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    F.D.A. Originally said to be approved, 23 Aricept to improve cognitive and global – function in patients with the disease – or in general. However, clinical trials have shown only a slight improvement in cognitive measures, and any improvement in the overall measure.
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    So how long after a drug is introduced by another manufacturer may make the generic equivalent? And how do they do it? Let’s find out.

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    The drug, Aricept 23, was approved in July 2010 against the advice of reviewers in the Office of the Food and Drug Administration.

    Therefore, if the generic version is exactly the same effect on the body in its original version, which is an advantage of generics? One word: price.

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    Marcia J. Diljak, Eisai spokeswoman, declined to comment on the safety of the drug, but said Eisai and Pfizer decided to develop a higher dose of 10 milligrams of Aricept after version was approved in 2005. “It was assumed that patients with more advanced disease Alzheimer’s could benefit from a higher dose of Aricept,” he said. The representative of Pfizer, questions about the drug to Eisai.
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