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Ranolazine interactions

Full monograph for RanolazineCheck it against another medicine

Medicines

454 documented

Medicines documented to interact with Ranolazine, worst severity first.
MedicineSeverityMechanismEffectSources
Amiodarone HydrochlorideMajorSynergyClass IA (e.g., disopyramide, quinidine, procainamide) and class III (e.g., amiodarone, dofetilide, sotalol) antiarrhythmic agents can cause dose-related…45 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 + AtorvastatinMajorMetabolism · UnknownCoadministration with ranolazine may increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The mechanism…2 documented mechanisms84 sources — open the full entry
ApalutamideMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
AprepitantMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
ArmodafinilMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 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 + LumefantrineMajorSynergyArtemether-lumefantrine may cause prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…2 documented mechanisms16 sources — open the full entry
Atorvastatin + EzetimibeMajorMetabolism · UnknownCoadministration with ranolazine may increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The mechanism…2 documented mechanisms84 sources — open the full entry
Atorvastatin CalciumMajorMetabolismCoadministration with ranolazine may increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The mechanism…84 sources — open the full entry
Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + LidocaineMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
Betamethasone + ClotrimazoleMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
Betamethasone + Clotrimazole + GentamicinMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 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
Bosentan MonohydrateMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 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
CabozantinibMajorSynergyCabozantinib can cause prolongation of the QT interval.7 sources — open the full entry
Calcium Dobesilate + Lidocaine + DexamethasoneMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
CarbamazepineMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
CenobamateMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
CeritinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of ranolazine, which is primarily metabolized by the…7 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
Ciprofloxacin + DexamethasoneMajorMetabolism · SynergyCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.2 documented mechanisms19 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
ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of ranolazine, which is primarily metabolized by the…7 sources — open the full entry
ClotrimazoleEar dropEye ointmentTopicalVaginal tabletMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
Clotrimazole + HydrocortisoneMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
ColchicineMajorExcretionCoadministration with inhibitors of P-glycoprotein (P-gp) may significantly increase the serum concentrations of colchicine. The mechanism involves enhanced…78 sources — open the full entry
CrizotinibMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
DexamethasoneMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
Dexamethasone + ChloramphenicolMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
Dexamethasone + LevofloxacinMajorMetabolism · SynergyCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.2 documented mechanisms19 sources — open the full entry
Dexamethasone + Neomycin + Glacial Acetic AcidMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
Dexamethasone + Neomycin Sulphate + Polymyxin B SulphateMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
Dexamethasone + TobramycinMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
Diltiazem HydrochlorideMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
EfavirenzMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
EnzalutamideMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
ErythromycinLotionOralMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
Escitalopram OxalateMajorSynergyEscitalopram can cause dose-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…13 sources — open the full entry
Esomeprazole + Amoxicillin + ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of ranolazine, which is primarily metabolized by the…7 sources — open the full entry
FluconazolebaseOphthalmicMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
Fluvoxamine MaleateMajorMetabolismCoadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme. Because…4 sources — open the full entry
Fosphenytoin SodiumMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
GatifloxacinMajorSynergyCertain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically…28 sources — open the full entry
Gatifloxacin + DexamethasoneMajorMetabolism · SynergyCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.2 documented mechanisms40 sources — open the full entry
Griseofulvin [Ultra Microsize]MajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
HaloperidolMajorSynergyHaloperidol can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…14 sources — open the full entry
Hydroxychloroquine SulphateMajorSynergyChloroquine 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
IloperidoneMajorSynergyIloperidone may cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…9 sources — open the full entry

Food & lifestyle

Conditions

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