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Artificial Blood Experiment: Is Your City Participating?
2006-07-07, ABC News
http://abcnews.go.com/WNT/story?id=2166058&page=1&WNT=true

Northfield Lab's experimental blood substitute Polyheme is currently in randomized phase III clinical trials recruiting patients without informed consent all over the country. At one point, it was being tested in as many as 27 cities; it is still being tested in 23 hospitals in 20 cities. With the FDA's approval, Northfield Lab has recruited hospitals to participate in the trial study with exemption from informed consent requirements on study participants. Although Northfield Lab claims that extensive information on the study has been made public, a vast majority of the general public has never heard of the trial.

Traumas create unwitting test subjects
2006-06-13, USA Today
http://www.usatoday.com/news/health/2006-06-13-traumas-trials_x.htm?POE=NEWISVA

With waived-consent studies becoming more prevalent, critics question whether the public understands how they work and whether test subjects get adequate protection. [A] trial, which is reported in today's Journal of the American Medical Association (JAMA), was halted because a device called the AutoPulse, which was used to revive cardiac-arrest victims, failed to save more lives than when rescuers performed cardiopulmonary resuscitation. Patients in these types of studies...are treated under a broad federal rule that allows researchers to test emergency treatments on patients with specific, life-threatening medical conditions without their explicit consent as long as they remain under close watch of independent reviewers. Studies have included large, multi-city, randomized trials, which scientists consider the gold standard for medical research. The [PolyHeme] trial has raised concern among some ethicists and alarm in Congress, where Sen. Charles Grassley, R-Iowa, chairman of the Finance Committee, is conducting an investigation. Grassley is concerned that people who live in the 19 states where PolyHeme is being tested have had inadequate notice about the trial. The FDA requires that community input be sought in the regions around test sites. "It is outrageous that, for all intents and purposes, the FDA allowed a clinical trial to proceed, which makes every citizen in the United States a potential 'guinea pig,' without providing a practical, informative warning to the public," Grassley wrote in a letter to the FDA in February.

Informed Consent Waived in Public Crisis
2006-06-08, CBS News/Associated Press
http://www.cbsnews.com/stories/2006/06/08/ap/health/mainD8I3MMRO0.shtml

In a public health emergency, suspected victims would no longer have to give permission before experimental tests could be run to determine why they're sick, under a federal rule published Wednesday. Privacy experts called the exception unnecessary, ripe for abuse and an override of state informed-consent laws. Health care workers will be free to run experimental tests on blood and other samples taken from people who have fallen sick as a result of a bioterrorist attack, bird flu outbreak, detonation of a dirty bomb or any other life-threatening public health emergency, according to the rule issued by the Food and Drug Administration. The rule took effect Wednesday but remains subject to public comment until Aug. 7. The FDA said it published the rule without first seeking comments because it would hinder the response to an outbreak of bird flu or other public health emergency.

Vaccine makers helped write Frist-backed shield law
2006-05-08, The Tennessean
http://tennessean.com/apps/pbcs.dll/article?AID=/20060508/NEWS02/605080356

Vaccine industry officials helped shape legislation behind the scenes that Senate Majority Leader Bill Frist secretly amended into a bill to shield them from lawsuits, according to e-mails obtained by a public advocacy group. E-mails and documents written by a trade group for the vaccine-makers show the organization met privately with Frist's staff and the White House about measures that would give the industry protection from lawsuits filed by people hurt by the vaccines. Frist, along with House Speaker Dennis Hastert, R-Ill., ordered the vaccine liability language inserted in a defense spending bill in December without debate and in violation of usual Senate practice. In a written statement, Frist spokeswoman Amy Call stated that the senator had promised publicly to include the vaccine liability protection in the defense spending bill. She did not address the issue of the influence of industry lobbyists.

Note: For one-paragraph summaries of media articles showing why the vaccine makers want this protection, click here.

