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The active ingredient is exemestane. Let your doctor know if you are taking or applying any medication that has estrogen in it including hormone replacement therapy or birth control pills or patches, or if you are taking any other medicines including over-the counter medicines, herbal supplements, and vitamins as they can affect how well AROMASIN works. If you become pregnant while taking AROMASIN, talk to your doctor immediately to learn about the potential risks to the baby. Taking AROMASIN during pregnancy or within 1 month of becoming pregnant can harm your unborn baby. Use effective birth control (contraceptive) during treatment with AROMASIN and for 1 month after your last dose of AROMASIN. A serious side effect of AROMASIN is bone loss over time that may increase your risk of bone fractures and weak and brittle bones (osteoporosis). The health of your bones should be carefully monitored by your doctor for any bone loss before and during treatment with AROMASIN. Any bone loss should be treated appropriately. Before starting to take AROMASIN, have your blood levels checked for Vitamin D deficiency. This is a common condition in women with early breast cancer and should be treated with Vitamin D supplements. A small number of women had chest pain, heart failure or stroke while taking AROMASIN. Tell your doctor if you are breastfeeding or plan to breastfeed. It is not known if AROMASIN passes into your breast milk. Do not breast-feed during treatment with AROMASIN and 1 month after your last dose of AROMASIN, steroids legal in bodybuilding. Common side effects of AROMASIN in women with early breast cancer were: hot flushes increased sweating trouble sleeping feeling tired joint pain, headache. Common side effects of AROMASIN in women with advanced breast cancer were: hot flushes feeling tired increased appetite nausea increased sweating. Before you take AROMASIN, tell your doctor about all of your medical conditions, including if you have liver or kidney problems. AROMASIN may cause decreased fertility in males and females. Talk to your doctor if you have concerns about fertility. AROMASIN is used in women who are past menopause for the treatment of: Early breast cancer (cancer that has not spread outside the breast) in women who: Have cancer that needs the female hormone estrogen to grow and Have had other treatments for breast cancer and Have taken tamoxifen for 2 to 3 years and Are switching to AROMASIN to complete 5 years in a row of hormonal therapy Advanced breast cancer (cancer that has spread) after treatment with tamoxifen, and it did not work or is no longer working. Ask your doctor to prescribe brand-name AROMASIN and to indicate “DAW” (Dispense As Written)—or the language used in your state—on all of your AROMASIN prescriptions. Tell the pharmacist that you want brand-name AROMASIN—and be sure to use the AROMASIN Savings Card if eligible. Check your pills to be sure they’re brand-name AROMASIN—not the generic—and also check that you’ve saved on your prescription if eligible. Make Sure You Have Brand-Name AROMASIN. Look for the distinctive shape and marking of AROMASIN, so you get the brand-name medication you want—from a company you know—pill to pill and month to month.
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The recommended therapeutic dosage is 2 mg to 3 mg/day for patients with signs and symptoms of Parkinson’s disease. Cabergoline should be given as a single daily dose. The safety and efficacy of cabergoline has not been investigated in children as Parkinson’s disease does not affect this population. The tablets are for oral administration. For long-term treatment: ‘ Evidence of cardiac valvulopathy as determined by pre-treatment echocardiography. As with other ergot derivatives, cabergoline should be given with caution to patients with severe cardiovascular disease, Raynaud’s syndrome, peptic ulcer or gastrointestinal bleeding, or with a history of serious, particularly psychotic, mental disorders. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine. The effects of alcohol on overall tolerability of Cabergoline are currently unknown. Lower doses of cabergoline should be considered in patients with severe hepatic insufficiency. Compared to normal volunteers and those with lesser degrees of hepatic insufficiency, an increase in AUC has been seen in patients with severe hepatic insufficiency (Child-Pugh Class C) who received a single 1 mg dose. Postural hypotension can occur following administration of cabergoline, particularly during the first days of administration of cabergoline. Care should be exercised when administering cabergoline concomitantly with other drugs known to lower blood pressure. Fibrosis and Cardiac Valvulopathy and Possibly Related Clinical Phenomena. Fibrotic and serosal inflammatory disorders such as pleuritis, pleural effusion, pleural fibrosis, pulmonary fibrosis, pericarditis, pericardial effusion, cardiac valvulopathy involving one or more valves (aortic, mitral and tricuspid) or retroperitoneal fibrosis have occurred after prolonged usage of ergot derivatives with agonist activity at the serotonin 5HT 2B receptor, such as cabergoline. In some cases, symptoms or manifestations of cardiac valvulopathy improved after discontinuation of cabergoline, steroids legal in bodybuilding. Erythrocyte sedimentation rate (ESR) has been found to be abnormally increased in association with pleural effusion/fibrosis. Chest x-ray examination is recommended in cases of unexplained ESR increases to abnormal values. Serum creatinine measurements can also be used to help in the diagnosis of fibrotic disorder. Following diagnosis of pleural effusion/pulmonary fibrosis or valvulopathy, the discontinuance of cabergoline has been reported to result in improvement of signs and symptoms (see section 4. Valvulopathy has been associated with cumulative doses, therefore patients should be treated with the lowest effective dose. At each visit, the risk benefit profile of cabergoline treatment for the patient should be reassessed to determine the suitability of continued treatment with cabergoline. Before initiating long-term treatment. All patients must undergo a cardiovascular evaluation, including echocardiogram, to assess the potential presence of asymptomatic valvular disease. It is also appropriate to perform baseline investigations of erythrocyte sedimentation rate or other inflammatory markers, lung function/chest x-ray and renal function prior to initiation of therapy. 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