,Chapter 01: Information Sources, Regulatory Agencies, Drug Legislation, and Prescription Writ
WS WS WS WS WS WS WS WS WS WS
ing
Haveles: Applied Pharmacology for the Dental Hygienist, 9th Edition
WS WS WS WS WS WS WS WS
MULTIPLE CHOICE WS
1. Knowledge of pharmacology aids the dental professional in WS WS WS WS WS WS WS
a. obtaining a patient’s health history. WS WS WS WS
b. administering drugs in the office. WS WS WS WS
c. handling emergency situations. WS WS
d. selection of a nonprescription medication. WS WS WS WS
e. All of the above. WS WS WS
ANS: E W S
All of the choices are true. Because many of our patients are being treated with drugs, knowledge of p
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
harmacology helps in understanding and interpreting patients’ responses to health history questions. K
WS WS WS WS WS WS WS WS WS WS WS WS
nowledge of the therapeutic and adverse effects of medications obviously helps in their proper admini
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
stration in the office. Emergency situations may be caused by drugs or treated by drugs; thus, knowle
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
dge of pharmacology is of great help, especially because a rapid response is sometimes required. A cl
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
ear understanding of the concepts of drug action, drug handling by the body, and drug interactions wil
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
l allow the dental practitioner to make proper judgments and grasp the concepts relevant to new drug t
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
herapies on the market. WS WS WS
DIF: Application
REF: Role of the Dental Hygienist (Medication/Health History), Role of the Dental Hygienist (Medicatio
W S WS WS WS WS WS WS WS WS WS WS WS WS
n Administration), Role of the Dental Hygienist (Emergency Situations), Role of the Dental Hygienist (No
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
nprescription Medication) | pp. 2-3 OBJ: 1 WS WS WS WS
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
2. Which of the following statements is true regarding planning appointments?
WS WS WS WS WS WS WS WS WS
a. Whether or not patients are taking medication for systemic diseases is of little
WS WS WS WS WS WS WS WS WS WS WS WS
consequence in the dental office. WS WS WS WS
b. Asthmatic patients should have dental appointments in the morning. WS WS WS WS WS WS WS WS
c. Diabetic patients usually have fewer problems with a morning appointment co
WS WS WS WS WS WS WS WS WS WS
mpared with afternoon appointments. WS WS WS
d. Both B and C are true. WS WS WS WS WS
ANS: D W S
Asthmatic patients who experience dental anxiety should schedule their appointments when they are n
WS WS WS WS WS WS WS WS WS WS WS WS WS
ot rushed or under pressure early in the morning. Diabetic patients usually have relatively fewer probl
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
ems with a morning appointment. Patients taking medication for systemic diseases may require special
WS WS WS WS WS WS WS WS WS WS WS WS WS
handling in the dental office.
WS WS WS WS WS
DIF: Comprehension
REF: Role of the Dental Hygienist (Appointment Scheduling) | p.
W S WS WS WS WS WS WS WS WS WS
3 OBJ: 1
WS TOP: NBDHE, 6.0. Pharmacology
W S W S WS WS
,3. Nutritional or herbal supplements WS WS WS
a. carry the U.S. Food and Drug Administration (FDA) approval for disease states.
WS WS WS WS WS WS WS WS WS WS WS
b. are not drugs. WS WS
c. can cause adverse effects. WS WS WS
d. will not interact with other drugs the patient may be taking.
WS WS WS WS WS WS WS WS WS WS
ANS: C W S
Nutritional or herbal supplements are quite capable of causing adverse effects. The majority of nutrition
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
al or herbal supplements do not carry FDA approval for treating disease states. These supplements are
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
drugs and can cause adverse effects and interact with different drugs.
WS WS WS WS WS WS WS WS WS WS
DIF: Comprehension
REF: Role of the Dental Hygienist (Nutritional or Herbal Supplements) | p.
W S WS WS WS WS WS WS WS WS WS WS WS
3 OBJ: 1
WS TOP: NBDHE, 6.0. Pharmacology
W S W S WS WS
4. Which type of drug name usually begins with a lowercase letter?
WS WS WS WS WS WS WS WS WS WS
a. Brand name WS
b. Code name WS
c. Generic name WS
d. Trade name WS
ANS: C W S
Before any drug is marketed, it is given a generic name that becomes the “official” name of the drug.
