Page 24 - RxExam's Naplex Theory Book Part 2
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                                Dose               Special Notes

                Everolimus      1. Renal           1). Everolimus (Zortress) inhibits antigenic and interleukin stimulated
                (Tablet)        Transplant:        activation and proliferation of T and B lymphocytes.

                                0.75 mg PO BID     2). Everolimus (Zortress) is indicated for the prophylaxis of organ
                                with reduced dose  rejection in adult patients at low-moderate immunologic risk receiving
                                of Cyclosporine.   a kidney transplant. It is to be administered in combination with
                                                   basiliximab induction and concurrently with reduced doses of
                                                   cyclosporine and corticosteroids.

                                                   3). Everolimus (Zortress) tablets should be swallowed whole with a
                                                   glass of water and not crushed before use. Administer Everolimus
                                                   (Zortress) consistently approximately 12 hours apart with or without
                                                   food to minimize variability in absorption and at the same time as
                                                   cyclosporine.

                                                   4). Both cyclosporine doses (standard doses) and the target range for
                                                   whole blood trough concentrations should be reduced, when given in
                                                   a regimen with Everolimus (Zortress), in order to minimize the risk of
                                                   nephrotoxicity.

                                                   5). Routine everolimus whole blood therapeutic drug concentration
                                                   monitoring is recommended for all patients using appropriate assay
                                                   methodology. The recommended everolimus therapeutic range is 3 to
                                                   8 ng/ml.

                                                   6). Everolimus (Zortress) is mainly metabolized by CYP3A4 in the liver
                                                   and to some extent in the intestinal wall and is a substrate for the
                                                   multidrug efflux pump, P-glycoprotein. Therefore, absorption and
                                                   subsequent elimination of systemically absorbed everolimus may be
                                                   influenced by medicinal products that affect CYP3A4 and/or P-
                                                   glycoprotein. Concurrent treatment with strong inhibitors (e.g.,
                                                   ketoconazole, itraconazole, voriconazole, clarithromycin,
                                                   telithromycin, ritonavir) and inducers (e.g., rifampin, rifabutin) of
                                                   CYP3A4 is not recommended. Inhibitors of P-glycoprotein (e.g.,
                                                   digoxin, cyclosporine) may decrease the efflux of everolimus from
                                                   intestinal cells and increase everolimus blood concentrations.

                                                   7). Hypersensitivity reactions, serious infections, angioedema,
                                                   hyperlipidemia, and nephrotoxicity are reported side effects of
                                                   Everolimus (Zortress).

                C). TNF Alfa Inhibitors

                Infliximab                         Please Refer To Page 329 (Part 1) of Chapter 36-Rheumatoid Arthritis.



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