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Manufacturer : Beligas Pharmaceuticals Substance : Anastrozole Pack : 50 tabs (1 mg/tab) Antreol 1 mg. Manufacturer : Knoll Healthcare Pvt. Substance : Anastrozole Pack : 30 tabs (1 mg/tab) Santra. Santra is an aromatase inhibitor which is used for adjuvant treatment of postmenopausal women with hormone receptor-positive early breast cancer. First-line treatment of postmenopausal women with hormone receptor-positive or hormone receptor unknown locally advanced or metastatic breast cancer and treatment of advanced breast cancer in postmenopausal women with disease progression following Tamoxifen therapy. Due to the fact that Santra act as anti-estrogens, this medication is used offlabel by male bodybuilders as part of their Post Cycle Therapy (PCT) to restore the natural level of testosterone in the body, so that they can avoid the undesirable effects of estrogen such as gynecomastia that can become apparent at the end of a steroid cycle. The active ingredient present in Santra is Anastrozole. Each Santra tablet contains 1 mg of Anastrozole. Santra is used in women who have finished menopause for treatment of early breast cancer. It is used in the following areas: after surgery, with or without radiation, in women whose breast cancer is hormone receptor-positive, first treatment of locally advanced or metastatic breast cancer in women whose breast cancer is hormone receptor-positive or the hormone receptors are not known, treatment of advanced breast cancer, if the cancer has grown, or the disease has spread after Tamoxifen therapy. The recommended dosage of Santra is 1 mg tablet taken once daily. Take Santra exactly as prescribed by your doctor. Keep taking Santra for as long as your doctor prescribes it for you, injectable steroids for sale uk. Take one tablet each day with or without food. If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose. Take your next regularly scheduled dose. Do not take two doses at the same time. If you have taken more Santra than your doctor has prescribed, contact your doctor right away. Do not take any additional Santra tablet until instructed to do so by your doctor. Talk with your doctor about any health changes you have while taking Santra. During clinical trials dosages up to 60 mg in a single dose given to healthy male volunteers and up to 10 mg daily given to postmenopausal women with advanced breast cancer; these dosages were tolerated. There is no specific antidote to Santra overdosage and the treatment must be symptomatic. In the management of an overdose, consider that multiple agents may have been taken. Vomiting can be induced if the patient is alert.
Table 2: Demographic Characteristics of Women in the NSABP P-1 Trial Characteristic Placebo Tamoxifen # % # % Age (yrs, injectable steroids for sale uk.

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Injectable steroids for sale uk, cheap price legal steroids for sale bodybuilding drugs. Ductal Carcinoma in Situ: NSABP B-24, a double-blind, randomized trial included women with ductal carcinoma in situ (DCIS). This trial compared the addition of tamoxifen or placebo to treatment with lumpectomy and radiation therapy for women with DCIS. The primary objective was to determine whether 5 years of tamoxifen therapy (20 mg/day) would reduce the incidence of invasive breast cancer in the ipsilateral (the same) or contralateral (the opposite) breast. In this trial 1804 women were randomized to receive either tamoxifen or placebo for 5 years: 902 women were randomized to tamoxifen 10 mg tablets twice a day and 902 women were randomized to placebo. As of December 31, 1998, follow-up data were available for 1798 women and the median duration of follow-up was 74 months. The tamoxifen and placebo groups were well balanced for baseline demographic and prognostic factors. Over 80% of the tumors were less than or equal to 1 cm in their maximum dimension, were not palpable, and were detected by mammography alone. Over 60% of the study population was postmenopausal, injectable steroids for sale uk. In 16% of patients, the margin of the resected specimen was reported as being positive after surgery. Approximately half of the tumors were reported to contain comedo necrosis. For the primary endpoint, the incidence of invasive breast cancer was reduced by 43% among women assigned to tamoxifen (44 cases-tamoxifen, 74 cases-placebo; p=0. No data are available regarding the ER status of the invasive cancers. The stage distribution of the invasive cancers at diagnosis was similar to that reported annually in the SEER data base. Results are shown in Table 1. For each endpoint the following results are presented: the number of events and rate per 1000 women per year for the placebo and tamoxifen groups; and the relative risk (RR) and its associated 95% confidence interval (CI) between tamoxifen and placebo. Relative risks less than 1. The limits of the confidence intervals can be used to assess the statistical significance of the benefits of tamoxifen therapy. If the upper limit of the CI is less than 1. Table 1: Major Outcomes of the NSABP B-24 Trial Type of Event Lumpectomy, radiotherapy, and placebo Lumpectomy, radiotherapy, and tamoxifen RR 95% CI Limits No. At 5 years from study entry, survival was 97% for both groups. Reduction in Breast Cancer Incidence in High Risk Women: The Breast Cancer Prevention Trial (BCPT, NSABP P-1) was a double-blind, randomized, placebo-controlled trial with a primary objective to determine whether 5 years of tamoxifen citrate therapy (20 mg/day) would reduce the incidence of invasive breast cancer in women at high risk for the disease (see INDICATIONS AND USAGE ). Secondary objectives included an evaluation of the incidence of ischemic heart disease; the effects on the incidence of bone fractures; and other events that might be associated with the use of tamoxifen, including: endometrial cancer, pulmonary embolus, deep-vein thrombosis, stroke, and cataract formation and surgery (see WARNINGS ). The Gail Model was used to calculate predicted breast cancer risk for women who were less than 60 years of age and did not have lobular carcinoma in situ (LCIS). The following risk factors were used: age; number of first-degree female relatives with breast cancer; previous breast biopsies; presence or absence of atypical hyperplasia; nulliparity; age at first live birth; and age at menarche. A 5-year predicted risk of breast cancer of greater than or equal to 1.

 

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. Most of the adverse reactions observed in all treatment groups were mild to moderate in severity and it was generally not possible to distinguish adverse reactions due to treatment from the consequences of the patient’s metastatic breast cancer, the effects of estrogen deprivation, or intercurrent illness. Tamoxifen and N-desmethyl tamoxifen plasma concentrations have been shown to be reduced when coadministered with rifampin or aminoglutethimide. Induction of CYP3A4-mediated metabolism is considered to be the mechanism by which these reductions occur; other CYP3A4 inducing agents have not been studied to confirm this effect, injectable steroids for sale
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. Based on these findings, tamoxifen is genotoxic in rodent and human MCL-5 cells. Tamoxifen produced impairment of fertility and conception in female rats at doses of 0, injectable steroids usa
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