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Zortress is indicated for the prophylaxis of allograft rejection in adult patients receiving a liver transplant. Zortress is to be administered no earlier than 30 days posttransplant concurrently in combination with reduced doses of tacrolimus and with corticosteroids [s ee Warnings and Precautions (5. 5), Clinical Studies (14.2)].
Zortress is indicated for the prophylaxis of organ rejection in adult patients at low-moderate immunologic risk receiving a kidney transplant [see Clinical Studies (14.1)]. Zortress is to be administered in combination with basiliximab induction and concurrently with reduced doses of cyclosporine and with corticosteroids.
Zortress is supplied as tablets for oral administration containing 0.25 mg, 0.5 mg, and 0.75 mg of everolimus together with butylated hydroxytoluene, magnesium stearate, lactose monohydrate, hypromellose, crospovidone and lactose anhydrous as inactive ingredients.
Important Product Information, including Boxed WARNINGS, for ZORTRESS, myfortic, Neoral, and SANDIMMUNE. For Patients: Call 1-877-952-1000 if you are in urgent need of your medication, and are unable to fill your prescription or need help paying for it.
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The Zortress brand of everolimus is used to prevent organ rejection after a kidney or liver transplant. Zortress is used together with cyclosporine, steroids, and other medications. Afinitor is another brand of everolimus used to treat certain types of cancer. This medication guide provides information only about about Zortress. Important ...