The 'vaccines are adequately tested' lie (Inadequate safety studies & done by makers)
Lies  Medical study ploys

“They (vaccine safety trials) all only use benign placebos – we use the safest most pure vaccines as a placebo."---David Salisbury (source  The Arnica Network)

[If vaccines were properly tested their ineffectiveness and danger would be obviously apparent.  "Testing" is carried out by the makers only!  No long term tests have ever been done, (they are doing them now on the whole population), no vaccine has ever been tested against 100% unvaccinated children, and using the Antibody Theory to test effectiveness is junk science!  The best way not to find vaccine contaminants is not to test for them in the first place.  Testing is limited, if carried out at all, to days or weeks, and often is done in third world countries!  In truth all vaccines are experimental, safety tests are carried out by the makers, and, barring a vaccine disaster, they carry on the uninformed, unconsented longer term vaccine trial on your children.  An obvious proof to this lie is to look at the long line of withdrawn vaccines and vaccine disasters.  To see the real purpose of these diseases have a look at the beliefs of Homeopathy,  Naturopathy on measles, and the effectiveness of Nutritional medicine,  to get some idea about it's experimental nature, the need for it, and the lack of informed consent.  This ones equally evil twin is the  'Safe' vaccine lie.]

Michael Belkin on "science based" vaccine information

Dr. Kwai Chan testified on 29 April 1999, "The long-term safety of the vaccine has not yet been studied."

See: Healthy trial babies only  Never unvaccinated controls Medical study ploys Study data kept secret Secrecy Placebos, Third world guinea pigs Foreign studies.]

See: DPT Mouse tests Mouse toxicity test  Kendrick mouse test  Hist test

[Swine flu vax 2009 Aug] Injecting one thing for testing and then adding adjuvant later

ABC NEWS Commentary On Vaccine Debate Written by Nicholas Regush

Quotes

Russell L. Blaylock, M.D.

Russell L. Blaylock, M.D.

I decided that I was going to review all of the safety studies about measles and measles containing vaccines because if I was going to get into a fight, I needed to know what I was talking about. If I was going to challenge the status quo and say things that might have an adverse effect on vaccine uptake, I had to know what I was talking about. So I read all the papers and I was appalled. I was absolutely appalled that the quality of the safety studies of the single and combined MMR vaccine in particular and then I wrote to my colleagues in advance of the paper coming out and I said this is going attract a lot of attention in the media and I have to tell you, that I have now read all these studies. I have written a 250-page report which I'm willing you, I'm very happy for you to read and I cannot support the continued use of the MMR vaccine. I will continue vigorously to support the use of the single vaccine but I cannot support the use of the MMR.
    Now at that stage, the dean of the medical school Arie Zuckerman had decided that he was going to have a press briefing, a press conference. Get people together, tell them about the findings of the study. And, I wrote to him, I copied this letter to him so he had an opportunity at this stage to say no press briefing. We don't want to get into the vaccine issue. Wakefield doesn't attend the press briefing or if the question is raised at the press briefing, it doesn't go to Wakefield. He had three opportunities to diffuse this, he didn't. As soon as the question came up at the press briefing which inevitably it was going to do, he directed it straight to me. And I responded in exactly the same way that I said I would respond in advance of that press briefing.
    Now, it wasn''t based upon the observations in 12 children, it was based upon reading all of the safety studies and producing a 250-page safety report on those studies which I'd offered to my colleagues to read. And that was the basis for my recommendation that parents be allowed to use the option of the single vaccines.[2010 April] Andrew Wakefield Interview by Dr Mercola

The lie [The best-tested thing! See: Rationalization]
"If they were willing to look at all the studies that were done with vaccines, they would find that they are, I think without question, the safest, best-tested thing we put into our bodies," says Offit." (CBS) 60 MinutesOctober 20, 2004

Safety studies for days or weeks
"Safety studies on vaccinations are limited to short time periods only: several days to several weeks. There are NO (NONE) long term (months or years) safety studies on any vaccination or immunization. For this reason, there are valid grounds for suspecting that many delayed-type vaccine reactions may be taking place unrecognized at to their true nature. Dr Buttram MD

"There have never been any safety studies done for any vaccine in use today that would meet the criteria of scientific proof. All we have are epidemiologic studies, which are indicators but not proof in and of themselves." [Oct 2004] Letter to the British Medical Journal by Harold E Buttram, MD,

"Longest safety trial of of the triple vaccine (MMR, all live attenuated viruses) was three weeks."--Dr Fudenburg MD

JABS has not been able to find any properly conducted trials where the safety of the vaccines has been monitored for more than a few weeks. Why Does The MMR Vaccine Need To Be Suspended?

