Respected international scientists who examined the evidence, concluded that annual influenza campaigns are likely an utter waste of time and money." But officials at the US Centers for Disease Control disregard science and accept commercial propaganda as their guide for setting public health policy.
Besides these cases, 1,833 children from the Chacha Nehru Bal Chikitsalaya (the paediatric hospital affiliated with MGM Medical College) and 233 mentally ill patients had been enrolled in clinical trials without any consent, according to documents submitted to the Supreme Court.
Three newly published peer-reviewed studies confirm that infants exposed to mercury in utero suffer serious harm–including death.
The negative finding of a comprehensive review of 50 published reports by the highly credible Cochrane Collaboration should discourage healthy people from getting a flu shot.
FDA, a complicit partner in crimes and corrupt industry practices have resulted in an epidemic of preventable injuries and deaths.
Part III. The Untouchable Third Rail in Healthcare—The Vaccine Controversy: Core Issues
Part II. What Do We Get for All That Money? A preventable epidemic of injury and death from prescription drugs; FDA’s contribution to the epidemic; Big Pharma’s business model: manufactured myths, propaganda and a hidden agenda;
Part I. America’s commercially profitable healthcare system is wasteful, inefficient and exceedingly harmful. Medical interventions are the third Leading cause of death.
Why didn’t Barbara Starfield’s Findings (JAMA 2000) cause a major overhaul of US medicine?
FDA’s preeminent authority to determine whether a drug or device is approved is its assumed scientific expertise and honest, independent review of safety and performance data from scientifically valid, controlled clinical trials. However, surveys of FDA scientists and numerous independent investigations by highly credible entities have all confirmed serious deficiencies…
Since 1995 FDA scientists have been at odds against FDA managers who routinely override sientists’ safety concerns to approve dubious prescription drugs.
Since 1995 FDA scientists have been at odds against FDA managers who routinely override sientists’ safety concerns to approve dubious prescription drugs.
