FDA NEWS RELEASE
Media Inquiries: Erica Jefferson, 301-796-4988, erica.jefferson@fda.hhs.gov
Consumer Inquiries: 888-INFO-FDA
Consumer Inquiries: 888-INFO-FDA
FDA approves Xarelto to reduce risk of blood clots after hip, knee replacements
On
July 1, the U.S. Food and Drug Administration approved Xarelto
(rivaroxaban) to reduce the risk of blood clots, deep vein thrombosis
(DVT), and pulmonary embolism (PE) following knee or hip replacement
surgery.
Xarelto is a pill taken once daily. Those undergoing a
knee replacement should take the medication for 12 days and patients
undergoing a hip replacement procedure should take Xarelto for 35 days.
The
safety and effectiveness of Xarelto was evaluated in patients
undergoing hip replacement surgery and patients undergoing knee
replacement surgery. Clinical studies were designed to identify
occurrence of venous thromboembolic events (VTE), DVT, PE or death in
patients treated. Treatment with Xarelto was compared to treatment with
enoxaparin, a drug that prevents DVTs or blood clotting.
“Xarelto
represents a new oral treatment option to help prevent blood clotting in
patients receiving a hip or knee replacement,” said Richard Pazdur,
M.D., director of the Office of Oncology Drug Products in the FDA’s
Center for Drug Evaluation and Research. Xarelto was reviewed by the
Division of Hematology Products within the Office of Oncology Drug
Products.
More than 6,000 patients undergoing hip or knee
replacement surgery received Xarelto in clinical studies. Among patients
undergoing knee replacement surgery, 9.7 percent of those treated with
Xarelto had VTE compared with 18.8 percent of patients who received
enoxaparin. In a study involving hip replacement surgery, 1.1 percent of
patients who received Xarelto had VTE compared with 3.9 percent of
those who received enoxaparin. In another study of hip replacement
patients, 2.0 percent of those treated with Xarelto had VTE compared
with 8.4 percent of those who received enoxaparin.
The most common side effect observed in patients treated with Xarelto was bleeding.
Other
FDA approved drugs to prevent blood clotting include Lovenox
(enoxaparin), generic versions of enoxaparin, Arixtra (fondaparinux),
Fragmin (dalteparin) for hip replacement surgery only, Coumadin
(warfarin) and heparin.
Xarelto is marketed in the U.S. by
Raritan, N.J.- based Janssen Pharmaceuticals, Inc., a member of the
Janssen Pharmaceutical Companies of Johnson & Johnson.
For more information:
The
FDA, an agency within the U.S. Department of Health and Human Services,
protects the public health by assuring the safety, effectiveness, and
security of human and veterinary drugs, vaccines and other biological
products for human use, and medical devices. The agency also is
responsible for the safety and security of our nation’s food supply,
cosmetics, dietary supplements, products that give off electronic
radiation, and for regulating tobacco products.
No comments:
Post a Comment