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PHAR 115: PTCB Cert Review Ch 2

Total questions: 15

Worksheet time: 11mins

Name
Class
Date
1.

Which of the following is NOT a drug label requirement for a Unit Dose Label?

a)

Lot number

b)

Prescriber's Name

c)

Drug name

d)

Expiration date

2.

If a pharmacy knowingly bills for a brand-name drug but dispenses a generic, this is an example of:

a)

Abuse

b)

Waste

c)

Neglect

d)

Fraud

3.

Any agent that promotes the formation of cancer is said to have:

a)

Carcinogenicity

b)

Teragenicity

c)

Reproductive toxicity

d)

Genotoxicity

4.

Which schedule of drugs has the highest potential for abuse and are illegal?

a)

Schedule I

b)

Schedule II

c)

Schedule III

d)

Schedule IV

5.

The legislation that required child-resistant containers for most prescription and OTC drugs to prevent accidental ingestion and poisoning is known as the:

a)

Occupational Safety and Health Act

b)

Orphan Drug Act

c)

Anabolic Steroids Control Act

d)

Poison Prevention Packaging Act

6.

Which of the following is NOT a duty that may be legally performed by a pharmacy techncian?

a)

Preparing doses of a premanufactured product

b)

Counseling customers on drugs

c)

Customer service for prescriptions

d)

Checking and replenishing drug inventory

7.

What do the initials REMS stand for?

a)

Random Evaluation Medical Statute

b)

Radical Event and Migration Strategies

c)

Rare Emergency and Medical Services

d)

Risk Evaluation and Mitigation Strategy

8.

What federal agency is responsible for supervising and enforcing laws related to the use and sale of legal (and illegal) controlled substances?

a)

The Drug Enforcement Administration

b)

Occupational Safety and Health Administration

c)

The Food and Drug Administration

d)

Centers for Disease Control and Prevention

9.

What two organizations can release an official drug recall?

a)

The manufacturer and the FDA

b)

The FDA and the CDC

c)

The Joint Commission and the White House

d)

The CDC and the FBI

10.

Which act mandates that pharmacies complete a drug utilization review (DUR) for medication dispensing to identify potential drug or supplement interactions or allergy warnings?

a)

Patient Protection and Affordable Care Act (ACA)

b)

Biologics Price Competition and Innovation Act (BCPI)

c)

Omnibus Budget Reconciliation Act of 1990 (OBRA-90)

d)

Health Insurance Portability and Accountability Act (HIPAA)

11.

Technicians must legally document the purchase of over-the-counter

a)

natural supplements

b)

vitamins

c)

pseudoephedrine or ephedrine

d)

homeopathic products

12.

Which of the following is not considered protected health information (PHI) under HIPAA?

a)

model of car

b)

social security number

c)

address

d)

date of birth

13.

Which of the following is not a list of hazardous waste?

a)

The U list

b)

The K list

c)

The F list

d)

The X list

14.

Which of the following is not a criteria that may identify a drug as hazardous?

a)

Carcinogenity

b)

Elasticity

c)

Genotoxicity

d)

Reproductive toxicity

15.

The only 501 (c) (3) nonprofit organization devoted entirely to preventing medication errors is the

a)

Centers for Disease Control (CDC)

b)

Institute for Safe Medication Practices (ISMP)

c)

The Joint Commission (TJC)

d)

The Food and Drug Administration (FDA)