Quotes & Sayings About Fda

A biologist with a history of tooth decay invents a symbiotic microbe which lives in the human mouth and feeds by cleaning our teeth. It secreted calcium, which is poisonous to it, controlling its growth and preventing it from eating the teeth themselves. So this guy, he wants to spread the thing to the world, but it'd never fly, FDA and human squeamishness and all, so he becomes a party animal. He throws wild partys at the lab, kisses female grad students, where's, babies. He backwashes in sodas left on tables. He bums drags of cigarettes. He grants humanity eternally clean and healthy teeth but dies of a terrible cocktail of STDs. — James Curcio

What about the FDA? Please, are you serious? Back then the FDA was one of the most underfunded, mismanaged organizations in the country. I think they were still high-fiving over getting Red No. 218 out of M&Ms. — Max Brooks

If you go to the FDA with a drug that's only meant to treat 50 people, and it's a 95 percent cure rate, you'll get your drug approved. — Leroy Hood

Dean Burk, PhD, of the National Cancer Institute (head of their Cytochemistry Section and 32-year veteran at the agency) declared in a (May 30,1972) letter to (congressman Louis Frey, Jr.) that high officials of the FDA, AMA and ACS (American Cancer Society), were deliberately falsifying information, literally lying ... and in other ways thwarting potential cancer cures to which they were opposed. — Barry Lynes

I think that the FDA has not been able to catch some of these things as quickly as I expect them to catch. And so we're gonna be doing a complete review of FDA operations ... at bare minimum, we should be able to count on our government keeping our kids safe when they eat peanut butter ... that's what Sasha eats for - for lunch - probably three times a week. — Barack Obama

2. One of the governmental agencies responsible for the cosmetics industry is the FDA, but it doesn't review cosmetics before they go on the market, it can't recall a product if there's a problem, and it has banned only about a dozen toxic chemicals from beauty products, compared with the more than 1,300 that are banned in the European Union. — Anonymous

Consider the clinicaltrials by which drugs are tested in human subjects.5 Before a new drug can enter the market, its manufacturer must sponsor clinicaltrials to show the Food and Drug Administration that the drug is safe and effective, usually as compared with a placebo or dummy pill. The results of all the trials (there may be many) are submitted to the FDA, and if one or two trials are positive - that is, they show effectiveness without serious risk - the drug is usually approved, even if all the other trials are negative. — Marcia Angell

The ... experts of the FDA have declared Laetrile to be worthless ... quackery and fraud ... These experts are the professional descendants of experts ... confident that mental illness should be cured by drilling holes in the skull, the better to let the demons out ... This is the Orwellian fashion in which the medical establishment throws its weight around ... — James J. Kilpatrick

FDA, which regulates the safety of vegetables, doesn't have those kinds of rules because Congress doesn't want it to. It's not that the vegetables themselves have anything wrong with them; it's that they're contaminated with animal manure. One of the rationales for a single food safety agency is that you can't separate animals from vegetables. — Marion Nestle

doctors & druggists wash each other's hands — Geoffrey Chaucer

I think FDA's concerns are patient-safety. — Dilip Shanghvi

The FDA and the EPA are supposed to be protecting us, not the people who make the poison. — Kenneth Eade

It's a terrible thing that we cannot really trust the FDA or NCI (National Cancer Institute). We need, therefore, an independent scientific investigation. — Paul Douglas

In 15 years, we've raised $225 million, sequenced the myeloma genome, and opened 45 trials of 23 drugs - six approved by the FDA - which have doubled the life span of multiple myeloma patients. I've taken both Velcade and Revlimid, which we helped develop. — Kathy Giusti

The food industry, its trade associations, and research foundations, is well financed and highly organized to pressure the FDA. — Ralph Nader

The FDA is redefining birth control as abortion. The FDA is setting the bar higher for this kind of drug. — Patty Murray

And thirdly, the FDA occasionally does some genuine public good with whatever energies it has left over after serving the vested political and commercial interest of its first two activities. — G. Edward Griffin

Today's political leaders demonstrate their low opinion of the public with every social law they pass. They believe that, if given the right to chose, the citizenry will probably make the wrong choice. Legislators do not think any more in terms of persuading people; they feel the need to force their agenda on the public at the point of a bayonet and the barrel of a gun, in the name of the IRS, the SEC, the FDA, the DEA, the EPA, or a multitude of other ABCs of government authority. — Mark Skousen

