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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.

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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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