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Equimax is a simple and effective worming treatment that treats most major equine worms, such as Tapeworm and bots. In just one single dose, Equimax treats and controls both adult and immature gastro-intestinal Roundworms, Lungworms, Tapeworms and Bots. Using the powerful ingredient Ivermectin, Equimax also contains Praziquantel for one of the most powerful and effective Tapeworm treatment on the market.
The presence of worms can be checked in your horse using a Worm Testing Kit.
See how to worm your horse below:
A white homogenous, oral gel containing:
1.87% w/w ivermectin Ph.Eur.
14.03% w/w praziquantel Ph.Eur.
For the treatment and control of adult and immature gastrointestinal roundworms, lungworms, bots and tapeworms of horses, including:
Strongylus vulgaris adults and 4th larval (arterial) stages
Strongylus edentatus adults and 4th larval (tissue) stages
Strongylus equinus adults
Triodontophorus spp adults
Small strongyles, adults
Trichostrongylus axei adults
Oxyuris equi adults and immatures
Parascaris equorum adults and immatures
Strongyloides westeri adults
Large-mouth stomach worms
Habronema muscae adults
Onchocerca spp. (microfilariae)
Dictyocaulus arnfieldi adult and immature
Gasterophilus spp. oral and gastric larval stages
Equimax Oral Paste for Horses is given by mouth at the recommended dose rate of 200 micrograms of ivermectin and 1.5mg of praziquantel per kg of bodyweight as a single dose, corresponding to 1.07g of paste per 100kg bodyweight. The first syringe division delivers sufficient paste to treat 100kg of bodyweight. Each subsequent syringe division delivers sufficient paste to treat 50kg of bodyweight. The syringe delivers sufficient paste to treat 700kg bodyweight at the recommended dose rate.
The horse’s weight should be accurately determined to ensure use of the correct dose of product.
Before administration adjust the syringe to the calculated dosage by setting the ring on the plunger.
Up to 100kg
The animal’s mouth must be free of food. The syringe should be placed between the front and back teeth and the paste deposited at the base of the tongue. Immediately elevate the head for a few seconds to ensure that the product is swallowed. Treatment is recommended at least twice a year, in spring and autumn or according to veterinary advice. Intermediate roundworm treatment is advisable.
For animal treatment only.
Not to be used in foals under two weeks of age.
Some horses carrying heavy infection of Onchocerca microfilariae have experienced reactions with swelling and itching after treatment. It is assumed to be the result of death of large numbers of microfilariae.
These signs resolve within a few days but symptomatic treatment may be advisable.
Equimax Oral paste for Horses has been formulated specifically for use in horses. Dogs and cats may be adversely affected by the concentration of ivermectin in this product, if they are allowed to ingest spilled paste or have access to used syringes.
As ivermectin is extremely dangerous to fish and aquatic life, treated animals should not have direct access to surface water and ditches during treatment.
Wash hands after use.
Avoid eye contact.
Do not smoke or eat while handling the product.
Horses may be slaughtered for human consumption only after 35 days from the last treatment.
Any unused product or waste material should be disposed of in accordance with local requirements. Ivermectin is EXTREMELY DANGEROUS TO FISH AND AQUATIC LIFE. Do not contaminate surface water or ditches with the product or used containers.
Keep out of the reach of children. Store below 30° C. Part-used syringes should be stored below 25° C.
Following withdrawal of the first dose, use the product within 6 months.
12 syringes, each containing 7.49g of 1.87% w/w ivermectin and 14.03% w/w praziquantel paste.
No known interaction with other equine medicaments.
Studies in other species showed no teratogenic or embryotoxic effect from either ivermectin or praziquantel at the recommended doses during therapy.
A tolerance study performed in foals from 2 weeks of age with doses up to 5 times the recommended dosage showed no adverse reactions.
Safety studies conducted with Equimax administered to mares at 3 times the recommended dosage at 14 day intervals during the whole gestation and lactation did not show any abortions, any adverse effects on the gestation, parturition and on the mares general health, nor any abnormalities on the foals.
Safety studies conducted with Equimax administered to stallions at 3 times the recommended dosage did not show any adverse effects in particular on the reproductive performances.
