Health Professions, 9th Edition Bruce Colbert
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
1. Which of the following require(s) a prescription but not a DEA number?
a. Standards
b. Controlled (schedule) drug
c. Legend drug
d. FDA
ANSWER: c
FEEDBACK: a. Incorrect. Standards do not require a prescription or DEA number.
b. Incorrect. Controlled (schedule) drugs require a DEA number.
c. Correct. Legend drugs need a prescription, but not a DEA number.
d. Incorrect. The FDA is the U.S. Food and Drug Administration.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 4:12 AM
DATE MODIFIED: 9/30/2022 5:12 AM
2. Which of these was/were established by the 1906 Pure Food and Drug Act?
a. Standards
b. Controlled (schedule) drugs
c. Legend drugs
d. FDA
ANSWER: a
FEEDBACK: a. Correct. Standards were established by the 1906 Pure Food and Drug
Act.
b. Incorrect. Controlled (schedule) drugs were not established by the 1906
Pure Food and Drug Act.
c. Incorrect. Legend drugs were not established by the 1906 Pure Food and
Drug Act.
d. Incorrect. The FDA is the U.S. Food and Drug Administration and was
not established by the 1906 Pure Food and Drug Act.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 4:45 AM
DATE MODIFIED: 8/18/2022 8:42 PM
3. Which of the following require(s) a prescription and DEA number?
a. Standards
b. Controlled (schedule) drug
c. Legend drug
d. FDA
ANSWER: b
FEEDBACK: a. Incorrect. Standards do not require a prescription or DEA number.
b. Correct. Controlled (schedule) drugs require a DEA number and a
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
prescription.
c. Incorrect. Legend drugs need a prescription but not a DEA number.
d. Incorrect. The FDA is the U.S. Food and Drug Administration.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 4:47 AM
DATE MODIFIED: 8/22/2022 4:01 AM
4. What is the name of the enforcement agency established by the 1970 Controlled Substances Act?
a. DEA
b. FBI
c. SWAT
d. FDA
ANSWER: a
FEEDBACK: a. Correct. The DEA was established by the 1970 Controlled Substances
Act.
b. Incorrect. The FBI was not established by the 1970 Controlled
Substances Act.
c. Incorrect. SWAT was not established by the 1970 Controlled Substances
Act.
d. Incorrect. The FDA is the U.S. Food and Drug Administration and was
not established by the 1970 Controlled Substances Act.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 4:49 AM
DATE MODIFIED: 8/22/2022 4:05 AM
5. Which of the following is the approval agency established by the 1938 Federal Food, Drug, and
Cosmetic Act?
a. Standards
b. Controlled (schedule) drug
c. Legend drug
d. FDA
ANSWER: d
FEEDBACK: a. Incorrect. Standards were not established by the 1938 Federal Food,
Drug, and Cosmetic Act.
b. Incorrect. Controlled (schedule) drugs were not established by the 1938
Federal Food, Drug, and Cosmetic Act.
c. Incorrect. Legend drugs were not established by the 1938 Federal Food,
Drug, and Cosmetic Act.
d. Correct. The FDA is the U.S. Food and Drug Administration and was
established by the 1938 Federal Food, Drug, and Cosmetic Act.
POINTS: 1
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 4:51 AM
DATE MODIFIED: 9/30/2022 5:09 AM
6. Which of the following best describes the uniform strength, purity, and quality of drugs?
a. Orphan drug
b. Drug standards
c. NDC
d. USP/NF
ANSWER: b
FEEDBACK: a. Incorrect. Orphan drugs treat diseases that affect a very small number of
people.
b. Correct. Drug standards describe the uniform strength, purity, and
quality of drugs.
c. Incorrect. NDC is a directory listing drugs by manufacturer and
packaging type(s).
