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Evaluation of certain veterinary drug residues in food : fortieth report of the Joint FAO/WHO Expert Committee on Food Additives [meeting held in Geneva from 9 to 18 June 1992] = Evaluación de ciertos residuos de fármacos de uso veterinario en los alimentos : 40 informe del Comité Mixto FAO/OMS de Expertos en Aditivos Alimentarios [se reunió en Ginebra del 9 al 18 de junio de 1992] / Food and Agriculture Organization of the United Nations

Tác giả : Food and Agriculture Organization of the United Nations

Nhà xuất bản : World Health Organization

Năm xuất bản : 1993

ISBN : 9241208325

Tùng thư : WHO technical report series

Chủ đề : 1. Drug Residues -- analysis. 2. Drug Therapy -- veterinary. 3. Food Contamination.

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62 p. Presents the conclusions of an expert committee commissioned to evaluate the safety of residues of selected veterinary drugs used in food-producing animals, to establish acceptable daily intakes for humans, and to recommend maximum residue limits. On the basis of a rigorous review of all available safety and residue data, the committee establishes international standards intended to promote food safety and facilitate the harmonization of international trade in animal products. The report has two parts. The first explains several methodological issues that are specific to the safety assessment of veterinary drug residues in food. Noting problems posed by the inadequacy of data on veterinary drugs with a long history of use, the report establishes general principles of evaluation and requirements for toxicological data needed to ensure that the safety of these older products is established according to rigorous contemporary standards. The second and most extensive part provides succinct summaries of the toxicological data examined and factors considered when evaluating each substance, identifying any potential hazards to consumer health, and allocating an acceptable daily intake and maximum residue limit. Veterinary drugs considered include five anthelminthics (closantel, flubendazole, ivermectin, tiabendazole, and triclabendazole), two antimicrobial agents (furazolidone and nitrofural), two production aids (bovine somatotropins and ractopamine), and a trypanocide (isometamidium). Acceptable daily intakes and maximum residue limits were established for seven of these drugs. For the remaining substances, the report identifies deficiencies in the available data and specifies the further information required for a re-evaluation

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Thông tin dữ liệu nguồn

Thư viện	Ký hiệu xếp giá	Dữ liệu nguồn
Tổ chức y tế thế giới		https://iris.who.int/handle/10665/38637

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245	__	$aEvaluation of certain veterinary drug residues in food : fortieth report of the Joint FAO/WHO Expert Committee on Food Additives [meeting held in Geneva from 9 to 18 June 1992] =$bEvaluación de ciertos residuos de fármacos de uso veterinario en los alimentos : 40 informe del Comité Mixto FAO/OMS de Expertos en Aditivos Alimentarios [se reunió en Ginebra del 9 al 18 de junio de 1992] /$cFood and Agriculture Organization of the United Nations
260	__	$bWorld Health Organization ,$c1993
490	__	$aWHO technical report series $v832
520	__	$a62 p.
520	__	$aPresents the conclusions of an expert committee commissioned to evaluate the safety of residues of selected veterinary drugs used in food-producing animals, to establish acceptable daily intakes for humans, and to recommend maximum residue limits. On the basis of a rigorous review of all available safety and residue data, the committee establishes international standards intended to promote food safety and facilitate the harmonization of international trade in animal products. The report has two parts. The first explains several methodological issues that are specific to the safety assessment of veterinary drug residues in food. Noting problems posed by the inadequacy of data on veterinary drugs with a long history of use, the report establishes general principles of evaluation and requirements for toxicological data needed to ensure that the safety of these older products is established according to rigorous contemporary standards. The second and most extensive part provides succinct summaries of the toxicological data examined and factors considered when evaluating each substance, identifying any potential hazards to consumer health, and allocating an acceptable daily intake and maximum residue limit. Veterinary drugs considered include five anthelminthics (closantel, flubendazole, ivermectin, tiabendazole, and triclabendazole), two antimicrobial agents (furazolidone and nitrofural), two production aids (bovine somatotropins and ractopamine), and a trypanocide (isometamidium). Acceptable daily intakes and maximum residue limits were established for seven of these drugs. For the remaining substances, the report identifies deficiencies in the available data and specifies the further information required for a re-evaluation
650	_2	$aDrug Residues $xanalysis
650	_2	$aDrug Therapy $xveterinary
650	_2	$aFood Contamination
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