CPJE Pharmacy Law 2026 | Questions with Correct
Answers | Latest Update | Exam Prep | Graded A+
1. If a pharmacy receives a prescription for a controlled substance written by a
prescriber who has recently passed away, what should the pharmacist do?
The pharmacist should contact the prescriber's office for confirmation.
The pharmacist can fill it if the patient is in urgent need.
The pharmacist can fill it for 30 days.
The pharmacist should not fill the prescription as it is invalid.
2. Describe the purpose of the REMS program for Clozapine and its
significance in pharmacy practice.
The REMS program for Clozapine is a requirement for all antipsychotic
medications.
The REMS program for Clozapine focuses on managing weight gain in
patients.
The REMS program for Clozapine is intended to enhance patient
counseling about side effects.
The REMS program for Clozapine is designed to monitor and
mitigate the risk of agranulocytosis, ensuring patient safety.
3. Describe the refill policy for schedule II drugs and its significance in
controlled substance management.
Schedule II drugs can be refilled up to 5 times within 6 months.
Schedule II drugs can be refilled once with a verbal authorization.
Schedule II drugs can be refilled up to 10 times if authorized by a
physician.
, Schedule II drugs cannot be refilled; a new prescription is required
for each dispensing.
4. If a pharmacist dispenses a medication known to impair driving, what steps
should they take to ensure patient safety?
Only provide the medication without any additional information.
Suggest the patient drive only during the day.
Advise the patient to avoid taking the medication altogether.
Provide counseling on the risks and attach an appropriate warning
label.
5. Two drug formulation is said to be therapeutically equivalent if they exhibit
the ff:
Same active ingredient
Same dosage form
Same route of administration
Same safety profile
All of the above
6. Describe the significance of refill limits for schedule V drugs in the context of
controlled substance management.
Refill limits only apply to schedule II drugs.
Refill limits for schedule V drugs help prevent misuse and ensure
safe medication practices.
Refill limits are determined by the pharmacist's discretion.
Refill limits are irrelevant for schedule V drugs.
,7. Describe the REMS requirement for Saxenda and its significance in the
dispensing process.
Saxenda can be dispensed without any patient counseling.
Saxenda requires a Risk Evaluation and Mitigation Strategy (REMS)
to ensure safe use and monitoring of potential risks.
Saxenda is approved for dispensing without any monitoring
requirements.
Saxenda does not have any specific requirements for dispensing.
8. Describe the significance of the exemption period for continuing education
in the first license cycle for pharmacists.
The exemption period applies only to pharmacists working in
telepharmacies.
The exemption period allows new pharmacists to focus on practical
experience without the immediate pressure of continuing education.
The exemption period is designed to encourage pharmacists to take
more courses immediately after graduation.
The exemption period is a temporary measure that will eventually be
eliminated.
9. Why are Patient Package Inserts (PPI) included?
Clinical Trial Data
Patient Request
Legal Requirement by FDA
Doctor's Recommendation
, 10. A Louisiana pharmacy license expires on
June 30th of every year
December 31st of every other year
June 30th of every other year
December 31st of every year
11. Describe the main purpose of Retrospective Drug Utilization Review (DUR)
in pharmacy practice.
To prevent potential medication errors before they happen.
To ensure compliance with pharmacy regulations during dispensing.
To evaluate the appropriateness of medication use after
prescriptions have been dispensed.
To provide real-time patient counseling during medication therapy.
12. If a pharmacy clerk is found to be dispensing medications without
pharmacist supervision, what regulatory issue could arise?
Violation of prescription handling laws
Failure to meet sales targets
Improper inventory management
Inadequate customer service
13. What does PPI stand for in the context of pharmacy regulations?
Pharmacy Practice Instruction
Patient Package Insert
Pharmaceutical Product Insert
Answers | Latest Update | Exam Prep | Graded A+
1. If a pharmacy receives a prescription for a controlled substance written by a
prescriber who has recently passed away, what should the pharmacist do?
The pharmacist should contact the prescriber's office for confirmation.
The pharmacist can fill it if the patient is in urgent need.
The pharmacist can fill it for 30 days.
The pharmacist should not fill the prescription as it is invalid.
2. Describe the purpose of the REMS program for Clozapine and its
significance in pharmacy practice.
The REMS program for Clozapine is a requirement for all antipsychotic
medications.
The REMS program for Clozapine focuses on managing weight gain in
patients.
The REMS program for Clozapine is intended to enhance patient
counseling about side effects.
The REMS program for Clozapine is designed to monitor and
mitigate the risk of agranulocytosis, ensuring patient safety.
3. Describe the refill policy for schedule II drugs and its significance in
controlled substance management.
Schedule II drugs can be refilled up to 5 times within 6 months.
Schedule II drugs can be refilled once with a verbal authorization.
Schedule II drugs can be refilled up to 10 times if authorized by a
physician.
, Schedule II drugs cannot be refilled; a new prescription is required
for each dispensing.
4. If a pharmacist dispenses a medication known to impair driving, what steps
should they take to ensure patient safety?
Only provide the medication without any additional information.
Suggest the patient drive only during the day.
Advise the patient to avoid taking the medication altogether.
Provide counseling on the risks and attach an appropriate warning
label.
5. Two drug formulation is said to be therapeutically equivalent if they exhibit
the ff:
Same active ingredient
Same dosage form
Same route of administration
Same safety profile
All of the above
6. Describe the significance of refill limits for schedule V drugs in the context of
controlled substance management.
Refill limits only apply to schedule II drugs.
Refill limits for schedule V drugs help prevent misuse and ensure
safe medication practices.
Refill limits are determined by the pharmacist's discretion.
Refill limits are irrelevant for schedule V drugs.
,7. Describe the REMS requirement for Saxenda and its significance in the
dispensing process.
Saxenda can be dispensed without any patient counseling.
Saxenda requires a Risk Evaluation and Mitigation Strategy (REMS)
to ensure safe use and monitoring of potential risks.
Saxenda is approved for dispensing without any monitoring
requirements.
Saxenda does not have any specific requirements for dispensing.
8. Describe the significance of the exemption period for continuing education
in the first license cycle for pharmacists.
The exemption period applies only to pharmacists working in
telepharmacies.
The exemption period allows new pharmacists to focus on practical
experience without the immediate pressure of continuing education.
The exemption period is designed to encourage pharmacists to take
more courses immediately after graduation.
The exemption period is a temporary measure that will eventually be
eliminated.
9. Why are Patient Package Inserts (PPI) included?
Clinical Trial Data
Patient Request
Legal Requirement by FDA
Doctor's Recommendation
, 10. A Louisiana pharmacy license expires on
June 30th of every year
December 31st of every other year
June 30th of every other year
December 31st of every year
11. Describe the main purpose of Retrospective Drug Utilization Review (DUR)
in pharmacy practice.
To prevent potential medication errors before they happen.
To ensure compliance with pharmacy regulations during dispensing.
To evaluate the appropriateness of medication use after
prescriptions have been dispensed.
To provide real-time patient counseling during medication therapy.
12. If a pharmacy clerk is found to be dispensing medications without
pharmacist supervision, what regulatory issue could arise?
Violation of prescription handling laws
Failure to meet sales targets
Improper inventory management
Inadequate customer service
13. What does PPI stand for in the context of pharmacy regulations?
Pharmacy Practice Instruction
Patient Package Insert
Pharmaceutical Product Insert