d. Incorrect. The USP/NF describes a directory listing of officially
approved drugs.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 4:52 AM
DATE MODIFIED: 8/18/2022 7:01 AM
7. Drug that treats a disease affecting a very small number of people are called _____.
a. orphan drug
b. drug standards
c. NDC
d. USP/NF
ANSWER: a
FEEDBACK: a. Correct. Orphan drugs treat diseases that affect a very small number of
people.
b. Incorrect. Drug standards describe the uniform strength, purity, and
quality of drugs.
c. Incorrect. NDC is a directory listing drugs by manufacturer and
packaging type(s).
d. Incorrect. The USP/NF describes a directory listing of officially
approved drugs.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:00 AM
DATE MODIFIED: 8/18/2022 7:02 AM
8. Which of the following is a directory listing drugs by manufacturer and packaging type(s)?
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
a. Orphan drug
b. Drug standards
c. NDC
d. USP/NF
ANSWER: c
FEEDBACK: a. Incorrect. Orphan drugs treat diseases that affect a very small number of people.
b. Incorrect. Drug standards describe the uniform strength, purity, and quality of drugs.
c. Correct. NDC is a directory listing drugs by manufacturer and packaging type(s).
d. Incorrect. The USP/NF describes a directory listing of officially approved drugs.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:02 AM
DATE MODIFIED: 8/18/2022 7:02 AM
9. Which of the following is a directory listing of officially approved drugs (it was originally two
references)?
a. Orphan drug
b. Drug standards
c. NDC
d. USP/NF
ANSWER: d
FEEDBACK: a. Incorrect. Orphan drugs treat diseases that affect a very small number of
people.
b. Incorrect. Drug standards describe the uniform strength, purity, and
quality of drugs.
c. Incorrect. NDC is a directory listing drugs by manufacturer and
packaging type(s).
d. Correct. The USP/NF describes a directory listing of officially approved
drugs.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:04 AM
DATE MODIFIED: 8/18/2022 8:42 PM
10. Which of these describe(s) drugs that require no prescription for purchasing?
a. OTC
b. Drug standards
c. NDC
d. USP/NF
ANSWER: a
FEEDBACK: a. Correct. OTC drugs require no prescription.
b. Incorrect. Drug standards describe the uniform strength, purity, and
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
quality of drugs.
c. Incorrect. NDC is a directory listing drugs by manufacturer and
packaging type(s).
d. Incorrect. The USP/NF describes a directory listing of officially
approved drugs.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:05 AM
DATE MODIFIED: 9/30/2022 5:03 AM
11. The pharmaceutical manufacturer has the authority to add additional active ingredients to a previously
approved pharmaceutical product.
ANSWER: False - According to the 1938 Federal Food, Drug, and Cosmetic Act and
Amendments of 1951 and 1962, all labels must be accurate and include a
listing of all active and inactive ingredients.
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:07 AM
DATE MODIFIED: 8/18/2022 5:08 AM
12. Drug strength may vary with each lot number of a medication.
ANSWER: False - The 1906 Pure Food and Drug Act established that all drugs
marketed in the United States must meet minimal standards of uniform
strength, purity, and quality.
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:08 AM
DATE MODIFIED: 8/18/2022 5:08 AM
13. The Pure Food and Drug Act of 1906 established drug standards and official drug references.
ANSWER: True
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:09 AM
DATE MODIFIED: 8/18/2022 5:09 AM
14. The 1906 Pure Food and Drug Act established consumer protections to prevent the inclusion of
“dangerous ingredients” without the knowledge of the consumer.
ANSWER: True
POINTS: 1
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:09 AM
DATE MODIFIED: 8/18/2022 5:10 AM
15. Medication labels need to only include the trade name of the drug.
ANSWER: False - Labels must include a listing of all active and inactive ingredients,
warning labels on certain preparations, and generic names for the
medication.
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:10 AM
DATE MODIFIED: 9/30/2022 2:24 AM
16. The prescriber of a medication is the only health care professional who is responsible for being aware
of new medications, laws, and restrictions.
ANSWER: False - The health care workers involved in dispensing and administering a
medication are also responsible for being aware of the laws and restrictions
pertinent to that medication.
