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Equest Pramox 19.5 mg/g + 121.7 mg/g oral gel (POM-VPS) Equest Pramox 19.5 mg/g + 121.7 mg/g oral gel (POM-VPS)
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Equest Pramox 19.5 mg/g + 121.7 mg/g oral gel (POM-VPS)

Equest Pramox 19.5 mg/g + 121.7 mg/g oral gel -  Active substances Moxidectin 19.5 mg Praziquantel 121.7 mg

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Equest Pramox 19.5 mg/g + 121.7 mg/g oral gel (POM-VPS)
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Product Description

Equest Pramox 19.5 mg/g + 121.7 mg/g oral gel

Active substances Moxidectin 19.5 mg Praziquantel 121.7 mg Excipients Benzyl alcohol (E1519) 220.0 mg Butylhydroxytoluene (E321) 0.8 mg For a full list of excipients, see section 6.1 Oral Gel. Pale yellow to orange/pink oral gel. CLINICAL PARTICULARS 4.1 Target species Horses. 4.2 Indications for Use, specifying the target species In horses: For the treatment of mixed cestodes and nematodes or arthropods infections, caused by moxidectin and praziquantel sensitive strains of:

Large strongyles: . Strongylus vulgaris (adult stages) .

Strongylus edentatus (adult stages) 

Triodontophorus brevicauda (adults) .

Triodontophorus serratus (adults) .

Triodontophorus tenuicollis (adults)

Small strongyles (adults and intraluminal larval stages):

Cyathostomum spp

Cylicocyclus spp .

Cylicostephanus spp .

Cylicodontophorus spp .

Gyalocephalus spp

Ascarids:

Parascaris equorum (adults)

Other species:

Oxyuris equi (adult stages) .

Habronema muscae (adults) .

Gasterophilus intestinalis (L2, L3)

Gasterophilus nasalis (L2, L3) .

Strongyloides westeri (adults) .

Trichostrongylus axei (adult stages)

Tapeworm (adults): .

Anoplocephala perfoliata .

Anoplocephala magna .

Paranoplocephala mammillana The egg reappearance period of small strongyles is 90 days.

The product is effective against (developing) intramucosal L4 stages of small strongyles.

At 8 weeks after treatment, early (hypobiotic) EL3 stages of small strongyles are eliminated.

Contraindications Do not administer to young foals less than 6.5 months old Do not use in case of hypersensitivity to the active substance or to any of the excipients The product has been formulated specifically for use in horses only. Dogs and cats may be adversely affected by the concentration of moxidectin in this product if they are allowed to ingest spilled gel or have access to used syringes.

Veterinary advice should be given on appropriate dosing programs and stock management to achieve adequate parasite control and reduce the likelihood of anthelmintic resistance developing. In the event that a product is suspected of being ineffective, the animal owner is advised to seek veterinary advice

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