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Faking Medical Reality

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Jon Rappoport’s Blog

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“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” —Marcia Angell, MD

“The secret of acting is sincerity. If you can fake that, you’ve got it made.” —George Burns

The faking of medical reality is, at bottom, an operation designed to bolster the power of the medical cartel, one of the most important forces on the planet.

What do doctors rely on? What do medical schools rely on? What do medical journals and mainstream medical reporters and drug companies and the FDA rely on?

The sanctity of published clinical trials of drugs. These trials determine whether the drugs are safe and effective. The drugs are tested on human volunteers. The results are tabulated. The trial is described in a paper that is printed by a medical journal.

This is science. This is rationality. This is the rock. Without these studies, the whole field of medical research would fall apart in utter chaos.

Upon this rock, and hence through media, the public becomes aware of the latest breakthrough, the newest medicine. Through doctors in their offices, the public finds out what drugs they should take—and their doctors know because their doctors have read the published reports in the medical journals, the reports that describe the clinical trials. Or if the doctors haven’t actually read the reports, they’ve been told about them.

It all goes back to this rock.

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Iatrogenesis and the Poisonous Nature of Fluoroquinolone Antibiotic Drugs Such as Cipro

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Duty to Warn

By Gary G. Kohls, MD

Definition: An iatrogenic disease is an illness that occurs as a result of a therapeutic or diagnostic procedure undertaken on a patient; a healthcare professional-caused disease, usually due to properly-prescribed prescription drugs, vaccines or surgical procedures.

Noroxin® (norfloxacin)—Merck and Co.

Cipro® Cipro XR® (ciprofloxacin)—Bayer HealthCare

Levaquin® (levofloxacin)—Janssen (subsidiary of J & J) Pharmaceuticals

Avelox® (moxifloxacin)—Bayer HealthCare

Factive® (gemifloxacin)—Cornerstone Therapeutics

Ofloxacin—gen

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The following information concerns the serious toxic effects of fluoroquinolone antibiotics – which include Bayer’s Cipro, Janssen’s Levaquin, Bayer’s Avelox, Merck’s Noroxin, Pfizer’s Trovan and the generic drug Ofloxacin.

The information outlined below is excerpted from three sources that I have only become aware of recently.

1) a 29-page FDA document that discusses fluoroquinolone antibiotic-caused peripheral neuropathy. The document can be found in its entirety at https://drive.google.com/file/d/0BzLMHZg5q0Y3VkVJUmhxSlQtbWs/edit.

This document totally ignores the equally serious poisonous effects of fluoroquinolone drugs such as the antibiotic’s toxic effects on cellular mitochondria, which is the likely cause of the tendonopathies, neuropsychiatric disorders, chronic fatigue syndromes, muscular disorders, cardiomyopathies, cardiac dysrhythmias, neurodegenerative disorders, etc

2) Some of the information has been excerpted from http://www.saferpills.org/wp-content/uploads/2014/08/Citizen-Petition-from-the-Southern-Network-on-Adverse_Reactions.pdf.

3) I also attach a relevant abstract from a 2001 British Medical Journal article about Pfizer’s malfeasance in its testing of ts fluoroquinolone drug (Trovan) during a 1996 Nigerian meningitis epidemic.

I feel that such information about once popular prescription drugs – that have been deceptively advertised by Big Pharma as safe – is particularly important because I have been among the multitude of healthcare providers that were intentionally deceived by Big Pharma into believing their false claims of safety for any number of now-known to be dangerous vaccines, psych drugs, arthritis drugs, heart drugs, etc. More

Beware the Drug Companies:Pertinent Quotes from Marcia Angell, MD and Author Helen Epstein

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strip bannernew-logo25Compiled by Dr Gary Kohls,MD

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Pertinent Quotes from Marcia Angell, MD and Author, Helen Epstein

Note: Dr Marcia Angell was fired from her long-held job as executive editor of the once prestigious New England Journal of Medicine because of an editorial that she wrote criticizing the pharmaceutical industry, criticisms that she elaborated on in her book, “The Truth About the Drug Companies: How They Deceive Us and What to Do About It”.

Here are some quotes from Dr Angell’s writings and/or interviews. Some of them were published at Jon Rappoport’s website:

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“…Similar conflicts of interest and biases exist in virtually every field of medicine, particularly those that rely heavily on drugs or devices. It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” — Marcia Angell, M, author of “The Truth About the Drug Companies: How They Deceive Us and What to Do About It” More

War On Health

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We have long maintained that the FDA is a threat to public health.  Routinely approving drugs for use on the public that they have neither tested nor questioned, tens of thousands of people die each year as a result.  No one is prosecuted.  No one is held accountable.  Not one pharmaceutical CEO will be held accountable or liable.