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
Each drug is assigned only one generic name selected by the U.S. Adopted Name Council, and the na
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
me is not capitalized. The brand name is equivalent to the trade name and is capitalized. Although the
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS W
brand name is technically the name of the company marketing the product, this term is often used inter
S WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
changeably with the trade name. The code name is the initial term used within a pharmaceutical comp
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
any to refer to a drug while it is undergoing investigation and is often a combination of capital letters
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
and numbers, the letters representing an abbreviation of the company name.
WS WS WS WS WS WS WS WS WS WS
DIF: Comprehension
REF: Drug Names | p. 4 OBJ: 3 W S WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology W S WS WS
5. A drug’s generic name is selected by the
WS WS WS WS WS WS WS
a. pharmaceutical company manufacturing it. WS WS WS
b. Food and Drug Administration (FDA). WS WS WS WS
c. U.S. Adopted Name Council. WS WS WS
d. Federal Patent Office. WS WS
ANS: C W S
Each drug is assigned only one generic name (e.g., ibuprofen). It is selected by the U.S. Adopted Na
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
me Council. The generic name is not selected by the FDA or the Federal Patent Office. The pharmace
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
utical company manufacturing the drug clearly has an influence on the generic name given its drug, bu
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
t the final decision is not the company’s.
WS WS WS WS WS WS WS
DIF: Recall REF: Drug Names | p. 4 W S WS WS WS WS
OBJ: 3 TOP: NBDHE, 6.0. Pharmacology
W S WS W S WS WS
6. Which of the following is true concerning generic and trade names of drugs?
WS WS WS WS WS WS WS WS WS WS WS WS
a. A drug may only have one generic name and one trade name.
WS WS WS WS WS WS WS WS WS WS WS
, b. A drug may only have one generic name, but it may have several trade names.
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
c. A drug may have several generic names, but it may only have one trade name.
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
d. A drug may have several generic names and several trade names.
WS WS WS WS WS WS WS WS WS WS
ANS: B W S
Each drug has only one generic name but may have several trade names. For each drug, there is only o
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
ne generic name. It is not capitalized, and it becomes the “official” name of the drug. The pharmaceuti
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
cal company discovering the drug gives the drug a trade name. The trade name is protected by the Fed
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
eral Patent Law for 20 years from the earliest claimed filing date, plus patent term extensions. Althoug
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
h the brand name is technically the name of the company marketing the product, it is often used interc
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
hangeably with the trade name. WS WS WS WS
DIF: Comprehension
REF: Drug Names | p. 4 OBJ: 3
W S WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
7. Two drugs that are found to be chemically equivalent, but not biologically equivalent or
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
therapeutically equivalent are said to differ in WS WS WS WS WS WS
a. potency.
b. efficacy.
c. bioavailability.
d. therapeutic index. WS
ANS: C W S
A preparation can be chemically equivalent yet not biologically or therapeutically equivalent. These p
WS WS WS WS WS WS WS WS WS WS WS WS WS
roducts are said to differ in their bioavailability. The potency of a drug is a function of the amount of d
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
rug required to produce an effect. The efficacy is the maximum intensity of effect or response that can
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
be produced by a drug. The therapeutic index is the ratio of the lethal dose for 50% of the experiment
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
al animals divided by the effective dose for 50% of the experimental animals. If the value of the thera
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
peutic index is small, toxicity is more likely.
WS WS WS WS WS WS WS
DIF: Recall
REF: Drug Names (Drug Substitution) | p. 5 OBJ: 4
W S WS WS WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
8. How many years must pass after a drug patent expires before other drug companies can market the
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
same compound as a generic drug?
