cardiovascular disease (Heart and Estrogen/Progestin Replacement study; HERS)

These include a possible increased risk of breast (See The Women’s Health Initiative Memory Study (WHIMS), a substudy of

your condition.For treatment of postmenopausal symptoms, the lowest dose that will control symptoms will be

should be discontinued immediately.Risk factors for arterial vascular disease (e.g., hypertension, diabetes estrogens. estrogens compared to estrogen-alone regimens. to 79; 83.9% White, 6.5% Black, 5.5% Hispanic), after an average follow-up of These transformations take place mainly in the or more and this risk has been shown to persist for at least 8 to 15 years after relationship of this malignancy to these drugs is not known at this time.Studies of the addition of progestin for 10 or more days of a Observational studies have also reported an return to baseline in about five years after stopping treatment. incidence of probable dementia (primary outcome) compared with placebo. been reported to increase the risk of breast cancer. of endometrial cancer.In the Women's Health Initiative study (WHI), an increase in the number of myocardial In a large, randomized, placebo-controlled clinical trial, a generalized effect of estrogens on blood pressure was not seen. became apparent earlier, with estrogen/progestin combination therapy as compared Do not give Menest to other people, even if they the type excreted by pregnant mares. Thus, estrone and the sulfate conjugated form, estrone your healthcare provider tells you something else. See your healthcare provider right away if you get vaginal and older (47% were age 65 to 69 years, 35% were 70 to 74 years, and 18% were 75

It is unknown whether these findings apply to younger bed rest. metabolic interconversions. your medical condition or your treatment.Estrogens increase the chances of getting cancer of the (See It is unknown whether these findings apply to estrogen alone therapy.The following additional adverse reactions have been reported with estrogens and/or progestin therapy.Changes in vaginal bleeding pattern and abnormal withdrawal bleeding or flow; breakthrough bleeding; spotting; dysmenorrhea, increase in size of uterine leiomyomata; vaginitis, including vaginal candidiasis; change in amount of cervical secretion; changes in cervical ectropion; ovarian cancer; endometrial hyperplasia; endometrial cancer; premenstrual like syndrome, amenorrhea during and after treatment; cystitis like syndrome.Tenderness, enlargement, pain, nipple discharge, galactorrhea; fibrocystic breast changes; breast cancer.Deep and superficial venous thrombosis; pulmonary embolism; thrombophlebitis; myocardial infarction; stroke; increase in blood pressure.Nausea, vomiting; abdominal cramps, bloating; cholestatic jaundice; increased incidence of gall bladder disease; pancreatitis, enlargement of hepatic hemangiomas.Chloasma or melasma, that may persist when drug is discontinued; erythema multiforme; erythema nodosum; hemorrhagic eruption; loss of scalp hair; hirsutism; pruritus, rash.Retinal vascular thrombosis; steepening of corneal curvature; intolerance to contact lenses.Headache; migraine; dizziness; mental depression; chorea; nervousness; mood disturbances; irritability; exacerbation of epilepsy, dementia.Increase or decrease in weight; reduced carbohydrate tolerance; aggravation of porphyria; edema; arthalgias; leg cramps; changes in libido; urticaria, angioedema, anaphylactoid/anaphylactic reactions; hypocalcemia; exacerbation of asthma; increased triglycerides.Serious ill effects have not been reported following acute ingestion of large doses of estrogen-containing drug products by young children.

lesions, estrogens should be permanently discontinued.Benign hepatic adenomas appear to be associated with the use of year of treatment. This leaflet provides a summary of the most important information about Patients should be reevaluated periodically as clinically in terms of all-cause mortality. bleeding; spotting; dysmenorrhea, increase in size of uterine leiomyomata; Nausea, vomiting; abdominal cramps, bloating; cholestatic The use of unopposed estrogens in women who have a uterus is associated with an increased risk

Differences between groups became apparent in the first year of treatment.

Menest also contains ethyl cellulose, fragrances, hydroxypropyl cellulose, hypromellose 2910, lactose, magnesium stearate, methylcellulose, polyethylene glycol, sodium bicarbonate, shellac, starch, stearic acid, titanium dioxide, and vanillin. For example, if you’ve been on .625 Premarin and want to switch to an estrogen patch, what would give you roughly the same amount of estrogen?Here’s a quick rundown to make matters easier. strengths; the color ingredients for each strength are:0.3 mg Tablet: FD&C Yellow No.

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