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Application for the Reassessment of a Hazardous Substance under ...

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―Dichlorvos has been <strong>for</strong>mulated <strong>for</strong> use as dusts, granules, pellets/tablets,impregnated resin strips and concentrates.―Household and public health uses represent <strong>the</strong> main sources <strong>of</strong> human exposureto dichlorvos. Exposure may also occur during its production and application.“5.2 Carcinogenicity in humans―One case-control study <strong>of</strong> leukaemia in <strong>the</strong> USA found an association with use <strong>of</strong>dichlorvos on animals; <strong>the</strong>re were few exposed subjects, and <strong>the</strong>y had potentialexposure to many pesticides.“5.3 Carcinogenicity in experimental animals―Dichlorvos was tested <strong>for</strong> carcinogenicity by oral administration in twoexperiments in mice and in three experiments in rats. A few rare oesophagealsquamous-cell tumours were found in mice treated with dichlorvos in <strong>the</strong> diet. Adose-related increase in <strong>the</strong> incidence <strong>of</strong> squamous-cell tumours (mainlypapillomas) was noted in <strong>the</strong> <strong>for</strong>estomachs <strong>of</strong> mice that received dichlorvos incorn oil by gavage. In rats that received dichlorvos in water by gavage, a fewsquamous-cell papillomas <strong>of</strong> <strong>the</strong> <strong>for</strong>estomach were seen. In rats that receiveddichlorvos in corn oil by gavage, a dose-related increase in <strong>the</strong> incidence <strong>of</strong>mononuclear-cell leukaemia and an increased incidence <strong>of</strong> pancreatic acinar-celladenomas were observed in males.“5.4 O<strong>the</strong>r relevant data―A variety <strong>of</strong> studies in several species did not demonstrate developmentaltoxicity due to dichlorvos.“In vitro, dichlorvos phosphorylates esterases to a greater extent than itmethylates nucleophiles; <strong>the</strong> likelihood <strong>of</strong> DNA methylation in vivo is extremelysmall.―Immunosuppression has been noted after short-term administration <strong>of</strong> high doses<strong>of</strong> dichlorvos which are associated with pr<strong>of</strong>ound cholinergic hyperstimulation.―No data were available on <strong>the</strong> genetic and related effects <strong>of</strong> dichlorvos inhumans.―Dichlorvos was not shown to have genetic activity in various assays in mammalsin vivo. It induced gene mutation and chromosomal damage in culturedmammalian cells and in insects, plants, fungi, yeast and bacteria.“5.5 Evaluation―There is inadequate evidence in humans <strong>for</strong> <strong>the</strong> carcinogenicity <strong>of</strong> dichlorvos.―There is sufficient evidence in experimental animals <strong>for</strong> <strong>the</strong> carcinogenicity <strong>of</strong>dichlorvos.“Overall evaluation―Dichlorvos is possibly carcinogenic to humans (Group 2B).‖Dichlorvos reassessment – application Page 204 <strong>of</strong> 436

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