Organic Food Fends Off Pesticides
2006-02-20, ABC News
http://abcnews.go.com/Health/Healthology/story?id=1642533

If you are looking to banish pesticides from your child's diet, new research suggests that organic food will do the trick, at least when it comes to two common pesticides. Researchers found that pesticide levels in children's bodies dropped to zero after just a few days of eating organic produce and grains. "After they switch back to a conventional diet, the levels go up," said study co-author Chensheng Lu, an assistant professor of environmental and occupational health at Emory University. Lu said the impetus for the new study was a previous research project that examined pesticide levels in 110 children and only found one child whose body was pesticide-free -- a child who regularly ate organic food. The findings were to be discussed Sunday at the annual meeting of the American Association for the Advancement of Science in St. Louis. The study, funded by the U.S. Environmental Protection Agency, appeared online last September in the journal Environmental Health Perspectives. Learn more about organic diets from CNN.com.

The deadly terror lurking around the corner may not be such a big, ominous threat after all
2006-02-19, San Francisco Chronicle (San Francisco's leading newspaper)
http://www.sfgate.com/cgi-bin/article.cgi?f=/c/a/2006/02/19/INGDDH8E2V1.DTL

Americans receive a steady stream of warnings and alarms about new and horrific perils that await them. Pandemics, dirty bombs, cyber attacks, bioterror and other exotic threats are always on the verge of being unleashed onto a shamefully unprepared republic. Yet, judging from statistics on life expectancy, violent deaths and war, we live in much less perilous times than any generation before us. Avian flu, for example. We are cautioned that a pandemic...is only months away. One World Health Organization estimate says 2 million to 7 million people will die in the next pandemic. But it is not 1918. The WHO reports that since 2003, there have been 152 cases of avian flu, resulting in 83 deaths. A flu pandemic has been regularly predicted since 1997 and (knock on wood) it has never arrived. Dirty bombs -- conventional explosives mixed with radioactive material -- present another example of overreaction. In 2004, experts warned in the normally staid Wall Street Journal that a terrorist attack with a dirty bomb was an imminent certainty. They announced: "Shame on our leaders and on us if the lamentations of the next blue-ribbon panel will be intoned over the graves of hundreds of thousands of Americans, the collapse of our economy, and perhaps a fatal blow to our way of life." But the Nuclear Regulatory Commission says a dirty bomb would contaminate "up to several city blocks." The commission's advice, if one goes off, is to walk away and take a shower.

Note: This informative article, by a program director of the Center for Strategic and International Studies in Washington, demonstrates clearly how the hype and fear around terror is much more damaging than terrorism itself. For more on this from both BBC and my own experience as a presidential interpreter, click here.

6 Ex-Chiefs of E.P.A. Urge Action on Greenhouse Gases
2006-01-19, New York Times/Associated Press
http://www.nytimes.com/2006/01/19/national/19enviro.html?ex=1295326800&en=a4e...

Six former heads of the Environmental Protection Agency, including five who served Republican presidents, said Wednesday that the Bush administration needed to act more aggressively to limit the emission of greenhouse gases linked to climate change. Speaking on a panel that also included the current agency chief, Stephen L. Johnson, they generally agreed that the need to address global warming was growing urgent and that the continuing debate over what percentage of the problem was caused by human activities was a waste of time. The blunt opinions of [the current EPA chief's] Republican predecessors served as a sharp reminder that since Mr. Bush took office in 2001, neither the president nor the Republican-led Congress has proposed any comprehensive plan to limit carbon emissions from vehicles, utilities and other sources, a problem that Mr. Bush's own Department of Energy predicts will grow worse.

Maker of drug admits hiding its risks
2005-07-24, Miami Herald
http://www.miami.com/mld/miamiherald/news/front/9231611.htm

The maker of a billion-dollar antipsychotic medication has acknowledged misleading doctors and other healthcare providers about the safety of its product, minimizing potentially deadly side effects. On Wednesday, drug maker Janssen Pharmaceutica wrote a two-page letter to doctors, warning them that the company, in promotional material, had "minimized potentially fatal risks, and made misleading claims" that the medication was more safe in treating mental illness than other drugs in the same category. Risperdal is the leading drug used to combat schizophrenia and other types of psychotic disorders, earning Janssen about $2.1 billion in annual sales. The drug was first marketed about eight years ago, and is prescribed to more than 10 million people worldwide. The "important correction of drug information" came shortly after federal regulators had accused Janssen of "disseminating" advertising and marketing material that was "false or misleading."

