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Concomitant strong CYP3A4 inhibitors
The concomitant use of strong CYP3A4 inhibitors should be avoided (including, but not limited to, ketoconazole, itraconazole, clarithromycin, atazanavir, indinavir, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, voriconazole). Should treatment with any of these agents be required, it is recommended that therapy with Tasigna be interrupted. If interruption of treatment with Tasigna is not possible, patients who require treatment with a drug that prolongs QT or strongly inhibits CYP3A4 should be closely monitored for prolongation of the QT interval, and a dose reduction to 1/2 the daily dose is recommended (400 mg once daily). If the strong inhibitor is discontinued, a washout period should be allowed before Tasigna is adjusted upward to the indicated dose. Close monitoring for prolongation of the QT interval is indicated for patients who cannot avoid strong CYP3A4 inhibitors. Grapefruit products and other foods that are known to inhibit CYP3A4 should also be avoided.
Concomitant strong CYP3A4 inducers
The concomitant use of strong CYP3A4 inducers should be avoided
(including, but not limited to, dexamethasone, phenytoin, carbamazepine,
rifampin, rifabutin, rifapentin, phenobarbital). Patients should also
refrain from taking St John's Wort. If patients must be co-administered a
strong CYP3A4 inducer, the dose of Tasigna may need to be increased,
depending on patient tolerability. If the strong inducer is discontinued,
the Tasigna dose should be reduced to the indicated dose. Tasigna is a
competitive inhibitor of CYP3A4, CYP2C8, CYP2C9, CYP2D6, and UGT1A1. Since
warfarin is metabolized by CYP2C9 and CYP3A4, it should be avoided if
possible. Tasigna inhibits human P-glycoprotein. If Tasigna is administered
with drugs that are substrates of Pgp, increased concentrations of the
substrate are
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