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ition by Elena Bablenis Haveles
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Complete Test Bank
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,Chapter 01: Information Sources, Regulatory Agencies, Drug Legislation, and Prescription Writin
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g
Haveles: Applied Pharmacology for the Dental Hygienist, 9th Edition
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MULTIPLE CHOICE z
1. Knowledge of pharmacology aids the dental professional in z z z z z z z
a. obtaining a patient’s health history. z z z z
b. administering drugs in the office. z z z z
c. handling emergency situations. z z
d. selection of a nonprescription medication. z z z z
e. All of the above. z z z
ANS: E z
All of the choices are true. Because many of our patients are being treated with drugs, knowledge of phar
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macology helps in understanding and interpreting patients’ responses to health history questions. Knowle
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dge of the therapeutic and adverse effects of medications obviously helps in their proper administration in
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zthe office. Emergency situations may be caused by drugs or treated by drugs; thus, knowledge of pharma
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cology is of great help, especially because a rapid response is sometimes required. A clear understanding
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of the concepts of drug action, drug handling by the body, and drug interactions will allow the dental pract
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itioner to make proper judgments and grasp the concepts relevant to new drug therapies on the market.
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DIF: Application
REF: Role of the Dental Hygienist (Medication/Health History), Role of the Dental Hygienist (Medication Ad
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ministration), Role of the Dental Hygienist (Emergency Situations), Role of the Dental Hygienist (Nonprescri
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ption Medication) | pp. 2-3
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TOP: NBDHE, 6.0. Pharmacology
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2. Which of the following statements is true regarding planning appointments?
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a. Whether or not patients are taking medication for systemic diseases is of little
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consequence in the dental office. z z z z
b. Asthmatic patients should have dental appointments in the morning. z z z z z z z z
c. Diabetic patients usually have fewer problems with a morning appointment com
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pared with afternoon appointments. z z z
d. Both B and C are true. z z z z z
ANS: D z
Asthmatic patients who experience dental anxiety should schedule their appointments when they are not r
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ushed or under pressure early in the morning. Diabetic patients usually have relatively fewer problems wi
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th a morning appointment. Patients taking medication for systemic diseases may require special handling
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in the dental office.
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DIF: Comprehension
REF: Role of the Dental Hygienist (Appointment Scheduling) | p. 3 O
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BJ: 1 z TOP: NBDHE, 6.0. Pharmacology z z z
,3. Nutritional or herbal supplements z z z
a. carry the U.S. Food and Drug Administration (FDA) approval for disease states.
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b. are not drugs. z z
c. can cause adverse effects. z z z
d. will not interact with other drugs the patient may be taking.
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ANS: C z
Nutritional or herbal supplements are quite capable of causing adverse effects. The majority of nutritional o
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r herbal supplements do not carry FDA approval for treating disease states. These supplements are drugs an
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d can cause adverse effects and interact with different drugs.
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DIF: Comprehension
REF: Role of the Dental Hygienist (Nutritional or Herbal Supplements) | p. 3 O
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BJ: 1 z TOP: NBDHE, 6.0. Pharmacology z z z
4. Which type of drug name usually begins with a lowercase letter?
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a. Brand name z
b. Code name z
c. Generic name z
d. Trade name z
ANS: C z
Before any drug is marketed, it is given a generic name that becomes the ―official‖ name of the drug. Each
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drug is assigned only one generic name selected by the U.S. Adopted Name Council, and the name is not c
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apitalized. The brand name is equivalent to the trade name and is capitalized. Although the brand name is t
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echnically the name of the company marketing the product, this term is often used interchangeably with th
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e trade name. The code name is the initial term used within a pharmaceutical company to refer to a drug w
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hile it is undergoing investigation and is often a combination of capital letters and numbers, the letters rep
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resenting an abbreviation of the company name. z z z z z z
DIF: Comprehension
REF: Drug Names | p. 4 OBJ: 3 z z z z z z z
TOP: NBDHE, 6.0. Pharmacology z z z
5. A drug’s generic name is selected by the
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a. pharmaceutical company manufacturing it. z z z
b. Food and Drug Administration (FDA). z z z z
c. U.S. Adopted Name Council. z z z
d. Federal Patent Office. z z
ANS: C z
Each drug is assigned only one generic name (e.g., ibuprofen). It is selected by the U.S. Adopted Name C
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ouncil. The generic name is not selected by the FDA or the Federal Patent Office. The pharmaceutical co
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mpany manufacturing the drug clearly has an influence on the generic name given its drug, but the final de
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cision is not the company’s. z z z z
DIF: Recall REF: Drug Names | p. 4 z z z z z
OBJ: 3 TOP: NBDHE, 6.0. Pharmacologyz z z z z
6. Which of the following is true concerning generic and trade names of drugs?
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a. A drug may only have one generic name and one trade name.
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, b. A drug may only have one generic name, but it may have several trade names.
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c. A drug may have several generic names, but it may only have one trade name.
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d. A drug may have several generic names and several trade names.
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ANS: B z
Each drug has only one generic name but may have several trade names. For each drug, there is only one g
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eneric name. It is not capitalized, and it becomes the ―official‖ name of the drug. The pharmaceutical com
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pany discovering the drug gives the drug a trade name. The trade name is protected by the Federal Patent L
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aw for 20 years from the earliest claimed filing date, plus patent term extensions. Although the brand name
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is technically the name of the company marketing the product, it is often used interchangeably with the tra
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de name. z
DIF: Comprehension
REF: Drug Names | p. 4 OBJ: 3
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TOP: NBDHE, 6.0. Pharmacology
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7. Two drugs that are found to be chemically equivalent, but not biologically equivalent or the
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rapeutically equivalent are said to differ in z z z z z z
a. potency.
b. efficacy.
c. bioavailability.
d. therapeutic index. z
ANS: C z
A preparation can be chemically equivalent yet not biologically or therapeutically equivalent. These prod
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ucts are said to differ in their bioavailability. The potency of a drug is a function of the amount of drug requ
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ired to produce an effect. The efficacy is the maximum intensity of effect or response that can be produced
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zby a drug. The therapeutic index is the ratio of the lethal dose for 50% of the experimental animals divide
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d by the effective dose for 50% of the experimental animals. If the value of the therapeutic index is small, t
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oxicity is more likely. z z z
DIF: Recall
REF: Drug Names (Drug Substitution) | p. 5 OBJ: 4
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TOP: NBDHE, 6.0. Pharmacology
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8. How many years must pass after a drug patent expires before other drug companies can market the sam
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e compound as a generic drug?
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a. 20 years z
b. 17 years z
c. 7 years z
d. 0 years z
ANS: D z
Once a drug patent expires, competing companies may immediately market the same compound in generi
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c form. The pharmaceutical company discovering the drug gives the drug a trade name. The trade name is
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protected by the Federal Patent Law for 20 years from the earliest claimed filing date, plus the patent term
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extensions.
DIF: Application
REF: Drug Names (Drug Substitution) | p. 5 OBJ: 4
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TOP: NBDHE, 6.0. Pharmacology
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