WASHINGTON, Sept. 14 (Xinhua) -- The U.S. Food and
Drug Administration approved Evista on Friday for reducing the risk of invasive
breast cancer in postmenopausal women with osteoporosis and in postmenopausal
women at high risk for invasive breast cancer.
In 1997, FDA approved Evista, which is manufactured
by Eli Lilly and Company, for the prevention of osteoporosis in postmenopausal
women and, in 1999, for the treatment of postmenopausal women with osteoporosis.
Previously as a drug for osteoporosis, Evista is now
only the second drug approved to reduce the risk of breast cancer. Evista is
commonly referred to as a selective estrogen receptor modulator(SERM). In
reducing the risk of invasive breast cancer, SERMs may act by blocking estrogen
receptors in the breast.
"Today's action provides an important new option for
women at heightened risk of breast cancer," said Steven Galson, director of
FDA's Center for Drug Evaluation and Research. "Because Evista can cause serious
side effects, the benefits and risks of taking Evista should be carefully
evaluated for each individual woman."
The serious side effects include blood clots in the
legs and lungs, and death due to stroke. Women with current or prior blood clots
in the legs, lungs, or eyes should not take Evista. Other potential side effects
include hot flashes, leg cramps, swelling of the legs and feet, flu-like
symptoms, joint pain, and sweating.
Evista should not be taken by premenopausal women and
women who are or may become pregnant because it may cause harm to the
unbornbaby, warned FDA in its statement.
In addition, Evista should not be taken with
cholestyramine (a drug used to lower cholesterol levels) or estrogens.
Evista does not completely prevent breast cancer.
Breast examinations and mammograms should be done before starting Evista and
regularly thereafter, said FDA.
Breast cancer is the second leading cause of cancer
death in American women and accounts for 26 percent of all cancers among women.
An estimated 178,480 new cases of invasive breast cancer are expected to occur
among women in the United States during 2007.