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　　US - The US Food and Drug Administration’s Center for Veterinary Medicine (CVM) has taken the first step toward withdrawing its approval of the use of carbadox to treat swine as the drug may leave trace amounts of a carcinogenic residue.CVM’s action comes after the center recently reexamined the safety profile of the drug and conducted a preliminary risk characterization that indicated there could be potential risk to human health from ingesting pork, especially pork liver, derived from carbadox-treated pigs.“The manufacturer of carbadox has failed to provide sufficient scientific data to demonstrate the safety of this drug given evidence that carbadox may result in carcinogenic residues,” said Michael R. Taylor, FDA deputy commissioner for foods and veterinary medicine.

　　由于卡巴多(carbadox)約摸留下微量的致癌殘渣，美國食品和藥物管理局(FDA)的獸醫(yī)中央(CVM)已經(jīng)邁出首席步，收歸藥物卡巴多在生豬飼養(yǎng)中的使用審批。獸醫(yī)中央最近在舉動之前重新審查了藥物的安全性并進行初步風險評估。評估能顯示出攝取豬肉對人體健康的潛在風險，尤其是使用卡巴多的生豬豬肝。美國食品和藥物管理局副局長邁克爾·泰勒(Michael R. Taylor)說：“有證據(jù)顯示卡巴多約摸引起致癌殘渣，而卡巴多創(chuàng)造商不能提供充沛的科學(xué)依據(jù)證明藥品的安全性?！?/p>