Help your patients alleviate their moderate-to-severe vasomotor symptoms with low-dose Evamist®, the first and only estradiol transdermal spray. Evamist provides flexible dosing with 1, 2, or 3 sprays once daily and is designed to provide consistent delivery of estradiol in a quick-drying invisible spray.1,2
   
Choose Evamist for efficacy, convenience, and patient satisfaction
 
  • Proven efficacy
    Proven to reduce frequency and severity of moderate-to-severe hot flashes1
  • Transdermal delivery
    Evamist delivers a low dose of 17ß-estradiol sprayed on a small area of the forearm1,2
  • Unique dosing
    Flexible titration with 3 dosing options in 1 applicator1
  • Convenient therapy
    Convenient spray application that fits easily into her daily routine2
  • Patient satisfaction
    Evamist has high patient satisfaction and is recommended by 8 out of 10 patients*2
 
Prescribe Evamist for your patient experiencing moderate-to-severe vasomotor symptoms
 
Read more about the pivotal Phase 3 study on the efficacy and safety of Evamist published by the American College of Obstetricians and Gynecologists in the June 2008 edition of its prestigious journal, Obstetrics & Gynecology. View the abstract here.
 
*Based on an experience study of 247 women using Evamist.2
» References
 
Important Safety Information

Indication
Evamist® is indicated for the treatment of moderate-to-severe vasomotor symptoms due to menopause.

WARNING—ENDOMETRIAL CANCER, CARDIOVASCULAR, AND OTHER RISKS

ENDOMETRIAL CANCER Adequate diagnostic measures, including endometrial sampling when indicated, should be undertaken to rule out malignancy in all cases of undiagnosed persistent or recurring abnormal vaginal bleeding.

CARDIOVASCULAR AND OTHER RISKS Estrogens with or without progestins should not be used for the prevention of cardiovascular disease or dementia. The Women’s Health Initiative (WHI) estrogen-alone substudy reported increased risks of stroke and deep vein thrombosis (DVT) in postmenopausal women (50 to 79 years of age) during 6.8 years and 7.1 years, respectively, of treatment with daily oral conjugated estrogens (CE 0.625 mg), relative to placebo. The estrogen plus progestin WHI substudy reported increased risk of myocardial infarction, stroke, invasive breast cancer, pulmonary emboli, and DVT in postmenopausal women (50 to 79 years of age) during 5.6 years of treatment with daily oral CE 0.625 mg combined with medroxyprogesterone acetate (MPA 2.5 mg), relative to placebo. The Women’s Health Initiative Memory Study (WHIMS), a substudy of the WHI, reported increased risk of developing probable dementia in postmenopausal women 65 years of age or older during 5.2 years of treatment with daily CE 0.625 mg alone and during 4 years of treatment with daily CE 0.625 mg combined with MPA 2.5 mg, relative to placebo. It is unknown whether this finding applies to younger postmenopausal women. In the absence of comparable data, these risks should be assumed to be similar for other doses of CE and MPA and other combinations and dosage forms of estrogens and progestins. Because of these risks, estrogens with or without progestins should be prescribed at the lowest effective doses and for the shortest duration consistent with treatment goals and risks for the individual woman.

Evamist should not be used in women with undiagnosed abnormal genital bleeding; known, suspected, or history of breast cancer; known or suspected estrogen-dependent neoplasia; active deep vein thrombosis, pulmonary embolism, or history of these conditions; active or recent arterial thromboembolic disease; liver dysfunction or disease; or known or suspected pregnancy.

In a clinical trial with Evamist, the most common side effects were headache, breast tenderness, nasopharyngitis, nipple pain, back pain, nausea, and arthralgia.

Please see full prescribing information for Evamist, including boxed warnings.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

   
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