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March 14, 2026Russian veterinary journal0 citations

Fluralaner (Vepripak®) for demodicosis, otodectosis, and sarcoptic mange in dogs: evaluation of efficacy and safety based on multicenter studies

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LKLidiya KupriyanovaNSNatal'ya ShagovaYBYuliya Burdukova

Key Points

  • To evaluate the efficacy and safety of fluralaner (Vepripak®) for treating acarosis in dogs.
  • Analyzed pilot clinical observation and prospective multicenter open study data from 986 dogs.
  • Evaluated palatability of Vepripak® in a separate study with 520 dogs.
  • Fluralaner was administered orally as a single dose of 25-56 mg/kg body weight.
  • Achieved 100% therapeutic efficacy in diagnosed acarosis cases.
  • Demodex canis and Otodectes cynotis were not detected in skin scrapings after respective treatment durations.
  • No adverse events were reported during a 12-week follow-up.

Abstract

Relevance. Acarosis in dogs (demodicosis, otodectosis, and sarcoptic mange) is one of the reasons for visiting a veterinarian; long-acting systemic acaricides with high compliance are important for controlling infestations and reducing the risk of re-infestation. Objective. To summarize the data on the therapeutic efficacy of Vepripak® (fluralaner, chewable tablet) in the treatment of demodicosis, otodectosis, and sarcoptic mange in dogs. Materials and methods. The data of a pilot clinical observation and a prospective multicenter open study (total 986 dogs, aged 6 months to 10 years) were analyzed, as well as a study of palatability (n=520). Vepripak® was administered orally once at a dose of 25…56 mg of fluralaner/kg of body weight; in the protocol – at least 2 hours after the last feeding. The efficacy in acarosis was assessed by the dynamics of clinical signs and microscopy (skin scrapings/ear secretions). Results. 100% therapeutic efficacy was observed in dogs with diagnosed acarosis. demodicosis, otodectosis, and sarcoptic mange: Demodex canis was not detected in scrapings after 14 days, Otodectes cynotis was not detected after 28 days, and clinical improvement in sarcoptic mange was observed after 2 to 4 weeks. In a multicenter study, no adverse events were reported during a 12-week period, and the voluntary consumption of the chewable form was 99.8%. Conclusion. Vepripak® demonstrated high clinical efficacy in a series of observations of major acaroses in dogs and high consumption, which may increase adherence to therapy in dermatological practice.

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Cite This Study

Kupriyanova et al. (2026) studied this question.

synapsesocial.com/papers/69b4ba0818185d8a39802741https://doi.org/10.32416/2500-4379-2026-1-38-46
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