New UK data finds prescription drugs 62,000 times more likely to kill than supplements
Wednesday, August 15, 2012 by: Tony Isaacs
(NaturalNews) According to data just released by the UK-based Alliance for Natural Health International (ANH-Intl), pharmaceutical drugs are 62,000 times more likely to kill you than supplements. In fact, the data collected by ANH-Intl demonstrates that food supplements are the safest substances regularly consumed by UK citizens even though they are the target of increasingly restrictive European legislation aimed at ‘protecting consumers.’
The newly released data found that pharmaceutical drugs were also 7,750 times more likely to result in death than herbal remedies. Both food supplements and herbal remedies were placed in the ‘supersafe’ category of individual risk – with a less than one in ten million risk of death.
The stark contrast between the safety of supplements and mainstream medicine
By contrast, being admitted to a UK hospital or taking prescription drugs exposes a person to one of the greatest preventable risks in society. Overall, preventable medical injuries in UK hospitals expose patients to the same risk of death as being deployed on military service to Afghanistan – both of which are around 300,000 times greater than the risk of death from taking natural health products.
ANH-Intl executive and scientific director, Dr. Robert Verkerk, PhD, hailed the figures as shedding new light on the question of natural healthcare’s safety. “These figures tell us not only what activities an individual is most or least likely to die from, but also what the relative risks of various activities are to society as a whole. It puts some real perspective on the actual risk of death posed by food supplements and herbal remedies at a time when governments are clamping down because they tell us they’re dangerous.”
Verkerk added, “When compared with the risk of taking food supplements, an individual is around 900 times more likely to die from food poisoning and nearly 300,000 times more likely to die from a preventable medical injury during a spell in a UK hospital. The latter is on a par with the risk of death from active military service in Iraq or Afghanistan.”
According to Dr. Verkerk, the new figures should put pressure on UK and European authorities to reduce regulatory burdens on natural health products. “Governments justify the increasingly elaborate and restrictive new laws affecting natural health products on grounds of public safety,” said Verkerk. “They argue that reducing consumer access to food supplements and herbal remedies, with the consequent negative impacts on small businesses manufacturing, distributing and selling such products, is in society’s interest. But the evidence is simply not there – where are the bodies?”
Among other key points presented in the data were:
* Pharmaceutical drugs pose nearly double the risk of death than motorcycle accidents on UK roads
* While herbal medicines can both be regarded as ‘supersafe,’ preventable medical injuries in UK hospitals are in the ‘Dangerous’ category, with a risk of death greater than 1 in 1,000.
About that bone scan and the meds that follow…
Wednesday, August 15, 2012 by: Craig Stellpflug
The scoop on bone meds
Long-term use of bone meds like Actonel, Boniva, Fosamax and Reclast have been linked to femur fractures. One study found bones on these meds turning brittle at four years. Two studies found an increased risk of fracture at five years on these meds in healthy, active women. These bad drugs are linked to esophageal cancer, necrosis of the jaw, heartburn, abdominal pain, fever, bone and muscle pain, low energy and low levels of calcium in the blood.
The treatment with the drug Infuse for bone growth, causes the overall cancer risk (including pancreatic) to shoot up by more than 250 percent in one year and 500 percent by three years. Infuse also gives about 50 percent of patients the “side effects” of infection, male sterility, pain, bone loss, and unwanted bone growth.
The most damning vaccination study not publically disclosed to date
Wednesday, August 15, 2012 by: Paul Fassa
Japanese study summary
Here’s the conclusion quoted from the Kobe University study’s journal report:
“Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organize criticality.” (Emphasis added.)
The initial purpose of this independently funded study was to understand how autoimmune diseases develop from autoimmunity. It was not an effort to prove vaccination safety or danger.
The researchers used mice that were bred to avoid autoimmune diseases and injected them with solutions that contain antigens. Antigens generate antibodies to protect against invading disease pathogens. Antibodies can turn against the host if they become self generated, causing autoimmune diseases.
A vaccination injects cultured vaccine antigens of weakened or dead viruses to create an immune response of antibodies to that antigen, supposedly for creating immunity to that particular disease.
It’s not very unusual for cytokine storms (immune system overreactions) to overwhelm one who has been vaccinated. Vaccine adverse reactions have caused injuries of permanent disability, autism spectrum disorders, or death more often than publicly disclosed.
The Kobe researchers injected the mice that were bred to not develop autoimmune diseases repeatedly with antigens, much like vaccinations are administered to infants and children, to study how an immune system could turn on itself to create autoimmune diseases.
