From Hell To Veins

November 17, 2010

RVF vaccine causes liver disease, death

Editor’s Note
I am right at the moment involved in a ‘preliminary’ investigation on the viral strains and, viral strain sequencing of vaccines given to the animals we later eat. Particularly pork and ask, can viral matter from vaccines withstand heating to later ‘recombine’ with viral matter from the latest live viral DNA vaccines that ‘just so happen to be’ in the latest flu shots? My guess is YES using altered lab DNA / RNA and Nano technology. See Nano vaccines.

My reasoning for doing this is to find out why, right after these pandemic live flu virus vaccines have made their way into the veins of the population (the last two flu seasons), do we see an increase in H3N2 cases AND H1N1 mutation. Why has the spread of H3N2 from hogs occurred so easily this year from people visiting or involved with county fairs? If the ‘true’ viral sequencing of vaccines for both people and hogs were made public would it prove the rise in pandemic A/H1N1 and H3N2 cases are in fact vaccine in origin?
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RVF vaccine causes liver disease, death.
Source: Natural News

Wednesday, November 17, 2010 by: Ethan A. Huff, staff writer

(NaturalNews) Many governments are pushing a new livestock vaccine for Rift Valley Fever (RVF), a serious and deadly virus that infects both humans and animals, and that spread across various regions of Africa earlier this year. But a recent study shows that the vaccine itself causes serious liver problems as well as abortions in pregnant animals, which are the same problems caused by the virus itself. Consequently, researchers are advising many farmers not to use the vaccine in their livestock.

The study, which took place at the Animal Health Research Institute in Egypt, evaluated the effects of the RVF vaccine on experimental goats. Since the injection is designed for such animals, researchers expected to observe considerable benefits from the vaccine. But they discovered that it basically causes the same harm as the virus itself, rendering it ineffective.

According to the report, RVF is transmitted by mosquitoes to both humans and animals. And it causes liver problems and death, just like the vaccine. But that has not stopped many media outlets from urging farmers to vaccinate their animals anyway, including even their pregnant animals (http://www.eyewitnessnews.co.za/art…).

Like the H1N1 / swine flu vaccine that was pushed heavily last year, the RVF vaccine contains a “live attenuated” strain of the disease right in the syringe. So injecting it into animals exposes them to the exact same live virus that the vaccine is touted as preventing, which typically causes the same harmful symptoms and side effects.

Whether alive or dead, the disease strains formulated in vaccines often do little to actually prevent disease. Drug companies mix these straings with dangerous, immune-destroying chemicals and preservatives as well, which compromise health. Thousands, if not millions, of people are injured every year by vaccines, but the vast majority of them continue to be pushed on populations as supposed safe and effective ways to prevent disease (http://www.naturalnews.com/030025_v…).

For more reading and linked sources click on link provided above.

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May 21, 2010

Pig virus contaminates rotavirus vaccines, but FDA says no problem

My Commentary:
What is interesting to me about the NON surprise ruling by the bought and paid for FDA is that the initial contamination was supposed to be limited just to the Rotarix vaccine. If the FDA is including both GlaxoSmithKline and Merck vaccine manufactures, this is where your ‘story’ lay. That is a huge detail AND a big deal! The question should be asked, why was it reported initially that Rotarix was the SOLE vaccine contaminated with this pig virus? Now the obvious question is, how can this be an accident when BOTH the Rotarix manufacture and the Merck’s Rotateq vaccine have the SAME contaminated vaccines? Also, why does this pig virus wind up in a ‘Rotavirus vaccine’ by two completely different companies as opposed to being in completely different types of vaccines? Last, these DNA strands ARE NOT THE ONLY VIRAL CONTAMINATES IN THESE VACCINES. Barbara Loe Fisher did an excellent ‘in depth’ report on this issue, and really should be read by all.
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(NaturalNews) Rotavirus vaccines are commonly given to children, and this year’s batch of vaccines made by GlaxoSmithKline and Merck are contaminated with a pig virus, the FDA recently discovered. So the FDA called a meeting to determine whether injecting a pig virus into the bodies of young children might be some sort of problem requiring a recall of the vaccines.

Can you guess what conclusion the agency reached? As reported by Reuters, the FDA concluded “…it was safe for doctors to resume giving patients Glaxo’s Rotarix and continue using Merck’s Rotateq. The agency said there was no evidence the contamination caused any harm…”

In other words, as long as they can bury the evidence and deny any link between vaccines and health problems — which has been the standard excuse of the FDA for decades — they can continue to claim the vaccines are safe enough to inject into little children.

