Dave Mihalovic, Prevent Disease
Waking Times

Other than a depressed immune system with a side serving of carcinogenic, immunotoxic, neurotoxic, and sterility agents, this year’s flu shot has nothing to offer you but the usual poisons based on previous formulations. Moreover, their effectiveness in preventing the flu is less than a placebo. Although the FDA gave a two year deadline to remove thimerosal from vaccines after they were banned in 1997, they continue to appear in vaccine formulations and ironically the FDA is now only supporting these drugs, not prohibiting them.

In 2009, eight out of ten H1N1 vaccines had thimerosal. For last year’s 2011/2012 flu vaccine season, three out of five FDA approved vaccines has thimerosal.

If you have any doubts on the neurotoxic potential of thimerosal, please review the following scientific publications which document the adverse effects of mercury, merthiolate and ethyl mercury.

This year, the 2012/2013 season offers three out of six flu vaccines which contain thimerosal and all are FDA approved of course.

Note that for every single 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.

////// 2012/2013 FDA APPROVED FLU VACCINES ////// 

1. AFLURIA 2012/2013
Manufactured by CSL Limited

Ingredients/Excipients: 
Beta-Propiolactone: Carcinogen
Monobasic Potassium Phosphate: Immunotoxin
Neomycin: Immunotoxin
Polymyxin: Neurotoxin
Potassium Chloride: Neurotoxin
Sodium Deoxycholate: Immunotoxin

Safety and effectiveness of AFLURIA have not been established in
pregnant women or nursing mothers.

AFLURIA is not approved for use in children less than 5 years of age.

AFLURIA has not been evaluated for carcinogenic or mutagenic potential.

***************************************************

2. FLUVARIX 2012/2013
Manufactured 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.

FLUARIX has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.

***************************************************

3. FLULAVAL 2012/2013
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.

FLULAVAL has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.

***************************************************

4. FLUMIST 2012/2013
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 2012/2013
Manufactured by Novartis Vaccines

Ingredients/Excipients: 
Beta-Propiolactone: Carcinogen
Neomycin: Immunotoxin
Polymyxin: Neurotoxin
Thimerosal: Neurotoxin

FLUVIRIN is not indicated for children less than 4 years of age because there is evidence of diminished immune response in this age group

FLUVIRIN has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.

***************************************************

6. FLUZONE 2012/2013
Manufactured 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.

Fluzone has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.

***************************************************

I recently wrote on how every single vaccine is now being exposed for the lack of demonstrated evidence to actually prevent a single case of disease over a placebo.

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.

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.

The authors found that vaccines administered parenterally, that is, outside the digestive tract, usually meaning by injection, reduced influenza-like symptoms by 4%. They found no evidence that vaccination prevents viral transmission putting the whole herd immunity myth once again into question.

The maximum success rate of the flu vaccine is 6.25% which is a pretty big under-achievement, considering that the average reaction to placebo injections of distilled water is 30%.

The Cochrane Collaboration, an international not-for-profit organization providing up-to-date information about the effects of health care, has compiled data from 40 flu seasons worldwide.

The institute has concluded from the studies that there is no clear evidence to suggest that the flu jab offers any more protection than cheaper, hygiene-based methods such as hand-washing.

“Our analysis is compiled using millions of data from 40 seasons worldwide. What we have seen is that the influenza vaccine can at best have a very small effect,” said Thomas Jefferson, one of the authors of the report, to the newspaper.

More independent scientific studies are also coming forth 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.

About the Author

Dave Mihalovic is a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment.

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