A patient tells the nurse that he likes to eat large amounts of garlic to help lower his cholesterol levels naturally. The nurse reviews his medication history and notes which drug has a potential interaction with the garlic?
Warfarin
Acetaminophen
Phenytoin
Digoxin
The Correct Answer is A
Choice A reason: Garlic can enhance warfarin’s anticoagulant effect by inhibiting platelet aggregation and potentially increasing INR, raising bleeding risk. Its sulfur compounds may also induce hepatic enzymes, affecting warfarin metabolism. Patients on warfarin should avoid high garlic intake to maintain stable anticoagulation and prevent hemorrhage.
Choice B reason: Acetaminophen has no significant interaction with garlic. Acetaminophen is metabolized by the liver, primarily via glucuronidation, and garlic’s effects on platelet function or enzymes do not notably affect its pharmacokinetics or analgesic efficacy, making this an unlikely interaction concern.
Choice C reason: Phenytoin, an anticonvulsant, is metabolized by hepatic CYP450 enzymes, but garlic’s weak enzyme induction does not significantly alter phenytoin levels. Garlic’s primary interaction is with anticoagulants like warfarin, not anticonvulsants, making this drug less relevant for garlic-related concerns.
Choice D reason: Digoxin has no major interaction with garlic. Digoxin’s pharmacokinetics are primarily renal, and garlic’s effects on platelets or minor enzyme induction do not significantly alter digoxin levels or cardiac effects. Warfarin’s bleeding risk is more impacted by garlic’s antiplatelet properties.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
Choice A reason: Levofloxacin, a fluoroquinolone, is associated with tendonitis and tendon rupture, particularly in older adults. It disrupts collagen synthesis, weakening tendons like the Achilles, especially in patients over 60 or on corticosteroids. Monitoring for tendon pain is critical to prevent debilitating injury during therapy.
Choice B reason: Hypotension and tachycardia are not primary adverse effects of levofloxacin. Fluoroquinolones may cause QT prolongation, but cardiovascular effects are rare. Their main toxicities include tendon damage and CNS effects, making this an incorrect choice for monitoring in this patient.
Choice C reason: Double vision and floaters are not typical levofloxacin side effects. Fluoroquinolones may cause CNS effects like dizziness or confusion, but visual disturbances like these are more associated with drugs like chloroquine. Tendon issues are a more significant concern with levofloxacin.
Choice D reason: Numbness and tingling are not common with levofloxacin. While fluoroquinolones can cause CNS side effects like seizures in rare cases, peripheral neuropathy is less frequent. Tendonitis and rupture are more prominent risks, especially in older patients, making this an incorrect monitoring priority.
Correct Answer is B
Explanation
Choice A reason: Hair loss is not a common side effect of isoniazid, nor is it prevented by pyridoxine. Isoniazid primarily causes hepatotoxicity or neurotoxicity due to its metabolism and pyridoxine depletion. Hair loss may occur with other drugs, but pyridoxine supplementation is unrelated to this effect.
Choice B reason: Pyridoxine (vitamin B6) is given with isoniazid to prevent peripheral neuropathy. Isoniazid depletes pyridoxine by forming inactive complexes, impairing nerve function and causing numbness or tingling. Supplementation restores pyridoxine levels, protecting peripheral nerves while allowing isoniazid to effectively treat tuberculosis by inhibiting mycolic acid synthesis.
Choice C reason: Heart failure is not associated with isoniazid or prevented by pyridoxine. Isoniazid’s primary toxicities are hepatic and neurological. Pyridoxine supports nerve health, not cardiac function, and heart failure is more linked to drugs like anthracyclines, not antitubercular therapy.
Choice D reason: Renal failure is not a common side effect of isoniazid, nor is it prevented by pyridoxine. Isoniazid is metabolized by the liver, and its toxicities include hepatotoxicity and neuropathy. Pyridoxine addresses neurological side effects, not renal function, making this an incorrect choice.
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