Drug Interactions between Duavee and eltrombopag
This report displays the potential drug interactions for the following 2 drugs:
- Duavee (bazedoxifene/conjugated estrogens)
- eltrombopag
Interactions between your drugs
conjugated estrogens eltrombopag
Applies to: Duavee (bazedoxifene / conjugated estrogens) and eltrombopag
Consumer information for this interaction is not currently available.
MONITOR CLOSELY: Venous thromboembolic events, including deep vein thrombosis (DVT) and pulmonary embolism (PE) have occurred during treatment with eltrombopag. Concurrent use of other agents such as combined hormonal contraceptives, hormone replacement therapy (HRT), or estrogen receptor modulators may potentiate this risk. Eltrombopag is a thrombopoietin (TPO) receptor agonist that initiates signaling cascades leading to proliferation and differentiation of megakaryocytes, which increases platelet production. Thromboembolic events have been observed in Immune Thrombocytopenia Purpura (ITP) patients receiving eltrombopag even with low or normal platelet counts. In controlled clinical studies of thrombocytopenic patients with hepatitis C receiving interferon-based therapy (n=1,439), thromboembolic events occurred in 4% of patients receiving eltrombopag versus 1% receiving placebo. Additionally, a case report described the development of DVT and PE in a patient taking eltrombopag and hormonal contraceptives, although the event occurred 10 days after eltrombopag discontinuation. Hormonal contraceptives and HRT are listed among risk factors for thromboembolism in patients receiving eltrombopag. This risk may be further increased in individuals with inherited or acquired coagulation disorders, advanced age, prolonged periods of immobilization, malignancies, surgery, trauma, obesity, or smoking.
MANAGEMENT: Caution and close clinical monitoring are advised when eltrombopag is coadministered with combined hormonal contraceptives, HRT, and/or estrogen receptor modulators. Platelet counts should be closely monitored throughout treatment with consideration given to a dose reduction or discontinuation of eltrombopag if the platelet count exceeds the target levels. Patients and their caregivers should also be advised to seek medical attention if they experience signs and symptoms of a thromboembolic event, such as shortness of breath, chest pain, hemoptysis, or arm or leg swelling or pain.
eltrombopag bazedoxifene
Applies to: eltrombopag and Duavee (bazedoxifene / conjugated estrogens)
Consumer information for this interaction is not currently available.
MONITOR CLOSELY: Venous thromboembolic events, including deep vein thrombosis (DVT) and pulmonary embolism (PE) have occurred during treatment with eltrombopag. Concurrent use of other agents such as combined hormonal contraceptives, hormone replacement therapy (HRT), or estrogen receptor modulators may potentiate this risk. Eltrombopag is a thrombopoietin (TPO) receptor agonist that initiates signaling cascades leading to proliferation and differentiation of megakaryocytes, which increases platelet production. Thromboembolic events have been observed in Immune Thrombocytopenia Purpura (ITP) patients receiving eltrombopag even with low or normal platelet counts. In controlled clinical studies of thrombocytopenic patients with hepatitis C receiving interferon-based therapy (n=1,439), thromboembolic events occurred in 4% of patients receiving eltrombopag versus 1% receiving placebo. Additionally, a case report described the development of DVT and PE in a patient taking eltrombopag and hormonal contraceptives, although the event occurred 10 days after eltrombopag discontinuation. Hormonal contraceptives and HRT are listed among risk factors for thromboembolism in patients receiving eltrombopag. This risk may be further increased in individuals with inherited or acquired coagulation disorders, advanced age, prolonged periods of immobilization, malignancies, surgery, trauma, obesity, or smoking.
MANAGEMENT: Caution and close clinical monitoring are advised when eltrombopag is coadministered with combined hormonal contraceptives, HRT, and/or estrogen receptor modulators. Platelet counts should be closely monitored throughout treatment with consideration given to a dose reduction or discontinuation of eltrombopag if the platelet count exceeds the target levels. Patients and their caregivers should also be advised to seek medical attention if they experience signs and symptoms of a thromboembolic event, such as shortness of breath, chest pain, hemoptysis, or arm or leg swelling or pain.
Drug and food/lifestyle interactions
eltrombopag food/lifestyle
Applies to: eltrombopag
Food may reduce the absorption and blood levels of eltrombopag. In addition, minerals such as aluminum, calcium, iron, magnesium, and zinc can also interfere with eltrombopag absorption into the bloodstream, which may make the medication less effective in treating your condition. You should take eltrombopag on an empty stomach one hour before or two hours after a meal. Eltrombopag should also be taken at least 2 hours before or 4 hours after products like antacids, mineral supplements, dairy products, and fortified juices. Talk to your doctor or pharmacist if you have questions on how to take this or other medications you are prescribed. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
conjugated estrogens food/lifestyle
Applies to: Duavee (bazedoxifene / conjugated estrogens)
Information for this minor interaction is available on the professional version.
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.