost of genetic research.
D)educating health care providers to its use.
Question
The identifying number on every prescription that is required by federal law is called the

A)National Drug Code.
B)label alert.
C)barcode symbol.
D)lot number.
Question
How does a surgical technologist know if he or she can handle and administer medications in his or her state?

A)By asking the surgeon
B)By asking the facility's risk management
C)By researching the state's policy online
D)By contacting the AORN
Question
How should an outdated multiuse vial of a local anesthetic be handled?

A)By finishing the vial
B)By returning it to pharmacy
C)By giving it to anesthesia team
D)By discarding the vial
Question
Which categories of medications under the FDA's pregnancy categories are considered to be within safe limits for use during pregnancy?
Question
In the phases of human medication testing,what is the last phase?
Question
Which medication reference is published annually and updated quarterly by the American Society of Health-System Pharmacists,Bethesda,Md.?

A)AHFS
B)USP-NF
C)PDR
D)WHO
Question
Which source is the most reliable way to check that medication information is accurate online?

A)Searching the Internet
B)Using a government website
C)Asking a clinical coordinator
D)Calling the FDA
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Deck 2: Medication Development,regulation,and Resources
1
Who assigns a brand name to a new medication?

A)The FDA
B)Manufacturer
C)Pharmacist
D)Drug reference publishers
Manufacturer
2
The full quantity contained in a medication bottle is its

A)control number.
B)administration route.
C)total volume.
D)supply dosage.
total volume.
3
Nonprescription medications are also known as which one of the following?

A)Addictive medications
B)Over-the-counter medications
C)Controlled substances
D)Schedule C-II medications
Over-the-counter medications
4
Which federal action sets the standards for quality and requires proper medication labeling for preparations containing morphine?

A)Durham-Humphrey Amendments
B)Food, Drug, and Cosmetic Act
C)Pure Food and Drug Act
D)Controlled Substances Act
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
5
Which government agency was established to enforce the Controlled Substances Act?

A)Occupational Safety and Health Administration (OSHA)
B)The U.S. Food and Drug Administration (FDA)
C)The Drug Enforcement Agency (DEA)
D)The Joint Commission
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
6
On some medication labels,the generic name is

A)placed inside parentheses.
B)capitalized.
C)not required.
D)most prominent.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
7
Coordination of research about drug abuse in another country is regulated by the

A)CDC
B)WHO
C)FDA
D)DEA
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
8
Drugs that are listed with a C-I are considered to

A)have a high-abuse potential with no medical use.
B)be appropriate for postoperative pain control.
C)have a low-abuse potential (e.g., steroids).
D)be available over the counter.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
9
All of the following are on the "Do Not Use" list of abbreviations except

A)U for unit.
B)the trailing zero.
C)QD for once daily.
D)zero before the decimal point.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
10
The organization that internationally regulates medications is

A)The Joint Commission.
B)FDA.
C)OSHA.
D)The World Health Organization.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
11
Which drug law established classifications,known as schedules,of medications that had potential for abuse?

A)Controlled Substances Act
B)Pure Food and Drug Act
C)Federal Food, Drug, and Cosmetic Act
D)Drug Enforcement Administration
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
12
Which of the following is an advantage of pharmacogenomics?

A)Complexity of the genetic research
B)Cost of the genetic research
C)Education in the use of this technology
D)Facilitate the medication approval process
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
13
Drugs from which controlled substance schedule have an accepted use in the surgical setting?

A)C-I
B)C-II
C)C-III
D)C-IV
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
14
A medication's generic name is

A)never capitalized on the label.
B)followed by the registered trademark (®) symbol.
C)its formula.
D)its proprietary name.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
15
All are found on medication labels,except

A)supply dosage.
B)control number.
C)label alert.
D)PDR number.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
16
What should be done to an otic suspension medication to dilute the particles before it is administered to the patient?

A)It must be liquefied.
B)It must be concentrated.
C)It must be shaken.
D)It must be sterilized.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
17
All of the following are disadvantages to pharmacogenetics except

A)its use to target specific diseases.
B)the complexity of its development.
C)the cost of genetic research.
D)educating health care providers to its use.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
18
The identifying number on every prescription that is required by federal law is called the

A)National Drug Code.
B)label alert.
C)barcode symbol.
D)lot number.
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
19
How does a surgical technologist know if he or she can handle and administer medications in his or her state?

A)By asking the surgeon
B)By asking the facility's risk management
C)By researching the state's policy online
D)By contacting the AORN
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
20
How should an outdated multiuse vial of a local anesthetic be handled?

A)By finishing the vial
B)By returning it to pharmacy
C)By giving it to anesthesia team
D)By discarding the vial
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
21
Which categories of medications under the FDA's pregnancy categories are considered to be within safe limits for use during pregnancy?
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
22
In the phases of human medication testing,what is the last phase?
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
23
Which medication reference is published annually and updated quarterly by the American Society of Health-System Pharmacists,Bethesda,Md.?

A)AHFS
B)USP-NF
C)PDR
D)WHO
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
24
Which source is the most reliable way to check that medication information is accurate online?

A)Searching the Internet
B)Using a government website
C)Asking a clinical coordinator
D)Calling the FDA
Unlock Deck
Unlock for access to all 24 flashcards in this deck.
Unlock Deck
k this deck
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Unlock Deck
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