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Peer-reviewed veterinary case report

Safety of metaflumizone plus amitraz spot-on for flea and tick

By Heaney, K & Lindahl, R G·Published in Veterinary parasitology·2007·Fort Dodge Animal Health, United States·View original on PubMed

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Original publication title: Safety of a topically applied spot-on formulation of metaflumizone plus amitraz for flea and tick control in dogs.

Species:
dog
Brain & nervesDogs

Plain-English summary

A group of Beagle dogs was tested for the safety of a new flea and tick treatment that combines metaflumizone and amitraz. The dogs received the treatment at normal and higher doses, and researchers monitored their health for any side effects. They found that even at higher doses, the dogs showed no significant health issues, though some had very mild and temporary increases in certain blood levels. Overall, the treatment was deemed safe for dogs as young as 8 weeks old when used as directed.

People also search for: dog flea treatment safety · metaflumizone amitraz side effects · Beagle flea and tick control

Abstract

Four laboratory studies were conducted in Beagle dogs to evaluate the safety of a novel ectoparasiticide combination of metaflumizone plus amitraz (ProMeris/ProMeris Duo for Dogs, Fort Dodge Animal Health, Overland Park, KS) when applied according to the recommended dosage of >/=20mgmetaflumizonekg(-1) plus >/=20mgamitrazkg(-1), at exaggerated and repeated dosages, and if accidentally orally ingested. Parameters evaluated included body weight, food consumption, clinical, physical and neurological examinations, clinical pathology and gross and microscopic pathology. Exaggerated and repeated topical treatment with metaflumizone plus amitraz administered at 1x, 3x and 5x the recommended dose had no effect on clinical findings, heart rates, body weight, food consumption, physical/neurological examinations, macroscopic and microscopic pathology. Very slight, transient, clinically insignificant increases in serum urea nitrogen were noted in some dogs treated at all dose rates tested. This effect was not persistent, was not dose-responsive, nor aggravated by repeated applications and was not associated with a corresponding increase in creatinine or renal pathology. Therefore, these increases in urea nitrogen were suspected to be of non-renal origin and were not considered toxicologically significant. Exaggerated doses (3x and 5x) caused very mild, transient hyperglycemia, most notably in some adult females. Transient and inconsistently noted mild increases in leukocytes, neutrophils and monocytes were observed in some 3x and 5x treated dogs at some intervals. None of the effects noted were aggravated by repeated administration. When 10% of the recommended topical dose was orally administered to mimic exposure due to licking the application, avoidance behaviors including spitting, head shaking, and salivation were noted immediately in all animals. Consequently, voluntary oral ingestion is considered unlikely. Transient decreased activity, slightly reduced body temperature and pale oral mucous membranes were noted in some animals beginning 1-2h posttreatment. Ataxia, resolving within 4h posttreatment, was noted in one female. Oral administration had no effect on clinical pathology. Results from these four studies indicate repeated use of metaflumizone plus amitraz causes no adverse health effects when used as recommended in dogs as young as 8 weeks of age.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/17928149/