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    The Agency’s Committee for Medicinal Products for Human Use (CHMP) has concluded that there arimidex is a need to harmonise the prescribing information for Arimidex in the European Union (EU) .
    What is Arimidex? arimidex Arimidex is a medicine that contains the active substance anastrozole .
    It is used to treat breast cancer in women who arimidex medicine arimidex patient information arimidex for gyno anastrozole kidney anastrozole dvt have already gone through the menopause .
    Arimidex belongs to a group of medicines called ‘aromatase inhibitors’ which reduce the amount of the hormone oestrogen made in the body by blocking arimidex the action of an enzyme in the body called ‘aromatase’ .
    Decreasing the production of oestrogen is a way of suppressing the growth of the breast cancer because arimidex the growth of breast tissue is stimulated by oestrogen .
    anastrozole cost uk anastrozole and dementia arimidex breast cancer forum arimidex gnc anastrozole The company that markets Arimidex is AstraZeneca .
    The medicine is available in all Member States arimidex of the European Union as well as Iceland and Norway .
    Why was Arimidex reviewed? Arimidex is authorised in the EU via mutual arimidex recognition and national procedures .
    This has led to divergences across Member States in the way the medicine can be used, as seen in the differences in the summaries of product characteristics (SmPCs), labelling and package leaflets in the arimidex countries where the medicine is marketed .
    arimidex Arimidex was identified as needing harmonisation by the Co-ordination Group on the Mutual and Decentralised Procedures – Human (CMD(h)) .
    On 22 July arimidex 2010, the European Commission referred the matter to the CHMP in order to harmonise the marketing authorisations for Arimidex in the EU .

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