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Indiana Pharmacist Licensure Exam With Practice Questions And Correct Answers (Verified Answers) Plus Rationales| Instant Download

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Practice questions and answers for the Indiana Pharmacist Licensure Exam, each with a rationale explaining the correct choice. Covers Indiana and federal pharmacy law, controlled substance dispensing, INSPECT requirements, USP 797 sterile compounding, vancomycin AUC dosing, warfarin and INR management, heart failure therapy, diabetes medications, and dose calculations. Use it to review key topics and test your knowledge before exam day.

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Indiana Pharmacist Licensure Exam with
Practice Questions And Correct Answers
(Verified A

1. A pharmacist in Indiana receives a faxed prescription for a Schedule II controlled
substance from an out-of-state prescriber. Which statement most accurately reflects
Indiana and federal requirements for dispensing?

A. The prescription must be an original written or electronically transmitted prescription;
faxed Schedule II prescriptions are never valid.
B. A faxed Schedule II prescription is valid if the prescriber is DEA-registered and the
pharmacist verifies authenticity, but Indiana limits such dispensing to a 7-day supply.
C. An out-of-state prescriber must be registered with the Indiana Board of Pharmacy in
addition to DEA registration for the prescription to be valid.
D. A faxed Schedule II prescription may be dispensed only for a patient in hospice or
long-term care, or when the prescriber certifies a medical emergency.

Answer: D. A faxed Schedule II prescription may be dispensed only for a patient in
hospice or long-term care, or when the prescriber certifies a medical emergency.
Rationale: Federal DEA rules allow faxed Schedule II prescriptions only in limited
circumstances (hospice, LTC, or medical emergency with follow-up). Indiana adopts these
federal exceptions; blanket validity or state board registration is incorrect. Option A is too
absolute, B invents a 7-day limit, and C misstates Indiana registration requirements.




Page 1 of 78

,2. A patient with heart failure with reduced ejection fraction is optimized on
guideline-directed therapy but remains symptomatic. Which addition has the
strongest evidence for reducing cardiovascular death and heart failure
hospitalization?

A. Ivabradine
B. Dapagliflozin
C. Hydralazine/isosorbide dinitrate
D. Digoxin

Answer: B. Dapagliflozin
Rationale: SGLT2 inhibitors (dapagliflozin, empagliflozin) have robust randomized
evidence for reducing CV death and HF hospitalization in HFrEF regardless of diabetes
status. Ivabradine reduces hospitalization but not mortality; hydralazine/ISDN is primarily
for self-identified Black patients or ACEi/ARB intolerance; digoxin reduces hospitalization
but not mortality.




Page 2 of 78

,3. A prescriber orders vancomycin 1.5 g IV q12h for a patient with a vancomycin
AUC target of 400-600 mg-h/L. Which monitoring strategy best reflects current
consensus guidelines?

A. Trough-only monitoring targeting 15-20 mcg/mL
B. Peak-only monitoring targeting 30-40 mcg/mL
C. AUC-guided dosing using two serum concentrations with Bayesian software
D. Routine monitoring of both peak and trough with a target peak of 20-30 mcg/mL

Answer: C. AUC-guided dosing using two serum concentrations with Bayesian
software
Rationale: The 2020 ASHP/IDSA/PIDS/SIDP vancomycin consensus guidelines recommend
AUC-guided dosing (AUC24 400-600 mg-h/L) over trough-only monitoring to reduce
nephrotoxicity while maintaining efficacy. Trough-only and peak-based strategies are
outdated; routine peak monitoring is not recommended.


4. A patient on warfarin for atrial fibrillation is prescribed a 7-day course of
fluconazole. Which INR monitoring approach is most appropriate?

A. No additional monitoring; fluconazole does not interact with warfarin.
B. Check INR in 3-5 days and consider empiric warfarin dose reduction due to CYP2C9
inhibition.
C. Check INR in 2 weeks; fluconazole only affects warfarin metabolism after 14 days.
D. Switch to a direct oral anticoagulant immediately to avoid interaction.
Answer: B. Check INR in 3-5 days and consider empiric warfarin dose reduction due
to CYP2C9 inhibition.
Rationale: Fluconazole is a potent CYP2C9 inhibitor and can significantly increase INR
within days; close monitoring and possible dose reduction are required. Option A is false,
C misstates the timeline, and D is not automatically indicated for a short antifungal course.




Page 3 of 78

, 5. A pharmacist is preparing a compounded sterile preparation (CSP) in a USP <797>
compliant facility. Which action is required for a medium-risk CSP with a beyond-use
date (BUD) exceeding 24 hours at room temperature?

A. Preparation must occur in an ISO Class 5 environment with no further requirements.
B. Preparation must occur in an ISO Class 5 PEC located in an ISO Class 7 buffer area,
and the CSP must be tested for sterility.
C. Preparation must occur in an ISO Class 5 PEC in an ISO Class 7 buffer area, with
demonstrated air quality and documented personnel competency.
D. Preparation must occur in an ISO Class 5 PEC in an ISO Class 8 clean room with
daily particle counts.

Answer: C. Preparation must occur in an ISO Class 5 PEC in an ISO Class 7 buffer
area, with demonstrated air quality and documented personnel competency.
Rationale: USP <797> requires medium-risk CSPs with extended BUDs to be prepared in
an ISO Class 5 PEC within an ISO Class 7 buffer area, with environmental monitoring and
validated personnel. Sterility testing is not routinely required for medium-risk CSPs, and
ISO Class 8 is insufficient for extended BUDs.


6. A patient is prescribed a continuous IV infusion of a drug with a narrow
therapeutic index. Which pharmacokinetic parameter is most critical to determine the
time to reach steady-state concentration?

A. Volume of distribution (Vd)
B. Clearance (CL)
C. Elimination half-life (t½)
D. Peak plasma concentration (Cmax)

Answer: C. Elimination half-life (t½)
Rationale: Time to steady state depends on elimination half-life (approximately 4-5
half-lives), which itself is determined by Vd and CL. Vd and CL individually do not directly
define time to steady state; Cmax is a result, not a determinant.




Page 4 of 78

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