Test bank for essentials of pharmacology for health professions, 8th edition, Bruce Col... Test bank for essentials of pharmacology for health professions, 8th edition, Bruce Colbert, Ruth Woodrow Test bank for essentials of pharmacology for health professions, 8th edition, Bruce Colbert, Ruth Wood...
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Test Bank for
Essentials of
Pharmacology for
Health
Professions, 8th
Edition, Bruce
Colbert, Ruth
Woodrow
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CHAPTER 1: CONSUMER SAFETY AND DRUG REGULATIONS
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TRUE/FALSE
1. The pharmaceutical manufacturer has the authority to add additional active ingredients
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to a previously approved pharmaceutical product.
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ANS: F O L
According to the 1938 Federal Food, Drug, and Cosmetic Act and Amendments of 195
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1 and 1962, all labels must be accurate and include a listing of all active and inactive in
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gredients.
PTS: 1 OLO L
2. Drug strength may vary with each lot number of a medication. ANS: F
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The 1906 Pure Food and Drug Act established that all drugs marketed in the
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United States meet minimal standards of strength, purity, and quality. PTS: 1
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3. The Pure Food and Drug Act of 1906 established drug standards and official drug refer
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ences.
ANS: T O L
This act established that all drugs marketed in the United States meet minimal standard
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s of strength, purity, and quality. It also established two official references that establish
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ed the standards for making each drug: The
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U.S. Pharmacopeia (USP) and the National Formulary (NF). PTS: 1
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4. The 1906 Pure Food and Drug Act established consumer protections to prevent the inc
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lusion of “dangerous ingredients” without the knowledge of the consumer.
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ANS: T O L
Morphine is one example of a dangerous ingredient that may have been included witho
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ut the knowledge of the consumer.
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PTS: 1 OLO L
5. Medication labels need only include the trade name of the drug. ANS: F OL OL OL OL OL OL OL OL OL OL O L O L
Labels must include a listing of all active and inactive ingredients, warning
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labels on certain preparations, and generic names for the medication
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PTS: 1 OLO L
6. The prescriber of the medication is the only health care professional who is responsibl
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e for being aware of new medications, laws, and restrictions.
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ANS: F O L
The health care worker involved in administration of a medication also bears the responsi
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bility of being aware of the laws and restrictions pertinent to that medication.
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PTS: 1 OLO L
7. A double-
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locked system is the recommended method for maintaining security of controlled substan
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ces.
ANS: T O L
A double-
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locked system may include two separate key entries or an electronic user identification a
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nd password access system.
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PTS: 1 OLO L
8. Health care workers are responsible for maintaining records of all controlled substances
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received, dispensed, and destroyed. OL OL OL
ANS: T O L PTS: 1 OLO L
9. Controlled substance records are to be kept for 10 years. ANS: F
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Records for the previous 2 years must be available at all times for inspection. PTS: 1
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MULTIPLE CHOICE OL
1. Identify the drug standard in the following list.
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a. Color c. Shape
b. Strength d. Taste
ANS: B O L
Feedback
A Color is not a standard. OL OL OL OL
B Correct!
C Shape is not a standard. OL OL OL OL
D Taste is not a standard. OL OL OL OL
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PTS: 1 OLO L
2. The risk of death from the use of street drugs versus prescription medicatio
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ns is mostly due to:
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a. a lack of control over quality, purity, and st
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rength makes street drugs dangerous. OL OL OL O L
b. the risk is the same for both sources of th
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e same substance.
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c. street drugs are approved for use. OL OL OL OL OL
d. the need for a prescription makes drug
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s hard to obtain.
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ANS: A O L
Feedback
A Correct!
B The lack of enforcement of drug stand
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ards in illegal street drugs poses a sign
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ificant danger for the consumer. OL OL OL O L
C The exact composition of a street drug is
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unknown, and it may contain dangerous c OL OL OL OL O L OL
ontaminants or undisclosed additional dru OL O L OL OL
gs.
D Street drugs are illegal. OL OL OL
PTS: 1 OLO L
3. Drug standards regulate drug manufacture so that medications of the same name will b
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e of the same:
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a. strength, purity, and quality. OL OL OL
b. shape, color, and taste. OL OL OL
c. purity, shape, and color. OL OL OL
d. quality, color, and shape. OL OL OL
ANS: A O L
Drug standards state that all preparations of the same drug name must be of uniform stre
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ngth, purity, and quality.
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PTS: 1 OLO L
4. The 1906 Pure Food and Drug Act includes which of the following provisions?
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a. Regulation of drugs sold in the OL OL OL OL OL
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