They were pushing the mice’s immune systems to see if and when they would no longer bend, but break. They used Staphylococcus entertoxin B (SEB) as their injected antigens.
The study report did not mention including any toxic adjuvants or preservatives such as mercury, aluminum, or formaldehyde used in vaccines. Antigens were used without the toxic additives normally used in vaccinations.
After seven injections the mice recovered each time with their immune systems intact. But after the eighth injection, problems with key immunity cells began arising.
Damaged cells were observed microscopically and showed signs of early autoimmunity. Their immune systems had started to self generate antibodies for autoimmune reactions after repeated antigen inoculations. (Source below)
FDA drug reviewer: ‘one manager threatened my children’
Wednesday, August 15, 2012 by: Jon Rappoport
Cavanaugh reviewed new drug applications made to the FDA by pharmaceutical companies. He was one of the holdouts at the Agency who insisted that the drugs had to be safe and effective before being released to the public.
But honest appraisal wasn’t part of the FDA culture, and Cavanaugh swam against the tide, until he realized his life and the life of his children was on the line.
What was his secret task at the FDA? “Drug reviewers were clearly told not to question drug companies and that our job was to approve drugs.” In other words, rubber stamp them. Say the drugs were safe and effective when they were not.
Cavanaugh’s revelations are astonishing. He recalls a meeting where a drug-company representative flat-out stated that his company had paid the FDA for a new-drug approval. Paid for it. As in bribe.
He remarks that the drug pyridostigmine, given to US troops to prevent the later effects of nerve gas, “actually increased the lethality” of certain nerve agents.
Cavanaugh recalls being given records of safety data on a drug—and then his bosses told him which sections not to read. Obviously, they knew the drug was dangerous and they knew exactly where, in the reports, that fact would be revealed.
Read the entire landmark interview for yourself and see what the FDA really is. We are not dealing with isolated incidents of cheating and lying. We are not dealing with a few isolated bought-off FDA employees. The situation at the FDA isn’t correctable with a few firings. This is an ongoing criminal enterprise, and any government official, serving in any capacity, who has become aware of it and has not taken action, is an accessory to mass poisoning of the population.
Twelve years ago, the cat was let out of the bag. Dr. Barbara Starfield, writing in the Journal of the American Medical Association, on July 26, 2000, in a review titled, “Is US health really the best in the world,” exposed the fact that FDA-approved medical drugs kill 106,000 Americans per year.
Eli Lilly admits to more than $200 million dollars worth of doctor payoffs
Wednesday, August 15, 2012 by: Willow Tohi
A history of questionable ethics
Beginning in 2012, all drug and medical device companies will be required to report their promotional expenditure numbers to the federal government, but several companies started disclosing their information in 2009. According to the disclosed information, last year Eli Lilly paid out more than $200 million in payments to doctors and healthcare providers for promoting their drugs. ProPublica.org’s Dollars for Docs database is tracking 11 other companies’ disclosures as well.
The reason this information has been disclosed in Eli Lilly’s case is because Eli Lilly was involved in a criminal settlement, and was ordered to disclose these payments, since 2009. They agreed to pay $1.4 billion to settle criminal and civil allegations of promoting drugs for unapproved uses. An official from the FDA testified in a court of law that Eli Lilly concealed the risks of its schizophrenia drug Zyprexa from U.S. officials, knowing the serious health risks it caused. They defrauded Medicare/Medicaid and blatantly put profit over the concern of the consumer.
The disclosure documents say the payments were for speaking, consulting, and research, as well as travel and meal reimbursement. You can look up the breakdown of the payments; how much was paid into your state, if your doctor was among those paid. The data provides insights into how firms adapt their strategies over time, even though complete analysis has proved challenging. So few companies report their data, and the data that is reported is inconsistent in both content and format. Its unclear exactly how much money is being spent where, and by whom. Needless to say, there will be more on this story in the future.
The transparency of the newly required disclosures has some companies reevaluating the current strategy. Most of the pharmaceutical giants have begun to reduce their promotional expenditures, since they started disclosing the figures. Most of them offer explanations such as, “normal year-to-year fluctuations.” Experts predict physicians will begin backing away from these arrangements as well, as the increased scrutiny of the pharmaceutical sales practices also exposes their names and pay. Some doctors are raking in a quarter of a million dollars, but actually claim they “wouldn’t want the appearance of being influenced by anything the company gave” them. Interesting choice of words, huh?
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