The field of U.S. cancer care is organized around a medical monopoly that ensures a continuous flow of money to the pharmaceutical companies, medical technology firms, research institutes, and government agencies such as the Food and Drug Administration (FDA) and the National Cancer Institute (NCI) and quasi-public organizations such as the American Cancer Society (ACS). — John Diamond

You wouldn't believe how many FDA officials or relatives or acquaintances of FDA officials come to see me as patients in Hanover. You wouldn't believe this, or directors of the AMA, or ACA, or the presidents of orthodox cancer institutes. That's the fact — Hans Alfred Nieper

I think every doctor should know the shocking state of affairs ... We discovered they (the FDA) failed to effectively regulate the large manufacturers and powerful interests while recklessly persecuting the small manufacturers ... (The FDA is) harassing (small) manufacturers and doctors ... (and) betrays the public trust. — Edward V. Long

The FDA is now warning people not to eat raw cookie dough this holiday season. Is that how fat we're getting in this country? Our ovens are too slow now? — Jay Leno

However, because of the great marketing hype surrounding the SSRIs, one of them, Prozac, now has the distinguished honor of having more adverse effects submitted to the FDA than any other drug in history. More than 40,000 adverse reactions were reported in its first ten years on the market. No other drug even comes close (Breggin and Cohen 67). — Gwen Olsen

Though the industrial logic that made feeding cattle to cattle seem like a good idea has been thrown into doubt by mad cow disease, I was surprised to learn it hadn't been discarded. The FDA ban on feeding ruminant protein to ruminants makes an exception for blood products and fat; my steer will probably dine on beef tallow recycled from the very slaughterhouse he's heading to in June. — Michael Pollan

When the FDA announced its intentions to join other countries and ban quinolone use on U.S. chicken farms, the drug manufacturer Bayer initiated legal action that successfully delayed the process for five years. — Michael Greger

Unfortunately, beer was only a short-term answer. And head transplants had yet to be approved by the FDA. — J.R. Ward

There had been a head of the FDA (who later turned out to be a fraud) his name was Fishbein and he was rampantly opposed to any alternative therapy. He went after Hoxsey, the Hoxsey therapy back in the 1940's and 50's, and destroyed Hoxsey. But not before Hoxsey sued the AMA and Fishbein and [proved] that the therapy actually worked. But it didn't help him because they closed him down anyhow — Gary Null

Our analyses of the FDA data showed relatively little difference between the effects of antidepressants and the effects of placebos. Indeed, the effects were so small that they did not qualify as clinically significant. The drug companies knew how small the effect of their medications were compared to placebos, and so did the FDA and other regulatory agencies. The companies found various ways to make the data seem more favorable to their products, and the FDA helped them keep their negative data secret. In fact, in some instances, the FDA urged the companies to keep negative data hidden, even when the companies wanted to reveal them. My colleagues and I hadn't really discovered anything new. We had merely revealed their 'dirty little secret'. — Irving Kirsch

Over the past two decades the pharmaceutical industry has moved very far from its original high purpose of discovering and producing useful new drugs. Now primarily a marketing machine to sell drugs of dubious benefit, this industry uses its wealth and power to co-opt every institution that might stand in its way, including the US Congress, the FDA, academic medical centers, and the medical profession itself. — Marcia Angell

You may have difficulty in obtaining some of these (non-drug) therapies..because the FDA has literally pressured Congress, under the guise of protecting the public, to keep time-honoured cultural and natural therapies out of the hands of the general public. If you look at the record of the FDA, it becomes obvious they are serving interests other than yours and mine. — Robert Willner

There's a certain libertarian right-wing view that there should be no FDA, that people can decide for themselves whether medicines are safe and effective. That's nonsense. Most people don't have the expertise or the resources to mount a proper study to find out whether a treatment is safe or effective. — Marcia Angell

22 of 52 top (FDA) officials have worked for regulated industries, or organizations that cater to those industries ... During a hearing held in 1969 by the House Inter-governmental Relations Subcommittee, it was disclosed that of 49 high ranking FDA officials who had recently resigned or retired, 37 joined or served as consultants to regulated industries. — Michael F. Jacobson

