Article: Keeping Track of Adverse Events

publication date: Mar 4, 2009
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The recall of a drug or medical device shakes everyone involved in the production, prescription or use of the product.  Patients worry, often needlessly, about how the recalled item may have affected their health.  Medical practitioners reconsider their decisions to prescribe any product from the company.  The company itself faces huge financial and regulatory risk.  Even more important is the potential loss of trust in its reputation and brand, not only among patients and prescribers but also among its employees...



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