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Pharmacology Fundamentals Flashcards

7 cards from real OSCE practice questions. Tap to flip, then mark Knew It or Still Learning โ€” missed cards come back until you master them.

Read the first 7 Pharmacology Fundamentals flashcards as text
  1. A patient is prescribed warfarin. Which enzyme system is primarily responsible for its metabolism?

    Answer: CYP2C9

    Warfarin is primarily metabolized by CYP2C9, making it susceptible to interactions with CYP2C9 inhibitors or inducers.

  2. A drug has a therapeutic index of 2. Which statement best describes this drug?

    Answer: It has a narrow safety margin between therapeutic and toxic doses

    A therapeutic index of 2 means the toxic dose is only twice the effective dose, indicating a narrow safety margin requiring close monitoring.

  3. Which pharmacokinetic parameter describes the fraction of an administered dose that reaches systemic circulation unchanged?

    Answer: Bioavailability

    Bioavailability (F) is the fraction of administered drug that reaches systemic circulation in its active form.

  4. A patient taking phenytoin starts rifampicin. The nurse should anticipate which change?

    Answer: Reduced phenytoin levels due to enzyme induction

    Rifampicin is a potent CYP enzyme inducer that accelerates phenytoin metabolism, lowering its plasma levels.

  5. Which receptor type uses a G-protein coupled mechanism to mediate its intracellular effects?

    Answer: Beta-adrenergic receptor

    Beta-adrenergic receptors couple to Gs proteins, activating adenylyl cyclase and increasing intracellular cAMP.

  6. A drug is described as having zero-order kinetics. What does this mean clinically?

    Answer: A constant amount of drug is eliminated per unit time regardless of concentration

    Zero-order kinetics means saturable elimination mechanisms are overwhelmed, so a fixed amount (not a fixed fraction) is removed per unit time.

  7. Which route of drug administration completely bypasses first-pass hepatic metabolism?

    Answer: Intravenous

    Intravenous administration delivers drug directly into systemic circulation, entirely bypassing hepatic first-pass metabolism.

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