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University of Texas, Arlington NURS 5334/NURS5334: Quiz 2 40 Questions and Answers (explained) | 100% correct 2025/26.

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University of Texas, Arlington NURS 5334/NURS5334: Quiz 2 40 Questions and Answers (explained) | 100% correct 2025/26. University of Texas, Arlington NURS 5334/NURS5334: Quiz 2 40 Questions and Answers (explained) | 100% correct 2025/26. University of Texas, Arlington NURS 5334/NURS5334: Quiz 2 40 Questions and Answers (explained) | 100% correct 2025/26.

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NURS 5334/NURS5334
b5 Stuvia: the best study material from your fellow students
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University of Texas, Arlington NURS 5334/NURS5334: Quiz 2 b5 b5 b5 b5 b5 b5 b5




40 Questions and Answers (explained) | 100% correct
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2025/26. b5




Section 1: Pharmacokinetics & Pharmacodynamics
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(Questions 1–12)
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1. A patient with end-stage renal disease (eGFR <15 mL/min) is prescribed a
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medication that is 70% renally excreted. The nurse practitioner should anticipate:
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A. Increasing the dose by 50% b5 b5 b5 b5




B. Decreasing the dosing frequency b 5 b5 b 5




C. Changing to a prodrug b5 b5 b5




D. Adding a diuretic to enhance excretion
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Answer: B — Reduced renal clearance leads to drug accumulation. Decreasing
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frequency 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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, NURS 5334/NURS5334
b5 Stuvia: the best study material from your fellow students
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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 decreasedb5 b5 b5 b5




Answer: B — High first-pass effect means the liver metabolizes much of the drug
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before it 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 b5 b5 b5 b5




B. Decrease INR and reduce anticoagulant effect b5 b 5 b 5 b5 b 5




C. Have no effect on INR
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D. Cause warfarin toxicityb5 b 5




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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