Never mind the fact that the pig virus found in the vaccines actually causes a wasting disease in baby pigs, giving them intense diarrhea and causing them to rapidly lose weight. DNA from these viruses was detected in the “master cells” used to make the vaccines.

Suppressing the evidence of harm

An FDA advisory panel said the risk to human health from the viral contamination was only “theoretical.” But of course it’s easy to claim anything is “theoretical” if you suppress the evidence that it’s real. By simply ignoring any reports of neurological side effects from the vaccine, the FDA can always claim there is “no evidence” of harm. Well, no evidence they’re willing to accept as real, anyway.

And that’s how vaccine science works these days: Suppress any evidence of harm, deny any links between vaccines and neurological problems, then okay practically any viral contamination from any animal and declare it’s all safe to be injected directly into the bodies of infants and children.

So much for science, huh? The vaccine industry operates more like a cult than a scientific organization, and anyone who questions the beliefs of their cult is immediately branded a heretic and publicly condemned.

By the way, even though these rotavirus vaccines are contaminated with a pig virus, the companies that make them claim there is “no manufacturing or safety issue” with the vaccines. In other words, this is normal!

Think about that for a moment: The discovery that a vaccine being injected into children is contaminated with a virus from a pig doesn’t even result in a product recall! It doesn’t raise any red flags! It’s just business as usual in the vaccine industry, where DNA from any number of diseased animals is often used in the vaccine formulas.

Last year, rotavirus vaccines earned nearly a billion dollars in revenues for Big Pharma. The risk of a child in the United States actually dying from a rotavirus infection is ridiculously small. What these kids need is good nutrition and vitamin D, not an injection of a questionable vaccine made with pig virus DNA.

Sources for this story include:
http://www.reuters.com/article/idUS...

April 7, 2010

In Depth Report On The Rotarix Contamination.

Thank you Barbara for digging into this story!

Where do I start? Oh yeah! By asking ,why would ANY sane individual be putting this junk not only into their bodies BUT, the bodies of their children?

I’m sure glad you brought up the fact that the contamination issue concerning vaccines has been an on going issue and, as far as I am concerned, is the #1 problem with vaccines.

As you know, the conventional wisdom of both corporate and government psychosis will simply tell us all not to pay ANY attention to all the nasty in those vaccines. They’re all safe as a sunday walk in the park.

Vaccine Contamination: Pig Virus DNA Found in Rotarix
by Barbara Loe Fisher
Vaccine Awakening

On March 22, 2010, Food and Drug Administration (FDA) officials adhering to the precautionary principle advised American doctors to suspend use of Rotarix 1 vaccine until the agency finds out why DNA from a swine virus (porcine circovirus 1 or PCV1) was found in the live rotavirus vaccine. The FDA said there is “no evidence at this time” that the vaccine manufactured by GlaxoSmithKline and given to babies at 2,4 and 6 months of age to prevent diarrhea poses any safety risk. 2

Independent Lab Using New Technology Found Contamination

The discovery that viral DNA is contaminating Rotarix vaccine was made by a team of scientists at an independent research lab in San Fransisco, California, where they used new technology to detect fragments of viral genetic material in vaccines using genetic sequencing. 3

More testing confirmed that many copies of DNA from the pig virus were present in all Rotarix vaccine lots released since the vaccine was licensed in 2008 because the pig virus DNA also contaminated the working cell bank and the original viral “seed” stock, from which Rotarix vaccine was first produced. 4

Two Other Live Virus Vaccines Contaminated

The surprising discovery reportedly was made after the independent lab used new technology to evaluate the purity of eight live virus vaccines for polio, rubella, measles, yellow fever, human herpes 3 (varicella or chicken pox), rotavirus (Rotarix and RotaTeq) and MMR. In addition to pig viral DNA found in Rotarix vaccine, low levels of DNA fragments from avian (bird) leukosis virus (a retrovirus) was found in measles vaccine and DNA fragments of a virus similar to simian (monkey) retrovirus was found in RotaTeq vaccine. 5

