Practice Questions Exam 1 Flashcards

1
Q

What is a rule?
A. A guideline set by administrative agency.
B. A system of enforceable rules.
C. A blueprint implemented to reach a common goal.
D. A guideline implement by an employer.

A

A. A guideline set by administrative agency.

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2
Q

Pharmacist can perform capillary blood tests for the purpose of diagnosing disease.

A. True
B. False

A

B. False (since they diagnose)

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3
Q

How many days does a pharmacist convicted of a felony have to report to the Board?

A. 3
B. 1
C. 7
D. 10

A

D. 10

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4
Q

How many pharmacists sit on the Georgia Board of Pharmacy?

A. 7
B. 4
C. 8
D. 5

A

A. 7 is a total of 8 but 1 is a consumer.

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5
Q

Georgia Drugs and Narcotics Agents may arrest a pharmacist who is violating pharmacy laws.

A. True
B. False

A

A. True

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6
Q

What is negligence?
A. Conduct that adheres to the expected standard of care.
B. An intentional act that a reasonable person would commit.
C. Conduct that deviates from the expected standard of care.
D. A criminal wrong-doing.

A

C. Conduct that deviates from the expected standard of care.

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7
Q

Which of the following are elements of negligence?
A. Duty to care
B. Behavior that conforms to your professional obligation.
C. No actual injury or damages occurred
D. A pharmacist cannot commit negligence.

A
A. Duty to care.
The other three elements are:
Breach of Duty
Injury actual damage
Causation/Proximate cause
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8
Q

Federal and state laws are expected to conflict.
A. True
B. False

A

B. False

They cannot conflict

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9
Q

What is policy?
A. A system of enforceable rules
B. A set of guidelines created by an administrative agency
C. A blueprint implemented to reach a common goal.
D. A set of guidelines created by legislation.

A

C. A blueprint implemented to reach a common goal.

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10
Q
Negligence is defines as:
A. Conduct that is careless and deviates from the standard of care.
B. The intentional commission of an act.
C. The intentional omission of an act.
D. A criminal wrong.
A

A. Conduct that is careless and deviates from the standard of care.

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11
Q
What type of law is created through the authority to promulgate regulations?
A. Administrative law
B. Civil law
C.	Criminal law
D.	Common law
A

A. Administrative law

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12
Q
The law was passed due to unsanitary conditions and poor labeling.
A.	Medical Device Amendment of 1976.
B.	Food Drug and Cosmetic Act of 1938.
C.	Kefauver-Harris Amendment of 1962.
D.	Pure Food and Drug Act of 1906.
A

D. Pure Food and Drug Act of 1906.

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13
Q

This law required new drugs to be proven safe before going to market.

A. Durham-Humphrey Amendment of 1951.
B. Food Drug and Cosmetic Act of 1938.
C. Pure Food and Drug Act of 1906.
D. Comprehensive Drug Abuse Prevent Control Act of 1970.

A

B. Food Drug and Cosmetic Act of 1938.

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14
Q

The legislation is also known as the Waxman-Hatch Amendment.

A. Orphan Drug Act of 1983
B. Medical Device Amendment of 1976
C. Drug Price Competition and Patent Restoration Act of 1984.
D. Prescription Drug Marketing Act of 1987

A

C. Drug Price Competition and Patent Restoration Act of 1984.

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15
Q

Which law required most legend drugs and controlled substances be packaged in child-resistant containers?

A. Durham-Humphrey Amendment of 1951.
B. Comprehensive Drug Abuse Prevention Control Act of 1970.
C. Poison Prevention Packaging Act of 1970.
D. Nutrition Labeling and Education Act of 1990.

A

C. Poison Prevention Packaging Act of 1970.

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16
Q

In Georgia, pharmacist must maintain patient records for at least two years.

A. True
B. False

A

A. True

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17
Q

A pharmacist can supervise one intern and two external at one time.
A. True
B. False

A

B. False

Because is only one extern

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18
Q

A pharmacist can supervise up to 3 registered technicians at one time if which scenario is true?

A. At least two technicians are certified
B. If all three technicians are certified
C. At least one technicians is certified
D. Pharmacists cannot supervise technicians

A

C. At least one technicians is certified

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19
Q

A non-pharmacist may hold a special permit if they want to distribute pharmaceuticals.

a. True
b. False.

A

B. False

Because is has to be a pharmacist

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20
Q

Melissa is the new PIC at Mercer Pharmacy. The Board of Pharmacy must be notified within 30 days of Melissa assuming her new role.

a. True
b. False

A

B. False

Is immediately

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21
Q

A pharmacist’s license may be suspended if they fail to keep accurate inventory records?
A. True
B. False

A

A. True

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22
Q

A pharmacist’s license may be suspended or revoked is they default of their student loan.

