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A safety trial with rafoxanide in sheep
Journal of the South African Veterinary Association
|June 1, 1981
Summary
This study found no adverse effects in lambs treated with rafoxanide at various dosages. Plasma rafoxanide assays are recommended for diagnosing potential toxicity in sheep.
Area of Science:
- Veterinary Pharmacology
- Animal Toxicology
- Sheep Health
Background:
- Rafoxanide is an anthelmintic used in livestock.
- Understanding its safety profile and potential toxicity is crucial for animal welfare.
- Establishing diagnostic methods for rafoxanide exposure is important.
Purpose of the Study:
- To evaluate the toxicological effects of rafoxanide in lambs.
- To determine safe dosage ranges and identify potential adverse reactions.
- To assess the utility of plasma-rafoxanide assays for diagnosis.
Main Methods:
- Oral administration of rafoxanide to six groups of lambs (6 lambs/group) at escalating doses (0-37.5 mg/kg).
- Post-mortem examinations conducted 27-31 days post-treatment.
- Clinical, ophthalmological, and pathological assessments performed.
Main Results:
- No clinical signs of toxicity were observed in any treatment group.
- No treatment-related ophthalmological or pathological changes were detected.
- Lambs tolerated rafoxanide well within the tested dosage range.
Conclusions:
- Rafoxanide exhibits a good safety margin in lambs at the tested dosages.
- Differential diagnoses and predisposing factors for potential toxicity warrant further investigation.
- Plasma-rafoxanide concentration assays are proposed as a valuable diagnostic tool for suspected toxicity.