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CSP Exam Practice Test (Specialty Pharmacy) – Questions & Correct Answers (2025/2026 Complete Study Guide)

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This document provides the complete 2025/2026 Certified Specialty Pharmacist (CSP) Practice Exam, aligned with the Specialty Pharmacy Certification Board (SPCB) Competency Blueprint. It includes 100 verified questions and correct answers covering clinical management, onboarding, fulfillment, regulatory compliance, and operational excellence. Key references include USP 797/800, FDA REMS, URAC/ACHC accreditation standards, and payer requirements. Designed for pharmacists and pharmacy professionals preparing for CSP certification, this guide also includes a concise Quick Review Sheet summarizing major topics and monitoring parameters.

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CSP EXAM PRACTICE TEST (SPECIALTY
PHARMACY) – QUESTIONS & CORRECT
ANSWERS (2025

/2026)Introduction
This 2025/2026 CSP practice exam aligns with the SPCB Competency Blueprint,
emphasizing clinical management, onboarding, fulfillment, regulatory compliance, and
operations. Questions reflect USP <797>/<800>, FDA REMS, URAC/ACHC standards, and
payor requirements for specialty pharmacy certification. Use for exam prep; review SPCB
outline for disease-state focus and quality metrics.



Question [1]: In oncology specialty pharmacy, what is the primary monitoring parameter
for tyrosine kinase inhibitor (TKI) therapy?

A. Blood glucose levels
B. QT interval prolongation
C. Serum creatinine clearance

D. Liver function tests

Answer: D — Liver function tests

Rationale: TKIs (e.g., imatinib) require LFT monitoring for hepatotoxicity per NCCN
guidelines; QT for some (B), CrCl renal (C), glucose unrelated (A).

Question [2]: For a patient starting MS therapy with fingolimod, what baseline test is
required?

A. Echocardiogram
B. Varicella zoster titer
C. Pulmonary function test

D. Bone density scan

Answer: B — Varicella zoster titer

,Rationale: Fingolimod (Gilenya) REMS requires VZV screening to prevent reactivation per
FDA; echo cardiac (A), PFT respiratory (C), DEXA osteoporosis (D).

Question [3]: A patient on adalimumab for RA reports injection-site reaction; initial
management is?

A. Discontinue immediately
B. Apply cold compress and monitor
C. Switch to IV infusion

D. Increase dose

Answer: B — Apply cold compress and monitor

Rationale: Mild reactions common, managed conservatively per ACR guidelines;
discontinue severe (A), switch unnecessary (C), dose adjustment contraindicated (D).

Question [4]: In HIV management, what is the goal CD4 count for initiating ART if viral
load >100,000?

A. >500 cells/mm³
B. <200 cells/mm³
C. Any CD4 with high VL

D. >350 cells/mm³

Answer: C — Any CD4 with high VL

Rationale: DHHS guidelines recommend immediate ART regardless of CD4 if VL
>100,000; low CD4 opportunistic (B), high delay not (A,D).

Question [5]: For hemophilia A patient on factor VIII, what lab monitors efficacy?

A. PT/INR
B. aPTT
C. Platelet count

D. Fibrinogen

Answer: B — aPTT

Rationale: Factor VIII affects intrinsic pathway, monitored by aPTT per ASH guidelines;
PT extrinsic (A), platelets separate (C), fibrinogen common (D).

Question [6]: Patient on ustekinumab for psoriasis; what screening is needed before
initiation?

, A. PPD for TB
B. Hepatitis B surface antigen
C. Serum lipids

D. Thyroid function

Answer: A — PPD for TB

Rationale: IL-12/23 inhibitors increase TB reactivation risk; screen latent TB per AAD;
Hep B live vaccines (B), lipids metabolic (C), thyroid unrelated (D).

Question [7]: In cystic fibrosis, what is the mechanism of ivacaftor?

A. Mucolytic
B. CFTR potentiator
C. Antibiotic

D. Bronchodilator

Answer: B — CFTR potentiator

Rationale: Ivacaftor enhances CFTR channel gating in G551D mutation per CFF
guidelines; mucolytic N-acetylcysteine (A), antibiotic infection (C), bronchodilator
albuterol (D).

Question [8]: For Gaucher's disease enzyme replacement therapy, what monitors
response?

A. Bone density
B. Chitotriosidase levels
C. Liver biopsy

D. Hemoglobin only

Answer: B — Chitotriosidase levels

Rationale: Chitotriosidase/macrophage markers decline with velaglucerase per NORD;
bone/spleen response (A,C), anemia partial (D).

Question [9]: Patient on natalizumab for Crohn's; what is the primary risk?

A. Hepatotoxicity
B. PML (progressive multifocal leukoencephalopathy)
C. Nephrotoxicity

D. Cardiotoxicity

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