Clinical Pharmacy Flashcards
7 cards from real Pharmacy practice questions. Tap to flip, then mark Knew It or Still Learning — missed cards come back until you master them.
Read the first 7 Clinical Pharmacy flashcards as text
A patient on warfarin is started on fluconazole. What is the expected pharmacokinetic interaction?
Answer: Fluconazole inhibits CYP2C9, increasing warfarin levels and bleeding risk
Fluconazole is a potent CYP2C9 inhibitor that reduces warfarin metabolism, raising INR and bleeding risk.
Which parameter best describes the time required to reach steady-state plasma concentration?
Answer: Approximately 4-5 half-lives
Steady state is reached after approximately 4-5 half-lives regardless of dose or dosing interval.
A patient with a serum creatinine of 2.4 mg/dL requires vancomycin dosing. What adjustment is necessary?
Answer: Reduce dose frequency due to decreased renal clearance
Vancomycin is renally eliminated, so impaired renal function requires extending the dosing interval to prevent toxicity.
A pharmacist reviews a medication therapy management (MTM) encounter. Which of the following is a medication-related problem?
Answer: Unnecessary drug therapy with no medical indication
Unnecessary drug therapy — taking a medication without a valid clinical indication — is a recognized category of medication-related problems in MTM.
Which electrolyte imbalance is most commonly associated with loop diuretic use?
Answer: Hypokalemia
Loop diuretics inhibit the Na-K-2Cl transporter, increasing urinary potassium loss and causing hypokalemia.
A patient taking lithium presents with nausea, tremor, and a serum lithium level of 1.9 mEq/L. What is the appropriate action?
Answer: Hold lithium and consider dialysis if symptoms worsen
A lithium level above 1.5 mEq/L with symptoms indicates toxicity; holding the drug and monitoring for dialysis need is appropriate.
Which statement best describes pharmacodynamic tolerance?
Answer: Decreased receptor sensitivity with repeated drug exposure
Pharmacodynamic tolerance occurs when receptors downregulate or become desensitized, reducing drug effect at the same concentration.
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