Don't miss the highly revealing article on this vital topic by the New England Journal of Medicine's former editor in chief Marica Angell. Click here

Allegations of Fake Research Hit New High
2005-07-10, MSNBC/AP
http://msnbc.msn.com/id/8474936

Doctors accused of making up data in medical studies. Allegations of misconduct by U.S. researchers reached record highs last year as the Department of Health and Human Services received 274 complaints - 50 percent higher than 2003 and the most since 1989 when the federal government established a program to deal with scientific misconduct. Chris Pascal, director of the federal Office of Research Integrity, said its 28 staffers and $7 million annual budget haven't kept pace with the allegations. The result: Only 23 cases were closed last year. Of those, eight individuals were found guilty of research misconduct. In the past 15 years, the office has confirmed about 185 cases of scientific misconduct. Research suggests this is but a small fraction of all the incidents of fabrication, falsification and plagiarism. In a survey published June 9 in the journal Nature, about 1.5 percent of 3,247 researchers who responded admitted to falsification or plagiarism. (One in three admitted to some type of professional misbehavior.)

Debate over vaccines, autism won't die
2005-06-26, MSNBC
http://msnbc.msn.com/id/8336821

Mercury in shots blamed for rise in brain disorder among children. Vested interests make it tough to know who to believe. Many parents have filed lawsuits. Many scientists have ties to vaccine makers or are selling their expertise in court cases. Government officials don’t want people to turn away from vaccines, which have clearly benefitted public health. Flu vaccine sold in multidose vials still contains the [mercury] preservative, and the government urges flu shots for pregnant women and young children even though not enough thimerosal-free ones are available, critics say. Robert F. Kennedy, Jr....who has pushed the issue on news shows and in an article in Rolling Stone magazine, said that when he looked at the government’s evidence it was laughably flawed. “It was clear to me that the reports they’re relying on are ’cigarette science,”’ he said, referring to tobacco companies’ past arguments that there was no proof cigarettes caused cancer.

State Secret: Thousands Secretly Sterilized
2005-05-15, ABC News
http://abcnews.go.com/WNT/Health/story?id=708780

From the early 1900s to the 1970s, some 65,000 men and women were sterilized in this country, many without their knowledge, as part of a government eugenics program to keep so-called undesirables from reproducing. "The procedures that were done here were done to poor folks," said Steven Selden, professor at the University of Maryland. "They were thought to be poor because they had bad genes or bad inheritance, if you will. And so they would be the focus of the sterilization." Even though the practice ended more than 30 years ago, some say the time has come to make amends. North Carolina was one of the first states out of 33 that once practiced sterilization to offer an apology. State Rep. Larry Womble is crafting a bill to provide financial reparations.

2 Paths of Bayer Drug in 80's: Riskier One Steered Overseas
2003-06-22, New York Times
http://query.nytimes.com/gst/fullpage.html?sec=health&res=9A00E4DA1F3EF931A15...

A division of the pharmaceutical company Bayer sold millions of dollars of blood-clotting medicine for hemophiliacs -- medicine that carried a high risk of transmitting AIDS -- to Asia and Latin America in the mid-1980's while selling a new, safer product in the West. The Bayer unit, Cutter Biological, introduced its safer medicine in late February 1984 as evidence mounted that the earlier version was infecting hemophiliacs with H.I.V. Yet for over a year, the company continued to sell the old medicine overseas. Cutter officials were trying to avoid being stuck with large stores of a product. Yet even after it began selling the new product, the company kept making the old medicine for several months more. In Hong Kong and Taiwan alone, more than 100 hemophiliacs got H.I.V. after using Cutter's old medicine. Many have since died. Cutter also continued to sell the older product after February 1984 in Malaysia, Singapore, Indonesia, Japan and Argentina. While admitting no wrongdoing, Bayer and three other companies that made the concentrate have paid hemophiliacs about $600 million to settle more than 15 years of lawsuits accusing them of making a dangerous product. Federal regulators helped keep the overseas sales out of the public eye. The Food and Drug Administration's regulator of blood products, Dr. Harry M. Meyer Jr....asked that the issue be "quietly solved without alerting the Congress, the medical community and the public."

