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Five key messages to prevent AMR in aquaculture farms









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    Meeting
    Antimicrobial use in aquaculture and antimicrobial resistance. Report of a Joint FAO/OIE/WHO Expert Consultation on Antimicrobial Use in Aquaculture and Antimicrobial Resistance
    Seoul, Republic of Korea, 13-16 June 2006
    2006
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    The public health hazards related to antimicrobial use in aquaculture include the development and spread of antimicrobial resistant bacteria and resistance genes, and the occurrence of antimicrobial residues in products of aquaculture. The greatest potential risk to public health associated with antimicrobial use in aquaculture is thought to be the development of a reservoir of transferable resistance genes in bacteria in aquatic environments from which such genes can be disseminated by horizont al gene transfer to other bacteria and ultimately reach human pathogens. However, a quantitative risk assessment on antimicrobial resistance in aquaculture is difficult to perform owing to lack of data and the many different and complex pathways of gene flow.
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    Brochure, flyer, fact-sheet
    Action to support the implementation of Codex AMR texts (ACT) project - ACT and youth: Nepal's young leaders take on antimicrobial resistance
    Success story
    2025
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    The ACT Project supports countries to implement the three Codex AMR texts. One of the key pillars in achieving this goal is raising awareness. In Nepal, the Nepal Chapter of FAO’s World Food Forum (WFF), part of the Global Youth Action Initiative, is supporting the ACT Project and harnessing the power of youth networks to reach communities and individuals the project itself cannot directly engage. This story highlights how young volunteers and leaders are spreading awareness about antimicrobial resistance (AMR) among their peers and within their communities.
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    Book (series)
    Carryover in feed and transfer from feed to food of unavoidable and unintended residues of approved veterinary drugs
    Report of the Joint FAO/WHO expert meeting – 8–10 January 2019, FAO Headquarters, Rome, Italy
    2019
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    Carryover of veterinary drugs in feed can occur during feed processing, handling, transportation, delivery or in feeding animals on-farm. The risk of unavoidable and unintentional veterinary drug residues from feed carryover and/or transfer from feed to food of animal origin is unacceptable when it causes adverse health effects in target and/or non-target animals and/or humans consuming food originating from these animals. If carryover is not properly managed, contaminated feed can directly harm species that are sensitive to the unintended veterinary drug they consume, and /or can result in residues in food of animal origin such as meat, milk and eggs that render them unsafe for human consumption. Even if residues are not a safety hazard, they can pose regulatory and global trade issue as countries/markets may enforce a “zero” tolerance for residues when appropriate maximum residue limits have not been established. Upon request of the Codex Committee on Residues of Veterinary Drugs in Foods (CCRVDF), FAO and WHO convened an Expert Meeting to review the causes of veterinary drug carryover in animal feed and the transfer from feed to food, as well as the known risks to human health and international trade, and suggest appropriate risk management strategies. This report shows the results of the expert discussions, conclusions and recommendations.

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