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Gemcitabine interactions

Full monograph for GemcitabineCheck it against another medicine

Medicines

375 documented

Medicines documented to interact with Gemcitabine, 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
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
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
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
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
LeflunomideMajorSynergyThe use of leflunomide with other immunosuppressive or myelosuppressive agents may increase the risk of infections. The risk is thought to extend to…1 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
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
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
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
Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + LidocaineModerateSynergyCoadministration of chloramphenicol with other agents that can cause bone marrow depression or aplastic anemia may increase the risk and/or severity of…8 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
Bleomycin SulfateModerateSynergyThe 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
CapecitabineModerateSynergyThe 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
CarboplatinModerateSynergyThe 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
CarmustineModerateSynergyThe 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
ChlorambucilModerateSynergyThe 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
Chloramphenicol (Ophthalmic)ModerateSynergyCoadministration of chloramphenicol with other agents that can cause bone marrow depression or aplastic anemia may increase the risk and/or severity of…8 sources — open the full entry
Chloramphenicol (Oral)ModerateSynergyCoadministration of chloramphenicol with other agents that can cause bone marrow depression or aplastic anemia may increase the risk and/or severity of…8 sources — open the full entry
Chloramphenicol + Lidocaine HydrochlorideModerateSynergyCoadministration of chloramphenicol with other agents that can cause bone marrow depression or aplastic anemia may increase the risk and/or severity of…8 sources — open the full entry
CyclophosphamideModerateSynergyThe 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
CytarabineModerateSynergyThe 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
DacarbazineModerateSynergyThe 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
DaunorubicinModerateSynergyThe 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
DecitabineModerateSynergyThe 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
DenosumabModerateSynergyConcomitant use of immunosuppressive or myelosuppressive agents with denosumab may increase the risk of serious infections. Denosumab binds to and inhibits the…2 sources — open the full entry
Dexamethasone + ChloramphenicolModerateSynergy · UnknownCoadministration of chloramphenicol with other agents that can cause bone marrow depression or aplastic anemia may increase the risk and/or severity of…2 documented mechanisms8 sources — open the full entry
Diphtheria + Tetanus + Pertussis + Hepatitis B + Polio + HIBModerateAntagonismThe administration of inactivated, killed, or otherwise noninfectious vaccines to immunosuppressed patients is generally safe but may be associated with a…10 sources — open the full entry
Diroximel FumarateModerateSynergyThe use of monomethyl fumarate (MMF) or its prodrugs, dimethyl fumarate and diroximel fumarate, with other immunosuppressive or myelosuppressive agents may…1 sources — open the full entry
Docetaxel TrihydrateModerateSynergyThe 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
Doxorubicin HydrochlorideModerateSynergyThe 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
Doxorubicin Hydrochloride LiposomeModerateSynergyThe 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
EfavirenzModerateSynergyCoadministration of efavirenz with other agents known to induce hepatotoxicity may potentiate the risk of liver injury. Efavirenz has been associated with…7 sources — open the full entry
Epirubicin HydrochlorideModerateSynergyThe 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
FilgrastimModerateAntagonismINTERVAL: The safety and efficacy of hematopoietic growth factors such as colony-stimulating factors (G-CSF and GM-CSF) and stem cell factors (SCF) given…4 sources — open the full entry
Fludarabine PhosphateModerateSynergyThe 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
FluorouracilModerateSynergyThe 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
GanciclovirModerateSynergyThe use of ganciclovir with other potentially myelotoxic and/or nephrotoxic agents may increase the risk and severity of hematologic toxicity and/or…7 sources — open the full entry
Hepatitis B Vaccine [rDNA]ModerateAntagonismThe administration of inactivated, killed, or otherwise noninfectious vaccines to immunosuppressed patients is generally safe but may be associated with a…10 sources — open the full entry
HydroxyureaModerateSynergyThe 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
Idarubicin HydrochlorideModerateSynergyThe 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
IfosfamideModerateSynergyThe 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
Imatinib MesylateModerateSynergyThe 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
Inactivated Hepatitis A vaccineModerateAntagonismThe administration of inactivated, killed, or otherwise noninfectious vaccines to immunosuppressed patients is generally safe but may be associated with a…10 sources — open the full entry
Interferon Alfa-2a [Recombinant]ModerateSynergyThe 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

This source documents no food, condition or duplication entries for Gemcitabine.