Cancer Cure?
1923-06-04, Time Magazine
http://www.time.com/time/magazine/article/0,9171,715686,00.html

A reported remedy for cancer developed by Dr. W. Blair Bell, of Liverpool, seems, on the basis of the meager information at hand, to be the most promising of all recent " cures" that have been suggested. Dr. Bell's specific is a solution of colloidal lead (a colloid is a gluelike, noncrystalline organic substance that will not pass through a membrane), which appears to have a marked effect on malignant growths like cancer. Dr. Bell has been experimenting with it for 18 years and has recently employed it in 50 cases given up by surgeons as hopeless, checking the cancer in every case, with no recurrence. William Blair Bell is a prominent surgeon and professor of gynecology and obstetrics at the University of Liverpool. He has a high reputation in his specialties, is an authority on the pituitary gland, is author of several standard medical works, including The Sex Complex, has held professorships and won prizes at important hospitals and medical schools in London, Durham, Belfast. That he has not made public his discovery is because he desired to treat many more patients before submitting it to the medical and surgical professions. Dr. Bell's professional standing is in itself strong presumptive evidence of the importance of his treatment, and first-hand details will be eagerly awaited.

Note: For more powerful news articles from the major media on potential cancer cures, click here.

Doctors, Legislators Resist Drugmakers' Prying Eyes
2007-05-22, Washington Post
http://www.washingtonpost.com/wp-dyn/content/article/2007/05/21/AR20070521017...

Pediatrician Rupin Thakkar's first inkling that the pharmaceutical industry was peering over his shoulder ... came in a letter from a drug representative about the generic drops Thakkar prescribes to treat infectious pinkeye. In the letter, the salesperson wrote that Thakkar was causing his patients to miss more days of school than they would if he put them on Vigamox, a more expensive brand-name medicine made by Alcon Laboratories. "My initial thought was 'How does she know what I'm prescribing?' " Thakkar said. "It feels intrusive ... I just feel strongly that medical encounters need to be private." He is not alone. Many doctors object to drugmakers' common practice of contracting with data-mining companies to track exactly which medicines physicians prescribe and in what quantities -- information marketers and salespeople use to fine-tune their efforts. The concerns are not merely about privacy. Proponents say using such detailed data for drug marketing serves mainly to influence physicians to prescribe more expensive medicines, not necessarily to provide the best treatment. "We don't like the practice, and we want it to stop," said Jean Silver-Isenstadt, executive director of the National Physicians Alliance. (Thakkar is on the group's board of directors.) "We think it's a contaminant to the doctor-patient relationship, and it's driving up costs." The American Medical Association makes millions of dollars each year by helping data-mining companies link prescribing data to individual physicians. It does so by licensing access to the AMA Physician Masterfile, a database containing names, birth dates, educational background, specialties and addresses for more than 800,000 doctors.

Note: For more reliable, verifiable information about major corruption in the drug industry, click here.

Consumer group sues FDA over biotech foods
2006-06-07, San Diego Union Tribune/Reuters
http://www.signonsandiego.com/news/business/biotech/20060607-1051-food-gmo-la...

A lawsuit filed Wednesday seeks to force the U.S. government to conduct mandatory reviews of genetically engineered foods and require labeling of such foods once they are approved. The Center for Food Safety's suit against the Food and Drug Administration comes after years of lobbying by environmental and consumer groups for more stringent regulation and labeling of biotech crops. Genetically modified crops, such as soybeans, corn, and canola, are grown widely throughout the United States, and the world leader in development and marketing of the gene-altered crops is...Monsanto. Yet the United States requires no independent testing of these crops or the food products they are used in, does not mandate what data companies must submit for review, and does not require that foods that contain biotech crops be labeled. CFS and more than fifty consumer and environmental groups, filed a legal petition with the FDA in March 2000, asking the agency to adopt a more rigorous approach to biotech food regulation, but the CFS said Wednesday that the FDA had ignored the petition. At various times over the last several years, different scientists, including some within the FDA, have warned that altering the genetic makeup of a food plant by inserting genes from one organism into another...could trigger unexpected food allergies, create toxins in food, or spread antibiotic-resistant disease. CFS said the tests that exposed that potential hazard have not been conducted on any of the genetically modified foods currently marketed.

