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Arimidex

Arimidex is used to treat breast cancer in women after menopause. Some breast cancers are made to grow faster by a natural hormone called estrogen. Arimidex decreases the amount of estrogen the body makes and helps to slow or reverse the growth of these breast cancers.

Other names for this medication:
Altraz, Altrol, Anabrez, Anastrocare, Anastrozole, Anatero, Anazol, Armilon, Armotraz, Femistra, Femitraz, Qubol, Redest, Rimidex, Stazonex, Xenosoul

Similar Products:
Clarinex, Amoxil, Retin, Mircette, Xalatan, Alprostadil, Zebeta, Moduretic, Cardura, Indapril, Veromon, Fomicet, Vasotop, Inhibace, Antram, Zepcid, Clopicard, Albins, Zegra,

Also known as: Anastrozole

Description

Arimidex is approved to treat certain types of breast cancer in women who’ve gone through menopause.

What breast cancer is

Breast cancer develops when cells in your breast start to grow and multiply (make more cells) more quickly than usual. With most breast cancers, the abnormal cells are encouraged to grow by the hormone estrogen.

If your breast cancer is stimulated by hormones, such as estrogen, certain tests will show that the cancer cells have receptors (attachment sites) for those hormones. This type of breast cancer is called hormone receptor-positive (HR+).

HR+ cancers can be treated with hormone therapies that lower the estrogen level in your body. And because most breast cancer is HR+, hormone therapies are also sometimes used to treat breast cancer whose receptor status isn’t known.

What Arimidex does

Arimidex is a hormone therapy that’s used to treat certain forms of breast cancer. It’s a type of drug called an aromatase inhibitor. Arimidex works by stopping (inhibiting) the action of an enzyme called aromatase. (Enzymes are certain proteins that help chemical reactions to happen inside your body.)

The aromatase enzyme makes estrogen out of steroid hormones in your body, such as testosterone. Aromatase is found in various tissues, including your brain, fat, and skin.

Before menopause, estrogen is mainly produced by your ovaries. And just a small amount is made by the aromatase enzyme. But after menopause, your ovaries stop producing estrogen. At that point, the aromatase enzyme is the main way that your body makes estrogen. (And in men, estrogen is also mainly produced by the aromatase enzyme.)

By stopping aromatase from working, Arimidex lowers the amount of estrogen in your body. This helps to stop estrogen from encouraging breast cancer to grow and spread.

How long does it take to work?

Arimidex will start working soon after you begin taking it. But you won’t be able to notice this. Your doctor may order different kinds of tests during your treatment to check and see if the drug is working for you.

Dosage

This medicine may be taken on an empty stomach or with food. Take this by mouth exactly as directed usually once a day. This is a potent medication. Do not increase your dose, or take this more often than directed. If you want to achieve most effective results do not stop taking Generic Arimidex suddenly.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Storage

Store between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children in a container that small children cannot open.

Side effects

The most common side effects associated with Arimidex are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Generic Arimidex if you are allergic to Generic Arimidex components. This medicine has been shown to cause harm to the human fetus. It is unknown if this drug is excreted in breast milk. Use a non-hormonal method of birth control if you are a woman capable of becoming pregnant. Avoid alcohol. Avoid machine driving. Do not stop taking Generic Arimidex suddenly.

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A study on the possible occurrence of base-exchange reactions in vivo. Computational identification and comparative analysis of miRNA precursors in three palm species. Prevalence of migraine and cluster headache in Swedish men of 18. In Situ Grown TiO2 Nanospindles Facilitate the Formation of Holey Reduced Graphene Oxide by Photodegradation. Fetuses carrying this replacement activated Hoxd-11 transcription prematurely, which led to a rostral shift of its expression boundary and a consequent anterior transposition of the sacrum. The later stages of sporulation in oocysts of Eimeria brunetti were examined in samples which had been allowed to sporulate at 27 degrees C for 24, 36 and 48 hours.

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The prevalence of squamous intraepithelial lesions (SIL), the incidence of SIL and regression from low-grade SIL were studied according to CD4 count after controlling for HPV detection results. Glut1 expression in a cutaneous lesion strongly suggests a proliferative lesion of the squamous cell type. Known volumes of air samples from the output of an olfactometer, a device used to generate odor stimuli, were passed through charcoal sorbent tubes. Genetic variants of the lipoprotein lipase gene have been associated with dyslipidemia and coronary artery disease. Effects of chronic exposure to coal in wild rodents (Ctenomys torquatus) evaluated by multiple methods and tissues. To illustrate the potential of the validated model in studying corneal biomechanics, its use in modelling Goldmann applanation tonometry (GAT) is briefly described. Within 10 min, the mannosylated and non-mannosylated antigens co-localized with typical markers for major histocompatibility complex class II-enriched compartments and lysosomes. Molecular analysis of the deduced protein reveals a 33 kDa acidic and extremely hydrophilic protein with potential amphiphilic alpha-helical regions. We conclude that by facilitating more efficient phagocytic clearance of spores, antibodies against individual exosporium components can contribute to protection against B.

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Social comparisons allow individuals to gain knowledge of their traits and abilities. However, there are limitations associated with the currently used carriers, including the need for surgical implantation and the associated increase in infection risk. Assessment of non-invasive models for liver fibrosis in chronic hepatitis B virus related liver disease patients in resource limited settings. This report describes the principles and application of capillary gel electrophoresis and high-performance liquid chromatography for the analysis of synthetic DNA varying in base composition and length. The processes described in this study have an enormous potential for industrial production of bioethanol because they are environmentally friendly, highly productive, economic with low cost, and can be easily manipulated.

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Collagen IV-dependent ERK activation in human Caco-2 intestinal epithelial cells requires focal adhesion kinase. Malignant phaeochromocytoma with cavoatrial extension imaged with (123)I-MIBG. Taken together, our findings indicate that housing-type social buffering is sustained after a period of social housing. Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage. Their role during development and differentiation remains unclear. Synthesis of Aryldifluoroamides by Copper-Catalyzed Cross-Coupling. In patients with acute leukemias hemorrhage is the most frequent problem.

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