Veterinary Dermatology · 2008 · 33 citations · 16 references
Veterinary MedicineToxicologyVeterinary DermatologyCanine DermatologyPharmaceutical ToxicologyVeterinary Parasitic DiseasesParasitic Disease DiagnosisToxicologic EmergenciesAbcb1 Genetic VariationAnthelmintic ToxicitySerious Adverse Drug ReactionsSwab SamplingToxicity In AnimalsToxicology Of Veterinary Drugs
Twenty-two dogs diagnosed with generalized demodicosis were treated with milbemycin oxime (MO) because of poor response to previous therapies or because the dog was a breed known to be susceptible to ivermectin toxicosis. Fifteen of the 22 dogs were herding breeds. Doses of MO ranged from 1.0 to 2.2 mg kg(-1) day(-1) per os. Cheek swab samples were obtained in order to determine each dog's ABCB1 genotype. Adverse drug reactions were recorded for each dog by the owners and/or veterinarians. The ABCB1-1 Delta genotype was significantly associated with the development of an adverse reaction (neurological toxicity) after treatment with MO. None of the 19 dogs with the wild-type ABCB1 allele experienced adverse reactions, whereas two dogs homozygous for the ABCB1-1 Delta mutation developed ataxia. Assessing the ABCB1-1 Delta genotype prior to MO administration may prevent neurological toxicity in these patients.
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Mark W. Neff, Kathryn Robertson, Aaron K. Wong et al. · Proceedings of the National Academy of Sciences · 2004 · 199 citations · Full text
Clinical observations in collies given ivermectin orally.
Paul Aj, Tranquilli Wj, Seward Rl et al. · PubMed · 1987 · 164 citations