Note: Many laboratory animals died in scientific tests of GM foods, yet this news has yet to be reported in the major media. If you want to understand the risks involved with the ever-increasing numbers of genetically modified organisms in the food you eat, don't miss: http://www.WantToKnow.info/deception10pg

Ministers back 'terminator' GM crops
2006-03-05, Independent (one of the UK's leading newspapers)
http://news.independent.co.uk/environment/article349331.ece

Ministers are trying to scrap an international agreement banning the world's most controversial genetic modification of crops, grimly nicknamed "terminator technology", a move which threatens to increase hunger in the Third World. The Government is to push for terminator crops to be considered for approval on a "case-by-case basis" at two meetings this month; its position closely mirrors the stance of the United States and other GM [genetically modified organisms]-promoting countries. Terminator technology...would stop hundreds of millions of poor farmers from saving seeds from their crops for resowing for the following harvest, forcing them to buy new ones from biotech companies every year. The technique is officially known as genetic use restriction technology (Gurt), making crops produce sterile seeds. It could be applied to any crop, including maize and rice, widely grown in developing countries. The UK working group on terminator technology...says: "It could destroy traditional farming methods, damage farmers' livelihoods and threaten food security, particularly in developing countries." [Former UK Minister of Environment Michael] Meacher said: "For the first time in the history of the world, farmers would be stopped from using their own seeds."

Note: For more on this alarming development: http://www.WantToKnow.info/deception10pg

Royal Rife: Discovering a Cure for Cancer Can Be Dangerous to Your Health
2000-10-09, WantToKnow.info/Jeff Rense
http://www.WantToKnow.info/cancercuresroyalrife

Note: We usually limit ourselves to information which comes from sources known and respected by the public. For this message, we're making an exception. Jeff Rense of rense.com is a radio personality and researcher of major cover-ups with no strong credentials other than a large following of people convinced of the quality of his work. His popular website receives millions of visits a month. Below is vital information everyone should know.

Royal Raymond Rife was a brilliant scientist born in 1888 and died in 1971. He received 14 major awards and honors and was given an honorary Doctorate by the University of Heidelberg for his work. By 1933, he had ... constructed the incredibly complex Universal Microscope, which...was capable of magnifying objects 60,000 times their normal size. With this incredible microscope, Rife became the first human being to actually see a live virus. In 1934, the University of Southern California appointed a Special Medical Research Committee to bring terminal cancer patients ... to Rife's San Diego Laboratory and clinic for treatment. The team included doctors and pathologists assigned to examine the patients - if still alive - in 90 days. After the 90 days of treatment, the Committee concluded that 86.5% of the patients had been completely cured. On November 20, 1931, forty-four of the nation's most respected medical authorities honored Royal Rife with a banquet billed as The End To All Diseases. But by 1939, almost all of these distinguished doctors and scientists were denying that they had ever met Rife. The last thing in the world that the pharmaceutical industry wanted was ... a painless therapy that cured ... terminal cancer patients and cost nothing to use but a little electricity. It might give people the idea that they didn't need drugs. Medical journals, supported almost entirely by drug company revenues and controlled by the AMA, refused to publish any paper by anyone on Rife's therapy. Rife technology became public knowledge again in 1986 with the publication of The Cancer Cure That Worked, by Barry Lynes, and other material about Royal Rife and his monumental work.

Note: For excellent video documentaries, including interviews with Royal Rife: http://www.rifevideos.com. For an excellent website focused on Rife's work, click here. For more reliable, verifiable information on health cover-ups, click here.

NIH: Scientists Escape Ethics Punishment
2006-09-12, CBS News/Associated Press
http://www.cbsnews.com/stories/2006/09/12/ap/tech/mainD8K3IQO00.shtml