If a drug failed as often and had as many side effects as western marriage, the FDA probably would not approve it. — Ron Davison

If a State has reliable scientific information that demonstrates that a warning is needed for a particular food, then in the interest of public health, it should share that information with the FDA and petition for a new national standard. — Nathan Deal

Treating only terminal cancer patients, the Rand (anti-cancer) vaccine produced objective improvement in 35% of 600 patients while another 30% demonstrated subjective improvement. FDA stopped the vaccine's use in a federal court hearing where neither the cancer patients nor their doctors were allowed to testify. — Barry Lynes

The simple truth is, the short-term solution is for the FDA to allow more importation of safe vaccines from other nations. But the long-term solution is to get more vaccine production within the U.S. — Larry Craig

Everyone should know that the 'war on cancer' is largely a fraud. — Linus Pauling

It's time to get the FDA to reverse its 1994 decision not to label GM foods. — Marion Nestle

There's always something that's going to kill us all. A few years ago, tomatoes were going to kill us and a few years before that it was spinach. The FDA is run by a 7-year-old kid that hates vegetables! — Alonzo Bodden

I have smuggled so many ingredients across so many borders, like shallot confit from Thailand, or a new sauce from New Orleans not approved by the FDA. — Blake Lively

5-Hour Energy is not an energy drink, it's a focus drink. But we can't say that. The FDA doesn't like the word 'focus.' I have no idea why. — Manoj Bhargava

The FDA and much, but not all, of the orthodox medical profession are actively hostile against vitamins and minerals ... They are out to get the health food industry ... And they are trying to do this out of active hostility and prejudice. — William Proxmire

I think you know how it works, Senator. The big chemical companies fill the coffers of one of your colleagues who is a lawmaker from an agricultural state such as, well, let's take Iowa, for example, and the lawmaker recommends the president to install industry executives in high positions, such as the head of the FDA or the EPA, and, this way, the industry can approve its own products without safety testing. — Kenneth Eade

Labor law violations are alive and well in the USA. — Steven Magee

The FDA protects the big drug companies, and is subsequently rewarded, and using the government's police powers, they attack those who threaten the big drug companies. People think that the FDA is protecting them. It isn't. What the FDA is doing, and what the public thinks it is doing are as different as night and day. — Herbert L. Ley Jr.

For many years there have been treatments available which are successful and usually NOT harmful for diseases, such as AIDS, cancer, cystic fibrosis, diabetes, organ regeneration and other diseases. One by one these treatments and their creators or proponents have been targeted by the FDA, which I call the "office of orthodoxy enforcement," illegally using just powers derived from the consent of governed. These forms of tyranny are always accompanied by multi agency intrusions or harassment, confiscation of private medical files, censorship of written materials and threats or prosecution. — Charles C. Pixley

The FDA calls certain substances "controlled." But there are no "controlled substances," there are only controlled citizens. — Thomas Szasz

The FDA has formed a rapid response team. — Andrew Von Eschenbach

They're putting cement dust into cattle feed to make the cows heavier; the FDA knows all about it. — Dick Dale

When birth control pills were available in Europe but not in the United States, American women created an uproar about how the unwillingness to make the pill available showed a contempt for the lives of women ... When the Food and Drug Administration (FDA) released birth control pills with high dosages of hormones that were later found to be unnecessarily high, they were attacked for not caring about women enough to do the necessary tests. — Warren Farrell

When the FDA forces an old drug off the market, patients have very little say in the matter. Patients have even less of a say when the FDA chooses not to approve a new drug. Instead, we are supposed to rely on the FDA's judgment and be grateful. But can the FDA really make a choice that is appropriate for everyone? Of course not. — Alex Tabarrok

The rationale for the FDA's rigid standards is to avoid the sale of a drug like thalidomide. But the unintended consequence is almost certainly to allow many more people to die prematurely than would have died from side-effects under a less restrictive regime. We count and recount the costs of such side-effects. We do not count the costs of not allowing new drugs to be made available. — Niall Ferguson

It disturbs me mostly ... is the willful, deliberate denial (by the FDA, of) our own citizens, a fair chance to use Laetrile, when all the record (shows) it is not toxic, ... is safe, ... and is effective. — Luther L. Bohanon