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:10 AM
DATE MODIFIED: 8/18/2022 5:18 AM
17. A double-locked system is the recommended method for maintaining the security of controlled
substances.
ANSWER: True
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:11 AM
DATE MODIFIED: 8/18/2022 5:11 AM
18. Health care workers are responsible for maintaining records of all controlled substances received,
dispensed, and destroyed.
a. True
b. False
ANSWER: True
POINTS: 1
QUESTION TYPE: True / False
HAS VARIABLES: False
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,Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
DATE CREATED: 8/18/2022 5:18 AM
DATE MODIFIED: 8/18/2022 5:18 AM
19. Controlled substance records are to be kept for 10 years.
ANSWER: False - Records for the previous 2 years must be available at all times for
inspection.
POINTS: 1
QUESTION TYPE: Modified True / False
HAS VARIABLES: False
STUDENT ENTRY MODE: Basic
DATE CREATED: 8/18/2022 5:19 AM
DATE MODIFIED: 8/18/2022 5:19 AM
20. The NDC contains the manufacturer, product, and package information for all commercially available
products.
a. True
b. False
ANSWER: True
POINTS: 1
QUESTION TYPE: True / False
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:19 AM
DATE MODIFIED: 8/18/2022 5:20 AM
21. Identify the drug standard in the following list.
a. Color
b. Strength
c. Shape
d. Taste
ANSWER: b
FEEDBACK: a. Incorrect. Color is not a drug standard.
b. Correct. Strength is a drug standard.
c. Incorrect. Shape is not a drug standard.
d. Incorrect. Taste is not a drug standard.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:20 AM
DATE MODIFIED: 8/18/2022 11:00 AM
22. The risk of death from the use of street drugs versus prescription medications is mostly due to _____.
a. the lack of control over the quality, purity, and strength of street drugs, which makes them
dangerous
b. the need for a prescription, which makes drugs hard to obtain
c. street drugs being approved for use
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, Name: Class: Date:
Chapter 01 - Consumer Safety and Drug Regulations
d. The risk is the same for both sources of the same substance.
ANSWER: a
FEEDBACK: a. Correct. There is no control over the quality, purity, or strength of street drugs.
b. Incorrect. Street drugs are illegal.
c. Incorrect. The exact composition of a street drug is unknown, and it may contain danger
contaminants or undisclosed additional drugs.
d. Incorrect. The lack of enforcement of drug standards in illegal street drugs poses a signi
for the consumer.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:21 AM
DATE MODIFIED: 8/18/2022 11:01 AM
23. Drug standards regulate the manufacture of drugs so that medications with the same name will be of
the same ____.
a. strength, purity, and quality
b. shape, color, and taste
c. purity, shape, and color
d. quality, color, and smell
ANSWER: a
FEEDBACK: a. Correct. Drug standards regulate manufacture of drugs related to
strength, purity and quality.
b. Incorrect. Drug standards do not regulate tastes.
c. Incorrect. Drug standards do not regulate color.
d. Incorrect. Drug standards do not regulate smell.
POINTS: 1
QUESTION TYPE: Multiple Choice
HAS VARIABLES: False
DATE CREATED: 8/18/2022 5:23 AM
DATE MODIFIED: 9/27/2022 8:21 AM
24. The 1906 Pure Food and Drug Act includes which of the following provisions?
a. Regulates drugs sold in the United States and Canada
b. Requires labeling to indicate if a medication contains a “dangerous ingredient”
c. Regulates illicit (illegal) drugs
d. Requires information regarding medications to be handed down from one practitioner to the
next
ANSWER: b
FEEDBACK: a. Incorrect. The Pure Food and Drug Act regulates all drugs marketed in
the United States. If a drug is manufactured in Canada, it must meet U.S.
FDA requirements to be marketed here.
b. Correct. The 1906 Pure Food and Drug Act requires labeling to indicate
if a medication contains a dangerous ingredient.
c. Incorrect. Illicit drugs are not regulated.
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