"The anthrax vaccine was approved without every doing a controlled clinical  study. There is no long term safety data on the anthrax vaccine. The government admitted this in congressional hearings. It is a distortion of the truth to say there is substantial safety data."--Bart Classen

"Safety studies on vaccinations are limited to short time periods only: several days to several weeks. There are NO (NONE) long term (months or years) safety studies on any vaccination or immunization. For this reason, there are valid grounds for suspecting that many delayed-type vaccine reactions may be taking place unrecognized at to their true nature."--Dr Buttram MD

"A small but growing minority of physicians and scientists are becoming aware that safety testings for the various vaccines have been woefully inadequate. As one of many examples, in 1994, a special committee of the National Academy of Sciences published a comprehensive review of the vaccine safety of the hepatitis B vaccine. When the committee investigated 5 possible and plausible adverse effects, they were unable to come to any conclusion for 4 of them because, to their dismay, they found that relevant safety research had not been done."--Harold Buttram MD

"He said the normal trials on a new vaccine were not possible in Britain because of the relatively small numbers of people who contracted the disease. Instead scientists had tested whether the vaccine produced sufficient antibodies."--Media report on meningitis C vaccine

"One of the flaws in studies of vaccines is that there are no true placebo groups. The vaccine is tested in one group of immunized children and is compared to another group of immunized children."--Peter Baratosy

"To date there has never been an independent, controlled study which proves that their vaccines are safe or even effective."--Ingri Cassel

"While the myriad short-term hazards of most immunizations are known (but rarely explained), no one knows the long term consequences of injecting foreign proteins into the body of your child. Even more shocking is the fact that no one is making any structured effort to find out."--Dr Robert Mendelsohn MD

JABS has not been able to find any properly conducted trials where the safety of the vaccines has been monitored for more than a few weeks. JABS has not been able to find any studies of the long-term consequences of the use of the MMR vaccines.Why Does The MMR Vaccine Need To Be Suspended? http://www.argonet.co.uk/users/jabs/mmrsuspend.html

"The CDC immunization policy is disgraceful from a scientific, medical, or public policy point of view. It is a scientific disgrace because vaccines only get short-term or epidemiological tests, and not controlled tests for long-term side effects"--Roger Schlafly, PhD

"There is a wider problem because of the failure to carry out long-term, randomised, controlled studies — properly conducted scientific investigations which would monitor the effects of multiple, early vaccination versus non-vaccination into adulthood."--Dr Odent M.D.

"The central defect in the numerous, recent mandatory vaccination requirements is that the same people who are profiting from these vaccines are also in control of the research on[,] and publication of[,] the dangers of the vaccines. The fox is pretending to guard the henhouse. …foreign research has found problems with the Hepatitis B vaccine for children. Note that I said "foreign," because there is no independent US medical research on this.  Incredibly, even industry safety studies on the MMR vaccine have not extended beyond three weeks following vaccination."---Laura Reude.

"I have minutes from a CDC Study Group Meeting on the Hepatitis B vaccine held in March, 1997. The minutes of the meeting show that it would take at least a 60 day study to show the onset of MS. Clinical studies done by the two manufacturers were four and five days in length, respectively. It should be noted that the afternoon session of this meeting was chaired by Dr. Robert Sharrar of Merck. This group was to decide how to identify various types of adverse reactions such as MS and demylenating disease and to plan meaningful studies. When Dr. Sharrar appeared on ABC's 20/20 in January he said that he honestly believed that the Hepatitis B vaccine had not caused any problems. Can an employee of a pharmaceutical company that manufactures the vaccine be objective in designing experiments to show fault in a product that generates close to a billion dollars in sales for his company?"---Betty Fluck

Use flawed or fraudulent methods to get vaccines on market:
"The Prevnar pre-licensure clinical trials, which Wyeth Lederle paid Kaiser Permanente to conduct, compared two experimental vaccines against each other. To compound this basic methodological flaw, Kaiser and Wyeth Lederle, allowed most of the children in the trial to be given the more reactive DPT vaccine rather than use the safer, less reactive DTaP vaccine. This placed the children in that five-year experiment in greater danger and allowed the drug company to write off the seizures that occurred as being caused by DPT and not Prevnar, when in fact, they didn't know. Even so, the groups of children who got Prevnar suffered more seizures, higher fevers, more irritability and other reactions than did the children who got the other experimental vaccine. It was a no-brainer as far as I was concerned: Kaiser and Wyeth Lederle had proved nothing about Prevnar vaccine safety."--Barbara Loe Fisher