FDA Looking For Answers

After the team double checked their findings, researchers notified GlaxoSmithKline (GSK) on February 9, 2010 and GSK notified the FDA on March 15, 2010, which prompted the FDA’s action on March 22, 2010 to suspend use of Rotarix. The FDA says it “does not know how DNA from PCV1 came to be present in Rotarix” or whether “this means that intact virus is present. Additional studies are being conducted.” 6

Rotavirus Vaccines Use Monkey, Cow, Pig Materials for Production

Rotarix is a genetically engineered vaccine that GSK created by isolating human rotavirus strain infecting a child in Cincinnati and using African Green monkey kidney cells to produce the original viral seed stock from which all Rotarix vaccine has been made. 7 In the FDA licensing process, Rotarix had to meet certain FDA standards, that included demonstrating the vaccine was not contaminated with, for example TSE (Transmissable Spongiform Encephalopathy or “mad cow” disease, a brain wasting disease) 8 or with cow viruses because bovine (cow) serum was used to prepare the original viral seed stock. Porcine trypsin, an enzyme in the pancreatic juice of a pig, was also used to make the viral seed stock. 9
RotaTeq is a genetically engineered vaccine containing five human-cow reassortment strains of rotavirus that were created at the Children’s Hospital of Pennsylvania (CHOP), where strains of rotavirus that give cows diarrhea were combined with strains of rotavirus that cause diarrhea in humans. The reassortment viruses were transported to Merck, where master seeds were produced using African Green Monkey kidney cell cultures. Fetal bovine (cow) serum and porcine trypsin was used to make the “seed” stock. 10 There are small amounts of bovine serum and cell culture media (monkey viral DNA) that remain in RotaTeq vaccine. 11 12

FDA Suggests Drug Companies Test for Vaccine “Purity”

In a February 2010 FDA document, Guidance for Industry: Characterization and Qualification of Cell Substrates and Other Biological Materials Used in the Production of Viral Vaccines for Infectious Disease Indications, the FDA lists “non-binding recommendations” for drug companies making vaccines using animal and human cell substrates. 13 Under the heading “Testing for Adventitious Agents,” the FDA states “assurance that products are free of adventitious agents is a critical component of meeting the [FDA regulations] requirement for purity.” Under the heading “Testing for Residual Cellular DNA,” the FDA states, “Residual DNA might be a risk to your final product because of oncogenic (cancer causing) and/or infectivity potential.”

Déjà Vu: Monkey Viruses Contaminated Polio Vaccines

Contamination of vaccines with animal viruses is not new. In the 20th century, polio vaccines given to tens of millions of people worldwide were contaminated with simian virus 40 (SV40), which was found to cause cancer in animals and is associated with human brain, bone and lung cancers but the government denies SV40 is causing those cancers in humans. 14 15 16 17

There has been controversy about the link between experimental polio vaccines tested in Africa in the 1950’s and 1960’s that were contaminated with a monkey virus, simian immunodeficiency virus (SIV). Soon after the polio vaccine trials in Africa, the human immunodeficiency virus (HIV) emerged. 18 Many questions about the failure of researchers and technology to screen for monkey viruses in those vaccines remain to this day.

Using Cancer Cells to Produce Vaccines?

Vaccine manufacturers have long used cell material that comes from the bodies of mammals, including humans, monkeys, cows, pigs, dogs and rodents, as well as birds or insects to make vaccines now in use or to make experimental vaccines. There is an inherent risk of contamination with viruses and other microbes (or DNA from those microbes) that can escape detection during the vaccine development, testing, licensing, manufacturing and oversight process. 19 There has even been discussion among vaccine manufacturers and the FDA in the last decade about using neoplastic (cancer) cell substrates to make vaccines but the risk of contamination with cancer cell DNA is a big risk. 20

New Influenza Vaccines: Is Contamination Possible?

In searching for ways to make seasonal influenza vaccines in a faster, easier and less expensive way than relying on chicken eggs for production, drug companies have experimented with using dog kidney cells and human fetal retinal cells. However, these cell lines have been documented to cause tumors in animals, especially dog kidney cells (MDCK). 21

At a November 19, 2009 meeting of the FDA Vaccines & Related Biological Products Advisory Committee, a vaccine manufacturer asked for permission to use insect (caterpillar) cells to make pandemic influenza shots. But insect cells can be contaminated with insect viruses that are hard to detect. The FDA Committee, on that day, voted “no.” 22

Unanswered Questions about Rotarix Contamination

There are lots of questions about how the manufacturer of Rotarix vaccine and the FDA both missed the pig virus DNA contaminating the original seed stock and all doses of Rotarix vaccine given to more than one million American children in the past few years. 23

Is there state-of-the-art technology that is being used by private laboratories but not by drug companies and the FDA?

