Tarun Wadhwa

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BACKGROUND The Food and Drug Administration's (FDA) Adverse Event Reporting System (FAERS) is a repository of spontaneously-reported adverse drug events (ADEs) for FDA-approved prescription drugs. FAERS reports include both structured reports and unstructured narratives. The narratives often include essential information for evaluation of the severity,(More)
In the last eight years, there has been little progress made on updating our nation's outdated and ineffective privacy laws. While the cost of data has plummeted and entire new industries have been created around storing, analyzing, and sorting large sets of data, our legislators have done little to ensure that regulation has kept up with the pace of(More)
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