http://www.mercola.com/1999/may/31/more_on_vaccinations.htm
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More
on Vaccinations
From last week’s Congressional testimony
regarding the reporting of adverse vaccine reactions. "Answer: Selling vaccines is
extremely profitable and the process of mandating vaccines is fraught with
conflicts of interest between vaccine manufacturers, the ACIP and the
American Academy of Pediatrics. The business model of having the government
mandate everyone must buy your product is a monopolist's delight. Question: What studies are being done on
the data from the FDA's Vaccine Adverse Event Reporting System (VAERS)? Answer: Absolutely nothing. The 25,000
REPORTS ARE GOING INTO A DRAWER AND BEING FORGOTTEN. How many reports are
enough to show a drug or vaccine is dangerous -- 2,500? 25,000? 250,000? CHEN
of the CDC and Ellenberg of the FDA monitor this data, write reports and
deliver speeches about how VAERS hepatitis B ADVERSE REACTION REPORTS SHOW
NOTHING OUT of the ORDINARY and show "the relative safety of HB vaccine
when given to neonates and infants." VAERS SHOWS NOTHING OF THE KIND.
TAKE A LOOK AT THE VAERS DATA YOURSELF. The health authorities continue to
NEGLIGENTLY DOWNPLAY the STEADY STREAM of SERIOUS ADVERSE REACTIONS to this
vaccine and more infants and adults continue to die and suffer central
nervous system and liver damage after HB vaccination." [Emphasis added].
Belkin had obtained copies of the VAERS
reports and was astounded at what he found: "The total 24,775 VAERS hepatitis B
reports from July 1990 to October 31, 1998 show 439 deaths and 9673 serious
reactions involving emergency room visits, hospitalization, disablement or
death. Therefore, more than one third of total
reports were serious events. 17,497 of those total reports were for hepatitis
B vaccine only, the remainder were vaccine cocktails where hepatitis B was
administered along with DPT, HIB, IPV, OPV, etc. The hepatitis-B-vaccine-only reports
show a shocking cluster of reactions in females starting in their teenage
years (the male/female reporting ratio is balanced before age 16). For ages
16-55, 77% of VAERS reports are women -- more than three times as many women
as men are reporting adverse reactions to hepatitis B vaccine. The median
onset of adverse event after vaccination is one day, 70% of reactions happen
within four days of vaccination. Independent scientists should investigate
why females are more disposed to have adverse reactions to hepatitis B
vaccine and/or report them to VAERS. One possible explanation is that nurses
have to take this vaccine for their jobs and are thus more exposed than most
adults to hepatitis B vaccine adverse reactions. Rather than dismiss that
factor as an "over-reporting bias" as Dr. Chen of the CDC did at
the February ACIP meeting, perhaps investigators might consider that nurses
are alert health care workers and ought to be listened to with regard to the
dangers of adverse events with any vaccine (rather than ignored). Personal
case studies reported to the author have showed many teenage girls getting
severe, debilitating adverse reactions to hepatitis B vaccine, having nothing
to do with nursing. Do women have a greater vulnerability to auto-immune
reactions to hepatitis B vaccine? Is the government discriminating against
women by administering this vaccine without regard for genetic risk of CNS
and liver disease? Those are questions that independent scientists should
investigate. A second area of concern is the VAERS
reports involving hepatitis B vaccine administered with other vaccines
(vaccine cocktails). Health officials are fond of dismissing those reports as
being attributable to hepatitis B vaccine, because of the multiple other
antigens present (almost as if they wanted to cloak hepatitis B vaccine
reactions from scrutiny). Let's avoid that controversy and focus on the
extremely disturbing VAERS data of hepatitis B vaccine with other vaccines.
These reports amount to only one third of total reports (7,275), but account
for two thirds of total deaths (291). The median onset of those deaths was 2
days after vaccination -- displaying a clear temporal association. The median
age of death was 0.5 years in this group. 50% of all
hepatitis-B-vaccine-cocktail reports were serious (died, emergency room,
hospitalized, disabled). I grouped convulsive reactions together from the
hep-B-vaccine-cocktail data and found a deeply disturbing pattern. These were
anything labeled convulsions, seizures or tremors in the VAERS hep-B-cocktail
data. Of the 1189 such reports, fully 80% (950) were serious (died, ER,
hospitalized, disabled) median age 0.5 years, median onset after vaccination
0 days (less than one day). Someone should do follow-up and find out what
happened to those poor infants who suffered severe convulsions after a
hepatitis B-multi-vaccine cocktail. In the personal reports I've taken of
similar adverse reactions, the children were left brain damaged and
developmentally disabled. Looking beyond the debate over whether
VAERS reports of vaccine cocktails can be attributed to hepatitis B, the data
strongly suggests combining multiple vaccines may be convenient and
profitable for pediatricians -- but fatal or debilitating for infants. Where
are the scientific studies showing hepatitis B vaccine is safe to administer
with DPT, HIB, IPV, OPV, etc.? Did anyone doing cost/benefit analysis for
those studies include data showing the higher mortality and serious reactions
present in the VAERS data? Why not? Is there an identifiable genetic marker
in those who suffered convulsive reactions to screen out those vulnerable in
the future? These are all matters for independent scientists to audit." |
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