Most of the federal scientists who improperly accepted personal money from drug or biotechnology companies walked away with reprimands or were allowed to retire unscathed. Only two of the 44 scientists found to have violated rules governing private consulting deals are being investigated for possible criminal activity, and they remain on the government payroll. NIH spokesman John Burklow said his agency wanted eight others reviewed for possible crimes, but those cases were rejected by the investigating office at the U.S. Health and Human Services Department. The two still outstanding...both committed "serious misconduct," so grave that they would be fired if they were civilians, NIH internal ethics reports contend. [A Congressional] subcommittee is expected to question NIH officials about documents showing it approved several taxpayer-paid trips for [Dr. Trey] Sunderland to attend conferences and events in places like Hawaii and Toronto, even after recommending his firing. Of the 44 alleged offenders...the majority received reprimands or warnings for failing to properly obtain approvals for their outside consulting work. NIH ethics reports allege...two scientists had unauthorized, unreported deals with drug companies -- Sunderland earning more than $600,000 over eight years for consulting and speeches and [Dr. Thomas] Walsh more than $100,000 in five years -- and that their consulting improperly overlapped with government duties.

Note: The Los Angeles Times later reported that Dr. Sunderland was the first NIH scientist in 14 years to be found guily of conflict of interest laws. For more vital information on major collusion between government and the pharmaceutical companies: http://www.WantToKnow.info/healthcoverup.

EPA Charges DuPont Hid Teflon's Carcinogenic Risks
2005-01-18, Chicago Tribune
http://www.chicagotribune.com/news/nationworld/chi-0501180271jan18,1,1986717....

More than 50 years after DuPont started producing Teflon ... federal officials are accusing the company of hiding information suggesting that [the chemical] might cause cancer, birth defects and other ailments. Environmental regulators are particularly alarmed because scientists are finding perfluorooctanoic acid, or PFOA, in the blood of people worldwide and it takes years for the chemical to leave the body. The U.S. Environmental Protection Agency reported last week that exposure even to low levels of PFOA could be harmful. With virtually no government oversight, PFOA has been used since the early 1950s. Questions about potential effects on human health and the environment often aren't raised until years after a chemical is introduced to the marketplace. The long and mostly secret history of PFOA began to unravel down the road from DuPont's Teflon plant...where a Parkersburg family began asking questions in the late 1990s about a mysterious wasting disease killing their cattle. Their lawsuit ended with a monetary settlement ... but the legal battle uncovered a trove of industry documents about PFOA. One document detailed how DuPont scientists started warning company executives to avoid human contact with PFOA as early as 1961. Industry tests later determined the chemical accumulates in the body [and] doesn't break down in the environment. Tests on lab animals have found links to illnesses including liver and testicular cancer, reduced weight of newborns and immune-system suppression. The findings concern EPA officials because rats flush the chemical out of their bodies within days, while PFOA stays in human blood for at least four years.

Note: As this article is no longer available on the Chicago Tribune website, to read it in full, click here.

Psychiatrists, Children and Drug Industry’s Role
2007-05-10, New York Times
http://www.nytimes.com/2007/05/10/health/10psyche.html?ex=1336449600&en=027d7...

When Anya Bailey developed an eating disorder after her 12th birthday, her mother took her to a psychiatrist at the University of Minnesota who prescribed a powerful antipsychotic drug called Risperdal. Created for schizophrenia, Risperdal is not approved to treat eating disorders, but increased appetite is a common side effect and doctors may prescribe drugs as they see fit. Anya gained weight but within two years developed a crippling knot in her back. She now receives regular injections of Botox to unclench her back muscles. She often awakens crying in pain. Isabella Bailey, Anya’s mother, said she had no idea that children might be especially susceptible to Risperdal’s side effects. Nor did she know that Risperdal and similar medicines were not approved at the time to treat children. Just as surprising, Ms. Bailey said, was learning that the university psychiatrist who supervised Anya’s care received more than $7,000 from 2003 to 2004 from Johnson & Johnson, Risperdal’s maker, in return for lectures about one of the company’s drugs. The intersection of money and medicine, and its effect on the well-being of patients, has become one of the most contentious issues in health care. Nowhere is that more true than in psychiatry, where increasing payments to doctors have coincided with the growing use in children of a relatively new class of drugs known as atypical antipsychotics. These best-selling drugs, including Risperdal, Seroquel, Zyprexa, Abilify and Geodon, are now being prescribed to more than half a million children in the United States to help parents deal with behavior problems despite profound risks and almost no approved uses for minors.

Note: For lots more reliable information on cover-ups affecting your health, click here. To read an inspiring story on the benefits of healthy school diet for students' health, behavior and studies, click here.

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