For the first time since 2007, the FDA Has approved a new device to treat obesity. The amazing breakthrough is called a vegetable. — Conan O'Brien

I mean, how do you know if people are good for you or not? It's not like they come with an FDA approved sticker or anything. — Michael Thomas Ford

But perhaps the most alarming ingredient in a Chicken McNugget is tertiary butylhydroquinone, or TBHQ, an antioxidant derived from petroleum that is either sprayed directly on the nugget or the inside of the box it comes in to "help preserve freshness." According to A Consumer's Dictionary of Food Additives, TBHQ is a form of butane (i.e. lighter fluid) the FDA allows processors to use sparingly in our food: It can comprise no more than 0.02 percent of the oil in a nugget. Which is probably just as well, considering that ingesting a single gram of TBHQ can cause "nausea, vomiting, ringing in the ears, delirium, a sense of suffocation, and collapse." Ingesting five grams of TBHQ can kill. — Michael Pollan

However, FDA attempted to reverse this clear congressional intent in March, 1979, by proposing to regulate vitamins and minerals as 'Over-The-Counter' drugs.. — Orrin Hatch

And here's the kicker: food manufacturers are using a gasoline additive known as hexane to process soy products (and some vegetable oils). Soybeans are soaked in large vats of hexane to assist in the extraction of substances such as protein and oils from them. An independent lab has found hexane residue in soy-based foods, but the FDA does not require any testing for hexane, even in baby foods. It is used by the food industry because it is cheap to do so and because the FDA lets them get away with it. The soy industry is incredibly powerful and influential. The U.S. Environmental Protection Agency lists hexane, incidentally, as a hazardous chemical. — Nora T. Gedgaudas

If end-of-life discussions were an experimental drug, the FDA would approve it. — Atul Gawande

You can't treat an illness with cosmetic surgery, and that's why it would be great if there were qualified therapists in plastic surgeons' offices, and that people would go to a therapeutic meeting before plastic surgery. I think that should be part of the FDA requirement. — Sharon Stone

The FDA just ordered them off the market. The glaze is supposed to be poison - provided you drink at least forty cups of tea out of one of them every day of your life for twenty years. — Frederik Pohl

Coke and Pepsi, with the acquiescence of the FDA, are needlessly exposing millions of Americans to a chemical that causes cancer, — Michael F. Jacobson

According to an article in the Washington Post: The Food and Drug Administration has repeatedly urged antidepressant manufacturers not to disclose to physicians and the public that some clinical trials of the medications in children found that drugs were no better than sugar pills, according to documents and testimony released at a congressional hearing yesterday. Regulators supressed the negative information on the grounds that it might scare families and physicians away from the drugs, according to testimony by drug company executives. For at least three medications, they said, the FDA blocked the companies' plans to reveal the negative studies in drug labels. — Irving Kirsch

Food safety oversight is largely, but not exclusively, divided between two agencies, the FDA and the USDA. The USDA mostly oversees meat and poultry; the FDA mostly handles everything else, including pet food and animal feed. Although this division of responsibility means that the FDA is responsible for 80% of the food supply, it only gets 20% of the federal budget for this purpose. In contrast, the USDA gets 80% of the budget for 20% of the foods. This uneven distribution is the result of a little history and a lot of politics. — Marion Nestle

We have the opportunity to provide the first FDA reviewed and approved over-the-counter option that can help people lose weight and make changes to their lifestyle and diet. — Steve Burton

The FDA, NCI and ACS, and the large treatment centres work to eliminate choice of cancer therapies, particulary better ones. They openly attack breakthroughs made by "mavericks", which they define as anyone outside their ranks. Folks, any serious study of how these entities work together to destroy hopeful approaches to cancer reveals a trail of corruption, conspiracy, dishonesty, and inhumanity that warrants desigantion of evil ... We continue to use them not because they work, but because those who perform them have so vigorously eliminated any other choice. — Julian Whitaker

My manager says we've been working with the FDA on this. — Carlos Gonzalez

There is a nationwide shortage of drugs for Attention Deficit Disorder. The FDA says they're not sure how it happened. I guess somebody wasn't paying attention. — Jay Leno

