Mike Adams, the Health Ranger
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 I wonder what interested phrases might be found by reordering the letters in, "Food and Drug Administration?" To find out, I used various online anagram generators and scoured the results to come up with these interesting FDA anagrams:
Anagrams for "Food and Drug Administration"
SAD NATION FROM DRUG ADDITION
(Note that by throwing in an extra "C" this could read "addiction" instead of addition.)
If you throw in an extra "C" you also get:
DRUG ADS FORM ADDICTION NATION
(The FDA legalized TV drug ads in 1998. |
| To determine that, you don't need any hidden letter patterns -- all you need to do is watch what the FDA openly says and does, and from there, it's easy to realize the food and drug Administration has become a pro-pharma organization that poses a very real danger to the public.
That's why people in the know refer to it as the "Fraud and Drug Administration." And while we're playing games with the FDA letters, the agency itself is playing games with the lives of Americans. That's why I think the whole agency should be renamed to a new, more accurate name: THE PHARMA BOOSTER CLUB! |
| To find out, I used various online anagram generators and scoured the results to come up with these interesting FDA anagrams:
Anagrams for "Food and Drug Administration"
SAD NATION FROM DRUG ADDITION
(Note that by throwing in an extra "C" this could read "addiction" instead of addition.)
If you throw in an extra "C" you also get:
DRUG ADS FORM ADDICTION NATION
(The FDA legalized TV drug ads in 1998.)
Here are some more anagrams that use no extra letters:
DID NOT ADD SUGAR INFORMATION
(A fairly accurate description of the FDA's enforcement of food labeling laws. |
Mike Adams, the Health Ranger
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 Amendment to Bill S1082
Purpose of the amendment:
The bill, S1082: The food and drug Administration Revitalization Act, is hereby amended to eliminate any reference to the terms food or food ingredients, such that food and food ingredients will not be subject to any jurisdiction or control by the Reagan-Udall Foundation for the food and drug Administration.
Intent of amendment:
To eliminate from the bill any possibility that food or food ingredients would be treated like drugs either for safety review purposes or for assessment of their efficacy. |
Mike Adams, the Health Ranger
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 Food and Drug Administration (FDA) with a name that more accurately reflects the demonstrated aims of the agency. The FDA's reputation is in shambles this year, following the public revelation that the agency was aware of the dangers of heart-damaging medications years ago, yet failed to warn the public or pull the drugs from the market. The agency even went so far as to censor its own drug safety scientists who were attempting to warn the public about the dangers of antidepressant drugs and anti-inflammatory drugs. Accordingly, the agency has earned itself a new name. |
Mike Adams, the Health Ranger
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| Proposed amendment to S1082:
"The bill, S1082, is hereby amended to eliminate any reference to the terms food or food ingredients within Subtitle B - Reagan-Udall Foundation for the food and drug Administration, such that food and food ingredients will not be subject to any jurisdiction or control by the Reagan-Udall Foundation for the food and drug Administration."
Intent of amendment:
To eliminate from the bill any possibility that food or food ingredients would be treated like drugs either for safety review purposes or for assessment of their efficacy. |
Mike Adams, the Health Ranger
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| Keep Taking Action -- Revised sample letter
Anti S.1082 food and drug Revitalization Act
May 5, 2007
The Honorable (Senator First and Last Name)
[insert their address here]
Dear Senator Last Name;
The issue of drug safety and access to drugs at a fair price is of the utmost importance to myself and all Americans. In general, I am opposed to Senate bill S1082: food and drug Administration Revitalization Act, as it does not go far enough to protect myself and my family from the dangers of drugs. |
Mike Adams, the Health Ranger
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 There is nothing resembling public safety still operating at the food and drug Administration anymore.
Add aspartame to the FDA's Hall of Shame, right alongside Vioxx, Rezulin and the ordered destruction of recipe books that dared to mention the stevia herb as an ingredient. It's just one more way in which the FDA continues to betray the American people and subject them to life-threatening ingredients that any honest food and drug Administration would have banned long ago. |
Mike Adams, the Health Ranger
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| Amendment to Bill S1082
Purpose of the amendment:
The bill, S1082: The food and drug Administration Revitalization Act, is hereby amended to eliminate any reference to the terms food or food ingredients, such that food and food ingredients will not be subject to any jurisdiction or control by the Reagan-Udall Foundation for the food and drug Administration.
