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Shocking Story Reveals How the FDA Is Recklessly Abandoning Drug Safety

Prescription Drugs

Story at-a-glance -

  • Learn how the FDA bypassed or ignored safety issues on major drug approvals from Ronald Kavanagh, who was a drug reviewer for the FDA in the Center for Drug Evaluation and Research from 1998 to 2008
  • He reveals some of the internal rules of the FDA that are clearly designed to thwart serious safety reviews from the get-go, and other loopholes frequently used by drug companies to circumvent safety investigations
  • Five years ago, a Subcommittee on Science and Technology report entitled “FDA Science and Mission at Risk” detailed how the FDA cannot fulfill its mission, in part because its scientific base has eroded and its scientific organizational structure is weak
  • The subcommittee concluded the FDA’s failures place the health of Americans and the financial health of the nation at grave risk

By Dr. Mercola

In the wake of shocking reports on how the FDA, terrified of being outed for its questionable practices, spied on its own employees in the hopes of rooting them out before they could become whistleblowers, a new story has emerged on how deep the deceit goes. From marginalizing safety reports to not reading them at all―and then going ahead and approving the drugs in question―the FDA once more stands accused of being little more than a rubber-stamping agency for Big Pharma.


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