PTCB Federal Requirements Practice Test #1 - 2023 (20 Questions with Explained Answers)

PTCB Exam Prep・2 minutes read

The PTCB Federal Requirements Practice Test covers various aspects of pharmacy regulations, including controlled substances, prescription records, and safety standards. It highlights critical information such as DEA numbers, controlled substance ordering, and proper disposal of hazardous waste.

Insights

  • Prescription records are categorized into two files: C2 for controlled substances and non-controlled substances, with the addition of C3 to C5 for further classification.
  • The pharmacist in charge is responsible for verifying and documenting all received C2 medications, ensuring strict adherence to regulatory requirements and safety protocols.

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Recent questions

  • What is the maximum amount of Sudafed one can purchase in a 30-day period?

    9 grams

  • How long must pharmacy prescription records be retained on-site?

    2 to 5 years

  • What form is used to report controlled substance theft or significant loss?

    DEA 106 form

  • What is the appropriate source for instructions on storing hazardous substances?

    Safety data sheets

  • What is the purpose of the Combat Methamphetamine Epidemic Act of 2005?

    To restrict the sale and storage of certain medications

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Summary

00:00

Pharmacy Regulations and Safety Guidelines Overview

  • The PTCB Federal Requirements Practice Test consists of 40 questions with explained answers.
  • Class 2 recalls are issued by the FDA for medications causing temporary adverse health effects.
  • Prescription records can be stored in two files: C2 and non-controlled, plus C3 to 5.
  • The appropriate form to order controlled substances from a pharmacy supplier is the DEA 222 form.
  • Valid DEA numbers follow specific steps, with the last digit determined by calculations.
  • Pharmacy prescription records must be retained on-site for 2 to 5 years, depending on the state.
  • The Combat Methamphetamine Epidemic Act limits Sudafed purchases to 9 grams in a 30-day period.
  • The pharmacist in charge must verify and document all received C2 medications.
  • Transferred control substance prescriptions must include the DEA number of the transferring pharmacy.
  • OSHA sets standards for keeping pharmacy employees safe during tasks, focusing on hazardous materials.
  • Safety data sheets are the appropriate source for instructions on storing and handling hazardous substances.
  • Hazardous drug waste must be stored in a leak-proof container and labeled as such for proper disposal.
  • In case of conflict, the more strict law between state and federal pharmacy laws should be followed.
  • The DEA 106 form is used to report controlled substance theft or significant loss.
  • Schedule 3 to 5 controlled substance prescriptions allow a maximum of 5 refills within 6 months.
  • Common reasons for medication recalls include contamination, mislabeling, and impurities.
  • The online controlled substance ordering platform replacing paper formats is CSOS.
  • Fentanyl is a scheduled 2 narcotic control substance.
  • The Combat Methamphetamine Epidemic Act of 2005 places restrictions on the sale and storage of certain medications.
  • Schedule 2 controlled substances carry the highest risk of abuse, misuse, and addiction.
  • The Omnibus Budget Reconciliation Act of 1990 mandates pharmacists to perform drug reviews and patient counseling.
  • After discovering theft of controlled substances, the pharmacy must notify the local DEA office within one business day.
  • All controlled substances are permitted to be mailed via the United States Postal Service.
  • The third segment of an NDC number identifies the package size and type.
  • Examples of schedule 5 controlled substances include Tylenol with codeine and Robitussin AC.
  • Pharmacies must complete an inventory of controlled substances every two years as per federal law.
  • USB 795 provides guidance for compounding non-sterile formulations for human or animal administration.
  • Class 3 recalls involve violative substances not likely to cause adverse health consequences.

28:29

Healthcare Standards and Privacy Regulations in US

  • The USP develops standards for medications and dietary supplements, ensuring identity, strength, quality, and purity.
  • The TJC evaluates and accredits healthcare organizations and programs in the United States.
  • The Health Insurance Portability and Accountability Act of 1996 established the provision that all patient medical records and personal health information must be kept private.
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