Panvax H1N1 Vaccine
By Commonwealth Serum Laboratories (CSL)

For details see –
http://www.public.health.wa.gov.au/cproot/2487/2/Training PowerpointPanvax.pdf

Panvax H1N1 is not to be confused with CSL’s previous Panvax product which was designed for Avian Influenza. Panvax H1N1 is a monovalent vaccine, indicating the use of one antigen only, for immunizing against one specific pandemic only. At this time (Sept 11, 2009), it is an unregistered vaccine.

The Australian Government has granted an exemption allowing the dispensing of this vaccine, without it being approved by the Therapeutic Goods Administration (TGA). That means that client consent must be obtained and recorded in detail on special Commonwealth consent forms prior to injection.

Panvax H1N1 is “unadjuvanted”. The theory that vaccines prevent the spread of infectious disease is based upon the belief that, by injecting a small amount of a disease into the body, it will develop "antibodies". The theory is complicated by the fact that attenuated doses of pathogens alone will not initiate an "antigenic response." So, vaccines contain compounds known as "adjuvants" to intensify the body’s immune response.

Attenuation - reducing the virulence of a pathogen, so that it becomes harmless or less virulent, but still keeping it viable (or 'live').

So how can the CSL Panvax be an effective vaccination without the adjuvant? The answer (if there was such a thing as an effective vaccination) may be that Panvax is not attenuated. It contains H1N1 Subunits. It is claimed that Panvax is not a “live” vaccine. Technically it is true that it contains no complete live virus, just live virus portions (subunits), disrupted by detergent.

Included in the ingredients are two antibiotics, Neomycin and Polymyxin B Sulphate. Both are noted for serious side effects, predominantly kidney failure. It is warned both these antibiotics not be used by pregnant women. Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to an unborn baby. In the “first tier” of candidates to receive this unregistered, unapproved vaccine, pregnant women are on top of the list.

Panvax is formulated using chick embryos (Ovalbumin). People who suffer allergy to eggs or anaphylactic reactions may experience problems.

Beta-Propiolactone is another listed ingredient. Ranked as one of the most hazardous compounds (worst 10%) to humans and "reasonably expected to be a human carcinogen" (International Agency for Research on Cancer - IARC, 1999). Βeta-Propiolactone is a disinfectant

Listed in possible side effects is Guillian-Barre Syndrome (nervous system disorder featuring paralysis). GBS is in fact polio paralysis. Over 45 million Americans were vaccinated for swine flu in 1976. The vaccine was contaminated with polio virus, 565 cases of polio paralysis (GBS) were recorded with 60 deaths and other serious problems, including blindness and impotence.

Thiomersal (by weight, 50% mercury), is used as a preservative in Panvax multi dose packs. Health departments advise that: It is recommended that all children under 10 years of age wait for the thiomersal free vaccine. However they also advise that: if clients request the vaccine and are aware of the content, they may receive the thiomersal vaccine with out waiting for the thiomersal free vaccine.

Ok, that’s great news, if you would like to poison your children, and you are aware that you are poisoning your children, feel free, vaccine dispensaries will oblige.

More info - http://www.thebigstinkguide.com/wordpress/?p=371