Stop
The Shots - Forced Swine Flu Vaccines Litigation Hits Courts
A
"stop the shot" campaign has hit federal and state courts.
This past Friday, a group of New York doctors and health care workers
asked a federal judge in Washington, D.C., to order the federal
government not to distribute the H1N1 vaccine. Specifically, they're
challenging the legality of the licensing of the swine flu vaccine,
alleging it was approved too quickly without appropriate testing for
safety and effectiveness. Furthermore, the plaintiffs, who filed
their suit in the U.S. District Court in the District of Columbia,
are seeking an immediate court order to halt mandated H1N1 flu shots
in New York state. That mandate is also facing a legal challenge in
New York state trial court in Manhattan, where a lawsuit on behalf of
60,000 state health care workers has been filed against the state
health commissioner to halt the required flu shots. A similar lawsuit
has been filed in the state of Washington, where the Washington State
Nurses Association is suin g a multifacility health care provider
over a policy requiring nurses to get vaccinated for both the
seasonal and swine flu.
Tresa Baldas, The National Law Journal
Related Links:
*
Data
Shows Flu Shots Precipitate Swine Flu - Canada Cancels
Programme
Phred Dvorak & Betsy McKay, The Wall Street
Journal
* UK
Government Swine Flu Dealers Busted In Public
Daniel Martin,
Daily Mail/The One Click Group
* GSK’s
Pandemrix Swine Flu Vaccine - Pandora's Box Release
Lara,
Health Advocate
* Swine
Flu: To Vaccinate Or Not?
Dr Marc Girard, MSc, MD, France
Pharma/FDA
Conflicted Data - Swine Flu Vaccines Deadly Adjuvants
With
a pivotal and profitable role played by the pharmaceutical industry
in vaccine production, Dr Meryl Nass MD suggests that there is a lack
of "unconflicted data" available about adjuvants. "Nearly
all of the MF59 (adjuvant) data were derived from the manufacturer of
MF59, for example,"
she said. "It
is more the lack of reliable data, and gives the impression that
something is being hidden. Those of us who are familiar with the
subject are concerned that if these adjuvants were used en masse, we
would face some bad outcomes. The FDA has been sitting on them for 10
years, and usually, that means that the FDA is aware of significant
problems."
LJ Anderson, Palo Alto Daily News