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首页> 外文期刊>DVM Newsmagazine >FDA investigates adverse events tied to Greenies; maker changes label: Federal regulators seek owner reports of adverse events that might be linked to treats
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FDA investigates adverse events tied to Greenies; maker changes label: Federal regulators seek owner reports of adverse events that might be linked to treats

机译:FDA调查与Greenies相关的不良事件;制造商更改标签:联邦监管机构要求所有者报告可能与治疗有关的不良事件

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摘要

KANSAS CITY, Mo.—S&M NuTec plans to change the label of the nation's top selling canine dental treat Greenies in response to media reports that at least 13 dogs have died from complications tied to ingestion of the product. As of March 1, PDAs Centerfor Veterinary Medicine (CVM) confirmed 35 complaints involving 34 dogs and one cat, prompting a regulatory investigation, says Linda Grassie, director of CVM's communications staff. According to reports, the product fails to break down and can become lodged in the dog's esophagus or intestine. Although the agency did not order the label change— which S&M NuTec terms a clarification — its inquiry into adverse reactions has driven a call for additional cases.
机译:密苏里州堪萨斯市—S&M NuTec计划更改该国最畅销的犬牙治疗产品Greenies的标签,以回应媒体报道至少有13只狗因与该产品摄入有关的并发症而死亡。 CVM通讯人员主管Linda Grassie说,截至3月1日,PDA兽医中心(CVM)确认了35起投诉,涉及34只狗和一只猫,这促使进行了监管调查。据报道,该产品未能分解,并可能滞留在狗的食道或肠中。尽管该机构未下令更改标签(S&M NuTec对此予以澄清),但其对不良反应的询问促使人们要求更多案件。

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