Since the 1920s, virtually all continuing medical and public health education is funded by pharmaceutical companies. In fact, today, the FDA can't even tell health scientists the truth about vaccine contaminants and their likely effects. The agency is bound and gagged by proprietary laws and non-disclosure agreements forced upon them by the pharmaceutical industry. Let us not forget that the pharmaceutical industry, as a special interest group, is the number one contributor to politicians on Capital Hill. — Leonard Horowitz

the FDA's own Web site states that "dental amalgams contain mercury, which may have neurotoxic effects on the nervous systems of children and developing fetuses. When amalgam fillings are placed in teeth or removed from teeth, they release mercury vapor. Mercury vapor is also released during chewing. — Lindsey Biel

We need to get the government out of the way. Inflation hits the middle class and the poor the most. Those are the people who are losing it. We don't have enough competition. There's a doctor monopoly out there. We need alternative health care freely available to the people. They ought to be able to make their own choices and not controlled by the FDA preventing them to use some of the medications. — Ron Paul

The public properly relies upon FDA classification of drugs as nonprescription as a reflection of the agency's judgment regarding the safety and proper use of a drug without a doctor's prescription. — Loretta Lynch

I've heard drug experts say they believe if penicillin were discovered today, the FDA wouldn't license it. — Ronald Reagan

The sad irony here is that the FDA, which does not regulate fluoride in drinking water, does regulate toothpaste and on the back of a tube of fluoridated toothpaste ... it must state that "if your child swallows more than the recommended amount, contact a poison control center."
The amount that they're talking about, the recommended amount, which is a pea-sized amount, is equivalent to one glass of water.
The FDA is not putting a label on the tap saying don't drink more than one glass of water. If you do, contact a poison center ...
There is no question that fluoride - not an excessive amount - can cause serious harm. — Paul Connett

FDA clearance is an important step on the path towards getting genetic information integrated with routine medical care. — Anne Wojcicki

And so far, their most recent results had been perfect. Their meetings in Germany and Switzerland had gone brilliantly. The testing done in their laboratories there was even more rigorous than what had been done in the States. They were sure now. It was safe. They could move ahead to Phase One Human Trials, as soon as the FDA approved it, which meant giving low doses of the medication to a select number of willing, well-informed subjects, and seeing how they fared. — Danielle Steel

The Law waits for you to stumble on a mode of being, a soul different from the FDA-approved purple-stamped standard dead meat - & as soon as you begin to act in harmony with nature the Law garottes & strangles you - so don't play the blessed liberal middleclass martyr - accept the fact that you're a criminal & be prepared to act like one. — Hakim Bey

Secondly, as a result of this political favoritism, the FDA has become a primary factor in that formula whereby cartel-oriented companies in the food and drug industry are able to use the police powers of government to harass or destroy their free-market competitors. — G. Edward Griffin

Wilson-Donovan had already submitted their application to the FDA in January, months before. Based on the information they were developing now, they were going to ask for Vicotec to be put on the "Fast Track," pressing ahead with human trials of the drug, and eventually early release, once the FDA saw how safe it was and Wilson-Donovan proved it to them. The "Fast Track" process was used in order to speed the various steps toward approval, in the case of drugs to be used in life-threatening diseases. Once they got approval from the FDA, they were going to start with a group of one hundred people who would sign informed consent agreements, acknowledging the potential dangers of the treatment. They were all so desperately ill, it would be their only hope, and they knew it. The people who signed up for experiments like this were — Danielle Steel

When Iran starts to regulate USA nuclear facilities, it will be a step in the right direction for the safety and security of 300 million people. — Steven Magee

Even to this day, the government, the FDA is refusing to use the sophisticated biotechnology to evaluate the contaminants in the vaccines such as the polio vaccines that they are administering. I think (people) would be appalled that some of the vaccines that are currently being used are still laced with viruses. — Leonard Horowitz

If the FDA would spend a little less time and effort on small manufacturers of vitamins ... and a little more on the large manufacturers of ... dangerous drugs ... , the public would be better served. — Russell B. Long

I have no faith in the USA corporate government systems of protection of public health and safety. — Steven Magee

RBGH poses an even greater risk to human health than ever considered. The FDA and Monsanto have a lot to answer for. Given the cancer risks, and other health concerns, why is rBGH milk still on the market? — Samuel Epstein

