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Drug Interactions between fluconazole and Jakafi

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

fluconazole ruxolitinib

Applies to: fluconazole and Jakafi (ruxolitinib)

ADJUST DOSE: Coadministration of fluconazole with ruxolitinib may significantly increase the plasma concentrations of ruxolitinib and the risk of cytopenias. The proposed mechanism is decreased clearance due to fluconazole-mediated inhibition of CYP450 3A4 and 2C9, the isoenzymes responsible for the metabolic clearance of ruxolitinib. Following concomitant administration of fluconazole at doses of 100 mg to 400 mg daily, the AUC of ruxolitinib is predicted to increase by approximately 100% to 300%, respectively.

MANAGEMENT: Coadministration of ruxolitinib with fluconazole doses greater than 200 mg per day should be avoided except in patients with acute graft versus host disease (GVHD). For patients with myelofibrosis (MF) coadministered fluconazole 200 mg per day or less, ruxolitinib should be started at 10 mg twice a day when the platelet count is at least 100 X 10(9)/L or greater and 5 mg once a day when the platelet counts is at least 50 X 10(9)/L. and less than 100 x 10(9)/L. The recommended starting dose for patients with Polycythemia vera (PV) coadministered fluconazole 200 mg per day or less is ruxolitinib 5 mg twice a day. For patients with MF or PV who are stabilized on ruxolitinib 10 mg twice a day or greater and starting fluconazole (at a dose of 200 mg per day or less), the ruxolitinib dose should be reduced by 50% (rounded up to the closest available tablet strength). For patients with MF or PV stabilized on ruxolitinib 5 mg twice a day and starting fluconazole (at a dose of 200 mg per day or less), the ruxolitinib dose should be reduced to 5 mg once a day. For patients with MF or PV stabilized on ruxolitinib 5 mg once a day, avoid starting fluconazole or interrupt ruxolitinib therapy for the duration of fluconazole use. Additional dosage modifications should be made with careful monitoring of safety and efficacy.

References

  1. Cerner Multum, Inc. "UK Summary of Product Characteristics."
  2. (2011) "Product Information. Jakafi (ruxolitinib)." Incyte Corporation

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Drug and food interactions

Moderate

ruxolitinib food

Applies to: Jakafi (ruxolitinib)

GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of ruxolitinib. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits.

MANAGEMENT: Patients treated with ruxolitinib should avoid consumption of grapefruit, grapefruit juice, and any supplement containing grapefruit extract. Ruxolitinib may be administered with or without food.

References

  1. (2011) "Product Information. Jakafi (ruxolitinib)." Incyte Corporation

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Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.