PANACUR 10% Oral Suspension - 1L Dewormer for Animals

PANACUR 10% x 1L - Oral suspension with fenbendazole for cattle, sheep, goats, horses, dogs and cats.

DECLARATION OF ACTIVE SUBSTANCES AND OTHER INGREDIENTS

1 ml suspension contains:

Fenbendazole (FBZ INN) 100 mg

Methyl parahydroxybenzoate

Propyl parahydroxybenzoate

Anhydrous colloidal silicon

Sodium carboxymethylcellulose

povidone

Sodium citrate

Citric acid monohydrate

Purified water

Directions

In cattle, sheep, goats, horses, dogs and cats, in the treatment of parasites produced by mature and immature stages of gastrointestinal or respiratory tract nematodes. It has an ovicidal effect on broad worms. It also has an effect on cestodes in cattle.

For the treatment of infestation in dogs with mature stages of large gastrointestinal worms and tapeworms, and in cats in infestations with mature and immature stages of large gastrointestinal worms and tapeworms.

Horses: Large and small stongs, roundworms, pinworms and strongyloid species.

Cattle: Haemonchus spp., Ostertagia spp., Trichostrongylus spp., Cooperia spp., Nematodirus spp., Bunostomum spp., Trichuris spp.,

Strongyloides spp., Oesophagostomum spp., Chabertia spp., Gaigeria pachyscelis, Dictyocaulus filaria and Moniezia spp.

Sheep, goats: mature and immature stages of: Haemonchus, Ostertagia, Trichostrongylus, Cooperia, Nematodirus, Bunostomum, Trichuris,

Strongyloides, Oesophagostomum., Chabertia ovina, Dictyocaulus viviparous - Dictyocaulus

The mature stages of: Moniezia spp. In lambs and Mullerius capillaries in goats.

Dogs: Toxocara canis, Toxascaris leonina, Ancylostoma caninum, Uncinaria stenocephala, Trichuris vulpis, Taenia spp.

Cats: Toxocara mystax (mature stages), Ancylostoma tubaeforme (mature and immature stages), Taenia spp.

Puppies: Toxocara spp., Trichuris spp., Ancylostoma spp.

DOSAGE FOR EACH SPECIES, ROUTE (S) AND METHOD OF ADMINISTRATION

Cattle and Horses: It is administered orally 1ml product per 13 kg body weight (= 7.5 mg fenbendazole / kg body weight) according to the table:

Dosage recommendations:

65 kg 5 ml

135 kg 10 ml

200 kg 15 ml

265 kg 20 ml

335 kg 25 ml

400 kg 30 ml

Over 400 kg, an additional 3.75 ml is required for every 50 kg body weight.

Horses:

Recommended dosing schedule

All horses should usually be dewormed with a single dosing schedule every 6-8 weeks.

Treatment of inhibited cystic larvae and those fixed in the mucosa should be performed in autumn (ideally in October / November) and then repeated in spring (ideally in February). late October / November) and again in the Spring (ideally in February). However, in horses that are not in good physical shape or in newcomers with an unknown history of deworming, treatment can be done at any time of the year.

5 day treatment

For the control of larval stages and larvae in migration of large strongyls, stages 3 and 4 of larvae trapped in the mucosa of small strongyls as well as stages 3 of trapped larvae inhibited of small strongyls in the mucosa, 5 ml of product per 64 kg body weight is administered daily. for 5 days (= 7.5 mg fenbendazole / kg body weight daily for 5 days).

Single dose treatment

For the treatment of larval stages trapped in the mucosa of small strongyls, administer 3 ml of product per 10 kg body weight (= 30 mg fenbendazole / kg body weight).

For the treatment and control of larval stages in migration and tissue of large strongyls, 6 ml of product per 10 kg body weight is administered (= 60 mg fenbendazole / kg body weight).

For the treatment of diarrhea caused by Strongyloides westeri in infants aged 2 to 3 weeks, 5 ml of product per 10 kg body weight (= 50 mg fenbendazole / kg body weight) is administered.

For administration to horses, mix the product completely with concentrated feed or cereals and give the full dose in one administration.

Sheep and goats: It is administered orally 0.5 ml per 10 kg body weight. (= 5 mg fenbendazole / kg body weight) according to the table:

Practical dosing recommendations:

Up to 10 kg 0.5 ml

11 to 20 kg 1.0 ml

21 to 30 kg 1.5 ml

31 to 40 kg 2.0 ml

41 to 50 kg 2.5 ml

51 to 60 kg 3.0 ml

61 to 70 kg 3.5 ml

71 to 80 kg 4.0 ml

Over 80 kg, an amount of 0.5 ml is required for every 10 kg extra body weight. In cattle it is best to be administered with the `` Panacur 20ml Automatic Drencher`` Automatic dosing gun and in sheep with the 5 ml for sheep, but other standard types of dosing guns or administration equipment can be used.

Dogs and cats:

Routine treatment of dogs and cats is 50 mg fenbendazole / kg body weight administered for 3 consecutive days or the single dose of 100 mg fenbendazole / kg body weight (adults).

For dogs and cats the dose should be mixed with food or administered directly orally after feeding, e.g. with a plastic syringe.

Treatment should be repeated at regular intervals to prevent natural reinfestation of animals with endoparasites, e.g. 2-4 times a year.

Breed dogs should be treated at 6-8 week intervals. Special treatment regimens are indicated for puppies and cats, eg: treatment at the age of 2 weeks, 5 weeks and before leaving the kennel.

If animals are treated collectively rather than individually, they will need to be grouped into body weight groups and dosed accordingly to avoid under or overdose.

RECOMMENDATIONS FOR CORRECT ADMINISTRATION

For oral administration only.

Shake the vial before use.

No dietary control is required before or after treatment.

In order to ensure a correct dose administration, the body weight will be determined as accurately as possible, checking the proper functioning of the dosing device.

WAITING TIME

Cattle:

Edible tissues: 7 days

Milk: 4 days

Horses:

Edible tissues: 5 days.

Sheep:

Edible tissues: 15 days

Milk: 6 days

SPECIAL STORAGE PRECAUTIONS

Keep out of reach of children.

This veterinary medicinal product does not require any special storage conditions.

SPECIAL WARNINGS

Care will be taken to avoid the following actions that could increase the risk of developing resistance that could ultimately lead to inefficiency:

_ Too frequent or repeated use of anthelmintics in the same class over a long period of time

_ Underdose which may be due to incorrect assessment of body weight, incorrect administration of the product, or failure to calibrate the dosing device (if used)

Clinical cases of suspected anthelmintic resistance should be further investigated using appropriate tests (e.g., fecal egg count reduction test). When test results suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class of anthelmintics with a different mode of action will be used.