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University of Texas, ArlingtonNURS 5334/NURS5334: Quiz 2 ‘/ ‘/ ‘/ ‘/ ‘/ ‘/ ‘/
40 Questions and Answers (explained) | 100% correct 2025/26.
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Section1:Pharmacokinetics&Pharmacodynamics ‘/ ‘/ ‘/ ‘/
(Questions 1–12)
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1. A patient with end-stage renal disease (eGFR <15 mL/min) is prescribed a medication
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that is 70% renally excreted. The nurse practitioner should anticipate:
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A. Increasing the dose by 50% ‘/ ‘/ ‘/ ‘/
B. Decreasing the dosing frequency ‘ / ‘ / ‘ /
C. Changing to a prodrug ‘/ ‘/ ‘/
D. Adding a diuretic to enhance excretion ‘ / ‘ / ‘/ ‘ / ‘/
Answer: B — Reduced renal clearance leads to drug accumulation. Decreasing frequency
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maintains therapeutic levels without toxicity .
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2. Which cytochrome P450 enzyme is most commonly involved in clinically
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significant drug-drug interactions?
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A. CYP1A2
B. CYP2D6
C. CYP3A4
D. CYP2C9
Answer: C — CYP3A4 metabolizes approximately 50% of marketed drugs and is highly
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susceptible to inhibition and induction .
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3. A drug with high first-pass effect is given orally. The NP understands that:
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A. The drug will have increased bioavailability
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B. The drug must be given via a non-oral route to avoid extensive hepatic metabolism
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C. Gastric pH will alter absorption significantly
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D. Protein binding will be decreased ‘/ ‘ / ‘ / ‘/
Answer: B — High first-pass effect means the liver metabolizes much of the drug before it
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reaches systemic circulation .
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4. A patient takes warfarin. Starting rifampin (a potent CYP inducer) will likely:
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A. Increase INR and bleeding risk ‘/ ‘ / ‘ / ‘ /
B. Decrease INR and reduce anticoagulant effect ‘ / ‘ / ‘ / ‘ / ‘ /
C. Have no effect on INR
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D. Cause warfarin toxicity ‘ / ‘ /
Answer: B — Rifampin induces CYP enzymes that metabolize warfarin, reducing its
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anticoagulant effect .
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5. What is the study of drug movement throughout the body called?
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A. Pharmacodynamics
B. Pharmacokinetics
C. Pharmacotherapeutics
D. Pharmacogenomics
Answer: B — Pharmacokinetics encompasses absorption, distribution, metabolism, and
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excretion (ADME) .
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6. A patient with liver cirrhosis has reduced synthesis of albumin. The NP should
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anticipate that a highly protein-bound drug will have:
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