Baxter Pharmaceutical Company has been approved to provide upwards of 250,000 doses of Celvapan, a different H1N1 Swine Flu vaccine for German soldiers than German citizens.
…the more compatible vaccine for the soldiers will not contain any contended additives nor will it contain any mercury preservatives, has been reported by the Bielefelder “Westfalen-Blatt” under reference to military sources. Its about the Serum Celvapan manufactured by Baxter, original source in German http://de.news.yahoo.com/2/20091012/tts-soldaten-bekommen-angeblich-besonder-c1b2fc3.html and highlighted by
http://www.fightbackh1n1.com/2009/10/german-soldiers-to-receive-different.html
The other other EU-approved vaccines Pandemrix, made by British firm GlaxoSmithKline, and Focetria, manufactured by Swiss company Novartis contain controversial strengthening additive adjuvants and the preservative agent mercury, both of which appear to be contained in the shots.
Has the German government, in the interest of its “Homeland” security realized that the standard issue vaccine is too dangerous a risk? If Pandemrix and Focetria side effects are too risky for one group, wouldn’t common sense dictate it is not safe for any group? Common sense has been thrown out the door with PanFlu.
The German government, like most are doing the vaccine propaganda dance. With a variety of vaccines now approved throughout the world, are governments hedging bets on selective eugenics and who gets which vaccination and where it is distributed?
The Germans used phenol in killing Jews during the holocaust and the vaccine they just approved may in fact contain the closely related chemical Triton X100, a know carcinogen used in Baxter’s U.S. patent application on Method for Producing Vaccines. Traditionally companies apply for an international patent at the same time. http://www.theoneclickgroup.co.uk/documents/vaccines/Baxter%20Vaccine%20Patent%20Application.pdf Incidentally this patent was applied for two years prior to the H1N1 Pandemic https://ahrcanum.wordpress.com/2009/09/18/swine-flu-vaccine-patent-conspiracy/
Celvapan patient insert lists some patient warnings and ingredients: http://www.emea.europa.eu/humandocs/PDFs/EPAR/celvapan/package_leaflet/emea-pl-h982pu17en.pdf
The virus was propagated in mammalian cells. That’s not chicken scratch! Monkeys have been a common source for growing viruses as are human diploid cells- you know, the aborted fetus cells. There is also news of growing the virus in dog kidneys. Arf, arf.
In one trial of Influenza A (H1N1) 2009 Monovalent MF59-Adjuvanted Vaccine- from Novartis http://content.nejm.org/cgi/content/full/NEJMoa0907650v1 –
The seed virus was grown in Madin–Darby CanineKidney (MDCK) cell culture by means of standard processes similarto those used for the development of Optaflu vaccines againstinterpandemic influenza. The vaccine was formulated and producedby Novartis (Marburg, Germany) as an inactivated surface-antigenH1N1 vaccine…
Our vaccine wasproduced from a classical egg-derived seed virus propagatedin a MDCK cell line.. Optaflu® is the first influenza vaccine made in a mammalian cell line, rather than chicken eggs. https://ahrcanum.wordpress.com/2009/10/12/h1n1-swine-flu-vaccine-grown-in-dog-cells/
By all accounts Celvapan is the second influenza vaccine made in a mammalian cell line that has been approved. Optaflu was approved April 27, 2007 in the EU- wiki
The other notable ingredients from the Celvapan patient insert is the use of Polysorbate 80.
According to Annals of Allergy, Asthma and Immunology, Volume 95, Number 6, December 2005 , pp. 593-599(7), “it is of current relevance as a ‘hidden’ inductor of anaphylactoid reactions”, and “Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Conclusions: Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.”
Put in plain English, polysorbate 80 can affect your immune system and cause severe anaphylactic shock which can kill. The study included a pregnant woman who suffered anaphylactic shock after being given a IV drip of multi-vitamins containing polysorbate 80. http://infertility.suite101.com/article.cfm/polysorbate_80_causes_infertility
Did we forget to mention the insert also says Celvapan contains formaldehyde, benzonase, and sucrose? Mmmm, wash that down with a good German beer while you read http://www.emea.europa.eu/humandocs/PDFs/EPAR/celvapan/H-982-en1.pdf the public document.
Baxter International completed its first commercial batches of the H1N1 vaccine in late July 2009. “The swine flu vaccine, to be sold under the brand name Celvapan, is made using Baxter’s cell culture process.” http://www.reuters.com/article/internal_ReutersNewsRoom_ExclusivesAndWins_MOLT/idUSTRE5746VY20090805 Now go back up in this post and re- read about the virus being cultivated in a mammalian cell line!!!!!!!!!!! Damned, that was some pretty fast production as well. Say nothing of claims that vaccine makers have been experimenting with nanoparticles as a way to “turbo charge” vaccines for several years.
Baxter sent vaccines contaminated with deadly live H5N1 avian flu virus to 18 countries before someone caught the mistake and the vaccine got injected thousands of people. Baxter just missed creating its own pandemic then by mixing deadly H5N1 virus with a mix of H3N2 seasonal flu viruses, or did they? By possibly creating the pandemic, maybe Baxter already has the cure and that is why WHO has deemed them the appropriate pharmaceutical company to lead the way for a swine flu vaccine. Keep in mind- Just 50 miles from the H1N1 ground zero outbreak in Mexico City, lies Baxter’s manufacturing plant in Cuernavaca, Mexico. https://ahrcanum.wordpress.com/2009/05/05/baxter-pharmaceutical-plant-in-mexico-ground-zero-for-flu-outbreak/
Baxter “is not able to distribute pandemic vaccine in the U.S., because the U.S. government requires license for a seasonal vaccine first, and Baxter doesn’t currently have that license,” says Chris Bona, a spokesman for Baxter Biosciences.
