Prestigious Mainstream Editor Torpedoed The FDA

JonRappoport February 3 2014

Marcia Angell
Marcia Angell

Seven years ago, Marcia Angell, who, for two decades, edited one of the most famous medical journals in the world, the New England Journal of Medicine, wrote a piece for the Boston Globe.

It was titled, Talking Back to the FDA (February 26, 2007).

In his book, Medication Madness, Dr. Peter Breggin quotes Angell’s article:

“The FDA also refuses to release unfavorable research results in its possession without the sponsoring company’s permission…It’s no wonder that serious safety concerns about drugs such as Vioxx, Paxil, and Zyprexa have emerged very late in the day—years after they were in widespread use.”

Serious safety concerns? Heart attacks, strokes, suicide and homicide, etc.

What’s this ongoing bureaucratic insanity Marcia Angell is referring to?

The drug companies do the human studies on new drugs before they are submitted to the FDA, who then decides whether to approve the drugs for public consumption.

The FDA examines these studies. But here is the catch. A drug company might submit four studies on a new drug to the FDA. The FDA might choose to render a favorable decision based on two studies.

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Murder In The Medical Matrix: The FDA

Jon Rappoport’s Blog | December 27 2012

cartoon_fda_conflicts-of-interestI have to begin this article with a bow in the direction of a remarkable site, SSRI stories. There you will find a huge assembly of media articles documenting the death and destruction wrought by psychiatric drugs. In particular, read the index.

It previews the whole picture. It connects the dots.

Keep in mind that all the indicted psychiatric drugs have been approved by the FDA as safe and effective.

Over the years, I’ve written much about the the FDA. I thought I’d assemble a small fraction of it in one place, to reveal what this federal agency is really all about and why it should be dismantled, amid a blizzard of prosecutions and convictions for negligent homicide and, yes, murder.

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Hidden In Plain View ~ Jon Rappoport – May 18, 2012
www.nomorefakenews.com

The day of the Smoking Gun has arrived.

The discovery of a page, on the FDA’s own website, proves the FDA is fully aware that:

the drugs it certifies as safe have been killing Americans, at the rate of 100,000 per year.

The FDA website page is currently available under the heading, “Why Learn About Adverse Drug Reactions.”

The FDA takes no blame, no responsibility for its own actions, and yet it admits the death statistics are accurate.

As an investigative reporter, I have been tracking and writing about pharmaceutically-caused deaths for 10 years. I have, on numerous occasions, cited Dr. Barbara Starfield’s report in the July 26th, 2000, Journal of the American Medical Association, in which she presents the figure of 106,000 deaths per year, in America, as a direct result of these drugs. I have claimed that the federal government and, in particular, the FDA, are aware of these numbers.

And now the page on the FDA’s own website confirms the death toll. Yet, nowhere do we see the FDA taking one shred of responsibility for this ongoing holocaust.

Holocaust? Add up the figures. Medical drugs cause 100,000 deaths in America every year: that means a million Americans are killed every decade.

Understand this very clearly. No medical drug in America can be released for public use until and unless the FDA states it is safe. The FDA is the agency that makes every such decision on every drug. The buck stops there.

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