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AHRP Ethical and Scientific Objections to FDA's Proposed Licensure of Anthrax Vaccine |
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Tuesday, 29 March 2005 |
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When a federal judge ruled the vaccine to be an "investigational
drug and a drug being used for an unapproved purpose" on December
22, 2003, FDA hurriedly issued a Final Rule for anthrax vaccine.
The agency submitted its Final Rule just eight days after a federal
court injunction, having failed to do so for 19 years. In a January 7,
2004 court hearing the same judge called FDA's actions "highly suspicious."
On October 27, 2004 FDA's arbitrary and capricious promulgation
of this Final Rule resulted in a permanent injunction, remanding
the license to your agency to complete according to the law. The injunction
also halted what the judge called DoD's
"illegal" mandatory anthrax vaccination program.
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Testimony of Meryl Nass, MD - Senate HELP Committee, Subcommittee on Bioterrorism |
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Tuesday, 08 February 2005 |
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Thank you for the opportunity to submit this testimony for the record.
My name is Meryl Nass, M.D., and I have worked for the past twenty years
as an emergency physician and internist in community hospitals in the
northeastern US. I have also studied many aspects of bioterrorism since
1989. I am the person who first demonstrated, in 1992, that one could
investigate an epidemic retrospectively, and prove that it was due to
biological warfare, using Rhodesia's 1978-80 anthrax epidemic as a model.[1]
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US Gov Pesticide Exposure Experiments: Target Children--$970 per child - Wash Post |
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Wednesday, 03 November 2004 |
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The Washington Post reports (below) that the Environmental Protection
Agency (EPA) announced plans to enroll 60 young children in Duval County,
Florida - infants to age 3 - exposing them to pesticides to study how
the children absorb poisonous chemicals!
In this experiment children will literally be relegated to the status
of human guinea pigs. This experimental abuse of children demonstrates
what the chemical / pharmaceutical industry buys when it "contributes"
funds to government agencies, public officials, scientists and academic
institutions. |
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Press Statement - FDA & Concealment of Suicide-Related Risks of Antidepressants |
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Tuesday, 14 September 2004 |
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We are witnessing the unraveling of a system that was intended to ensure
that marketed drugs met high safety standards; that physicians were
informed about potential, serious adverse drug effects - so that they
would prescribe judiciously; and that the integrity of the scientific
literature was preserved. But that system has been hijacked by the drug
industry - which has infected medical practice and medical research
with detail men and informercials that make false claims while manipulating
partial data to conceal adverse drug effects. |
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AHRP Press Briefing: Antidepressants and Suicide-Related Risks for Children |
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Tuesday, 14 September 2004 |
Scientists' Presentations at AHRP Press Briefing in Conjunction
with FDA Hearings:
- Peter Mansfield, MD, University of Adelaide (Australia), Director
of Healthy Skepticism discussed the illusion of potency in light of
the meta-analyses in the British Medical Journal (which he co-authored)
and the Lancet.
Dr. Mansfield's power point presentation
- Peter Breggin, MD, a psychiatrist with a sub-specialty in clinical
psychopharmacology, who was among the first to recognize adverse antidepressant
drug reactions
Dr. Breggin's presentation
- Lawrence Diller, MD, a pediatrician and family therapist who has
evaluated and treated more than 2,500 children
Dr. Diller's presentation
- Stefan Kruszewski, MD, a clinical and academic psychiatrist, and
Associate Medical Director of Physicians' Health Programs, Pennsylvania
Medical Society
Dr. Kruszewski's presentation
- David Healy, MD, Director of the North Wales Department of Psychological
Medicine and Visiting Professor, University of Toronto,
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