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Showing posts with label drug contamination. Show all posts
Showing posts with label drug contamination. Show all posts

Health Effects of Vaccines: 'Mercury in Medicine' — Investigative Report Published in the Congressional Record

Photograph by Melissa Wiese.
Photograph by Melissa Wiese.

By Ronald David Jackson
The following "Mercury in Medicine" report was added to the Congressional Record on May 20, 2003.  The report was prepared by the staff of the Subcommittee on Human Rights and Wellness, Committee on Government Reform. The report is the result of a three-year investigation initiated in the Committee on Government Reform. The key findings of the investigation are highlighted with black outlines and in some cases with black and yellow outlines. Some of the key findings include:

1) No one knows for sure if vaccines are safe or unsafe because while there are studies comparing health outcomes in those who did and did not get the vaccine (epidemiological studies) - the vaccines themselves (and more importantly, the various ingredients in the vaccines) have never been thoroughly tested for safety in humans. Specifically: "The FDA [Food and Drug Administration] has never required manufacturers to conduct adequate safety testing on thimerosal and ethylmercury compounds."

2) As the rate of autism has grown at epidemic proportions during the last two decades, the number of childhood vaccines containing thimerosal was growing, increasing the amount of ethylmercury to which infants were exposed threefold.

3) The Institute of Medicine (an American non-profit, non-governmental organization founded in 1970) determined that a relationship between autism, attention deficit hyperactive disorder, and speech or language delay, and the increased use of thimerosal in vaccines is plausible and deserves more scrutiny (even though there was not enough evidence to support or reject this hypothesis).

4) In 1998, the FDA finalized a rule requiring that ethylmercury be removed from over-the-counter products like topical ointments and skin creams (suggesting that ethylmercury—used as a preservative in many vaccines—could be hazardous to health) . Yet it took the FDA 18 years to get around to doing this, even though an advisory committee determined that ethylmercury was unsalfe in these products in 1980.
5) The FDA and the CDC [Center for Disease Control] failed in their duty to be vigilant as new vaccines containing thimerosal were approved and added to the immunization schedule. When the Hepatitis B and Haemophilus Influenzae Type B vaccines were added to the recommended schedule of childhood immunizations, the cumulative amount of ethylmercury to which children were exposed nearly tripled.

6) The amount of ethylmercury to which children were exposed through vaccines exceeded the safety thresholds established by the Federal government for a closely related substance methylmercury, "experts agree that the methylmercury guidelines are a good substitute."

7) Federal health officials have conceded that the amount of thimerosal in vaccines exceeded the EPA threshold of 0.1 micrograms per kilogram of bodyweight. "In fact, the amount of mercury in one dose of DTaP or Hepatitis B vaccines (25 micrograms each) exceeded this threshold many times over.

8) The FDA has: a) Failed to require the pharmaceutical industry to conduct extensive safety studies on thimerosal or ethylmercury. b) Failed to require the pharmaceutical industry to conduct adequate testing to determine how thimerosal is metabolized. c) Failed to require the pharmaceutical industry to determine the maximum safe exposure level to thimerosal.

9) Over the course of two decades the FDA slowly removed ethylmercury from many medicinal products - WHY?

10) In June of 2000, the CDC's Advisory Committe on Immunization Practice met in Atlanta. One of the key factors that weighed against a recommendation for a preference for thimerosal-free vaccines was the financial health of the vaccine industry. A recommendation for thimerosal-free vaccine had "the potential for financial losses of existing inventories", "could harm one or more manufacturers and may then decreased the number of suppliers", and "could entail financial losses for all existing stocks of vaccines that contain thimerosal."

It appears that protecting the industry's profits took precedent over protecting children from mercury damage.


Mercury in Medicine

EPA Faked the Entire Science of Sewage Sludge Safety — Says Whistleblower: Absolutely Unsafe for Use As Fertilizer — It's Actually Lethal

Deer Island Waste Water Plant - Boston, MA. One of the many in the U.S. producing sewage sludge.
Deer Island Waste Water Plant - Boston, MA. One of the many in the U.S. producing sewage sludge.
(Photo by Doc Searls)

By David Lewis
US EPA’s 503 sludge rule (1993) allows treated sewage sludges, aka biosolids, to be land-applied to farms, forests, parks, school playgrounds, home gardens and other private and public lands. According to a recent EPA survey, biosolids contain a wide range of mutagenic and neurotoxic chemicals, which are present at a million-fold higher concentrations (ppm versus ppt) compared with their levels in polluted air and water (1). Biosolids contain all of the lipophilic (fat-soluble) chemical wastes that once polluted our rivers and lakes, but which now settle out at sewage treatment plants and become concentrated in sewage sludges. Most biosolids contain ppm concentrations of heavy metals, including chromium, lead, and mercury. They contain similarly high levels of polycyclic aromatic hydrocarbons (PAHs) and semi-volatiles, such as bis (2-Ethylhexyl) phthalate, Benzo(a)pyrene), and polybrominated diphenyl ether congeners (PBDE flame retardants). Most biosolids also contain pathogenic agents and ppm levels of many common drugs, including ciprofloxacin (Cipro), carbamazepine (Tegretol, Equetro), and fluoxetine (Prozac).

While working at EPA Dr David Lewis published evidence that teenager Shayne Conner (of New Hampshire) died and other neighbors were harmed from living near land applied with sewage sludge (Lewis et al 2002). He furthermore became involved after dairy herds of two Georgia farms (McElmurray and Boyce) were poisoned after grazing on sludged land. He testified in lawsuits following each incident, against his employer (EPA), which is where many of the following depositions were obtained. The following article is an excerpt from Chapter 4 (Sludge Magic) of his new book (Science for Sale: How the US Government Uses Powerful Corporations and Leading Universities to Support Government Policies, Silence Top Scientists, Jeopardize Our Health, and Protect Corporate Profits). The lawsuits referred to are Lewis v. EPA 1999; Lewis v. EPA 2003; and USA, ex rel. Lewis, McElmurray and Boyce v. Walker et al. 2009. The depositions below piece together an unprecedented and coordinated multi-agency scientific scheme involving EPA, USDA, local and city municipalities, Synagro Technologies (a waste management company), various universities, and the National Academies of Science. The effort was intended to misleadingly present sewage sludge as scientifically safe, to hide the evidence that it was not, to deliberately misreport the contents of municipal sludges, and smear David Lewis with a scientific misconduct charge after he blew the whistle.


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