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Ivermectin. Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 81st meeting 2015

JECFA Monographs 18









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    Diflubenzuron. Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 81st meeting 2015 2016
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    This monograph was also published in: Residue Evaluation of Certain Veterinary Drugs. Joint FAO/WHO Expert Committee on Food Additives (JECFA), 81st meeting 2015. FAO JECFA Monographs 18.

    Diflubenzuron (CAS No. 35367-38-5), besides its use in agriculture, horticulture and forestry against larvae of Lepidoptera, Coleoptera, Diptera, Hymenoptera, and in public health against larvae of mosquitoes, is used as a veterinary drug for the treatment of sea lice (Lepeophtheirus salmonis Kr øyer and Caligus rogercresseyi Boxshall and Bravo, 2000) infestations in Atlantic salmon (Salmo salar L.). Diflubenzuron acts by interference with the synthesis of chitin. Demand for chitin synthesis is greatest at the moult between growth stages and hence parasites are killed due to disruption of the moulting process.

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    Residue Evaluation of Certain Veterinary Drugs. Joint FAO/WHO Expert Committee on Food Additives (JECFA), 81st Meeting, 2015. FAO JECFA Monograph 18 2016
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    This volume of FAO JECFA Monographs contains residue evaluation of certain veterinary drugs prepared at the 81st Meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), held in Rome, Italy, 17–26 November 2015. This JECFA meeting was convened specifically to consider residues of veterinary drugs in food-producing animal species, to further elaborate principles for evaluating the safety of residues of veterinary drugs in food and for establishing acceptable daily intakes (ADIs) a nd/or acute reference doses (ARfDs), and to recommend maximum residue limits (MRLs) for substances on the agenda when they are administered to food-producing animals in accordance with good veterinary practice in the use of veterinary drugs. The monographs contained therein provide the scientific basis for the recommendations of MRLs.
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    Zilpaterol hydrochloride. Residue Monograph of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 81st meeting 2015 2016
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    The 78th meeting of the Committee, at the request of the 21st Session of CCRVDF (FAO/WHO, 2014a), evaluated zilpaterol HCl and established an ADI of 0–0.04 μg/kg bw on the basis of a LOAEL for a slight increase of tremor in humans in a single dose study (FAO/WHO, 2014b). The 78th meeting of the Committee also agreed that parent zilpaterol was an appropriate marker residue in muscle. Only limited data were available for tissues other than muscle, and the Committee was unable to determine a suitab le marker residue in other edible tissues. Liver and kidney contained the highest concentration of zilpaterol at all sampling times, followed by muscle. The ratios of the concentration of zilpaterol to the concentration of the total residues for liver and for kidney over the 96-hour withdrawal period after the last drug administration could not be determined with any confidence due to the very limited data available and lack of sensitivity of the methods used. The data provided were not sufficie nt to determine the total residue half-life in the liver after 96 hours. There are no measurable residues in adipose fat.

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