Intent of amendment:
To eliminate from the bill any possibility that food or food ingredients would be treated like drugs either for safety review purposes or for assessment of their efficacy. |
Mike Adams, the Health Ranger
See article keywords and concepts |
| Sample letter
Anti S.1082 food and drug Revitalization Act
May 2, 2007
The Honorable (Senator First and Last Name)
(List their address here)
Dear Senator Last Name; The issue of drug safety and access to drugs at a fair price is of the utmost importance to myself and all Americans. In general, I am opposed to Senate bill S1082: food and drug Administration Revitalization Act, as it does not go far enough to protect myself and my family from the dangers of drugs. |
Mike Adams, the Health Ranger
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 They reveal the food and drug Administration to be alarmingly out of touch with the concerns of the American people. Some of the most interesting results include:
96 percent agreed the government should have the power to require warning labels on drugs with known safety problems. As Consumer Reports explains, "Right now, the food and drug Administration must negotiate safety warning labels with a drug maker."
84 percent agree that drug companies have "too much influence over the government officials who regulate them. |
| REPPED: More than four out of five Americans think drug companies have too much influence over the food and drug Administration, and 84 percent believe that advertisements for prescription drugs with safety concerns should be outlawed, reveals a striking new survey from Consumer Reports.
The survey results, released today, are based on a telephone survey of 1,026 American adults conducted by the Consumer Reports National Research Center. They reveal the food and drug Administration to be alarmingly out of touch with the concerns of the American people. |
Mike Adams, the Health Ranger
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| Amendment to Bill S1082
Purpose of the amendment: The bill, S1082: The food and drug Administration Revitalization Act, is hereby amended to eliminate any reference to the terms food or food ingredients, such that food and food ingredients will not be subject to any jurisdiction or control by the Regan-Udall Foundation for the food and drug Administration.
Intent of amendment: To eliminate from the bill any possibility that food or food ingredients would be treated like drugs either for safety review purposes or for assessment of their efficacy. |
Craig Pepin-Donat
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 The food and drug Administration (FDA), drug manufacturers and traditional health care providers have purposely chosen to mask the symptoms rather than provide real solutions that could eliminate self-inflicted conditions before they damage us. The FDA, which could do so much more to protect people, has a curious way of dealing with the health issues of the twentieth-first century. |
Andreas Moritz
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 In July 2007, the U.S. food and drug Administration—believe it or not—gave Derma Sciences, a New Jersey-based manufacturer of wound-care products, clearance to sell Manuka wound and burn dressings as medical devices. Now Manuka honey can officially be used in wound and burn care in the United States. Manuka honey has already been used as wound dressing for several years in Great Britain, Australia, and its native New Zealand. Canada also approved it for use as an antimicrobial dressing in early 2007. |
| According to a report published in the New England Journal of Medicine (October 15, 2004), the two stents that are currently approved by the food and drug Administration (FDA), the Cordis Cypher sirolimus-eluting stent and the Boston Scientific Taxus Express paclitaxel-eluting stent, have been associated with highly publicized adverse events after they were approved for marketing.
Bypass, angioplasty and stent operations are really not about preventing heart attacks per se. The obvious purpose of these procedures is symptom relief. |
| Researchers from the American food and drug Administration discovered that vaccinations, particularly the hepatitis B shot, could cause hair loss. They estimate that 50,000 Americans suffer hair loss (alopecia) after immunization every year. The report was published by the Journal of the American Medical Association in 1997.
It is nearly impossible to estimate the damage and suffering that has been created and will occur in the future as a result of inadequate information about the dangers of modern immunization programs. |
| In the United States, BST was licensed by the American food and drug Administration (FDA) in 1994. This effectively gave farmers the legal permission to treat their herds with the controversial hormone. The license was accompanied with a new labeling policy, previously unheard of in the United States. Traditional dairy farmers are prohibited from labeling their milk as "hormone free"—while those using the hormone are not required to say that they use BST. |
Bottom Line Health
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| Along with providing optimal nutrition, breast milk also provides compounds that boost babies' immune system and help protect them from bacteria, viruses and parasites, according to the US food and drug Administration (FDA). In addition, breast-fed children have lower rates of childhood illnesses and tend to be leaner than their formula-fed counterparts.
And research has shown that breast-feeding benefits mothers as well, by helping the body return to normal faster after pregnancy, according to the FDA. |
| Breakthrough: The US food and drug Administration (FDA) recently approved a new drug, exenatide (Byetta), for people who cannot adequately control glucose levels using other drugs. Taken by injection twice daily, it's called a "smart" drug because it stimulates the pancreas to produce insulin based on the level of blood sugar.
