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Wisconsin Agriculturist www.FarmProgress.com – June 2015 19 Dairy & Livestock Make meat, milk safe to consume By SANDY STUTTGEN N 2012, the USDA reported 360 violative drug residues in meat, representing 0.01% of the 3.1 million dairy cows slaughtered in the U.S. that year. That same year, 63 violative meat residues were found in beef cows, representing 0.002% of the 3.5 million beef cows slaughtered. Keep this in perspective. Meat supplied by dairy and beef cows (about 25% of the total U.S. beef supply) is essentially free of residues. However, compared to the beef industry, dairy is responsible for a fivefoldhigher incidence of violations. I law to use the product as the label directs. Veterinarians within the scope of a valid veterinary patient relationship may use some, but not all, FDA-approved drugs in an extra-label fashion. Enrofloxacin and sulfamethazine are prohibited from extra-label drug use in food-producing animals. ELDU is permitted for the other drugs identified, and such use cannot result in violative food residues. The total number of violative residues is small; however, milk from individual treated cows is being sold for human consumption. Missing both on-farm treatment records and individual animal identification and increasing dosage without adjusting withdrawal times are the top three reasons given for why residues occur. Invalid veterinary oversight of ELDU is evident. Producers and veterinarians want to treat the animals in their care effectively, and both have an ethical responsibility to use the drugs entrusted to them carefully. Consumers expect no less. Stuttgen is the Taylor County Extension agriculture agent. Drug violations The drug violations identified from the dairy cows slaughtered in 2012 were due to the beta-lactam antibiotics desfuroylceftiofur and penicillin, plus a variety of non-beta-lactams and nonsteroidal anti-inflammatory drugs. Bulk tank milk is only tested for beta-lactam drugs under the Pasteurized Milk Ordinance, and in 2012, 0.02% of raw milk was violative for these antibiotics. In response to drug residue violations in dairy beef, the Food and Drug Administration set out to answer this question: Were those dairy farms responsible for violative meat residues more likely to also have raw milk residues, especially from non-beta-lactam drugs? Bulk tank milk samples taken from January through November 2012 were tested for 31 drugs — both beta-lactam and non-beta-lactam antibiotics, and nonsteroidal anti-inflammatory and antihistamine drugs. The results released in March indicated 15 confirmed positive samples out of 1,912 tested, or 0.7%. Statistical analysis determined those farms with prior history of meat residues were no more likely to have bulk tank milk residues than those farms without a history of meat residues. The findings of less than 1% of farms’ individual tanks is unlikely to result in violative residue levels in pooled milk. Five of the six violative drugs identified (enrofloxacin, florfenicol, gentamicin, tilmicosin and tulathromycin) are prescription products labeled for cattle under 20 months of age (nonlactating). The over-the-counter drug sulfamethazine, labeled for cattle under 20 months of age (nonlactating), was also identified. While producers can purchase sulfamethazine without veterinary involvement, they are required to use it per label directions; cows should not be treated with it. Every user of every drug is required by GROWING A STRONG STAND DEPENDS ON THE SEED IT’S GROWN FROM. We put more into our seed because you demand more out of it. WL 354HQ WL 356HQ.RR WL 372HQ.RR Learn more at wlbetterseed.com Do not export Genuity ® Roundup Ready ® Alfalfa seed or crop, including hay or hay products, to China pending import approval. In addition, due to the unique cropping practices do not plant Genuity® Roundup Ready ® Alfalfa in Imperial County, California, pending import approvals and until Monsanto grants express permission for such planting. Monsanto Company is a member of Excellence Through Stewardship® (ETS). Monsanto products are commercialized in accordance with ETS Product Launch Stewardship Guidance, and in compliance with Monsanto’s Policy for Commercialization of Biotechnology-Derived Plant Products in Commodity Crops. Commercialized products have been approved for import into key export markets with functioning regulatory systems. Any crop or material produced from this product can only be exported to, or used, processed or sold in countries where all necessary regulatory approvals have been granted. It is a violation of national and international law to move material containing biotech traits across boundaries into nations where import is not permitted. Growers should talk to their grain handler or product purchaser to confirm their buying position for this product. ALWAYS READ AND FOLLOW PESTICIDE LABEL DIRECTIONS. Roundup Ready ® crops contain genes that confer tolerance to glyphosate, the active ingredient in Roundup ® brand agricultural herbicides. Roundup ® brand agricultural herbicides will kill crops that are not tolerant to glyphosate. Genuity Design®, Genuity Icons, Genuity ®, Roundup Ready ® and Roundup® are trademarks of Monsanto Technology LLC. © 2015 W-L Research.