Posts Tagged ‘FDA’
Measles Hysteria; FDA Approves High Risk Dengue Vaccine
For the past four-five months, the New York Times has assumed the role the lead propaganda megaphone helping government bureaucrats stir up a measles frenzy with a barrage of daily headlines. How the Measles Outbreak Started Measles Outbreak Infects 695, Highest Number Since 2000 Measles Outbreak: Yeshiva’s Preschool Program Is Closed by New York…
Read MoreMissing, Hidden and Destroyed Adverse Event Data. Who Vaccinates?
Who are the anti-vaxxers, really? If I asked you whether you were for or against pharmaceutical drugs, you would think my question absurd. Obviously, each drug is different and should be judged on its own merits; furthermore, the usefulness of a drug depends on the specific needs of the person to whom it is…
Read MoreHow Monsanto Rigged the System: through Politics & Propaganda
A profit-enhancing policy trumps public safety & scientific integrity In the mid-1980s, the U.S. executive branch was persuaded that the biotechnology industry would boost the U.S. economy out of its doldrums. To accommodate this newly developing industry, the executive branch gave the industry “regulatory relief” in 1992. The US government public health safety policy shifted…
Read MoreMedical Research — Peeling the Onion from the Inside Out
A book review by AHRP board member, John J Noble Jr, Emeritus Professor, was recently published in the Indian Journal of Medical Ethics. The book, Reducing Adverse Events in Older Patients Taking Newly Released Drugs by Margaret T. Whitstock, an Australian research professional, is an indictment of the the U.S. Food and Drug Administration’ flawed drug…
Read MoreAccountability Demanded – NYC Foster Children AIDS drug trials
The efforts of AHRP to hold the medical research community and government administrators accountable for unethical exploitation of vulnerable children in medical experiments conducted in violation of federal regulations.
Read More2006: Fake Blood Experiments Without Consent: Is Your City Participating? FDA: Closed Door Meeting
Scientists and entrepreneurs have tried for years to develop a safe and universal blood substitute that did not spoil after 42 days. However, all such efforts have encountered serious safety problems.
Read More1990: Soldiers used as guinea pigs break their silence
December, 1990: FDA issued a waiver from informed consent to permit the Department of Defense to use unapproved, experimental drugs and vaccines – e.g. anthrax vaccine on soldiers. This violated the foremost “absolutely essential” mandatory ethical principle defined by the Nuremberg Code which was promulgated by U.S. judges under the authority of the U.S. Army.…
Read MoreTestimony Against SF 2841-Minnesota – Preschool Socioemotional Screening–Karen Effrem, MD.
I am here in vigorous opposition to SF 2841 that would implement mental health screening for three-year-old children entering public school.
Read MoreNora Coffey
Nora Coffey is a prominent women’s health advocate, activist and educator who founded the Hysterectomy Educational Resources and Services (HERS) Foundation in 1982. The foundation is the only independent nonprofit organization solely dedicated to the alternatives to and aftermath of hysterectomy. In 1978, Nora Coffey, then in her mid-thirties, had surgery which sent shock waves…
Read MoreBernice Eddy, PhD (1903–1989)
Bernice Eddy, PhD (1903–1989) a virologist and epidemiologist at NIH, identified SV40, a cancer-causing monkey virus that millions of children were exposed to from contaminated polio vaccines. In 1954, while the NIH was testing the first commercial polio vaccines, Eddy’s job was to test the vaccines from five different companies. She and her staff worked…
Read MoreCurt D. Furberg, MD
Curt D. Furberg, MD, an internationally recognized cardiovascular epidemiologist with expertise in clinical trials, drug safety and public health. Dr. Furberg is a Professor Emeritus of Public Health Sciences at Wake Forest University who has chaired NIH’s Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack (ALLHAT) Steering Committee and has been a vocal advocate for…
Read MoreDavid Graham, MD
David Graham, MD, FDA’s Associate Director of Science and Medicine who, throughout his career, has been a thorn for FDA managers by identifying hazardous drug effects. In 1999, his data helped identify the risk of liver damage from Pfizer’s diabetes drug Rezulin — which eventually was withdrawn from the market. In 2004, he emerged as…
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