Why did the independent team of scientists, who found the contamination, notify the vaccine manufacturer first rather than also immediately reporting their finding directly to the FDA?

What about the significance of finding bird viral DNA in measles vaccine and the monkey viral DNA in RotaTeq vaccine?

Wake Up Call for Industry & Government

The contamination of Rotarix vaccine is only the latest in a long history of vaccine contamination issues that require a re-examination of the way vaccines are made and tested. It is a wake-up call for industry and government

The big question people are asking is: why do drug companies making vaccines continue to use cells from animals, birds and insects that can be contaminated with viruses and other adventitious agents that are hard to detect?

The FDA was right to suspend use of Rotarix vaccine until they know more. Hopefully, this serious vaccine production and testing issue will be addressed immediately by vaccine manufacturers. If not, the next pandemic or serious health problem affecting large populations may be one that comes out of a vaccine lab.

REFERENCES:

1 National Vaccine Information Center (NVIC). Rotarix and Rotarix Vaccine.
http://www.nvic.org/Vaccines-and-Diseases/Rotavirus.aspx

2 FDA. News Release: Components of Extraneous Virus Detected in Rotarix Vaccine: No Known Safety Risk, FDA Recommends Clinicians Temporarily Suspend Use of Vaccine As Agency Learns More. March 22, 2010. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm205625.htm

3 Racaniello V. Deep sequencing reveals viral vaccine contaminants. http://www.virology.ws. March 29, 2010. http://www.virology.ws/2010/03/29/DEEP-SEQUENCING-REVEALS-VIRAL-VACCINE-CONTAMINANTS/?
UTM_SOURCE=FEEDBURNER&UTM_MEDIUM=EMAIL&UTM_CAMPAIGN=FEED%253A+VIROLOGYBLOG
+%2528VIROLOGY
+BLOG%2529%0A

4 FDA. Detection of DNA from PCV1 in Rotarix. March 22, 2010. http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm205545.htm

5 See Reference #3 above.

6 FDA. See Reference #4 above.

7 FDA. Memorandum: Review of Vero Cell Banks used for Vaccine Production and Adventitious Agent Testing of Virus Seeds and Vaccine Human Rotavirus Vaccine (HRV) – Rotarix. April 1, 2008. http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm134138.htm

8 FDA. Summary Basis for FDA Regulatory Action – Rotarix. June 4, 2007. http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm133543.htm

9 European Medicines Control Agency. Evaluation of Medicines for Human Use: Rotarix Vaccine (Control of Materials (Reagants) page 4). 2006. http://www.ema.europa.eu/humandocs/PDFs/EPAR/rotarix/063906en6.pdf

10 European Medicines Control Agency. Evaluation of Medicines for Human Use: RotaTeq Vaccine (Active Substance (Manufacture). Pages 3-10. http://www.ema.europa.eu/humandocs/PDFs/EPAR/Rotateq/066906en6.pdf

11 FDA. Memorandum: Clinical Review of New Biologics License Application – RotaTeq (Description of the Product). Page 12. April 6, 2005. http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM142304.pdf

12 European Medicines Control Agency. See Reference #10 above. Page 6.

13 FDA. Guidance for Industry: Characterization and Qualification of Cell Substrates and Other Biological Materials Used in the Production of Viral Vaccines for Infectious Disease Indications. February 2010. http://www.fda.gov/downloads/BiologicsBloodVaccines/
GuidanceComplianceRegulatoryInformation/Guidances/Vaccines/UCM202439.pdf

14 Bookchin D, Schumacher J. The Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus, Contaminated Polio Vaccine, and the Millions of Americans Exposed. St. Martin’s Press: New York. 2004. http://www.nvic.org/resource-center/books.aspx

15 Fisher BL. Congressional Testimony: The SV-40 Virus: Has Tainted Polio Vaccine Caused an Increase in Cancer? U.S. House Government Reform Committee. September 10, 2003. http://www.nvic.org/vaccines-and-diseases/Polio-SV40/BLFTestimonySV40.aspx

