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Clarithromycin interactions

Full monograph for ClarithromycinCheck it against another medicine

Medicines

768 documented

Medicines documented to interact with Clarithromycin, worst severity first.
MedicineSeverityMechanismEffectSources
AbemaciclibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of abemaciclib and its pharmacologically active…3 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
Amiodarone HydrochlorideMajorMetabolism · SynergyAmiodarone can cause dose-related prolongation of the QT interval. Coadministration with other agents that can prolong the QT interval such as macrolide…10 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 + AtorvastatinMajorMetabolismSome macrolide antibiotics inhibit CYP450 3A4 and may elevate the plasma concentrations of HMG-CoA reductase inhibitors that are metabolized by the isoenzyme…2 documented mechanisms43 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 · UnknownSome macrolide antibiotics inhibit CYP450 3A4 and may elevate the plasma concentrations of HMG-CoA reductase inhibitors that are metabolized by the isoenzyme…2 documented mechanisms38 sources — open the full entry
Atorvastatin CalciumMajorMetabolismSome macrolide antibiotics inhibit CYP450 3A4 and may elevate the plasma concentrations of HMG-CoA reductase inhibitors that are metabolized by the isoenzyme…38 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 PropionateMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 may increase the systemic exposure to fluticasone following intranasal administration or oral inhalation…2 documented mechanisms40 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
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 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
CabergolineMajorMetabolismCoadministration with certain macrolide antibiotics may significantly increase the plasma concentrations of ergot derivatives. The mechanism is macrolide…48 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
CarbamazepineMajorMetabolismSome macrolide antibiotics can significantly increase serum carbamazepine levels. The mechanism is probably inhibition of hepatic CYP450 3A4 isoenzymes. Severe…22 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
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
ColchicineMajorMetabolismCoadministration of colchicine with clarithromycin may significantly increase the serum concentrations of colchicine. The proposed mechanism is inhibition of…42 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)MajorMetabolismCoadministration with macrolide antibiotics that are potent inhibitors of CYP450 3A4 may significantly increase the blood concentrations of cyclosporine, which…37 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
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
DigoxinMajorExcretionCoadministration with clarithromycin may significantly increase the plasma concentrations of digoxin. The proposed mechanism is clarithromycin inhibition of…38 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 mechanisms25 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 mechanisms25 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 mechanisms25 sources — open the full entry
Econazole Nitrate + Triamcinolone AcetonideMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of triamcinolone.14 sources — open the full entry
ElacestrantMajorMetabolismCoadministration with potent or moderate inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of elacestrant, which is primarily…1 sources — open the full entry
Elagolix SodiumMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of elagolix, which is a substrate of the isoenzyme…3 sources — open the full entry
EplerenoneMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations and risk of adverse reactions of eplerenone, which…3 sources — open the full entry
ErdafitinibMajorMetabolismCoadministration of erdafitinib with potent inhibitors of CYP450 2C9 or 3A4 may increase the plasma concentrations and risk of toxicity of erdafitinib, which…1 sources — open the full entry
Ergometrine MaleateMajorMetabolismCoadministration with certain macrolide antibiotics may significantly increase the plasma concentrations of ergot derivatives. The mechanism is macrolide…48 sources — open the full entry
ErythromycinLotionOralMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may increase the plasma concentrations of erythromycin, which is primarily metabolized by the isoenzyme…11 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

Food & lifestyle

Conditions

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

Therapeutic duplication

Drug classes that overlap with Clarithromycin, so taking both doubles up the same effect. This source publishes no per-row citations for duplication.