A. True
B. False

A

A. True

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23
Q

How many hours of CE must a pharmacist in Georgia have in order to renew their license?

A.15 hours every year
B. 30 hours every 2 years
C. 30 hours every year
D. 15 hours every 2 year

A

B. 30 hours every 2 years

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24
Q

For how many days may a temporary pharmacist license be grandest?

A. 30
B. 45
C. 60
D. 90

A

D. 90

25
Q

What is the maximum number of times an applicant may take a board exam in Georgia before requesting special permission?

A. 5
B. 2
C. 4
D. 3

A

D. 3

26
Q

Which USP chapter provides minimum standards for preparing, compounding, dispensing, and packaging radio pharmaceuticals?

A. USP 800
B. USP 825
C. USP 797
D. USP 795

A

B. USP 825

27
Q

This law prohibited interstate commerce of adulterated and misbranded products.

A. Pure Food and Drug Act of 1906
B. Orphan Drug Act of 1983
C. Medicinal Devise Amendment of 1976
D. Non of above

A

A. Pure Food and Drug Act of 1906

28
Q
  1. Which USP chapter provides practice and quality standards for handling hazardous drugs?

A. USP 825
B. USP 795
C. USP 797
D. USP 800

A

D. USP 800

29
Q
  1. Which USP chapter provides standards for compounding quality sterile products?

A. USP 800
B. USP 797
C. USP 825
D. USP 795

A

B. USP 797

30
Q

Which USP chapter provides standards for compounding non-sterile products?

A. USP 795
B. USP 797
C. USP 800
D. USP 825

A

A. USP 795

31
Q
  1. The Medicaid Tamper-Resistant Law of 2007 required electronic prescriptions for all Medicaid patients.

a. True
b. False

A

B. False

Because is not all patients.

32
Q

The Omnibus Reconciliation Act of 1990 required pharmacist to counsel all patients. (Because is only medicare patients)

A. True
B. False

A

B. False

Because is only medicare patients

33
Q

The Medical Device Amendment of 1976 established which of the following?

A. Provided tax incentives for development of drugs to treat rare diseases.
B. Did not require devices to be manufactured according to GMP
C. Required medical devices be classified by their function.
D. Streamlined the generic device approval process.

A

C. Required medical devices be classified by their function.

34
Q

Which law required most legend drugs and controlled substances be packaged in child-resistant containers?

A. Durham-Humphrey Amendment of 1951
B. Comprehensive Drug abuse Prevention Control Act of 1970.
C. Poison Prevention Packaging Act of 1970
D. Nutrition Labeling and Education Act of 1990

A

C. Poison Prevention Packaging Act of 1970

35
Q

This law gave oversight of large-scale compounding facilities to the FDA.

A. Fast Tract Act of 1992
B. 21 st Century Cure Act of 2016
C. Patient Protection and Affordable Care Act of 2010.
D. Drug Quality and Security Act of 2013.

A

D. Drug Quality and Security Act of 2013.

36
Q

Which law provided tax incentives to manufactures who developed drugs to treat rare disease?

A. Orphan Drug Act of 1983
B. Prescription Drug Marketing Act of 1987
C. Drug Price Competition and Patent Restoration Act of 1984.
D. Omnibus Reconciliation Act of 1990.

A

A. Orphan Drug Act of 1983

37
Q

The Food Drug and and Cosmetic Act of 1938 established which of the following?

A. Required all new drugs be proven safe and effective.
B. Required all new drugs be proven safe.
C. Required pharmacists to counsel on all new prescriptions
D. Required all new drugs be proven effective.

A

B. Required all new drugs be proven safe.

38
Q

Which law required drugs to be proven safe and effective before going to market?

A. Food Drug and Cosmetic Act of 1938.
B. Durham-Humphrey Amendment of 1962.
C. Kefauver-Harris Amendment of 1962.
D. Wax man-Hatch Amendment of 1984.

A

C. Kefauver-Harris Amendment of 1962.

39
Q

What law created five schedules of controlled substances?

A. Poison Prevention PackagingAct of 1970.
B. Comprehensive Drug Abuse Prevention Control Act of 1970.
C. Kefauver-Harris Amendment of 1962
D. Orphan Drug Act of 1983.

A

B. Comprehensive Drug Abuse Prevention Control Act of 1970.

40
Q

Which law required informed consent from research subjects?

A. Food Drug and Cosmetic Act of 1938.
B. Poison Prevention Packaging Act of 1970.
C. Kefauver-Harris Amendment of 1962
D. Durham-Humphrey Amendment 0f 1951.

A

C. Kefauver-Harris Amendment of 1962.

41
Q

Which of the following is considered an “exception to the rule” for child-resistant packaging?

