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Med Rx.

Ketoconazole + Zinc Pyrithione + Aleovera interactions

Checked as Ketoconazole in this data source.

Full monograph for Ketoconazole + Zinc Pyrithione + AleoveraCheck it against another medicine

Medicines

618 documented

Medicines documented to interact with Ketoconazole + Zinc Pyrithione + Aleovera, 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 + Zinc Pyrithione + Aleovera needs care, as documented in this source.