By giving the FDA adequate resources and authority to both prevent outbreaks and intervene once they appear, we can support the administration's efforts to reassure the parents of America that the food they feed their children is the product of the safest system in the world. — Diana DeGette

If these restrictions were necessary, the FDA would have promulgated them in the first place, ... The FDA knows how to evaluate scientific information. Congress knows nothing about that. — Gloria Feldt

In other words, our decision making in medicine has failed so spectacularly that we have reached the point of actively inflicting harm on patients rather than confronting the subject of mortality. If end-of-life discussions were an experimental drug, the FDA would approve it. Patients — Atul Gawande

Some of the FDA's own scientists have charged that politics, not science, is behind the FDA's actions. — Joseph Crowley

As was noted in the Wall Street Journal, last March 21st, FDA approval of drug labelling, ' ... requires seven to ten years, and costs each applicant an average of $70 million.' — Orrin Hatch

Wilson-Donovan wanted to move ahead as quickly as possible to clinical trials on patients, which was why it was so important to test Vicotec's safety now before the FDA hearings in September, which would hopefully put it on the "Fast Track." Peter was absolutely sure that the testing being concluded by Paul-Louis Suchard, the head of the laboratory in Paris, would only confirm the good news he had just been given in Geneva. — Danielle Steel

Over the years, HIV/AIDS activists and their allies have been pioneers in creating new frontiers in the medical establishment. Through their efforts, the FDA drug approval procedures were reformed so promising new therapies could reach desperate patients quicker. — David Mixner

Only the big food manufacturers have the wherewithal to secure FDA-approved health claims for their products and then trumpet them to the world. Generally, it is the products of modern food science that make the boldest health claims, and these are often founded on incomplete and often bad science. — Michael Pollan

In 2004, the FDA urged drug companies to adopt a 'Don't ask, don't tell' policy with respect to their clinical-trial data showing that antidepressants are not better than placebos for depressed children. If the data were made public, they cautioned, it might lead doctors to not prescribe antidepressants. The FDA believed that the jury was still out on antidepressants for children. Even if the clinical trials show negative results, an FDA spokesperson was reported to have said to a Washington Post reporter, it doesn't mean that the drugs are ineffective. The assumption seems to have been that doctors should prescribe medications that have not been shown to work, until it has been proven that they don't work. — Irving Kirsch

Remember, FDA employees are serious about fear. We pay these people to panic about an iota of rodent hair in our chili, even when the recipe calls for it. FDA employees are first-class agonizers, world champions at losing sleep. When Meryl Streep got hysterical about Alar, they actually checked the apples instead of Meryl's head. — P. J. O'Rourke

The FDA has received over a million comments from citizens demanding labeling of GMOs. 90 percent of Americans agree. So, why no labeling? — Dennis Kucinich

The harm done by the FDA does not result from defects in the people in charge - unless it be a defect to be human. Many have been able and devoted civil servants. However, social, political, and economic pressures determine the behavior of the people supposedly in charge of a government agency to a far greater extent than they determine its behavior. No doubt there are exceptions, but they are rare - almost as rare as barking cats. That does not mean that effective reform is impossible. But it requires taking account of the political laws governing the behavior of government agencies, not simply berating officials for inefficiency and waste or questioning their motives and urging them to do better. The — Milton Friedman

The government has a monopoly on the supply of marijuana that you can use in FDA-approved research. So even though there are 20 states and the District of Columbia [that have legalized medical marijuana], and there's marijuana everywhere, we've spent seven years trying to get 10 grams of marijuana for vaporizer research. We're the only people in America that can't get 10 grams of marijuana. — Rick Doblin

At FDA, our mission is to promote and protect the health of the public. As commissioner, I've worked hard to galvanize people around that idea. I want employees to be thinking about the unique and essential contribution they are making to our mission. — Margaret Hamburg

If you're trying to develop a new drug, that costs you a billion dollars to get through the FDA. If you want to start a software company, you can get started with maybe $100,000. — Peter Thiel

Such letters ... from the FDA, are, filled with objectively demonstrable lies, practiced deceptions and deviousness, red herrings, directed misinformation, misdirected information, etc ... Once FDA-NCI-AMA-ACS ... concedes that Laetrile anti-tumor efficacy was indeed even once observed ... a permanent crack in bureaucratic armor has taken place. — Dean Burk