Drug General Information (ID: DDI5GCYOX3)
  Drug Name Teriflunomide Drug Info Olaparib Drug Info
  Drug Type Small molecule Small molecule
  Therapeutic Class Selective Immunosuppressants Poly (Adp-Ribose) Polymerase Inhibitors
  Structure

 Mechanism of Teriflunomide-Olaparib Interaction (Severity Level: Major)
     Additive immunosuppressive effects Click to Show/Hide Mechanism Graph
Could Not Find 2D Structure
      Drug Name Teriflunomide Olaparib
      Mechanism 1 Immunosuppressive effects Immunosuppressive effects
      Key Mechanism Factor 1
Factor Name Immunosuppressive effects
Factor Description Immunosuppression is when your immune system is not functioning as it should. The immune system is made up of cells, tissues and organs that help the body fight off infections. If the immune system is suppressed, an infection that your body was able to control may become serious or even fatal.
      Mechanism Description
  • Additive immunosuppressive effects by the combination of Teriflunomide and Olaparib 
     Additive myelosuppressive effects Click to Show/Hide Mechanism Graph
Could Not Find 2D Structure
      Drug Name Teriflunomide Olaparib
      Mechanism 2 Myelosuppressive effects Myelosuppressive effects
      Key Mechanism Factor 2
Factor Name Myelosuppressive effects
Factor Description Myelosuppression, also known as bone marrow suppression, is a decrease in bone marrow activity that leads to a decrease in the production of blood cells. Some blood cell disorders include: erythrocytopenia (anemia), leukopenia (neutropenia), and thrombocytopenia (thrombocytopenia).
      Mechanism Description
  • Additive myelosuppressive effects by the combination of Teriflunomide and Olaparib 

Recommended Action
      Management Close monitoring for the development of infection is recommended if leflunomide or teriflunomide is used in patients who are currently receiving or have recently received other immuno- or myelosuppressive agents, and vice versa. Platelet, white blood cell count, and hemoglobin or hematocrit should be evaluated at baseline and regularly during therapy. Patients should be advised to contact their physician if they develop signs and symptoms of infection such as fever, chills, diarrhea, sore throat, muscle aches, shortness of breath, blood in phlegm, weight loss, red or inflamed skin, body sores, and pain or burning during urination. If evidence of serious infection or bone marrow suppression occurs, treatment should be stopped, and cholestyramine or charcoal administered to accelerate elimination of leflunomide's active metabolite from plasma, which otherwise may take up to two years.

References
1 Product Information. Arava (leflunomide). Hoechst Marion-Roussel Inc, Kansas City, MO.
2 Product Information. Aubagio (teriflunomide). Genzyme Corporation, Cambridge, MA.