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Immune-related Adverse Events from Immune Checkpoint Inhibitor Therapy

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11 Contraindications and Cautions AZA is contraindicated in patients who have shown hypersensitivity to the drug. Patients with rheumatoid arthritis previously treated with alkylating agents (cyclophosphamide, chlorambucil, melphalan, or others) may have a prohibitive risk of malignancy if treated with AZA. Warning that patients receiving immunosuppressants, including AZA, are at increased risk of developing lymphoma and other malignancies, particularly of the skin. Physicians should inform patients of the risk of malignancy with AZA. As usual for patients with increased risk for skin cancer, exposure to sunlight and ultraviolet light should be limited. Contraindications include hypersensitivity to cyclophosphamide and urinary outflow obstruction. Warnings include urinary tract and renal toxicity. Cardiotoxicity, which may be fatal, has been reported. Monitor patients, especially those with risk factors for cardiotoxicity or pre-existing cardiac disease. Pulmonary toxicity leading to respiratory failure may also occur. Monitor patients for signs and symptoms of pulmonary toxicity. Secondary malignancies, veno-occlusive liver disease, and embryo-fetal toxicity can occur. Advise female patients of reproductive potential to avoid pregnancy. Contraindicated in patients with a hypersensitivity to cyclosporine and/or polyoxyethylated castor oil. Only physicians experienced in immunosuppressive therapy and management of organ transplant patients should prescribe cyclosporine. Patients receiving the drug should be managed in facilities equipped and staffed with adequate laboratory and supportive medical resources. Cyclosporine should be administered with adrenal corticosteroids but not with other immunosuppressive agents. Increased susceptibility to infection and the possible development of lymphoma may result from immunosuppression. Cyclosporine, when used in high doses, can cause hepatotoxicity and nephrotoxicity. No contraindications. Warnings that eltrombopag may cause hepatotoxicity, increase the risk for development or progression of reticulin fiber deposition within the bone marrow, and may increase the risk for hematological malignancies. Contraindicated in patients with a hypersensitivity to etoposide products. Warnings that etoposide may cause Myelosuppression, secondary leukemias with long-term use, hypersensitivity reactions, and embryo-fetal toxicity. Use of hydroxychloroquine is contraindicated in patients with known hypersensitivity to 4 aminoquinoline compounds. Use with caution in patients with gastrointestinal, neurologic, or blood disorders. Prolonged used requires ophthalmologic monitoring for retinal toxicity.

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