test bank for essentials of pharmacology for health professions 8thedition bruce colbert ruth woodrow.

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Test Bank for Essentials of
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Pharmacologyfor Health s ss ss




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Professions, 8 Edition, Br ss ss ss




uce Colbert, Ruth Woodr
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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 activ
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e ingredients to a previously approved pharmaceutical product.
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ANS: F s s




According to the 1938 Federal Food, Drug, and Cosmetic Act and Amendm e
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nts of 1951 and 1962, all labels must be accurate and include a listing of al l
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active and inactive ingredients. ss ss ss




PTS: 1 s s




2. Drug strength may vary with each lot number of a medication.
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ANS: F s s




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.
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PTS: 1 s s




3. The Pure Food and Drug Act of 1906 established drug standards and offici al
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ss drug references. ss




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This act established that all drugs marketed in the United States meet min i
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mal standards of strength, purity, and quality. It also established two offici
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al references that established the standards for making each drug: The
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U.S. Pharmacopeia (USP) and the National Formulary (NF).
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4. The 1906 Pure Food and Drug Act established consumer protections to p
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revent the inclusion of “dangerous ingredients” without the knowledge
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of the consumer.
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Morphine is one example of a dangerous ingredient that may have been incl
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uded without the knowledge of the consumer.
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PTS: 1 s s




5. Medication labels need only include the trade name of the drug.
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ANS: F s s




Labels must include a listing of all active and inactive ingredients, warning l a
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bels on certain preparations, and generic names for the medication
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6. The prescriber of the medication is the only health care professional who i
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s responsible for being aware of new medications, laws, and restrictions
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.


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The health care worker involved in administration of a medication also bear
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s the responsibility of being aware of the laws and restrictions pertinent to t
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hat medication.
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7. A double-
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locked system is the recommended method for maintaining security of contr
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s olled substances. ss




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A double-ss




locked system may include two separate key entries or an electronic user id
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entification and password access system. ss ss ss ss




PTS: 1 s s




8. Health care workers are responsible for maintaining records of all controlle
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s d substances received, dispensed, and destroyed.
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9. Controlled substance records are to be kept for 10 years.
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