Exenatide mimics the effects of the intestinal hormone incretin, which is not produced adequately in diabetics. The drug slows stomach emptying.. .inhibits increases in postprandial glucose levels.. .and acts as an appetite suppressant. |
| Eszopiclone (Lunesta) was approved by the US food and drug Administration (FDA) in 2004. Research indicates that Lunesta may be the most effective nonbenzodiazepine for preventing nighttime waking. It lasts eight hours—two hours longer than Ambien—but it's still too soon to tell if daytime drowsiness is a commonly experienced side effect.
Best if you: Need help increasing the amount of time you sleep to a full seven or eight hours. BENZODIAZEPINES
This class of drugs includes temazepam (Re-storil), estazolam (ProSom), triazolam (Halcion) and flurazepam (Dalmane). |
Jonny Bowden, Ph.D., C.N.S.
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 But Lipitor is only approved by the food and drug Administration to reduce the risk of heart attack if you have multiple risk factors for heart disease, and its benefits are based largely on its supposed ability to lower cholesterol, which may or may not have anything to do with preventing cardiovascular events and death. In fact, if you read the small print on television ads for Lipitor a couple of years ago, you'd briefly see the following words flash on the screen in tiny letters: "Lipitor has not been shown to prevent heart disease or heart attacks. |
Craig Pepin-Donat
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| Sidney Wolfe, director of Public Citizen Health and Research Group, a non-profit consumer advocate organization, "In the 31 years that I've been monitoring the food and drug Administration...there have been an unprecedented number and percentage of drugs taken off the market, in many cases, drugs with known problems before they came on the market."12 Since every individual reacts differently it is important to know your own body, your allergies and how well you tolerate drugs. It's also important to follow dosage instructions. |
Jonny Bowden, Ph.D., C.N.S.
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| Questionable Safety Concerns
You used to be able to buy L-tryptophan as a separate nutritional supplement, but the food and drug Administration—in what I still believe to be an incredible act of bureaucratic stupidity— took it off the market around 1990 after an outbreak of eosinophilia myalgia syndrome (EMS), which was linked to the use of tryptophan.
EMS is a dangerous and potentially deadly blood disease that is usually associated with parasitic infections or severe allergy. |
Mike Adams, the Health Ranger
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 But I'm not in the aloe vera business, I'm in the business of helping people heal, and I will not censor the truth about the healing powers of aloe vera merely to appease a corrupt food and drug Administration that continues to censor and oppress information about the healing benefits of natural medicine.
Here's what I know about aloe vera's health benefits:
Aloe vera boosts immune function and destroys cancer tumors
Scientific research shows strong immunomodulatory and antitumour properties for aloe vera polysaccharides. |
Andreas Moritz
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| The American food and drug Administration (FDA) has labeled nitrosamines "one of the most formidable and versatile groups of carcinogens yet discovered." In other words, if you are a smoker or if you drink beer, wine, or tea and eat meat, you produce one of the most deadly toxins that can be found anywhere. As it turns out, most meat-eaters also drink wine or beer, and many of them smoke, too. |
Mike Adams, the Health Ranger
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| These changes, all contained in the amendment which was approved yesterday, make clear that there are no new dietary supplement requirements in the food and drug Administration Revitalization Act. It is my hope this will reassure the many who have expressed concern that Congress was inadvertently repealing Public Law 109-462.
The voice of the people has been heard. Let us not forget these promises nor let the FDA forget them -- as the questionable language regarding the Reagan-Udall Foundation for the FDA still remains. |
Marshall Editions
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 Ephedra has been banned for sale in the United States by The US food and drug Administration due to its potential to cause cardiovascular problems, such as heart attack and stroke. Despite this, many still believe it is safe when administered for right reason and in the right dose. Always consult a health professional about ephedra, and use this powerful natural product only under his or her guidance.
507
DIAGNOSIS
Bronchitis is an obstructive pulmonary disease. |
Mike Adams, the Health Ranger
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| That law authorizes a new program so that reports of serious adverse events related to the use of a dietary supplement or over-the-counter drug would be reported to the food and drug Administration, FDA, on a priority basis.
As I said, the Durbin amendment contemplates a new adulterated food registry. Under the provisions establishing that registry, reports of adulterated foods would be made by many, if not all, of the same parties who are required to file reports of serious adverse events associated with the use of dietary supplements under Public Law 109-462. |
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