"The evaluation of safety and efficacy and federal approval of Prevnar is laden with ethical questions. Many of the doctors directly involved in the testing and approval process appear to have significant conflicts of interest. The efficacy of the vaccine is questionable and safety testing has been terribly inadequate. There are no long-term studies (i.e. more than 5 years) of the chronic, debilitating and life threatening diseases that this vaccine may cause. The fact that the vaccine is bio-engineered by combining various types and portions of bacteria should require it to undergo considerable scrutiny. Assuming the vaccine has any efficacy at all, the need for universal vaccination needs to be reexamined in light of the small number of children who might be at risk from serious complications from pneumococcal disease. "---Michael Horwin, MA

No government vaccine testing:
"FDA virologist Peter Reeve........ acknowledged that the FDA suspended its own independent tests of vaccine purity 15 years ago, leaving it entirely up to the manufacturers to ensure the vaccine is contaminant free."--'The Virus and the Vaccine': Atlantic Monthly  http://www.whale.to/vaccines/sv409.html

"In addition, the U.S. Office of Technology, one of the few semi-reliable agencies of the U.S. government, says there is no current system utilized by the CDC to determine if the vaccines do work or how dangerous they really are."--Dr Douglass M.D.

Keep safety data secret from government regulators:
"FDA virologist Peter Reeve........ acknowledged that the FDA suspended its own independent tests of vaccine purity 15 years ago, leaving it entirely up to the manufacturers to ensure the vaccine is contaminant free."--'The Virus and the Vaccine': Atlantic Monthly  http://www.whale.to/vaccines/sv409.html

"Since the 1920s, virtually all continuing medical and public health education is funded by pharmaceutical companies. In fact, today, the FDA can't even tell health scientists the truth about vaccine contaminants and their likely effects. The agency is bound and gagged by proprietary laws and non-disclosure agreements forced upon them by the pharmaceutical industry. Let us not forget that the pharmaceutical industry, as a special interest group, is the number one contributor to politicians on Capital Hill."--Leonard Horowitz

"Since vaccine development information is considered proprietary (protected by nondisclosure policies) government officials and researchers must shield potential safety issues from public scrutiny. This censorship is rationalized by the all too persuasive argument that vaccines cannot be criticized lest the public become non-compliant in taking them. Finally, this silence is buttressed by the small number of people capable of critically evaluating vaccine manufacturing and safety testing procedures. In essence, health care professionals and the general public know little about the possible dangers of live viral vaccines."--Dr Martin

Disregard for safety can be seen in the selling of withdrawn vaccines to third world, and unethical vaccine experiments;
"Using kids as guinea pigs in potentially harmful vaccine experiments is every parents' worst nightmare. This actually happened in 1989-1991 when Kaiser Permanente of Southern California and the Centers for Disease Control (CDC) jointly conducted a measles vaccine experiment. Without proper parental disclosure,  the Yugoslavian-made "high titre" Edmonston-Zagreb measles vaccine was tested on 1,500 poor, primarily black and Latino,  inner city  children in Los Angeles. Highly recommended by the World Health Organization (WHO),    the high-potency experimental vaccine was previously injected into infants in Mexico, Haiti, and Africa. It was discontinued in these countries when it was discovered that the children were dying in large numbers."--Dr Alan Cantwell MD

"To determine the effect of different amounts of the vaccines, researchers at the hospital inoculated newborns from mostly lower-income black families with doses ranging up to more than 100 times the dose recommended for adults."--Media

On september 14, 1992 two measles vaccines (Pluserix & Immravax) were banned in the UK after it was revealed that children had developed meningitis.  On Sept 16, 1992 the New Zealand government withdrew Pluserix

1997 Brazil:
OUTBREAK OF ASEPTIC MENINGITIS ASSOCIATED WITH MASS VACCINATION WITH A URABE CONTAINING MMR VACCINE

2002:
"Officers are also investigating how a consignment of potentially dangerous mumps vaccine was sent to one of Direct Health 2000's suppliers. The vaccine sent by a German distributor turned out to be of the Urabe strain, banned in Britain since 1992 as it can cause viral meningitis in babies. "--Media 2002

And in continuing to use proven unsafe vaccines, sometimes for years or decades:
"DOCTORS have been told to come clean about Infanrix, the safer whooping cough jab available on the NHS - but only if directly challenged about it by parents. The compromise means that parents who ask no questions will have their children injected with the cheaper DTwP jab laced with ethyl mercury - a substance ordered out of US medicine on health grounds."--Media Feb 2003

"For decades, American pharmaceutical companies have known how to produce the safer DPT vaccine but decided not to bring it to market because it would increase production costs and lower the drug's 50% or higher profit margins."--Money Magazine