WS WS WS WS WS
a. 20 years WS
b. 17 years WS
c. 7 years WS
d. 0 years WS
ANS: D W S
Once a drug patent expires, competing companies may immediately market the same compound in ge
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
neric form. The pharmaceutical company discovering the drug gives the drug a trade name. The trade
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
name is protected by the Federal Patent Law for 20 years from the earliest claimed filing date, plus the
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
patent term extensions. WS WS
DIF: Application
REF: Drug Names (Drug Substitution) | p. 5 OBJ: 4
W S WS WS WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
WS WS WS WS WS WS WS WS WS WS
ing
Haveles: Applied Pharmacology for the Dental Hygienist, 9th Edition
WS WS WS WS WS WS WS WS
MULTIPLE CHOICE WS
1. Knowledge of pharmacology aids the dental professional in WS WS WS WS WS WS WS
a. obtaining a patient’s health history. WS WS WS WS
b. administering drugs in the office. WS WS WS WS
c. handling emergency situations. WS WS
d. selection of a nonprescription medication. WS WS WS WS
e. All of the above. WS WS WS
ANS: E W S
All of the choices are true. Because many of our patients are being treated with drugs, knowledge of p
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
harmacology helps in understanding and interpreting patients’ responses to health history questions. K
WS WS WS WS WS WS WS WS WS WS WS WS
nowledge of the therapeutic and adverse effects of medications obviously helps in their proper admini
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
stration in the office. Emergency situations may be caused by drugs or treated by drugs; thus, knowle
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
dge of pharmacology is of great help, especially because a rapid response is sometimes required. A cl
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
ear understanding of the concepts of drug action, drug handling by the body, and drug interactions wil
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
l allow the dental practitioner to make proper judgments and grasp the concepts relevant to new drug t
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
herapies on the market. WS WS WS
DIF: Application
REF: Role of the Dental Hygienist (Medication/Health History), Role of the Dental Hygienist (Medicatio
W S WS WS WS WS WS WS WS WS WS WS WS WS
n Administration), Role of the Dental Hygienist (Emergency Situations), Role of the Dental Hygienist (No
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
nprescription Medication) | pp. 2-3 OBJ: 1 WS WS WS WS
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
2. Which of the following statements is true regarding planning appointments?
WS WS WS WS WS WS WS WS WS
a. Whether or not patients are taking medication for systemic diseases is of little
WS WS WS WS WS WS WS WS WS WS WS WS
consequence in the dental office. WS WS WS WS
b. Asthmatic patients should have dental appointments in the morning. WS WS WS WS WS WS WS WS
c. Diabetic patients usually have fewer problems with a morning appointment co
WS WS WS WS WS WS WS WS WS WS
mpared with afternoon appointments. WS WS WS
d. Both B and C are true. WS WS WS WS WS
ANS: D W S
Asthmatic patients who experience dental anxiety should schedule their appointments when they are n
WS WS WS WS WS WS WS WS WS WS WS WS WS
ot rushed or under pressure early in the morning. Diabetic patients usually have relatively fewer probl
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
ems with a morning appointment. Patients taking medication for systemic diseases may require special
WS WS WS WS WS WS WS WS WS WS WS WS WS
handling in the dental office.
WS WS WS WS WS
DIF: Comprehension
REF: Role of the Dental Hygienist (Appointment Scheduling) | p.
W S WS WS WS WS WS WS WS WS WS
3 OBJ: 1
WS TOP: NBDHE, 6.0. Pharmacology
W S W S WS WS
,3. Nutritional or herbal supplements WS WS WS
a. carry the U.S. Food and Drug Administration (FDA) approval for disease states.
WS WS WS WS WS WS WS WS WS WS WS
b. are not drugs. WS WS
c. can cause adverse effects. WS WS WS
d. will not interact with other drugs the patient may be taking.
WS WS WS WS WS WS WS WS WS WS
ANS: C W S
Nutritional or herbal supplements are quite capable of causing adverse effects. The majority of nutrition
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
al or herbal supplements do not carry FDA approval for treating disease states. These supplements are
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
drugs and can cause adverse effects and interact with different drugs.
WS WS WS WS WS WS WS WS WS WS
DIF: Comprehension
REF: Role of the Dental Hygienist (Nutritional or Herbal Supplements) | p.
W S WS WS WS WS WS WS WS WS WS WS WS
3 OBJ: 1
WS TOP: NBDHE, 6.0. Pharmacology
W S W S WS WS
4. Which type of drug name usually begins with a lowercase letter?
WS WS WS WS WS WS WS WS WS WS
a. Brand name WS
b. Code name WS
c. Generic name WS
d. Trade name WS
ANS: C W S
Before any drug is marketed, it is given a generic name that becomes the “official” name of the drug.
