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Ketoconazole interactions

Full monograph for KetoconazoleCheck it against another medicine

Medicines

618 documented

Medicines documented to interact with Ketoconazole, worst severity first.
MedicineSeverityMechanismEffectSources
AbemaciclibMajorMetabolismCoadministration with ketoconazole may significantly increase the plasma concentrations of abemaciclib and its pharmacologically active metabolites. The…2 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 Besilate + AtorvastatinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 including azole antifungal agents may significantly increase the plasma concentrations of HMG-CoA…2 documented mechanisms61 sources — open the full entry
Amlodipine Besilate + Benazepril HydrochlorideMajorMetabolism · SynergyUse of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury.2 documented mechanisms43 sources — open the full entry
Amoxicillin + Clavulanic AcidMajorSynergyUse of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury.3 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
Arsenic TrioxideMajorSynergyArsenic trioxide can cause QT interval prolongation and complete atrioventricular block. Theoretically, coadministration with other agents that can prolong the…4 sources — open the full entry
Artemether + LumefantrineMajorMetabolism · SynergyCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of artemether and lumefantrine, both of which are primarily metabolized…3 documented mechanisms13 sources — open the full entry
Atorvastatin + EzetimibeMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 including azole antifungal agents may significantly increase the plasma concentrations of HMG-CoA…2 documented mechanisms21 sources — open the full entry
Atorvastatin CalciumMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 including azole antifungal agents may significantly increase the plasma concentrations of HMG-CoA…21 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
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
Bromocriptine MesylateMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of bromocriptine. Orally administered bromocriptine…7 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 FumarateMajorMetabolism · SynergyCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…2 documented mechanisms49 sources — open the full entry
Budesonide + Glycopyrronium Bromide + Formoterol FumarateMajorAbsorption · Metabolism · SynergyCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…3 documented mechanisms50 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
Cefpodoxime Proxetil + Clavulanic AcidMajorSynergyUse of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury.3 sources — open the full entry
Cefuroxime Axetil + Clavulanic AcidMajorSynergyUse of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury.3 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
Chloroquine PhosphateMajorSynergyChloroquine and hydroxychloroquine can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong…22 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
Citalopram HydrobromideMajorSynergyCitalopram can cause dose-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…15 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
ClozapineMajorSynergyClozapine has the potential to prolong QT interval of the electrocardiogram. Theoretically, coadministration with other agents that can cause QT prolongation…13 sources — open the full entry
ColchicineMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 such as ketoconazole may significantly increase the serum concentrations of colchicine, which is…22 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 such as ketoconazole may significantly increase the bioavailability of dabigatran following oral…4 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
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
Drospirenone + Ethinyl Estradiol + LevomefolateMajorMetabolismCoadministration 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 Ketoconazole needs care, as documented in this source.