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October 3, 2013

Despite Thimerosal (Mercury) Ban Imposed By The FDA, 60 Percent of All Flu Vaccines Still Contain This Deadly Neurotoxin

Dave Mihalovic, Prevent Disease
Waking Times
Although the FDA gave a two year deadline to remove thimerosal from vaccines after the deadly neurotoxin was banned in 1999, they continue to appear in vaccine formulations to this day. The FDA now supports thimerosal in up to 60 percent of flu vaccines, many which are approved for children for the 2013/2014 flu season.
The public is still so propagandized by mainstream medicine and the media, that they are blind to the facts relating to the FDA’s reversal on their decision of allowing thimerosal into vaccines. 




Factually, Thimerosal is a mercury-containing compound that is a known human carcinogen, mutagen, teratogen and immune-system disruptor at levels below 1 part-per-million, and a compound to which some humans can have an anaphylactic shock reaction. It is also a recognized reproductive and fetal toxin with no established toxicologically safe level of exposure for humans.
In November, 1997, the U.S. Congress passed the Food and Drug Administration Modernization Act, requiring the study of mercury content in FDA-approved products. The review disclosed the hitherto-unrecognized levels of ethylmercury in vaccines. 
In July 1999, public-health officials announced that thimerosal would be phased out of vaccines. The CDC, American Academy of Pediatrics, and FDA insisted that the measure was purely precautionary. They requested of all vaccine manufacturers to eliminate mercury from vaccines.
The requests were denied by vaccine manufacturers and continued every year thereafter.

In 2009, eight out of ten H1N1 vaccines had thimerosal. Last year’s 2011/2012 flu vaccine season saw three out of five FDA approved vaccines containing thimerosal. The 2012/2013 season offered three out of six flu vaccines which contained thimerosal and all were FDA approved.
Under specific codes of conduct for manufacturers as dictated by the FDA, they must prove that any compound used as a preservative is “sufficiently nontoxic so that the amount present in the recommended dose of the product will not be toxic to the recipient” and the vaccine makers have never done this for Thimerosal used as a preservative in US-FDA-approved vaccines. 

Thimerosal, is now used as a preservative in four (4) out of the seven (7) FDA approved flu vaccines for the 2013/2014 flu season noted below.
Thimerosal-Derived Ethylmercury in vaccines is now well established as a mitochondrial toxin in human brain cells.
There are dozens of scientific inquiries and studies on the adverse effects of thimerosal, including gastrointestinal abnormalities and immune system irregularities.
In ongoing negotiations, the World Health Organization and other global distributors of vaccines have defended the continuing use of mercury, especially in vaccines. They maintain that there is no evidence of harm from Thimerosal. Dr. Mark R. Geier, a CoMeD director, cautions, “Recent statements by those holding national and global responsibility for vaccine safety are difficult to reconcile with the known and published toxicity of Thimerosal.” Eight decades of scientific literature have shown that Thimerosal poses a significant health risk and its manufacturers acknowledge it can cause mild to severe mental retardation in children.
According to Coalition for Mercury-Free Drugs (CoMeD), numerous scientific studies and extensive peer-reviewed scientific and medical papers have all concluded that Thimerosal poses a significant health risk. Thimerosal manufacturers also acknowledge that the preservative can cause mild to severe mental retardation in children.
Reverend Lisa K. Sykes, President of CoMeD, stated “The most vulnerable among us continue to be intentionally exposed to mercury from Thimerosal in childhood vaccines. This exposure is entirely avoidable, and must be stopped.”
Note that for every single flu vaccine, the carcinogenic or mutagenic potential has not been evaluated, or for impairment of fertility. . This means that none of the carcinogenic excipients (inside every vaccine) are ever studied and their effects on the human body are unknown. This declaration also indicates that there is no responsible authority that can state to a parent, that their son or daughter will not become infertile as a consequence of receiving the influenza vaccine.
Another remarkable fact is that although all pregnant women are encouraged to receive the flu vaccine by health and medical authorities, the safety and effectiveness for pregnant women or nursing mothers has also not been established. Perhaps this is why studies show many spontaneous abortions and stillbirths after pregnant women are vaccinated.
////// 2013/2014 FDA APPROVED FLU VACCINES ////// 
1. AFLURIA 2013/2014
Manufactured by CSL Limited

Ingredients/Excipients: 
Beta-Propiolactone: Carcinogen
Monobasic Potassium Phosphate: Immunotoxin
Neomycin: Immunotoxin
Polymyxin: Neurotoxin
Potassium Chloride: Neurotoxin
Sodium Deoxycholate: Immunotoxin
Thimerosal: Neurotoxin
Safety and effectiveness of AFLURIA have not been established in
pregnant women or nursing mothers.
All multi-dose formulations of this vaccines contain Thimerosal.
AFLURIA is not approved for use in children less than 5 years of age.
AFLURIA has not been evaluated for carcinogenic or mutagenic potential or for impairment of fertility.
***************************************************
2. FLUVARIX 2013/2014Manufactured by GlaxoSmithKline

