TEST BANK FOR ESSENTIALS OF
PHARMACOLOGY FOR HEALTH
PROFESSIONS 8TH EDITION BY
BRUCE COLBERT RUTH 2026 2027
VERIFIED ANSWERS ACTUAL
UPDATED PRACTICE QUESTIONS
HIGH YIELD STUDY GUIDE GRADED
A+
CHAPTER 1: CONSUMER SAFETY AND DRUG REGULATIONS
TRUE/FALSE
1. The pharmaceutical manufacturer has the authority to add additional active ingredients to a
previously approved pharmaceutical product.
ANS: F
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.
PTS: 1
2. Drug strength may vary with each lot number of a medication.
ANS: F
The 1906 Pure Food and Drug Act established that all drugs marketed in the United States meet
minimal standards of strength, purity, and quality.
, , ,,
, PTS: 1
3. The Pure Food and Drug Act of 1906 established drug standards and official drug references.
ANS: T
This act established that all drugs marketed in the United States meet minimal standards
of strength, purity, and quality. It also established two official references that established
the standards for making each drug: The U.S. Pharmacopeia (USP) and the National
Formulary (NF).
PTS: 1
4. The 1906 Pure Food and Drug Act established consumer protections to prevent the inclusion of
“dangerous ingredients” without the knowledge of the consumer.
ANS: T
Morphine is one example of a dangerous ingredient that may have been included without the
knowledge of the consumer.
PTS: 1
5. Medication labels need only include the trade name of the drug.
ANS: F
Labels must include a listing of all active and inactive ingredients, warning labels on certain
preparations, and generic names for the medication
, , ,,
, ,
PTS: 1
6. The prescriber of the medication is the only health care professional who is responsible
for being aware of new medications, laws, and restrictions.
ANS: F
The health care worker involved in administration of a medication also bears the
responsibility of being aware of the laws and restrictions pertinent to that medication.
PTS: 1
7. A double-locked system is the recommended method for maintaining security of controlled
substances.
ANS: T
A double-locked system may include two separate key entries or an electronic user
identification and password access system.
PTS: 1
8. Health care workers are responsible for maintaining records of all controlled substances
received, dispensed, and destroyed.
ANS: T PTS: 1
9. Controlled substance records are to be kept for 10 years.
ANS: F
Records for the previous 2 years must be available at all times for inspection.
PTS: 1
MULTIPLE CHOICE
1. Identify the drug standard in the following list.
a. Color c. Shape
b. Strength d. Taste
ANS: B
Feedback
, , ,,
, ,
A
Color is not a standard.
B
Correct!
C
Shape is not a standard.
D
Taste is not a standard.
PTS: 1
2. The risk of death from the use of street drugs versus prescription
medications is mostly due to:
a.
a lack of control over quality, purity, and
strength makes street drugs dangerous.
b. the risk is the same for both sources of the
same substance.
c. street drugs are approved for use.
d. the need for a prescription makes drugs
hard to obtain.
ANS: A
Feedback
A
Correct!
B
The lack of enforcement of drug
standards in illegal street drugs poses a
significant danger for the consumer.
C
The exact composition of a street drug is
unknown, and it may contain dangerous
contaminants or undisclosed additional
drugs.
D Street drugs are illegal.
PTS: 1
3. Drug standards regulate drug manufacture so that medications of the same
name will be of the same:
, , ,,
PHARMACOLOGY FOR HEALTH
PROFESSIONS 8TH EDITION BY
BRUCE COLBERT RUTH 2026 2027
VERIFIED ANSWERS ACTUAL
UPDATED PRACTICE QUESTIONS
HIGH YIELD STUDY GUIDE GRADED
A+
CHAPTER 1: CONSUMER SAFETY AND DRUG REGULATIONS
TRUE/FALSE
1. The pharmaceutical manufacturer has the authority to add additional active ingredients to a
previously approved pharmaceutical product.
ANS: F
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.
PTS: 1
2. Drug strength may vary with each lot number of a medication.
ANS: F
The 1906 Pure Food and Drug Act established that all drugs marketed in the United States meet
minimal standards of strength, purity, and quality.
, , ,,
, PTS: 1
3. The Pure Food and Drug Act of 1906 established drug standards and official drug references.
ANS: T
This act established that all drugs marketed in the United States meet minimal standards
of strength, purity, and quality. It also established two official references that established
the standards for making each drug: The U.S. Pharmacopeia (USP) and the National
Formulary (NF).
PTS: 1
4. The 1906 Pure Food and Drug Act established consumer protections to prevent the inclusion of
“dangerous ingredients” without the knowledge of the consumer.
ANS: T
Morphine is one example of a dangerous ingredient that may have been included without the
knowledge of the consumer.
PTS: 1
5. Medication labels need only include the trade name of the drug.
ANS: F
Labels must include a listing of all active and inactive ingredients, warning labels on certain
preparations, and generic names for the medication
, , ,,
, ,
PTS: 1
6. The prescriber of the medication is the only health care professional who is responsible
for being aware of new medications, laws, and restrictions.
ANS: F
The health care worker involved in administration of a medication also bears the
responsibility of being aware of the laws and restrictions pertinent to that medication.
PTS: 1
7. A double-locked system is the recommended method for maintaining security of controlled
substances.
ANS: T
A double-locked system may include two separate key entries or an electronic user
identification and password access system.
PTS: 1
8. Health care workers are responsible for maintaining records of all controlled substances
received, dispensed, and destroyed.
ANS: T PTS: 1
9. Controlled substance records are to be kept for 10 years.
ANS: F
Records for the previous 2 years must be available at all times for inspection.
PTS: 1
MULTIPLE CHOICE
1. Identify the drug standard in the following list.
a. Color c. Shape
b. Strength d. Taste
ANS: B
Feedback
, , ,,
, ,
A
Color is not a standard.
B
Correct!
C
Shape is not a standard.
D
Taste is not a standard.
PTS: 1
2. The risk of death from the use of street drugs versus prescription
medications is mostly due to:
a.
a lack of control over quality, purity, and
strength makes street drugs dangerous.
b. the risk is the same for both sources of the
same substance.
c. street drugs are approved for use.
d. the need for a prescription makes drugs
hard to obtain.
ANS: A
Feedback
A
Correct!
B
The lack of enforcement of drug
standards in illegal street drugs poses a
significant danger for the consumer.
C
The exact composition of a street drug is
unknown, and it may contain dangerous
contaminants or undisclosed additional
drugs.
D Street drugs are illegal.
PTS: 1
3. Drug standards regulate drug manufacture so that medications of the same
name will be of the same:
, , ,,