At best, this is racketeering. At worst, it is aiding and abetting in mass murder.

It would appear that money fixes everything.  Vioxx killed an estimated 400,000 people…….before Merck pulled it off the market.  Conservative writer and activist Ron Unz  has concluded that data indicate that the death toll from Vioxx was closer to 500,000 just in 2004.

This agency, which has been responsible for more deaths than many wars, the hyped up gun arguments, and assorted other hot button topics, has never once been smacked down for its collusion with its pharmaceutical corporate partners.  And never once has it been held liable for the massive number of deaths that are a result of its “for profit at the expense of human life” business practices.

About half of the drugs put into the market will be recalled in five years because they cause death, heart attacks and numerous other adverse effects…..and not one FDA “I was just following orders” employee on any level will see one day in jail.

Maybe public hangings should be reconsidered.  How many people are going to be seriously harmed or die before we close this abomination down?

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The FDA: Close this abomination down!

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Marti Oakley  2012/All rights Reserved

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One of the greatest threats we face today is what many refer to as the “Food and Death Administration”. (FDA) Far from being a protector of the public health, the true intent of this agency was revealed in the ongoing senate hearings regarding S 3187.

The American public has become increasingly alarmed over the use of the word “modernization” in connection with anything coming out of the District of Criminals. Modernization generally means we are about to get another federal corporate agency expansion that will subject us to foreign agreements, which will grossly infringe on our rights to be left alone by government, and, which will effectively militarize some federal agency against the public. These “modernizations” generally conflict with constitutional protections and grossly expand or create enforcement arms of various agencies.

S 3187 is primarily concerned with increasing the pay-to-play administrative fees; in other words they are going to charge those who contract with them more while at the same time shortening the time it takes to get all pharmaceuticals approved. Well! My goodness! That is exactly what we need to do. We need to fast track the approval process for more drugs that kill, harm and impair the public.

Sen. Tom Harkin (D) IA, introduced the bill claiming it had broad support and acknowledging that they had a great deal of input from stakeholders: THE PRESCRIPTION DRUG MANUFACTURERS, THE PHARMACISTS, THE DRUGSTOREs. He also claimed that consumer groups were involved in the process. More

The FDA as it exists: A clear and present danger to the public

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Marti Oakley (c)copyright 2011 All Rights Reserved

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On August 20th, 2010, the FDA issued a recall and alert of an estimated 300 million (or was it billion?) eggs that were produced at Wright County Egg in Galt, Iowa. Far from being the first time this egg company had been sited for unsanitary conditions or other FDA violations, the FDA subsequent to the latest infractions which affected consumers in many states, issued a warning letter (yet again) to the company. No one from Wright Egg Company was arrested; no product was seized or destroyed and not one person associated with Wright Egg was taken to court or charged with any crimes. What did follow was a letter of warning.

The letter states: “Failure to take prompt corrective action may result in regulatory action being initiated by the Food and Drug Administration without further notice.  These actions include, but are not limited to, seizure and/or injunction.” 

No seizure or injunction occurred.  In fact,Wright County Egg really never missed a day of production, or was penalized in any meaningful way for their ongoing disregard of FDA standards.

The FDA is in ongoing communications with Wright County Egg to ensure that appropriate preventive measures are put in place to reduce the risk of recurrence.” 

I bet they were really shakin’ in their shoes! (sarc) More

FDA begins its propaganda campaign against dietary supplements: Be afraid! Very afraid….of the FDA

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 Marti Oakley (c) copyright 2010 All Rights Reserved

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Is there any requirement on pharmaceutical labels to state that they are safe and effective?

Do pharmaceuticals in fact, state that they are safe and effective?  No! They do not!   

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Consumer Reports has just come out with the first volley against dietary supplements in order to help the FDA justify the illegal and unlawful assumption of power the agency recently claimed it “believed” it had.  As the FDA attempts to exert unlawful authority over alternative’s to toxic pharmaceuticals, it appears Consumer Reports will do what it can to propagandize this campaign for CODEX and the coming attempts to regulate alternative natural supplements and herbs in order to profit corporate pharmaceutical companies.  

With this report surfacing behind the recent claims of FDA, saying they believed they had the authority to override DSHEA , ending our protected rights to dietary supplements, if that’s what we chose, and implementing CODEX standards which have been thoroughly rejected by the public, FDA will be surfacing more in the news with exaggerated claims of danger from contamination and unverifiable claims of harm from dietary supplements. 

It is unfortunate that FDA is not as tenacious or concerned with the lethal drugs it sets loose on the population on behalf of corporate partners who pay to play. More

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