"Drug companies keep DTP alive because it is less-expensive to make, offers a bigger profit margin and can be easily dumped on developing countries......Because many pediatricians prefer to reduce office visits by giving the combined DTP-HiB shot and because many HMOs use about 50 percent DTPH, as many as 30 percent of American infants still get reactive whole-cell pertussis."--NVIC  http://www.909shot.com/gnssafet.htm  

"The British drug company Glaxo Wellcome allowed thousands of British babies to be inoculated with toxic whooping cough vaccines it knew had not passed crucial safety tests."--Media July 2001

"MERCURY, one of the most dangerous substances known to man, is being used in a series of infant vaccines - in spite of a warning from NHS advisers that its use as a cheap preservative "may be toxic" to babies aged under six months..... "The very low thiomersal concentrations present in the pharmacological and biological products are relatively non-toxic in adults," the UKMI report says. "But it may be toxic in utero [in the foetus] and during the first six months of life."  It is the first time any UK health official has admitted to the danger posed by mercury in vaccines.....The list includes four out of the seven flu vaccines issued this year by the government, a pneumonia vaccine and four of the 11 child vaccines. The main source is the triple DTwP jab, for whole-cell diphtheria, tetanus and pertussis. "--Media Jan 2003

"Michigan had made too much DPT in its Lansing laboratory and wanted to sell it to other states. That required FDA testing and approval, as with any other manufacturer. However, the FDA denied approval and returned the vaccine, saying It was 300 percent too potent. State health officials disagreed and decided to test the vaccine on children in Ingham County (Lansing). Despite more adverse reactions than usual, health officials released 400,000 doses of the DPT vaccine for use throughout the state a month later."---Fresno Bee DPT report 1984

"They began using MMR in April 1989 and by July doctors were already warning of side-effects, but the government didn’t take any notice because it was not convenient for them. They kept using it for another 3 years, securing the profits for the manufacturers".---Shunsuke Fuji

"Congress requires records to be kept of the lot numbers of vaccines for which unusually large number of "adverse events" (side effects) are reported. But the information is then simply ignored. The "hot lots," as they are called, are not destroyed, but continue to be injected into infants and children. (no use throwing out expensive vaccines--dollars are worth more than lives, just as in the U.K.) "---Dr Rimland

"SENIOR government advisers said as early as 1989 that vaccines could provide a route by which BSE could be transferred to human beings."--Media report

"Up to 300 cases relate to this brand of vaccine - Pluserix - which was banned by the Department of Health in 1992 after being linked with meningitis. This was two years after an identical vaccine was banned in Canada."--Media

"THE Department of Health has told doctors they must use stocks of a mercury-based vaccine for infants even though it is being phased out for safety reasons."--Media Aug 2001

"According to one memo, SV40 was found in three of 15 lots of the oral vaccine seven months after the federal directive was issued in March 1961. Lederle released the contaminated vaccine to the public anyway, the memo shows. The documents also suggest that the company failed to test the monkey- kidney seed strains used to make the bulk polio vaccine for contamination, despite a written warning from Dr. Albert Sabin, who developed the oral vaccine."--Media

"In 1990, scientists from the Queen’s Medical Centre Nottingham found some children developed a form of meningitis after receiving it. But despite this the Government went on using it for more than two years.  The Canadian Government, also using the vaccine, immediately switched to a safer version. It was not until September 1992 that the UK Department of Health issued pharmacists with emergency supplies of a safer brand with instructions to withdraw existing batches."--Sunday Express

"The British drug company Glaxo Wellcome allowed thousands of British babies to be inoculated (late 60's-early 70's) with toxic whooping cough vaccines it knew had not passed crucial safety tests."--Media July 2001

From Pediatric News:
Don't Be First or Last to Use a Drug or Vaccine---Mike Bykowski, Senior Writer [Pediatric News 33(7):13, 1999. International Medical News Group] Hilton Head, S.C.
    Don't be the first or the last in your community to use a new drug or vaccine, Dr. Jerome O. Klein advised at a meeting on clinical pediatrics sponsored by Boston Medical Center.
    When a new drug comes on the market, it's typically based on 5,000-10,000 subjects who have received it because that's all you need for FDA approval, said Dr. Klein, director of pediatric infectious diseases at Boston Medical Center.
    If there's an adverse event with an incidence of 1 in 20,000 associated with the drug or vaccine, it won't be detected right away. Unless the new drug or vaccine fills a critical void, Dr. Klein recommended staying away from it until the first 100,000 individuals have been treated. After that "you can feel a lot more comfortable that the adverse event profile is as it has been
described."