Drug General Information (ID: DDI351F6U0)
  Drug Name Lenalidomide Drug Info Mestranol Drug Info
  Drug Type Small molecule Small molecule
  Therapeutic Class Antineoplastics Estrogens
  Structure

 Mechanism of Lenalidomide-Mestranol Interaction (Severity Level: Major)
     Additive thrombogenic effects Click to Show/Hide Mechanism Graph
Could Not Find 2D Structure
      Drug Name Lenalidomide Mestranol
      Mechanism Thrombogenic effects Thrombogenic effects
      Key Mechanism Factor 1
Factor Name Thrombogenic effects
Factor Description Drug-induced thrombosis disrupts the balance between thrombogenic factors and protective mechanisms and tends to produce thrombosis. Drug-induced thrombosis usually causes venous thrombotic events, and arterial thrombotic events are also noted as a result of drug administration
      Mechanism Description
  • Additive thrombogenic effects by the combination of Lenalidomide and Mestranol 

Recommended Action
      Management The use of estrogen-containing medications including combined oral contraceptive pills should be undertaken with caution in patients receiving lenalidomide, particularly multiple myeloma patients receiving lenalidomide with dexamethasone. Patients should be apprised of the increased risk of venous thromboembolic events if a combined oral contraceptive pill is chosen as one of two effective methods of contraception that must be used simultaneously and continuously for 4 weeks before, during (even in case of dose interruption), and for 4 weeks after lenalidomide therapy. Input from a gynecologist or similar expert on adequate contraception should be sought as needed. Patients should be advised to seek medical attention if they develop potential signs and symptoms of thromboembolism such as chest pain, shortness of breath, and pain or swelling in the arms or legs. It is not known whether prophylactic anticoagulation or antiplatelet therapy may lessen the risk of venous thromboembolic events. The decision to take prophylactic measures should be done carefully after an assessment of underlying risk factors. If a thromboembolic event occurs during therapy with lenalidomide, treatment must be discontinued and standard anticoagulation therapy started. Once anticoagulation is stabilized and complications of the thromboembolic event under control, lenalidomide may be restarted at the original dose if benefit is deemed to outweigh the risks. Anticoagulation therapy should be continued during the remaining course of lenalidomide treatment.

References
1 Cerner Multum, Inc. "UK Summary of Product Characteristics.".
2 Gunston GD, Mehta U "Potentially serious drug interactions with grapefruit juice." S Afr Med J 90 (2000): 41. [PMID: 10721388]
3 Product Information. Revlimid (lenalidomide). Celgene Corporation, Summit, NJ.