Table 2

Interactions between chemotherapeutic agents and immunosuppressants with NOACs based on known metabolic pathway activity

DabigatranRivaroxabanApixaban
Interaction effect*P-glycoproteinP-glycoprotein CYP3A4P-glycoprotein CYP3A4
Increases NOAC plasma levels Cyclosporine Cyclosporine Cyclosporine 
Tacrolimus Tacrolimus Tacrolimus 
Tamoxifen Tamoxifen Tamoxifen 
Lapatinib Lapatinib Lapatinib 
Nilotinib Nilotinib Nilotinib 
Sunitinib Sunitinib Sunitinib 
Imatinib Imatinib 
Reduces NOAC plasma levels Dexamethasone Dexamethasone Dexamethasone 
Doxorubicin Doxorubicin Doxorubicin 
Vinblastine Vinblastine Vinblastine 
DabigatranRivaroxabanApixaban
Interaction effect*P-glycoproteinP-glycoprotein CYP3A4P-glycoprotein CYP3A4
Increases NOAC plasma levels Cyclosporine Cyclosporine Cyclosporine 
Tacrolimus Tacrolimus Tacrolimus 
Tamoxifen Tamoxifen Tamoxifen 
Lapatinib Lapatinib Lapatinib 
Nilotinib Nilotinib Nilotinib 
Sunitinib Sunitinib Sunitinib 
Imatinib Imatinib 
Reduces NOAC plasma levels Dexamethasone Dexamethasone Dexamethasone 
Doxorubicin Doxorubicin Doxorubicin 
Vinblastine Vinblastine Vinblastine 

CYP3A4, cytochrome P450 3A4.

*

Clinicians should consult with the pharmacist to determine if these and other drug interactions exist when NOACs are being considered.

Drugs that inhibit P-glycoprotein transport or CYP3A4 pathway can increase NOAC levels.

Drugs that induce P-glycoprotein transport or CYP3A4 pathway can lower NOAC levels.

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