16 U.S. Congress. Congressional Hearing: Preventing Another SV40 Tragedy: Are Today’s Vaccine Safety Protocols Effective? U.S. House Government Reform Committee. November 13, 2003. http://frwebgate.access.gpo.gov/cgi-bin/getdoc.cgi?dbname=108_house_hearings&docid=f:92772.wais

17 Carlsen W. Rogue Virus in the Vaccine: Early Polio Vaccine Harbored Virus Now Feared to Cause Cancer in Humans. San Francisco Chronicle. July 15, 2001. http://www.sfgate.com/cgi-bin/article.cgi?file=/chronicle/archive/2001/07/15/MN193825.DTL

18 Carlsen W. Quest for the Origin of AIDS: Controversial Book Spurs Search for How the Worldwide Scourge of HIV Began. San Francisco Chronicle. January 14, 2001. http://www.sfgate.com/cgi-bin/article.cgi?file=/chronicle/archive/2001/01/14/MN140641.DTL

19 See Reference # 13 above.

20 FDA. Designer Cells as Substrates for the Manufacture of Viral Vaccines. 2001. http://www.fda.gov/OHRMS/DOCKETS/AC/01/briefing/3750b1_01.pdf

21 WHO. Initiative for Vaccine Research: Use of Cell Lines for the Production of Influenza Virus Vaccines: the Appraisal of Technical, Manufacturing and Regulatory Considerations. April 10, 2007.
http://www.who.int/vaccine_research/diseases/influenza/WHO_Flu_Cell_Substrate_Version3.pdf

22 FDA. Vaccines & Related Biological Products Advisory Committee. Safety & Effectiveness of Purified Recombinant Influenza Hemagglutinin Vaccine for the Prevention of Influenza (FluBlok). November 19, 2009. http://www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMaterials/
BloodVaccinesandOtherBiologics/VaccinesandRelatedBiologicalProductsAdvisoryCommittee/UCM197912.pdf

23 FDA. Background on Rotavirus Vaccines: How Many Doses of Rotarix Have Been Sold? March 22, 2010. http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm205543.htm

Click below to watch the video:

http://www.nvic.org/NVIC-Vaccine-News/April-2010/Vaccine-Contamination-Pig-Virus-DNA-Found-in-Rota.aspx

March 24, 2010

Rotavirus Vaccine In The News AGAIN.

My Commentary:

It should be noted that the JACKASS that helped to develop this crap vaccine was none other Dr. Offit who said it was SAFE for a baby to be injected with up to 100,000 vaccines! This IS the JACKASS that the American Academy of Pediatrics got their ‘sound advise’ on vaccine safety from WHILE AT THE SAME TIME being enveloped in a CONFLICT OF INTEREST with the pharmaceutical companies, lining his pockets all the way to the bank. This is the same JACKASS that said he would publicly debate Dr. Blaylock on his 100,000 vaccine injection claim and the vaccine safety / dangers in general BUT CHICKENED OUT at the last minute.

Notice how the news agency that gets ‘generous’ money from big pharma down plays the ‘contamination’ as “no big deal”.

Yeah right!

I’m going to take this very revealing story a step further in the next few days and use it to explain my pet peeve with these vaccines that, in the wrong hands, (YES, THEY ARE IN WRONG HANDS!) vaccines are an excellent ‘tool’ to distribute viruses to human blood that in NO WAY would happen in nature. Or, in some cases, would be very, very difficult to transfer naturally to humans.

Besides the ‘science’ of transferring animal viruses to humans, along with the science of virus ‘recombination in this story, there are NO numbers given on how many babies, children have been INFECTED with this pig virus. You can be sure the company that produced this vaccine knows exactly ‘how many’ they infected with this pig virus. This information would be very important if another so-called pandemic was announced and our loving government wanted to start injecting vaccines with viral dna / rna that could prove to be a ‘lethal recombination’ and even worse, spread into the population.

Rotarix rotavirus vaccine contaminated, officials say
By Tom Watkins, CNN
March 22, 2010 4:22 p.m. EDT

(CNN) — Federal health authorities recommended Monday that doctors suspend using Rotarix, one of two vaccines licensed in the United States against rotavirus, saying the vaccine is contaminated with material from a pig virus.

Article

RELATED
We covered this on the Rotavirus vaccine not long ago…
The Rotavirus Vaccine Was Fast Tracked By The FDA As Safe YET Had To Be Recalled.

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