Raloxifene is an oral selective estrogen receptor modulator which is used in the prevention of osteoporosis in postmenopausal women. It was announced on April 17, 2006, that raloxifene is as effective as tamoxifen in reducing the incidence of breast cancer in certain high risk groups of females, [http://ca.today.reuters.com/news/newsArticle.aspx?type=topNews&storyID=2006-04-18T001012Z_01_N17276340_RTRIDST_0_NEWS-CANCER-BREAST-COL.XML&archived=False though with a reduced risk of thromboembolic events and cataracts in patients taking raloxifene versus those taking tamoxifen. It has not been approved by the FDA for this use, and there has been criticism in the mainstream oncology press of the way that the information was released ( A STARring role for raloxifene? Lancet Oncology 7 (6) Page 443 please wikify). There has been some confusion in the lay media about the meaning of the trial results. There is no specific clinical evidence for the use of Raloxifene in the adjuvant treatment of breast cancer over established drugs such as Tamoxifen or Anastrozole.
Raloxifene is produced by Eli Lilly Pharmaceuticals and is sold under the brand name Evista.
SERMs mimic estrogen in some tissues and have anti-estrogen activity in others. Other SERMs, such as Pfizer's lasofoxifene and Wyeth's bazedoxifene are in the late stages of clinical development.
For either osteoporosis treatment or prevention, supplemental calcium and/or vitamin D should be added to the diet if daily intake is inadequate.
Recently it was shown that Raloxifene is very potent drug for prevention of breast cancer. In a recent clinical trial, the drug was shown to be as effective as tamoxifen for breast cancer prevention with lesser side effects1.
Raloxifene may infrequently cause serious blood clots to form in the legs, lungs, or eyes. Other reactions experienced include leg swelling/pain, trouble breathing, chest pain, vision changes.Recently Eli Lilly, the manufactures of raloxifene had issued a warning that use of raloxifene may be associated with increased risk of death from stroke 2.
Benzothiophenes | Piperidines | Selective estrogen receptor modulators
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