Good luck to the German Army and anyone else who chooses to get vaccinated.
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Just saw the Asthma comment. If you’re taking inhaled cortisone or any other drug to dampen the immune system, you really, really want to take Pandemrix. It provokes a stronger immune response than a non-adjuvanted vaccine. Currently the US is testing whether a double dose of standard vaccine is better for asthmatics. I’m sure the answer will be yes.
But for now, you want Pandemrix.
The Celvapan is an ordinary power vaccine made a new way.
Pandemrix is made with the miracle ingredient AS03.
You get better protection against the flu and better protection in case the strain of the virus changes.
All that cost of some fish oil under your skin and an arm that may hurt more.
Canada’s vaccine is Pandemrix under a different name.
It’s also great for kids under 10 as a single half dose should protect.
The mercury is, honestly, an ignorant concern. It started out as a complaint of too many vaccines at one time in children. You’re an adult and you’re talking one vaccine. And if you go with Pandemrix the dose is even tinier one of 5-10 mcg than what the Americans which is 25mcg.
Hi, here in Ireland folks have 2 choices either Pandemrix which is given by GP’s (regular doctors) at their clinics or Celvapan which is given at special centres which have been setup nationwide. For Celvapan you can either make an appointment or just turn up at the vaccination centre and for Pandemrix you need to make a doctors appointment.
I wasn’t going to get the vaccine but think I will now, in fact I’ve just made an appointment for the Celvapan jab. The vaccines are being given to people with certain underlying medical conditions first including asthma which is widespread in Ireland (I have asthma) And after that group has been vaccinated it’s then rolled out to everyone else.
About 2 weeks ago I had booked a flight to Ukraine and a hotel in a city called Ternopil but the next day I cancelled my holiday, just had a change of mind. A few days later it seems that H1N1 or perhaps a variant of it had expolded in western Ukraine, the city where it had all started was Ternopil! Good thing I changed my mind on going there! So, I’m going to get the jab but not the mercury based one, Celvapan for me…….
BEIJING – The A/H1N1 influenza virus is responsible for nearly 80 percent of China’s total flu infections and most of the mass cases occurred in schools, according to a senior official with the Ministry of Health (MOH).
A/H1N1 accounts for 80% total flu cases Flu Pandemic Outbreak
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A/H1N1 accounts for 80% total flu cases H1N1 claims first Beijing victim
A/H1N1 accounts for 80% total flu cases Youths worst hit by H1N1
A/H1N1 accounts for 80% total flu cases WHO: China’s H1N1 vaccine safe, effective
A/H1N1 accounts for 80% total flu cases Obama declares H1N1 flu a national emergency
“As the weather keeps getting colder, many regions are entering the traditional period of possible flu outbreak, and prevention and control work is becoming tougher,” Liang Wannian, vice director of the health emergency office under the MOH, said Thursday during an online interview with the official website of the Chinese government.
According to Liang, as of Wednesday, a total of 1,502 mass cases were reported in 31 provinces, municipalities and autonomous regions of the Chinese mainland and 96.4 percent occurred in schools.
Liang said the country would act faster in providing vaccines for more people as it was still the most effective way to protect vulnerable groups and keep patients’ illness situation from deteriorating.
On Wednesday Beijing reported an A/H1N1 death case of a university student, also the fourth on the Chinese mainland.
Liang revealed that, based on clinical experiments, at least 85 percent of people receiving the vaccine would get protection from the virus and the effectiveness duration would last till this winter or next spring.
So far the side effects of the vaccine had been mostly slight, such as temporary fever and exhaustion, and the benefits from receiving the vaccine were “far greater” than harms.
Statistics from the ministry show that the Chinese mainland had reported 42,009 confirmed cases of the A/H1N1 flu by 3 p.m. Wednesday.
A total of 30,854 patients had recovered. Twenty-two of 66 patients in serious conditions had been cured, the ministry said.
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Thanks to you, I learned that cell-line vaccine was now being made. I called a local paper and asked them to raise with the government the issue of whether they would allow cell-line vaccine into the country for compassionate use by those with allergies to what’s in the egg-grown vaccine.
I’m not allergic so egg or not egg doesn’t make any difference.
I’ve seen that patent. Explain to me how that patent is evidence of nefarious intentions as opposed to an invention as they created the process of cell-line based vaccines.
The danger from Baxter’s contaminated virus material was pretty remote. There was a regular human flu virus and an avian flu virus. Avian flu virus except for one two cases hasn’t been transmitted person to person. Sure it would kill a person who got injected with it, but otherwise it wasn’t a problem. The danger wasi if the viruses swapped genes.
Under no circumstances can I see any advantage to Baxter. From the way it really happened it gave Baxter a black day and means it will be under more regulatory scrutiny.
If the viruses had mixed, there wouldn’t have been any advantage to Baxter because society would be collapsing or very close to collapsing. Spanish Flu killed 1.1% of Europeans. Avian flu kills about 30% of humans infected. If there was enough society left, there might be a lynching of everyone responsible at Baxter.
You’re not unusual in saying look at this, look at this, isn’t it awful, those who did may very well seeking advantage.
What’s better is to follow the logic to the end. When you do, there’s no reason for Baxte to purposely send out contaminated materials.