Oksavil

Oksavil

Product Group:Antiparasitics
Pharmaceutical Form:Oral Tablet
Active Ingredient:Oxfendazole, Oxyclozanide
Target Animal:Cattle, Sheep
Package Form:Blister containing 10 tablets

COMPOSITION

It is a white-cream colored, bisect tablet containing 375 mg oxfendazole and 750 mg oxyclozanide per tablet.

 

PHARMACOLOGICAL PROPERTIES

It is a broad-spectrum antiparasitic combination used in cattle and sheep against liver flukes, gastrointestinal nematodes, lungworms, and tapeworms.

Oxfendazole: A benzimidazole derivative anthelmintic. It inhibits fumarate reductase enzyme activity and disrupts energy metabolism in parasites. After oral administration, it is absorbed to a limited extent from the digestive tract and excreted via urine and feces.

Oxyclozanide: A salicylanilide derivative anthelmintic. It disrupts oxidative phosphorylation in parasites. After oral administration, it is largely absorbed from the digestive tract and reaches high concentrations in the liver, kidneys, and intestines. Excretion occurs via bile as glucuronide conjugates.

Oksavil Oral Tablet is also effective against larval stages of parasites at higher doses.

 

AREA OF USE/INDICATIONS

It is used for the treatment and prevention of mature and immature gastrointestinal and lung nematodes, liver flukes, and adult Moniezia spp. Tapeworms in cattle and sheep.

In cattle:

Liver flukes: Fasciola hepatica, F. gigantica (adult)

Gastrointestinal nematodes: Ostertagia spp., Haemonchus spp., Trichostrongylus spp., Cooperia spp., Oesophagostomum spp., Nematodirus spp., Strongyloides spp., Bunostomum spp., Trichuris spp.

Lungworms: Dictyocaulus viviparus (adult and larva)

Tapeworms: Moniezia spp.

In sheep:

Liver flukes: Fasciola hepatica, F. gigantica (adult)

Gastrointestinal nematodes: Ostertagia spp., Haemonchus spp., Trichostrongylus spp., Cooperia spp., Oesophagostomum spp., Nematodirus spp., Strongyloides spp., Chabertia spp., Trichuris spp.

Lungworms: Dictyocaulus filaria (adult and larva)

Tapeworms: Moniezia spp.

 

USAGE AND DOSAGE

Pharmacological dose:

Cattle: Oxyclozanide 10–15 mg/kg, Oxfendazole 4.5–5 mg/kg is administered orally

Sheep: Oxyclozanide 10–20 mg/kg, Oxfendazole 5–7.5 mg/kg is administered orally

Practical dose: 1 tablet /50 kg body weight

Tablets may be administered directly to the animal or dissolved in water. Tablets can be split at the bisect line if needed.

SPECIAL CLINICAL INFORMATION AND SPECIAL WARNINGS FOR TARGET SPECIES

Recommended to administer prophylactically twice a year, in spring and autumn.

Repeat the administration 1–2 months after the treatment.

Apply treatment before animals graze to prevent parasite infection.

Keep animals confined for 8–12 hours post-treatment to maximize ovisidal effect and prevent pasture contamination.

Administer medication two weeks prior to mating rams.

 

ADVERSE EFFECTS

Relatively low single doses (15 mg/kg) of oxyclozanide may cause temporary central neurvous system (CNS) and gastrointestinal disturbances (behavioral changes, diarrhea, anorexia) in cattle and sheep.

 

DRUG INTERACTIONS

When it is used with bromsalan, it may cause abortion in cows and death in sheep, so it should not be used with these products.

 

SYMPTOMS OF OVERDOSE, PRECAUTIONS AND ANTIDOTE

High doses may increase severity of toxic signs (anorexia, depression, ataxia, recumbency, rapid breathing, salivation, spasms). Doses ≥50 mg/kg may be fatal. In case of toxicity, provide supportive treatment based on clinical symptoms.

 

WITHDRAWAL PERIODS

Meat: 28 days for cattle, 21 days for sheep.

Milk: 5 days (10 milkings) for cow. Not to be used in lactating sheep producing milk for human consumption.

 

CONTRAINDICATIONS

It is not recommended for animals with hepatic failure.

Use during pregnancy: Contraindicated during mating season and first third of gestation due to embryotoxic and teratogenic effects of benzimidazoles.

 

GENERAL WARNINGS

Consult a veterinarian before use and in case of unexpected reactions. Keep out of reach of children.

 

PRECAUTIONS TO BE TAKEN BY THE ADMINISTRATOR AND WARNINGS FOR VETERINARY SURGEON

Avoid contact with the product. Wash hands after use.

 

STORAGE CONDITIONS AND SHELF LIFE

It should be stored in the original packages, protected from light, below 25°C, without refrigeration or freezing. Shelf life is 2 years.

 

COMMERCIAL PRESENTATION FORM

15x10 tablets in blister with boxes.

 

PLACE OF SALE AND CONDITIONS

Sold in pharmacies with a veterinary prescription, as well as in veterinary clinics, polyclinics, and animal hospitals. (VPR)

 

APPROVAL DATE OF LEAFLET: 17.12.2012

 

MARKETING AUTHORIZATION DATE AND NO: 31.12.2008-020/0100

 

NAME AND ADDRESS OF MARKETING AUTHORIZATION HOLDER

VİLSAN Veteriner İlaçları Tic. ve San. A.Ş.

Balıkhisar Mah. Balıkhisar Köy İçi Küme Evleri No:765A Akyurt/Ankara–Türkiye

 

MANUFACTURER COMPANY

VİLSAN Veteriner İlaçları Tic. ve San. A.Ş.

Balıkhisar Mah. Balıkhisar Köy İçi Küme Evleri No:765A Akyurt/Ankara–Türkiye

 

Made in Turkiye

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