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
Each drug is assigned only one generic name selected by the U.S. Adopted Name Council, and the na
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
me is not capitalized. The brand name is equivalent to the trade name and is capitalized. Although the
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS W
brand name is technically the name of the company marketing the product, this term is often used inter
S WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
changeably with the trade name. The code name is the initial term used within a pharmaceutical comp
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
any to refer to a drug while it is undergoing investigation and is often a combination of capital letters
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
and numbers, the letters representing an abbreviation of the company name.
WS WS WS WS WS WS WS WS WS WS
DIF: Comprehension
REF: Drug Names | p. 4 OBJ: 3 W S WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology W S WS WS
5. A drug’s generic name is selected by the
WS WS WS WS WS WS WS
a. pharmaceutical company manufacturing it. WS WS WS
b. Food and Drug Administration (FDA). WS WS WS WS
c. U.S. Adopted Name Council. WS WS WS
d. Federal Patent Office. WS WS
ANS: C W S
Each drug is assigned only one generic name (e.g., ibuprofen). It is selected by the U.S. Adopted Na
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
me Council. The generic name is not selected by the FDA or the Federal Patent Office. The pharmace
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
utical company manufacturing the drug clearly has an influence on the generic name given its drug, bu
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
t the final decision is not the company’s.
WS WS WS WS WS WS WS
DIF: Recall REF: Drug Names | p. 4 W S WS WS WS WS
OBJ: 3 TOP: NBDHE, 6.0. Pharmacology
W S WS W S WS WS
6. Which of the following is true concerning generic and trade names of drugs?
WS WS WS WS WS WS WS WS WS WS WS WS
a. A drug may only have one generic name and one trade name.
WS WS WS WS WS WS WS WS WS WS WS
, b. A drug may only have one generic name, but it may have several trade names.
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
c. A drug may have several generic names, but it may only have one trade name.
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
d. A drug may have several generic names and several trade names.
WS WS WS WS WS WS WS WS WS WS
ANS: B W S
Each drug has only one generic name but may have several trade names. For each drug, there is only o
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
ne generic name. It is not capitalized, and it becomes the “official” name of the drug. The pharmaceuti
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
cal company discovering the drug gives the drug a trade name. The trade name is protected by the Fed
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
eral Patent Law for 20 years from the earliest claimed filing date, plus patent term extensions. Althoug
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
h the brand name is technically the name of the company marketing the product, it is often used interc
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
hangeably with the trade name. WS WS WS WS
DIF: Comprehension
REF: Drug Names | p. 4 OBJ: 3
W S WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
7. Two drugs that are found to be chemically equivalent, but not biologically equivalent or
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
therapeutically equivalent are said to differ in WS WS WS WS WS WS
a. potency.
b. efficacy.
c. bioavailability.
d. therapeutic index. WS
ANS: C W S
A preparation can be chemically equivalent yet not biologically or therapeutically equivalent. These p
WS WS WS WS WS WS WS WS WS WS WS WS WS
roducts are said to differ in their bioavailability. The potency of a drug is a function of the amount of d
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
rug required to produce an effect. The efficacy is the maximum intensity of effect or response that can
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
be produced by a drug. The therapeutic index is the ratio of the lethal dose for 50% of the experiment
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
al animals divided by the effective dose for 50% of the experimental animals. If the value of the thera
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
peutic index is small, toxicity is more likely.
WS WS WS WS WS WS WS
DIF: Recall
REF: Drug Names (Drug Substitution) | p. 5 OBJ: 4
W S WS WS WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology
W S WS WS
8. How many years must pass after a drug patent expires before other drug companies can market the
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
same compound as a generic drug?
WS WS WS WS WS
a. 20 years WS
b. 17 years WS
c. 7 years WS
d. 0 years WS
ANS: D W S
Once a drug patent expires, competing companies may immediately market the same compound in ge
WS WS WS WS WS WS WS WS WS WS WS WS WS WS
neric form. The pharmaceutical company discovering the drug gives the drug a trade name. The trade
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
name is protected by the Federal Patent Law for 20 years from the earliest claimed filing date, plus the
WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS WS
patent term extensions. WS WS
DIF: Application
REF: Drug Names (Drug Substitution) | p. 5 OBJ: 4
W S WS WS WS WS WS WS WS W S
TOP: NBDHE, 6.0. Pharmacology
W S WS WS