Emerging drug resistance in bacteria is one of the world's greatest health threats, according to the CDC, the FDA, the World Health moncler jackets Organization, and a wide range of medical professional societies.
These groups cite "strong evidence" that many of these hard-to-treat germs arise in food animals and spread to humans. For this reason, the FDA argues strongly against unwise -- "injudicious" -- use of antibiotics in livestock. Yet over 80% of animal antibiotics are used in these ways.
In January 2012, the FDA prohibited some uses of the cephalosporin class of antibiotics in food animals. But these antibiotics make up less than a fraction of 1% of the 15,000 tons of antibiotics used in U.S. food animals each year.
This raises important questions. Here are WebMD's answers.
Why are antibiotics used in food animals?
There are two main reasons: To promote animal health, and to make animals grow faster.
The FDA has no problem with the antibiotics used to treat disease in animals. And it has no problem with antibiotics used under the direct supervision of a veterinarian who is treating specific animals.
But over 80% of antibiotics used in food animals is put into their feed or water by livestock producers, almost always on a herd-wide basis. This makes animals put on weight faster even if they don't eat more food.
Such "production use" of antibiotics is what the FDA, in its June 2010 guidance to the industry, deemed unwise or "injudicious."
How can antibiotics given to animals create drug-resistant germs?
If you get an antibiotic prescription moncler jacket from your doctor, you'll be warned to take every single one of the pills exactly as prescribed. That's because the last few pills mop up the most drug-resistant germs. If you take too low a dose, the most resistant germs remain.
The same thing happens in animals. Veterinarians treat sick animals with appropriate doses of antibiotics.
But when antibiotics are used to make animals grow faster, they are given at low doses over long periods of time. That's a recipe for growing drug resistant bacteria in food animals.
Can drug-resistant bacteria in food animals find their way to humans?
There are some researchers, such as an expert panel of the Institute of Food Technologists, who say the odds are low that any of these bugs will find their way into humans. But in testimony before Congress, the USDA, the FDA, and the CDC all said that the use of antibiotics in food animals leads to infections with drug resistant bacteria to humans.
And in a letter to Congress, 14 health groups -- including the American Medical Association and the American Academy of Pediatrics -- said "overuse and misuse of important antibiotics in food animals must end, in order to protect human health."
The World Health Organization has also warned that overuse of antibiotics in food animals can lead to drug-resistant infections in people.
In January 2012, the FDA banned certain uses of cephalosporin antibiotics in food animals effective April 5, 2012.
The ruling prohibits giving food animals the kinds of cephalosporins used to treat disease in humans or in pets. Exceptions allow off-label use by veterinarians to treat specific diseases, and allow the use of an older cephalosporin called cephapirin, which is not used in humans.
Cephalosporins are not one of the antibiotics used to increase animal growth.
Cephalosporins are important human drugs introduced in 1964. They are often used to treat pneumonia. Cephalosporins are also used to treat ear, skin, urinary tract, and other infections.
In 2010, U.S. meat and poultry producers used 27 tons of cephalosporins. That sounds like a lot. But it's only a fraction of the 14,600 tons of antibiotics used in food animals that year.
One consumer group called the FDA action a step forward -- but only a baby step.
Will the FDA ban use of other antibiotics in food animals?
There is no indication that the FDA plans to ban food-animal use of other antibiotics already approved for such uses.
Antibiotics have been used for what the FDA now calls "injudicious uses" since the 1950s. In the now famous "Swann Report," U.K. researchers in 1969 concluded that feeding low-dose antibiotics to animals posed a health risk to humans.
The U.S. government in 1970 formed its own task force to look at the issue. Eventually -- in 1977 -- the FDA issued a formal finding that all animal use of penicillins and low-dose animal use of tetracyclines should be banned.
But the FDA never acted on this finding. Environmental groups filed a lawsuit to force FDA to act. The FDA asked for more time. On Dec. 22, 2011, the FDA finally withdrew its 1977 finding.
Meanwhile, in 1999 and in 2005 environmental moncler jackets 2011 groups filed citizen petitions demanding that the FDA ban non-health-related antibiotic use in food animals. In November 2011, the FDA issued a statement saying it was "concerned" about injudicious food-animal use of antibiotics -- but that the petitions were denied.
What is the FDA doing about its concerns over antibiotic use in food animals?
The FDA says it takes too long and costs too much to formally ban unwise use of antibiotics in food animals. Instead, in a formal response to the citizen petition to ban such use, the FDA said it would ask the food industry to voluntarily stop "production use" of antibiotics.
That strategy is outlined in an unusual "draft guidance to industry" issued in June 2010 but not yet made final. Entitled "The Judicious Use of Medically Important Antimicrobial Drugs in Food-Producing Animals," the paper chronicles over 40 years of scientific and government reports linking antibiotic use in food animals to drug-resistant infections in humans.
The guidance stresses two main principles:
Antibiotics important to humans should be used in food animals only when necessary for the animals' health.
Use of these antibiotics in food animals should require the oversight of a veterinarian.
But the document makes it clear that the FDA expects industry to follow this guidance voluntarily. How has it worked so far?
The FDA tells WebMD that it hasn't worked yet because the guidance isn't yet final.
"There is no estimated time frame, but moving forward with strategies for implementing the recommendations outlined in the draft guidance is a priority for the agency," the FDA wrote in an email to WebMD in January 2012. "FDA intends to finalize the draft guidance (Guidance #209) in the near future as well as issue additional, cheap moncler more detailed guidance on implementing the recommendations."
Avinash Kar, a spokesman for the Natural Resources Defense Council, one of the environmental groups that had petitioned the FDA, is dubious.