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Itraconazole interactions

Full monograph for ItraconazoleCheck it against another medicine

Medicines

606 documented

Medicines documented to interact with Itraconazole, worst severity first.
MedicineSeverityMechanismEffectSources
AbemaciclibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of abemaciclib and its pharmacologically active…4 sources — open the full entry
AcalabrutinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of acalabrutinib, which is primarily metabolized by…4 sources — open the full entry
Alfuzosin HydrochlorideMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of alfuzosin, which is primarily metabolized by the…8 sources — open the full entry
AlprazolamMajorMetabolismCoadministration with itraconazole or ketoconazole may significantly increase the plasma concentrations and pharmacologic effects of benzodiazepines that are…28 sources — open the full entry
Amiodarone HydrochlorideMajorMetabolismCoadministration with azole antifungal agents may significantly increase the plasma concentrations of amiodarone. The proposed mechanism is azole inhibition of…8 sources — open the full entry
AmisulprideMajorSynergyAmisulpride can cause dose- and concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the…3 sources — open the full entry
Amlodipine BesilateMajorMetabolism · SynergyItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…36 sources — open the full entry
Amlodipine Besilate + AtenololMajorMetabolism · Synergy · UnknownItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms36 sources — open the full entry
Amlodipine Besilate + AtorvastatinMajorMetabolism · SynergyItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms61 sources — open the full entry
Amlodipine Besilate + Benazepril HydrochlorideMajorMetabolism · SynergyItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…36 sources — open the full entry
Amlodipine Besilate + Olmesartan MedoxomilMajorMetabolism · SynergyItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…36 sources — open the full entry
Amlodipine Besilate + TelmisartanMajorMetabolism · Synergy · UnknownItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms36 sources — open the full entry
Amlodipine Besilate + ValsartanMajorMetabolism · Synergy · UnknownItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms36 sources — open the full entry
ApixabanMajorAbsorption · MetabolismCoadministration with potent inhibitors of CYP450 3A4 that can also inhibit P-glycoprotein (P-gp) may significantly increase the plasma concentrations of…6 sources — open the full entry
Artemether + LumefantrineMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of artemether and lumefantrine, both of which are primarily metabolized…2 documented mechanisms9 sources — open the full entry
AsciminibMajorOthersCoadministration with itraconazole oral solution containing hydroxypropyl-beta-cyclodextrin may decrease the plasma concentrations of asciminib and reduce its…2 sources — open the full entry
Atorvastatin + EzetimibeMajorMetabolism · UnknownCoadministration with itraconazole may significantly increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The…2 documented mechanisms25 sources — open the full entry
Atorvastatin CalciumMajorMetabolismCoadministration with itraconazole may significantly increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The…25 sources — open the full entry
AvanafilMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the…10 sources — open the full entry
AxitinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of axitinib, which is primarily metabolized by the…7 sources — open the full entry
Azelastine Hydrochloride + Fluticasone PropionateMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may increase the systemic exposure to fluticasone following intranasal administration or oral inhalation…40 sources — open the full entry
BetrixabanMajorOthersCoadministration with inhibitors of P-glycoprotein (P-gp) may significantly increase the plasma concentrations of betrixaban, which is a substrate of the…11 sources — open the full entry
Bisoprolol Fumarate + Amlodipine BesilateMajorMetabolism · SynergyItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…36 sources — open the full entry
BrexpiprazoleMajorMetabolismCoadministration with inhibitors of CYP450 3A4 and/or 2D6 may significantly increase the plasma concentrations of brexpiprazole, which is metabolized by these…5 sources — open the full entry
BrigatinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of brigatinib, which is partially metabolized by the…4 sources — open the full entry
BudesonideInhalerNebuliser SuspensionTabletMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…19 sources — open the full entry
Budesonide + Formoterol FumarateMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…19 sources — open the full entry
Budesonide + Glycopyrronium Bromide + Formoterol FumarateMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…19 sources — open the full entry
CabozantinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may increase the plasma concentrations of cabozantinib, which is a substrate of the isoenzyme. High…7 sources — open the full entry
Capmatinib HydrochlorideMajorMetabolismCoadministration of capmatinib with strong CYP450 3A4 inhibitors may increase the risk and severity of capmatinib adverse effects, such as interstitial lung…3 sources — open the full entry
CariprazineMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of cariprazine and its major active metabolite…5 sources — open the full entry
CeritinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of ceritinib, which is a substrate of the isoenzyme…6 sources — open the full entry
CilostazolMajorMetabolismCoadministration with inhibitors of CYP450 3A4 and/or 2C19 may increase the plasma concentrations of cilostazol and or its pharmacologically active…12 sources — open the full entry
Clindamycin + TretinoinMajorMetabolismCoadministration with azole antifungal agents may increase the plasma concentrations and toxicities of tretinoin. The proposed mechanism is inhibition of…2 documented mechanisms15 sources — open the full entry
ColchicineMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may significantly increase the serum concentrations of colchicine, which is primarily metabolized by the…44 sources — open the full entry
CrizotinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of crizotinib, which is primarily metabolized by the…6 sources — open the full entry
Cyclosporine (Oral)MajorMetabolismCertain azole antifungal agents such as ketoconazole and itraconazole that are potent inhibitors of CYP450 3A4 may significantly increase the blood levels of…26 sources — open the full entry
Dabigatran Etexilate MesylateMajorAbsorptionCoadministration with potent inhibitors of P-glycoprotein (P-gp) may increase the bioavailability of dabigatran following oral administration of dabigatran…5 sources — open the full entry
DaclatasvirMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of daclatasvir, which is primarily metabolized by…4 sources — open the full entry
Daclatasvir + SofosbuvirMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of daclatasvir, which is primarily metabolized by…4 sources — open the full entry
DarifenacinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of darifenacin, which is partially metabolized by…7 sources — open the full entry
DasatinibMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations and pharmacologic effects of dasatinib, which is primarily metabolized by…8 sources — open the full entry
DeflazacortMajorMetabolismCoadministration with potent or moderate inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of 21-desdeflazacort, the active…3 sources — open the full entry
DigoxinMajorAbsorption · ExcretionCoadministration with itraconazole may significantly increase the serum concentrations of digoxin. The proposed mechanism is inhibition of the…24 sources — open the full entry
Diltiazem HydrochlorideMajorMetabolism · SynergyItraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…36 sources — open the full entry
Docetaxel TrihydrateMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma…21 sources — open the full entry
DrospirenoneMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…9 sources — open the full entry
Drospirenone + EstetrolMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…9 sources — open the full entry
Drospirenone + EstradiolMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms17 sources — open the full entry
Drospirenone + Ethinyl Estradiol0.02 mg0.03 mgMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms17 sources — open the full entry

Food & lifestyle

Conditions

Conditions in which Itraconazole needs care, as documented in this source.