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Med Rx.

Docetaxel Trihydrate interactions

Checked as Docetaxel in this data source.

Full monograph for Docetaxel TrihydrateCheck it against another medicine

Medicines

571 documented

Medicines documented to interact with Docetaxel Trihydrate, worst severity first.
MedicineSeverityMechanismEffectSources
AdalimumabMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
Amiodarone HydrochlorideMajorMetabolismCoadministration with amiodarone or dronedarone may significantly increase the plasma concentrations of docetaxel. The proposed mechanism is inhibition of the…19 sources — open the full entry
BaricitinibMajorSynergyCoadministration of baricitinib with other immuno- or myelosuppressive agents may potentiate the risk of infections as well as lymphoma and other malignancies…4 sources — open the full entry
CeritinibMajorMetabolismCoadministration 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
ClarithromycinMajorMetabolismCoadministration 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
ClozapineMajorSynergyCoadministration of clozapine with other agents that can cause neutropenia or agranulocytosis may increase the risk and/or severity of hematologic toxicity.9 sources — open the full entry
CrizotinibMajorMetabolismCoadministration 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
Cyclosporine (Oral)MajorMetabolismCoadministration 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
DeferiproneMajorSynergyCoadministration of deferiprone and other drugs that can cause neutropenia or agranulocytosis may increase the risk and/or severity of hematologic toxicity…5 sources — open the full entry
Diltiazem HydrochlorideMajorMetabolismCoadministration 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
ErythromycinLotionOralMajorMetabolismCoadministration 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
Esomeprazole + Amoxicillin + ClarithromycinMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma…2 documented mechanisms21 sources — open the full entry
EtanerceptMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
GolimumabMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
InfliximabMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
ItraconazoleMajorMetabolismCoadministration 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
KetoconazoleMajorMetabolismCoadministration 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
Ketoconazole + Zinc Pyrithione + AleoveraMajorMetabolismCoadministration 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
Lansoprazole + Amoxicillin + ClarithromycinMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma…3 documented mechanisms21 sources — open the full entry
LeflunomideMajorSynergyThe use of leflunomide with other immunosuppressive or myelosuppressive agents may increase the risk of infections. The risk is thought to extend to…2 sources — open the full entry
Lopinavir + RitonavirMajorMetabolismCoadministration 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
MifepristoneMajorMetabolismCoadministration 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
Mifepristone + MisoprostolMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma…2 documented mechanisms21 sources — open the full entry
NelfinavirMajorMetabolismCoadministration 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
Nirmatrelvir + RitonavirMajorMetabolismCoadministration 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
PosaconazoleMajorMetabolismCoadministration 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
Rabeprazole + Amoxicillin + ClarithromycinMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma…3 documented mechanisms21 sources — open the full entry
Rotavirus VaccineMajorOthersThe administration of live, attenuated viral or bacterial vaccines during immunosuppressant or intense antineoplastic therapy may be associated with a risk of…9 sources — open the full entry
ThalidomideMajorSynergyCoadministration of thalidomide with glucocorticoids and/or antineoplastic agents in the treatment of malignancy may potentiate the risk of thromboembolism…20 sources — open the full entry
TofacitinibMajorOthersCoadministration of tofacitinib with other immuno- or myelosuppressive agents may potentiate the risk of infections as well as lymphoma and other malignancies…1 sources — open the full entry
TucatinibMajorMetabolismCoadministration 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
UpadacitinibMajorOthersCoadministration of upadacitinib with other immuno- or myelosuppressive agents may potentiate the risk of infections as well as lymphoma and other malignancies.1 sources — open the full entry
Verapamil HydrochlorideMajorMetabolismCoadministration 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
Vonoprazan + Amoxicillin + ClarithromycinMajorMetabolism · UnknownCoadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma…2 documented mechanisms21 sources — open the full entry
VoriconazoleMajorMetabolismCoadministration 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
Yellow Fever VaccineMajorOthersThe administration of live, attenuated viral or bacterial vaccines during immunosuppressant or intense antineoplastic therapy may be associated with a risk of…2 documented mechanisms19 sources — open the full entry
AbametapirModerateMetabolismBased on in vitro inhibition data, a single topical application of abametapir lotion may increase plasma concentrations of drugs that are substrates of CYP450…1 sources — open the full entry
AlpelisibModerateExcretionCoadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)…5 sources — open the full entry
Amlodipine Besilate + AtorvastatinModerateSynergy · UnknownThe risk of peripheral neuropathy may be increased during concurrent use of two or more agents that are associated with this adverse effect. Patient risk…2 documented mechanisms4 sources — open the full entry
ApalutamideModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of docetaxel, which is a substrate of the isoenzyme. Rifampin and…14 sources — open the full entry
AprepitantModerateMetabolismCoadministration with inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may increase the plasma concentrations of docetaxel…18 sources — open the full entry
AsciminibModerateMetabolismCoadministration with asciminib may increase the plasma concentrations of drugs that are primarily metabolized by the CYP450 3A4 isoenzyme. The mechanism is…1 sources — open the full entry
Atorvastatin + EzetimibeModerateSynergy · UnknownThe risk of peripheral neuropathy may be increased during concurrent use of two or more agents that are associated with this adverse effect. Patient risk…2 documented mechanisms4 sources — open the full entry
Atorvastatin CalciumModerateSynergyThe risk of peripheral neuropathy may be increased during concurrent use of two or more agents that are associated with this adverse effect. Patient risk…4 sources — open the full entry
AzathioprineModerateSynergyThe use of azathioprine with other immunosuppressive or myelosuppressive agents may result in additive hematologic toxicities and increased risk of infections…3 sources — open the full entry
Azithromycin DihydratebaseOphthalmicModerateAbsorptionCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the blood concentrations of the taxanes, docetaxel and paclitaxel, which have been shown…22 sources — open the full entry
Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + LidocaineModerateMetabolism · UnknownCoadministration with inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may increase the plasma concentrations of docetaxel…3 documented mechanisms18 sources — open the full entry
BendamustineModerateSynergyThe concomitant or sequential administration of multiple antineoplastic agents may result in additive toxicities, particularly in the bone marrow and…9 sources — open the full entry
Beta carotene + Vitamin C + Vitamin EModerateOthersThe potential effects of vitamin E on cancer chemotherapy and radiation have not been established. Because vitamin E is an antioxidant, pharmacologic doses…9 sources — open the full entry
BicalutamideModerateMetabolismCoadministration with inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may increase the plasma concentrations of docetaxel…18 sources — open the full entry

Food & lifestyle

Conditions

Conditions in which Docetaxel Trihydrate needs care, as documented in this source.

Therapeutic duplication

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