1. What is the name under which a drug is listed by the U.S. Food and Drug Administration (FDA)?
a Brand
.
b Nonproprietary
.
c Official
.
d Trademark
.
2. Which source contains information specific to nutritional supplements?
a USP Dictionary of USAN & International Drug Names
.
b Natural Medicines Comprehensive Database
.
c United States Pharmacopoeia/National Formulary (USP-NF)
.
d Drug Interaction Facts
.
3. What is the most comprehensive reference available to research a drug interaction?
a Drug Facts and Comparisons
.
b Drug Interaction Facts
.
c Handbook on Injectable Drugs
.
d Martindale—The Complete Drug Reference
.
4. Which legislation authorizes the FDA to determine the safety of a drug before its marketing?
a Federal Food, Drug, and Cosmetic Act (1938)
.
b Durham-Humphrey Amendment (1952)
.
c Controlled Substances Act (1970)
.
d Kefauver-Harris Drug Amendment (1962)
. What would the FDA do to expedite drug development and approval for an outbreak of smallpox, forwhich
there is no known treatment?
a List smallpox as a health orphan disease.
.
b Omit the preclinical research phase.
.
c Extend the clinical research phase.
.
d Fast-track the investigational drug.
.
6. The nurse is administering Lomotil, a Schedule V drug. Which statement is true about this drug’s
classification?
a Abuse potential for this drug is low.
.
b Psychological dependency is likely.
.
c There is a high potential for abuse.
.
d This drug is not a controlled substance.
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