FDA’s Stealth Attack on Chelation Therapy for Cardio-Vascular Disease

January 30, 2008
Print This Post Print This Post

The Food and Drug Administration (FDA) recently released a Public Health Advisory on Edetate Disodium (EDTA).  The advisory reflects FDA’s current analysis of data available concerning this drug.  The advisory is meant to alert patients and healthcare professionals about EDTA.

In this relatively innocent looking letter, the FDA is warning hospital pharmacies that there have been 11 deaths associated with di-sodium EDTA since 1971.  They indicate that to improve safety and avoid potential medical errors, hospitals may want to consider not carrying di-sodium EDTA.  Finally, they hint they may be revisiting di-sodium EDTA’s safety record at some point in time.

They are responding to the death of a child in 2003 year because the physician mixed up di-sodium with Calcium EDTA.  Medical errors do take place and the majority of these reported cases.  In fact it is known that 450 people die each year from acetaminophen poisoning.  With the millions of di-sodium EDTA treatments each year, this product has a better safety record than Tylenol®.

The FDA is, of course, forbidden to regulate the practice of medicine but that doesn’t stop them from pushing the envelope.  Every time they have tried, they have lost in court.  One of the most important cases was the FDA v. Evers in 1978.  Guess what the drug in question was?  Yes, di-sodium EDTA.  So they never give up even when they have had their hands slapped.

In addition to the public advisory, the FDA is suggesting that they are revisiting the safety of di-sodium EDTA, essential for the treatment of cardiovascular disease to remove calcium from blocked arteries, while encouraging the use of Calcium-EDTA, which cannot remove the calcium plaque because it is already bonded to Calcium.

This is the same agency that refuses to classify the mercury component in dental fillings, which puts between 42 and 57 tons of mercury into people’s bodies every year.  The agency that has stated it may be unethical to try to find out whether mercury is “safe” in people’s bodies.  Also the same agency that approved Vioxx that killed 50,000 people and approved Viagra that killed well more than 11 people in its first week of use!  Yet, they are focused on the safety of di-Sodium EDTA because of potential confusion about treatment.

The American Association for Health Freedom is very concerned about where the FDA may take this.  The FDA cannot approve or disapprove of how a legally marketed drug is used by a physician in his practice. The agency approves of what a manufacturer may recommend about uses in its labeling (package insert) and advertising. We are meeting with our team of attorneys to make sure our response to this new threat to this very effective and inexpensive treatment for cardio-vascular disease.  We will be working with the physician groups that use di-sodium EDTA to make sure this unnecessary concern the FDA is displaying is not used as an excuse to end this effective and safe treatment.

2 Responses to “FDA’s Stealth Attack on Chelation Therapy for Cardio-Vascular Disease”

  1. [email protected] says:

    The FDA needs to know, and have it reinforced to them in writing, that the Nuremberg Code will be applicable to them and what they are trying to do. Legal precedent exists that if someone is coming to save another’s life, and if that person is prevented from doing so by another, then the person who prevented the individual from saving the other’s life can be held accountable for murder. Millions of people know that the FDA has already prevented good, alternative medical practitioners from saving the lives of countless millions. It’s obvious that this is not just about money for Big Pharma, but that it also involves a much more sinister aspect of “population reduction”. Records exist for what has been done in thousands of places. They thought they could get away with this in Nazi Germany, but they found out otherwise. It will be the same here in the U.S., but it will be much larger and more well documented.

       0 likes

  2. Hi Deborah,

    Thanks for all you do and one thing, in the article on CT make sure you check with Al Augustine in Chicago on the Dr. Keery thing, the child did not die due to CT, the doctor has his license reinstated and the courts found the child of a heart defect known to the parents, they are also doctors. We need to stop the story from being repeated, it was not the wrong kind of EDTA it was a preexisting heart problem according to all our data. Please check with Al and lets get it out on the air waves. Thanks C

       0 likes

Leave a Reply

Comment Policy:
ANH-USA provides a comment forum for our readers to share their constructive thoughts and criticisms about our newsletter articles and engage in civil debate with other readers. All comments are pre-moderated regardless of author. We never censor comments based on political or ideological point of view. We only remove those comments that are abusive, off-topic, use foul language, include personal attacks, or are otherwise discourteous and uncivil. Please do not post comments in ALL CAPS; on the internet this is considered "shouting."

 characters available

Follow us on...