Recently in Safety and Effectiveness Category

By MIKE STOBBE (AP) - Jul 17, 2009

ATLANTA -- The last time the government embarked on a major vaccine campaign against a new swine flu, thousands filed claims contending they suffered side effects from the shots. This time, the government has already taken steps to head that off.

Vaccine makers and federal officials will be immune from lawsuits that result from any new swine flu vaccine, under a document signed by Secretary of Health and Human Services Kathleen Sebelius, government health officials said Friday.

Since the 1980s, the government has protected vaccine makers against lawsuits over the use of childhood vaccines. Instead, a federal court handles claims and decides who will be paid from a special fund.

"If I had a child now, the last thing I would allow is vaccination."
-Retired Vaccine Researcher to Jon Rappoport
 
Editor's Note -- This interview was posted by Jon Rappoport in early January 2002. You will discover by reading it that the very issues we now face of FORCED vaccination of a laboratory-created vaccine to "protect" us against a laboratory-created "disease" (Swine Flu, Bird flu, etc.) was set into motion a long time ago.

The vaccine researcher quoted here flat out says that the World Homicide Organization, WHO, is driven by a DEPOPULATION agenda, and that many African leaders know full well that the explosive spread of HIV and AIDS in Africa was caused by WHO-sponsored vaccinations of the 1970s.

ScienceDaily (May 20, 2009) -- The inactivated flu vaccine does not appear to be effective in preventing influenza-related hospitalizations in children, especially the ones with asthma. In fact, children who get the flu vaccine are more at risk for hospitalization than their peers who do not get the vaccine, according to new research that will be presented on May 19, at the 105th International Conference of the American Thoracic Society in San Diego.

Flu vaccine (trivalent inactivated flu vaccine--TIV) has unknown effects on asthmatics.

"The concerns that vaccination maybe associated with asthma exacerbations have been disproved with multiple studies in the past, but the vaccine's effectiveness has not been well-established," said Avni Joshi, M.D., of the Mayo Clinic in Rochester, MN. "This study was aimed at evaluating the effectiveness of the TIV in children overall, as well as the children with asthma, to prevent influenza-related hospitalization."

A TEENAGER is fighting to prove that the MMR vaccine made her deaf.

Katie Stephen, 16, fell ill with a fever 10 days after being injected with an early form of the immunisation as a toddler in 1991.

Parents Wendy and Alistair believe the vaccine, which included a strain of mumps, was responsible for their daughter losing the hearing in her left ear.

Atlanta, GA -- The Advisory Committee on Immunization Practices (ACIP) will meet tomorrow at the CDC in Atlanta. Thimerosal, a controversial mercury- based vaccine preservative still used in flu shots, will be discussed. Health Reporters are encouraged to attend. Lyn Redwood of the National Autism Association and the Coalition for SafeMinds will be in attendance and available to speak with members of the press.

WHAT:
The Advisory Committee on Immunization Practices (ACIP) Meeting

WHEN:
Tomorrow, February 21st and Thursday, February 22nd from 7:00a.m.-6:00p.m.
Ethylmercury Thimerosal is scheduled to be discussed tomorrow at 10:55 am. 

Washington, D.C. - The National Vaccine Information Center (NVIC) today released a new analysis of the federal Vaccine Adverse Event Reporting System (VAERS) reports of serious health problems following HPV vaccination (Merck's GARDASIL) during the last six months of 2006. Out of the 385 individual GARDASIL adverse event reports made to VAERS, two-thirds required additional medical care and about one-third of all reports were for children 16-years-old and under, with nearly 25 percent of those children having received simultaneously one or more of the 18 vaccines that Merck did not study in combination with GARDASIL. NVIC is calling on the FDA and CDC to warn parents and doctors that GARDASIL should not be combined with other vaccines and that young girls should be monitored for at least 24 hours for syncopal (collapse/fainting) episodes that can be accompanied by seizure activity, as well as symptoms of tingling, numbness and loss of sensation in the fingers and limbs, all of which should be reported to VAERS immediately.

Greg Ciola Interviews Mary Tocco

When was the last time you heard an honest debate on the flu shot where experts from both conventional and alternative medicine were allowed to present their facts and debate the issues? There are plenty of independent researchers not beholden to the drug companies that have a wealth of interesting information to share that if disseminated widely, would cause many to stop and think twice before getting jabbed with a flu shot. The one good thing we’ve hopefully learned is to get a second opinion before making any major medical decision. Getting a flu shot is a major medical decision.

Crusador editor, Greg Ciola, is pleased to interview vaccine researcher Marry Tocco about the dangers of the flu shot. Before succumbing to fear thinking that you’ll die or become horribly sick if you don’t get a flu shot, listen to what Mary Tocco has to say first, pray about it, and decide for yourself whether you should take a shot after weighing all the facts.

A persistent criticism from opponents of the Pentagon’s anthrax vaccination program is the charge that defense officials purposely put squalene in some vaccine lots to boost troops’ immune responses and increase the length of time vaccine stocks would remain effective.

The Pentagon and the vaccine’s manufacturer have repeatedly denied those charges, but opponents continue to question whether the fatlike substance may have played a role in illnesses developed by some troops who got anthrax shots during the 1991 Persian Gulf War and in the early stages of the Pentagon’s mandatory anthrax vaccine program in the late 1990s.

BRISBANE, Calif., Dec. 18 /PRNewswire-FirstCall/ -- VaxGen, Inc. (Pink Sheets: VXGN.PK) announced today that the Food and Drug Administration's Center for Biologics Evaluation and Research (CBER) has informed the company that it is maintaining its clinical hold on the company's second Phase II trial for its investigational anthrax vaccine. The hold is due to CBER's continued concerns about the vaccine candidate's stability.

The Department of Health and Human Services (HHS), under its contract with VaxGen to purchase 75 million doses of its recombinant anthrax vaccine, rPA102, had imposed a deadline of today, December 18, for the company to initiate its next clinical trial for the vaccine candidate. The Office of Public Health Emergency Preparedness (OPHEP), the office within HHS that administers the contract, has yet to inform VaxGen what direction it intends to take with respect to the contract.

Kozhikode, INDIA - Tetanus vaccination has been temporarily suspended following the death of Rupisha (15), daughter of Rajan of Kuttiyadi. A temporarily ban was put on the vaccine of Mumbai based Afkin Company which is suspected to be the cause of death of the girl. The health department ordered to suspend the vaccine used in the Vattoli sector.

Though the authorities stated that the death was not due to the tetanus vaccine, suspicion arose after temporarily suspending it. The sample of the medicine used for the tetanus injection at the Vattoli High School has been sent for analysis to the National Virology Institute at Hasoli in Himachal Pradesh. The decision to ban the injection temporarily was taken since it takes at least one month to get the report.

source - Keral Online