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The National Vaccine Information Center (NVIC) is calling the "Biodefense
and Pandemic Vaccine and Drug Development Act of 2005"(S. 1873), which
passed out of the U.S. Senate HELP Committee one day after it was introduced
"a drug company stockholder's dream and a consumer's worst nightmare."
The proposed legislation will strip Americans of the right to a trial by jury
if harmed by an experimental or licensed drug or vaccine that they are forced
by government to take, whenever federal health officials declare a public health
emergency.
The legislation's architect, Senator Richard Burr (R-NC), Chairman of the HELP
Subcommittee on Bioterrorism and Public Health Preparedness, told the full HELP
Committee yesterday that the legislation" creates a true partnership"
between the federal government, the pharmaceutical industry and academia to
walk the drug companies "through the Valley of Death" in bringing
a new vaccine or drug to market. Burr said it will give the Department of Health
and Human Services "additional authority and resources to partner with
the private sector to rapidly develop drugs and vaccines." The Burr bill
gives the Secretary of DHHS the sole authority to decide whether a manufacturer
violated laws mandating drug safety and bans citizens from challenging his decision
in the civil court system.
The bill establishes the Biomedical Advanced Research and Development Agency
(BARDA), as the single point of authority within the government for the advanced
research and development of drugs and vaccines in response to bioterrorism and
natural disease outbreaks such as the flu. BARDA will operate in secret, exempt
from the Freedom of Information Act and the Federal Advisory Committee Act,
insuring that no evidence of injuries or deaths caused by drugs and vaccines
labeled as "countermeasures" will become public.
Nicknamed "Bioshield Two," the legislation is being pushed rapidly
through Congress without time for voters to make their voices heard by their
elected representatives. Co-sponsored by Republican Senate Majority Leader Bill
Frist (R-TN), Senate Health, Education, Labor and Pensions Committee Chairman
Mike Enzi (R-WY), and Senate Budget Committee Chairman Judd Gregg (R-NH), the
legislation will eliminate both regulatory and legal safeguards applied to vaccines
as well as take away the right of children and adults harmed by vaccines and
drugs to present their case in front of a jury in a civil court of law.
"It is a sad day for this nation when Congress is frightened and bullied
into allowing one profit making industry to destroy the seventh Amendment to
the Constitution guaranteeing citizens their day in court in front of a jury
of their peers," said Barbara Loe Fisher, president of NVIC. "This
proposed legislation, like the power and money grab by federal health officials
and industry in the Homeland Security Act of 2002 and the Project Bioshield
Act of 2004, is an unconstitutional attempt by some in Congress to give a taxpayer-funded
handout to pharmaceutical companies for drugs and vaccines the government can
force all citizens to use while absolving everyone connected from any responsibility
for injuries and deaths which occur. It means that, if an American is injured
by an experimental flu or anthrax vaccine he or she is mandated to take, that
citizen will be banned from exercising the Constitutional right to a jury trial
even if it is revealed that the vaccine maker engaged in criminal fraud and
negligence in the manufacture of the vaccine."
The federal Food and Drug Administration (FDA) is legally responsible for regulating
the pharmaceutical industry and ensuring that drugs and vaccines released to
the public are safe and effective. Drug companies marketing painkillers, like
Vioxx, and anti-depressants, which have resulted in the deaths and injuries
of thousands of children and adults, are being held accountable in civil court
while the FDA has come under intense criticism for withholding information about
the drugs' dangers from the public. Since 1986, vaccine makers have been protected
from most liability in civil court through the National Childhood Vaccine Injury
Act in which Congress created a federal vaccine injury compensation program
(VICP) that offers vaccine victims an alternative to the court system. Even
though the the program has awarded nearly $2 billion to victims of mandated
vaccines, two out of three plaintiffs are turned away.
"The drug companies and doctors got all the liability protection they needed
in 1986 but they are greedy and want more," said Fisher. "And the
federal health agencies want more power to force citizens to use vaccines without
having to worry about properly regulating them. If the Burr bill passes, all
economic incentives to insure mandated vaccines are safe will be removed and
the American people are facing a future where government can force them to take
poorly regulated experimental drugs and vaccines labeled as "countermeasures"
or go to jail. The only recourse for citizens will be to strike down mandatory
vaccination laws so vaccines will be subject to the law of supply and demand
in the marketplace. The health care consumer's cry will be: No liability? No
mandates."
The National Vaccine Information Center (NVIC) was founded by parents of vaccine
injured children in 1982 and co-founders worked with Congress on the National
Childhood Vaccine Injury Act of 1986.