Professional Documents
Culture Documents
1. The superscription section of the prescription contains the name of the drug and the quantities of ingredients.
a. True
b. False
ANSWER: False
2. The subscription section of the prescription contains directions to the pharmacist regarding the total quantity of the drug
and the form of the medication.
a. True
b. False
ANSWER: True
5. Drug flow sheets may be used to replace the physician’s initial dictation in the medical record.
a. True
b. False
ANSWER: False
6. Controlled substances may be flushed down the toilet when they have reached their expiration date.
a. True
b. False
ANSWER: False
7. The Harrison Narcotic Act of 1914 was the beginning of a long history of narcotic control legislation.
a. True
b. False
ANSWER: True
8. All controlled substances have a high potential for abuse and have no medical use.
a. True
b. False
ANSWER: False
10. Pharmacists do not provide medication instructions; that is entirely up to the medical office personnel.
a. True
b. False
ANSWER: False
Multiple Choice
11. The proprietary or trade name of a drug as copyrighted by the manufacturer is known as the
a. generic name. b. chemical name.
c. brand name. d. pharmacy name.
ANSWER: c
14. Vaporizers and nebulizers are examples of apparatus used to administer medication by means of
a. inhalation. b. injection.
c. injunction. d. instillation.
ANSWER: a
16. All methods of giving medications by means of a needle or cannula through the skin are referred to as
a. transdermal. b. parenteral.
c. topical. d. sublingual.
ANSWER: b
21. What is the correct term for a preparation with undissolved ingredients that must be shaken well before using?
a. Solution b. Suspension
c. Liquid d. Gel
ANSWER: b
22. What is the correct term for a liquid with ingredients that are dissolved evenly?
a. Gel b. Suspension
c. Ointment d. Solution
ANSWER: d
24. What is the name of the federal law passed in 1970 that requires the pharmaceutical industry to maintain physical
security and strict record keeping for intoxicating drugs?
a. The Volstead Act
b. The Food, Drug, and Cosmetic Act
c. The Controlled Substances Act
d. The Marijuana Tax Act
ANSWER: c
25. Which drugs in the Schedule of Controlled Substances have the highest potential for abuse?
a. Schedule V drugs b. Schedule IV drugs
c. Schedule II drugs d. Schedule I drugs
ANSWER: d
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26. Which part of a prescription includes instructions to the patient that are to appear on the label?
a. Signature or transcription b. Body
c. Inscription d. Subscription
ANSWER: a
27. Which part of a prescription contains information for the pharmacist on total quantity of the drug and the form in
which it should be provided?
a. Inscription b. Subscription
c. Transcription d. Superscription
ANSWER: b
29. When a patient calls the office to request a medication refill, the medical assistant should find out
a. the name of the medication.
b. the dosage and strength.
c. the quantity, such as number of tablets.
d. All of the above
ANSWER: d
32. Which drug name is proprietary, indicating its ownership by a particular manufacturer?
a. Official name b. Generic name
c. Registered name d. Brand name
ANSWER: d
33. Which federal agency is charged with enforcing drug legislation, looking out for consumer safety, and regulating the
manufacture and sale of prescription and nonprescription drugs?
a. Drug Enforcement Administration
b. Food and Drug Administration
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34. Physicians who administer, prescribe, or dispense drugs listen in the Controlled Substances Act must be registered
with the
a. IRS. b. state HIPAA agency.
c. FDA. d. DEA.
ANSWER: d
40. Besides the physician, who is the physician’s office allowed to administer medication?
a. No one except the physician.
b. Only medication aids.
c. Only state licensed personnel.
d. Medical assistants under the supervision of the physician.
ANSWER: d
41. Information sheets that explain the benefits and risks of vaccines are
a. called Vaccine Information Statements.
b. produced by the Centers for Disease Control.
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42. Select the correct statement regarding the disposal of unused or expired drugs.
a. Uncontrolled substances may be put in trash bins.
b. Controlled substances may be picked up by a return processor.
c. Uncontrolled substances may be given to other patients by the physician.
d. All of the above.
ANSWER: b
Completion
43. The federal agency that regulates the manufacture and dispensing of dangerous drugs is the FDA
ANSWER: False
44. Over-the-counter drugs are those that may be purchased without a prescription.
ANSWER: True
45. A comprehensive reference book used by physicians and medical staff to find information about prescription drugs is
the Monthly Prescribing Reference (MPR)
ANSWER: False
46. The expiration date of medications should be checked periodically to ensure that they have not exceeded their usable
shelf life.
ANSWER: True
47. Hazardous wastes are waste products that can cause death, illness, or injury to living things or destruction of the
environment if improperly discarded.
ANSWER: True
48. To protect from theft by drug abusers, the physician’s DEA license should never be left out in plain view or in a
location that is easily accessible to patients.
ANSWER: False
49. Medication taken in the correct dosage can still produce side effects, which patients should report to the doctor.
ANSWER: True
50. A(n) adverse reaction can be occur when certain medications are taken in conjunction with others.
ANSWER: True
51. Every time medication is prescribed, a patient should be asked if they have any medication ____________________.
ANSWER: allergies
52. An ____________________ tag should be placed on the patient’s medical record if they have ever had an adverse
reaction to any medication.
ANSWER: alert
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53. ____________________ are a suspension of infectious agents used to convey resistance to infectious diseases.
ANSWER: Vaccines
54. A ____________________ schedule can be given to patients, especially those taking multiple drugs, to help keep
track of drug names, correct doses, and the time(s) of day they should be taken.
ANSWER: medication
55. A ___________________________ is a record kept in the medical office to track frequency of drug refills.
ANSWER: medication log
Matching
74. agency, which regulates the manufacturing and dispensing of dangerous drugs
ANSWER: e
75. act, which required the first labeling of drugs with adequate directions for safe use
ANSWER: d
76. federal law, which requires the pharmaceutical industry to maintain physical security and strict recordkeeping for
certain types of drugs
ANSWER: f
77. act, which required a transfer tax for all who sold marijuana
ANSWER: c
79. law, that prohibited the manufacture, transportation, and sale of alcohol beverages
ANSWER: b
80. state act, passed to ensure that the seriously ill have the right to obtain and use marijuana for medical purposes
ANSWER: h
81. first act that begins a long history of narcotic control legislation
ANSWER: a
82. What is the difference between a Schedule I drug and a Schedule V drug?
ANSWER: Schedule I drugs are most easily abused and habit forming. Schedule V drugs are less dangerous to the user
and are not subject to as much abuse
84. Explain what it means for a generic drug to be bioequivalent to an original brand-name drug.
ANSWER: A bioequivalent generic drug contains the same active ingredients as the original drug. Filler ingredients that
do not affect the drug’s action can be different in a generic version, and the shape, size, or color of the product
may differ from the original.