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Procrit is used to treat anemia in patients suffering from Chronic Kidney Disease (CKD). It is also used to treat anemia in HIV-infected patients and people being treated with chemotherapy. Procrit is a man-made form of the protein that produces red blood cells in the body. It is manufactured by Amgen, Inc., and was approved by the FDA in 1989. Procrit is in a class of medications called erythropoiesis stimulating agents (ESA) and makes approximately $2 billion a year.
Procrit is a dangerous drug that has a black box label warning about serious risks. After a number of studies showed that Procrit may accelerate the progress of certain types of cancer, the FDA advised doctors not to prescribe the drug to patients suffering from breast, head and neck cancer.
The black-box warning placed on Procrit advises “ESAs shortened overall survival and/or increased the risk of tumor progression or recurrence in clinical studies of patients with breast, non-small cell lung, head and neck, lymphoid, and cervical cancers.”
Serious side effects have been seen when the patient was prescribed a high dose of Procrit. In 2007, a warning about high doses of Procrit was placed on the label. Serious side effects that have been linked to the drug are heart attack, stroke, blood clots, pulmonary embolisms, deep vein thrombosis, rapid growth of pre-existing tumors and death.
Serious side effects may include:
Less serious side effects may include:
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