Ingredients/Excipients: 
Formaldehyde : Carcinogen
Gentamicin Sulfate: Nephrotoxic
Hydrocortisone: Myelin Degenerator
Octoxynol 10 (TRITON X-100): Immunotoxin
Polysorbate 80 (Tween 80): Sterilie Agent
Sodium Deoxycholate: Immunotoxin
Safety and effectiveness of FLUARIX have not been established in pregnant women or nursing mothers.
All multi-dose formulations of this vaccines contain Thimerosal.
FLUARIX has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.
***************************************************

3. FLULAVAL 2013/2014
Manufactured by ID Biomedical Corporation

Ingredients/Excipients: 
Formaldehyde: Carcinogen
Sodium Deoxycholate: Immunotoxin
Thimerosal: Neurotoxin
Safety and effectiveness of FLULAVAL have not been established in pregnant women, nursing mothers, or children.
All multi-dose formulations of this vaccines contain Thimerosal.
FLULAVAL has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.
***************************************************

4. FLUMIST 2013/2014
Manufactured by MedImmune Vaccines Inc.

Ingredients/Excipients: 
Gelatin: Allergen
Gentamicin: Nephrotoxic
Monobasic Potassium Phosphate: Immunotoxin
Monosodium Glutamate: Neurotoxin
Safety and effectiveness of FLUMIST have not been established in pregnant women, nursing mothers, geriatric adults, or children less than 2 years of age.
FLUMIST has not been evaluated for its carcinogenic or mutagenic potential or its potential to impair fertility
***************************************************

5. FLUVIRIN 2013/2014
Manufactured by Novartis Vaccines

Ingredients/Excipients: 
Beta-Propiolactone: Carcinogen
Neomycin: Immunotoxin
Polymyxin: Neurotoxin
Thimerosal: Neurotoxin
Latex: Allergen
Safety and effectiveness of FLUVIRIN has not been established in pregnant women or nursing mothers or children less than 4 years of age. This vaccine was found to lower the immune response of young children.
All multi-dose formulations of this vaccines contain Thimerosal.
FLUVIRIN has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.
***************************************************

6. FLUZONE 2013/2014Manufactured by Sanofi Pasteur

Ingredients/Excipients: 
Gelatin: Allergen
Formaldehyde: Carcinogen
Octoxynol 10 (TRITON X-100): Immunotoxin
Thimerosal: Neurotoxin
Safety and effectiveness of Fluzone has not been established in pregnant women or nursing mothers.
All multi-dose formulations of this vaccines contain Thimerosal.
Fluzone has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.
***************************************************
7. FLUCELVAX 2013/2014
Manufactured by Novartis Vaccines

Ingredients/Excipients: 
Beta-Propiolactone: Carcinogen
Formaldehyde: Carcinogen
Polysorbate 80 (Tween 80): Sterilie Agent
FLUCELVAX is approved for use in persons 18 years of age and older.
Safety and effectiveness of Fluzone has not been established in pregnant women or nursing mothers.
Fluzone has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.
Never Tested and Never Effective 
Flu vaccines are never tested in humans before they are produced to scale. It doesn’t matter what type of flu vaccine it is…it is categorically impossible to test a flu vaccine before it is mass produced on the scale that flu vaccines are manufactured today. It takes several years for most vaccines to move from preclinical development to the marketplace.
Before a vaccine enters human testing, the developer conducts laboratory (in vitro) and laboratory animal (in vivo) testing to determine whether the product will be safe enough for researchers to proceed to clinical trials. If a flu vaccine were to follow the standard development procedures, by the time it would actually enter the marketplace it would be useless, since the strain it was testing against during clinical development has now changed. This is the nature of vaccine development versus flu viruses and something the vaccine industrial complex will never admit to.
Moreover, they estimate the probable strains meaning that 100 percent of influenza vaccines are a crap shoot in terms of effectiveness for any given population.
With more than 200 viruses known to cause influenza-like illness (ILI), a person can get a flu shot and still become sick with what is described as “the flu”. According to CDC data, in the past 11 years, 86% of all influenza-type illnesses were NOT caused by the influenza virus, thus influenza viruses are ONLY active 14% of the time.
The proportion of ILI caused by influenza viruses varies by year, and even varies within a specific year over the course of the winter.
Therefore, under a hypothetical scenario that influenza vaccines work 25% of the time (which is marginally high percentage for flu vaccine effectiveness), that means the maximum effectiveness of the flu vaccine would be 3.5% on influenza viral strains and nil for ILI.
A recent report which is again being highlighted by the alternative media is a remarkable study published in the Cochrane Library which found no evidence of benefit for influenza vaccinations and also noted that the vast majority of trials were inadequate.
More independent scientific studies have come out in recent years showing evidence of massive fetal toxicity associated with flu vaccines.Recent research I reported on is now published in the journal Human & Experimental Toxicology showing a 4,250% increase in fetal deaths according to Vaccine Adverse Event Reporting System (VAERS) data when comparing three consecutive influenza seasons.
Dave Mihalovic is a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment.
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