A. Oral contraceptives
B. Ibuprofen
C. Chewable children’s vitamins
D. Children’s Tylenol

A

A. Oral contraceptives

42
Q

This law lessened the burden of proof to bioequivalency only for generic manufactures.

A. Drug Price Competition and Patent Restoration Act of 1984.
B. Medical Device Amendment of 1976.
C. Prescription Drug Marketing Act of 1987.
D. Food Drug and Cosmetic Act of 1938.

A

A. Drug Price Competition and Patent Restoration Act of 1984.

43
Q

Which of the following defines a rare disease according to the Orphan Drug Act of 1938?

A. Affecting<2,000,000 persons worldwide
B. Affecting<200,000 Americans
C. Affecting<200,000 persons worldwide
D. Affecting<2,000,000 Americans

A

B. Affecting<200,000 Americans

44
Q
  1. Which law created a fast-track approval process for drug approvals?

A. Food and Drug Modernization Act of 1997.
B. Fast Tract Act of 1992.
C. Health Insurance Portability and Accountability Act of 1996.
D. Omnibus Reconcilliation Act of 1990.

A

A. Food and Drug Modernization Act of 1997.

45
Q

This law established sales limits and record-keeping requirements for pseudoephedrine.

A. Comprehensive Drug Abuse Prevention Control Act of 1970.
B. Combat Methamphetamine Act of 2005.
C. Food and Drug Administration Amendments Act of 2007.
D. Medicare Modernization Act of 2003.

A

B. Combat Methamphetamine Act of 2005.

46
Q

Four unique Medicare programs were created by this piece of legislation.

A. Food and Drug Administration Amendments Act of 2007.
B. Medicare Modernization Act of 2003
C. Combat Methamphetamine Act of 2005.
D. Omnibus Reconciliation Act of 1990.

A

B. Medicare Modernization Act of 2003

47
Q

his law required all individual to have health insurance.

A. Medicaid Tamper-Resistan Prescription Law of 2007.
B. Drug Quality and Security Act of 2013
C. Patient Protection and Affordable Care Act of 2010.
D. Food Drug and Administrative Amendment Act of 2007

A

C. Patient Protection and Affordable Care Act of 2010.

48
Q

The following scenario is an example of which type of action “A patient sues for medical expenses and lost wages following an injury that occurred due to a misfill”

A. Administrative action
B. Civil action
C. Criminal action

A

B. Civil action

49
Q

Is the following scenario an example of negligence? “A pharmacist purposely dispense Augmentin instead of the prescribed amoxicillin because that is all he has on hand at the time”

A. Yes
B. No

A

B. No

Because it was on purpose

50
Q

T/F: laws have to be followed, but regulations do not.

A. True
B. False

A

B. False

Because regulation also have to be follow.

51
Q

How long must a pharmacy maintain patient records?

A
a.	At least 2 years
Rx number 
Name of strength of medication
Quantity and date dispensed
Name of dispensing RPh
52
Q

What is the correct tech to RPh ratio? (select all that apply)

A. 2:1
B. 3:1 as long as at least one technician is licensed
C. 3:1 as long as at least one technician is certified
D. 4:1

A

A. 2:1

C. 3:1 as long as at least one technician is certified

53
Q

A pharmacist must renew his/her license every ___ years. The required number of containing education hours is _____.

A

2 years, 30 hours.

54
Q

Which of the following drugs is exempt from the Poison Prevention Packaging Act of 1970?

A. Azithromycin
B. Tylenol
C. Sublingual nitroglycerin
D. Carvedilol

A

C. Sublingual nitroglycerin

55
Q

The Orphan Drug Act of 1983 provides tax and exclusive licensing incentives to manufactures to develop and market drugs for rare diseases that affect less than __________ Americans.

A

200,000

56
Q

T/F: The Medicaid Tamper-Resistant Prescription Law of 2007 required use of electronic prescriptions or tamper-resistant prescription pads for Medicare patients.

A. True
B. False

A

B. False (because it was for Medicaid patients)

57
Q

The Board of Pharmacy is composed of ___ members. ____ pharmacists and ___ consumer.

A

8 members
7 pharmacist
1 consumer

58
Q

Which 3 drugs are regulated by the Combat Methamphetamine Epidemic Act of 2005?

A

Ephedrine
Pseudoephedrine
Phenylpropanolamine

59
Q

Match the following standards with their USP Chapter:

  1. Sterile and non sterile radiopharmaceuticals. A. USP 795
  2. Non-sterile products. B. USP 797
  3. Hazardous drugs. C. USP 800
  4. Sterile products. D. USP 825
A
  1. D. USP 825
  2. A. USP 795
  3. C. USP 800
  4. B. USP 797