Why Eli Lilly’s Alzheimer’s Imaging Test- Amyvid- Is NO Breakthrough
On Friday, April 6, the FDA approved another of Eli Lilly’s "breakthroughs" whose clinical value is questionable (at best).
On Friday, April 6, the FDA approved another of Eli Lilly’s "breakthroughs" whose clinical value is questionable (at best).
The single National Biodefense Science Board panelist who voted against the recommendation in support of an anthrax vaccine test in children was Patricia Quinlisk, M.D., M.P.H. State Epidemiologist and Medical Director Iowa Department of Public Health, who chaired the NBSB panel.
As of June 2011 there have been 68 deaths related to the HPV Gardasil vaccine were reported to VAERS.
A year after professor Susan M. Reverby, a historian at Wellesley College in Massachusetts, uncovered a heinous Guatemalan syphilis experiment conducted between 1946 and 1948, on at least 5,500 under the auspices of the US Public Health Service, a hearing was held this week about the findings of the…
Three new studies–one,, a pharmaco-genetic study, is groundbreaking–confirm that widely prescribed psychotropic drugs that pose serious risks of harm, offer no therapeutic benefit.
The Obama Administration has embarked on an aggressive course of action that will accelerate the pace at which the integrity of American medicine–is sullied beyond repair.
The primary promoters–inventors, one might say– of diagnosing children with "bipolar" disorder, who for over a decade, aggressively promoted the biopolar diagnosis and use of antipsychotics in children, were disciplined by Harvard University and its affiliated Massachusetts General Hospital.
The Alliance for Human Research Protection speaks out against a US government-proposed anthrax vaccine experiment on children. Such an experiment would sacrifice children’s welfare, much as canaries sent into the coal mines were sacrificed.
To date, the available evidence about the safety and efficacy of the anthrax vaccine is resoundingly negative. Three US government anthrax vaccine initiatives represent a reckless deviation from the precautionary principle of medical ethics and fiscal responsibility.
April 27, 2011: US Department of Health and Human Services Letter to National Biodefense Science Board seeks OK to Expose children to serious risks of Anthrax Vaccine.
July 1, 2005: Sen. Jeff Bingaman Letter of complaint to the Secretary of of Health and Human Services Stopped proposed Anthrax Vaccine Trial. in children.
FDA’s lax approval process for medical devices has shielded surgeons and manufacturers who have made a killing from a lucrative business venture. FDA has even awarded the seal of approval years after the rings were implanted in patients while still in the experimental stage–without their knowledge or informed consent.
Public Citzen petitioned FDA Commissioner to immediately removal from market Pfizer’s Alzheimer’s drug, Aricept 23 mg dose, because of serious safety hazards and failure to demonstrate efficacy. The petition also urges FDA to add a label warning on Aricept and generic donepezil (5 mg and 10 mg) stating: "Use of 20 mg per day is counter indicated."