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| (ral-OX-ih-FEEN) |
| Evista |
| Class: Hormone/selective estrogen receptor modulator |
Action Binds to and modulates effects of selected estrogen receptors. This results in estrogen-like effects on bone (increase in bone mineral density) and lipids (decrease in total and LDL cholesterol) but no effect on breast or uterine tissue.
Indications For the prevention and treatment of osteoporosis in postmenopausal women.
Contraindications Women who are or may become pregnant; women with active or history of venous thromboembolic events, including deep venous thrombosis, pulmonary embolism, and retinal vein thrombosis; allergy to raloxifene or other constituents of the tablet; coadministration of cholestyramine.
ADULT WOMEN: PO 60 mg qd.
Cholestyramine: Major reduction in absorption and enterohepatic cycling of raloxifene; avoid concurrent use. Warfarin: Raloxifene may decrease anticoagulant effect. Highly protein-bound drugs (eg, clofibrate, indomethacin, naproxen, ibuprofen, diazepam, diazoxide): May displace raloxifene from protein-binding sites, increasing the effects of raloxifene.
Lab Test Interferences None well documented.
CV: Hot flashes. CNS: Migraine; depression; insomnia. DERM: Rash; sweating. EENT: Sinusitis; pharyngitis; laryngitis. GI: Nausea; dyspepsia; vomiting; flatulence; gastroenteritis; abdominal pain. GU: Vaginitis; urinary tract infection; cystitis; leukorrhea; endometrial disorder. RESP: Cough; pneumonia. OTHER: Infection; flu-syndrome; leg cramps; chest pain; fever; weight gain; edema; arthralgia; myalgia; arthritis.
Pregnancy: Category X. Lactation: Undetermined. Children: Safety and efficacy not established. Venous thromboembolic events: Increased risk of thromboembolic events. Hepatic function impairment: Safety and efficacy not evaluated in patients with severe hepatic insufficiency. Premenopausal use: Safety and efficacy not established. Use is not recommended. Concurrent estrogen therapy: Concurrent use with systemic estrogens is not recommended. Lipid metabolism: Raloxifene lowers serum total and LDL cholesterol but does not affect total HDL or triglycerides. Endometrium: Because raloxifene does not affect endometrial proliferation unexplained uterine bleeding should be investigated as clinically indicated. Breast abnormality: Investigate any unexplained breast abnormality during therapy. Prior history of breast cancer: Raloxifene has not been adequately studied in women with prior history of breast cancer. Use in men: Safety and efficacy not established.
| PATIENT CARE CONSIDERATIONS |
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Popularity: 3% [?]
One Response
Janardhan
July 6th, 2007 at 6:29 am
1sir,
Please can you send the information of drug ralista sideeffects in bonemarrow of humans and animals. I will be very thankfull to u for receving message related to my topic
Thanking You sir
Your’s Faithfully
A.D.V.Janardhan
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