Cherry Investigation

I do not try to make jokes, what I do for a good roll on the floor every now and then just watch what the government is then to report just the facts. Consider the latest debacle or a bad joke, you, the FDA is trying to play on the public. The FDA has now said that the good old healthy cherries are eaten by millions of people for millennia, according to the FDA, unapproved drug! Tut, these are the same people who said eggs is bad for you 20 years ago.

1999 according to a report

According to a report of substantiated "Journal of natural products" in 1999, the facts bore out tart cherries less pain relief 33% better than the anti-inflammatory drugs and aspirin.

It's known for years for people who suffer from gout who consumed up to three liters more than three days to get rid of the pain. The problem is cherry with a lot of carbohydrates, so it's easier to take in capsule form, and reduces inflammation in a much smaller doses of aspirin.

Cherries then a rival anti-inflammatory drugs

In the above study 20 cherries reduces swelling when eating like that of aspirin without the side effects or depletion of minerals and vitamins in the body.

Growers are bloviating research pointing to their website what cherries can do for you when out of nowhere, the FDA sent letters to eight nine p.m. warning saying that it will take legal action if the breeders can not shake off science from their seats.

Does this sound like the FDA Power Mad?

If power is not crazy then extremely irrational behavior could be inferred from these agencies and behavior when you put the power in the mixture becomes very dangerous for breeders who are only trying to earn a living. It is, of course, is not at the news, the FDA had the power mad disorder in the past 20 years.

Government Accounting Office

GAO Report nailed almost twenty years, said: "The GAO found that of 198 drugs approved between 1976 and 1985 KB 102 (or 51.5%) had serious post-approval risks .... posted serious risks of approval. Included .. heart failure, myocardial infarction, anaphylaxis, respiratory depression and arrest, seizures, kidney and liver failure, several blood disorders, birth defects and fetal toxicity and blindness. "
With this abysmal record continues well into this century just need to watch the new ads for new drugs that are approved for the U.S. market by the FDA that they have at the end of the ad states, oh by the way this drug could kill you with a nice long list of things that would it might do to your body and brain (Vioxx comes to mind.)

Busy Drug Approval

The FDA has years of dueling against their right to use healthy organic foods and dietary supplements like vitamins and minerals in their diet, and they are putting their stamp of approval on the deadly patent drugs that could kill in a heartbeat!

FDA Science & Mission in danger

In 2007, former FDA Commissioner Mark McClellan, MD, said: "Over the last decade, complex scientific advances, globalization and challenging new safety issues have combined to multiply the responsibilities FDA as it is clearly a new report. Our expectations may not exceed the resources we give FDA to accomplish its mission. In this regard, more is definitely better. "There is no mention of hiring competent researchers and scientists to come to reasonable conclusions about the drug in the study.

FDA reform is needed

Some want additional resources to throw at the agency problem as well as more cash will always resolve what it takes! What is really needed is a reform that is overdue time. Firing of those who approve of the deadly dangerous patented prescription drugs to an unsuspecting public will not only enhance the credibility of the agency, but will set the standard that they themselves will have to live up to. Change is needed before or more types of drug Vioxx will be put in the hopper for mass consumption that could prove lethal to the FDA's reputation and image. Health for all of us should be the goal here.