Elestrin estradiol gel 0.06%
Patients
Important Risk
Information Below
Resize Text: A A A
Full Prescribing Information|Patient Information|Sign Up
  • About
    Elestrin
    • PK Profile
    • Common Side Effects
    • Elestrin Dosing and Administration
  • Advanced
    Transdermal Delivery
  • Proven
    Effectiveness
  • Treatment
    Options
  • Patient
    Benefits
    • Elestrin Coupon

Site
Map

  • Site Map

Site Map

  • Healthcare Provider Home
  • About Elestrin
    • PK Profile
    • Common Side Effects
    • Elestrin Dosing and Administration
  • Advanced Transdermal Delivery
  • Proven Effectiveness
  • Treatment Options
  • Patient Benefits
    • Elestrin Coupon
    • Contact Us
    • Sign Up
    • Unsubscribe
    • Full Prescribing Information
    • Patient Information
    • Privacy Policy
    • Site Map


    • Patient Home
    • Menopause & Treatment Options
      • Symptoms
      • Estrogen Therapy
      • Other Treatments
      • Menopause FAQ
    • About Elestrin
      • How It Works
      • Hot Flash Relief
      • Facts About Elestrin
      • Benefits
      • Using Elestrin
      • Elestrin FAQ
    • Assess Your Symptoms
    • Elestrin Coupon
    • Contact Us
    • Sign Up
    • Unsubscribe
    • Full Prescribing Information
    • Patient Information
    • Privacy Policy
    • Terms of Use
    • Site Map

    Sign Up | Privacy Policy | Site Map | Contact Us

    Advanced Transdermal Delivery (ATD™) is a registered trademark of Antares Pharma Inc.

    Meda logo © 2013 Meda Pharmaceuticals® All rights reserved.

    ELE-13-0009

    EXPAND ▲
    COLLAPSE ▼

    Elestrin (estradiol gel) is indicated for the treatment of moderate-to-severe vasomotor symptoms due to menopause. Please expand this section to read Important Risk Information.

    WARNING: ENDOMETRIAL CANCER, CARDIOVASCULAR DISORDERS, BREAST CANCER and PROBABLE DEMENTIA

    Estrogen-Alone Therapy

    Endometrial Cancer

    There is an increased risk of endometrial cancer in a woman with a uterus who uses unopposed estrogens. Adding a progestin to estrogen therapy has been shown to reduce the risk of endometrial hyperplasia, which may be a precursor to endometrial cancer. Adequate diagnostic measures, including directed or random endometrial sampling when indicated, should be undertaken to rule out malignancy in postmenopausal women with undiagnosed, persistent or recurring abnormal genital bleeding [see Warnings and Precautions (5.2)].

    Cardiovascular Disorders and Probable Dementia

    Estrogen-alone therapy should not be used for the prevention of cardiovascular disease or dementia [see Warnings and Precautions (5.1, 5.3), and Clinical Studies (14.2, 14.3)].

    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 7.1 years of treatment with daily oral conjugated estrogens (CE) [0.625 mg]-alone, relative to placebo.

    The WHI Memory Study (WHIMS) estrogen-alone ancillary study of the WHI reported an 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, 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 other dosage forms of estrogens.

    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.

    Estrogen Plus Progestin Therapy

    Cardiovascular Disorders and Probable Dementia

    Estrogen plus progestin therapy should not be used for the prevention of cardiovascular disease or dementia.

    The WHI estrogen plus progestin substudy reported increased risks of DVT, pulmonary embolism (PE), stroke and myocardial infarction (MI) 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 WHIMS estrogen plus progestin ancillary study of the WHI reported an increased risk of developing probable dementia in postmenopausal women 65 years of age or older 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.

    Breast Cancer

    The WHI estrogen plus progestin substudy also demonstrated an increased risk of invasive breast cancer. 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.

    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.

    OTHER WARNINGS AND PRECAUTIONS

    • The WHI estrogen plus progestin substudy reported a statistically non-significant increased risk of ovarian cancer
    • Estrogens increase the risk of gallbladder disease
    • Discontinue estrogen if severe hypercalcemia, loss of vision, severe hypertriglyceridemia, or cholestatic jaundice occurs
    • In a small number of case reports, substantial increases in blood pressure have been attributed to idiosyncratic reactions to estrogens
    • Monitor thyroid function in women on thyroid replacement therapy
    • Estrogens may cause fluid retention. Women with cardiac or renal dysfunction, warrant careful observation when estrogen-alone is prescribed
    • Estrogen therapy should be used with caution in women with hypoparathyroidism as estrogen-induced hypocalcemia may occur
    • Women known to have residual endometriosis post-hysterectomy, adding a progestin should be considered
    • Exogenous estrogens may exacerbate symptoms of angioedema in women with hereditary angioedema
    • Estrogen therapy may cause an exacerbation of asthma, diabetes mellitus, epilepsy, migraine, porphyria, systemic lupus erythematosus, and hepatic hemangiomas and should be used with caution with these conditions
    • Estradiol absorption was increased when sunscreen was applied 10 minutes before Elestrin application. Sunscreen should not be applied to the same site until at least 25 minutes after the application of Elestrin
    • Alcohol based gels are potentially flammable. Avoid fire, flame, or smoking until the gel has dried

    CONTRAINDICATIONS

    Elestrin should not be used in women with any of the following conditions:

    • Undiagnosed abnormal genital bleeding
    • Known, suspected, or history of breast cancer
    • Known or suspected estrogen-dependent neoplasia
    • Active DVT, PE, or history of these conditions.
    • Active arterial thromboembolic disease (for example, stroke and MI), or a history of these conditions
    • Known anaphylactic reaction or angioedema to Elestrin
    • Known liver impairment or disease
    • Known protein C, protein S, or antithrombin deficiency, or other known thrombophilic disorders
    • Known or suspected pregnancy

    ADVERSE EVENTS

    The most frequently reported adverse events in ≥ 5% of subjects were nasopharyngitis, breast tenderness, upper respiratory tract infection, and metrorrhagia.

    Please see full Prescribing Information, including Boxed Warning and Patient Information Sheet.

    You are encouraged to report negative side effects of prescription drugs to the FDA at 1-800-FDA-1088 or to Meda Pharmaceuticals Inc. at 1-877-999-8401