White, circular, biconcave tablet with brown spots.
Each chewable tablet of 3300 mg contains:
For the treatment of mixed cestode, nematode and arthropod infestations, due to adult and immature roundworms, lungworms, bots and tapeworms in horses:
Strongylus vulgaris (adult and arterial larvae)
Strongylus edentatus (adult and L4 tissue larval stages)
Strongylus equinus (adult and L4 larval stage)
Triodontophorus spp. (adult)
Cyathostomum (adult and non-encysted mucosal larvae): Cylicocyclus spp., Cylicostephanus spp., Gyalocephalus spp.
Parascaris equorum (adult and larvae).
Oxyuris equi (adult and larvae).
Trichostrongylus axei (adult)
Anoplocephala perfoliata,Anoplocephala magna, Paranoplocephala mamillana
As tapeworm infestation is unlikely to occur in horses before two months of age, treatment of foals below this age is not considered necessary.
Gasterophilus spp. (larvae).
Single oral administration.
200 µg of ivermectin and 1.5 mg of praziquantel per kg of bodyweight corresponding to 1 tablet per 100 kg bodyweight.
To ensure a correct dosage, body weight should be determined as accurately as possible.
up to 100 kg
101 - 200 kg
201 - 300 kg
301 - 400 kg
401 - 500 kg
501 - 600 kg
601 - 700 kg
701 - 800 kg
Once the correct dose has been determined, it should be administered in the following way:
Present the tablet in the palm of your hand. Repeat this gesture until the complete dose has been administered. During the initial administration, the tablet can be combined with a small amount of food or a treat to increase the acceptance by the horse.
In the event that the required dose is not ingested an alternative treatment should be administered. Seek the advice of your veterinary practitioner.
Advice regarding appropriate dosing programmes and stock management should be sought to achieve adequate parasite control for both tapeworm and roundworm infestations.
For animal treatment only.
Do not use in foals under 2 weeks of age.
Do not use in mares from which milk is taken for human consumption.
Do not use in horses known to be hypersensitive to the active ingredients or any of the other ingredients.
Special warnings for target species
Care should be taken to avoid the following practices because they increase the risk of development of resistance and could ultimately result in ineffective therapy:
-too frequent and repeated use of anthelmintics from the same class over an extended period of time,
-underdosing, which may be due to underestimation of body weight, misadministration of the product, or lack of calibration of the dosing device (if any).
Suspected clinical cases of resistance to anthelmintics should be further investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test). Where the results of the test(s) strongly suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class and having a different mode of action should be used.
Resistance to ivermectin has been reported in Parascaris equorum in horses in a number of countries including ones in the EU. Therefore the use of this product should be based on national (regional, farm) epidemiological information about susceptibility of nematodes and recommendations on how to limit further selection for resistance to anthelmintics
The product can be used safely in stallions.
Can be used during pregnancy and lactation.
Special precautions for use in animals
Avermectins may not be well tolerated in all non target species. Cases of intolerance are reported in dogs, especially Collies, Old English Sheepdogs and related breeds or crosses, and also in turtles and tortoises.
Dogs and cats should not be allowed to ingest spilled tablets or have access to used packaging due to the potential for adverse effects related to ivermectin toxicity.
Wash hands after use. Avoid contact with the eyes. In case of eye irritation, seek medical attention. Do not eat, drink or smoke while handling this product. Keep out of the reach of children. In the event of accidental ingestion, seek medical advice and show the leaflet to the physician so that he knows what you have taken.
Colic, diarrhoea and anorexia have been reported in very rare occasions post treatment, in particular when there is heavy worm burden. In very rare occasions, allergic reactions such as hypersalivation, lingual oedema and urticaria, tachycardia, congested mucus membranes, and subcutaneous oedema have been reported following treatment with the product.
Horses may be slaughtered for human consumption only after 35 days from the last treatment. Not to be used in horses producing milk for human consumption
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with national requirements. EXTREMELY DANGEROUS TO FISH AND AQUATIC LIFE. Do not contaminate surface waters or ditches with the product or used container.
Keep out of reach and sight of children. Do not store above 30°C
Shelf life of the veterinary medicinal product as packaged for sale : 18 months
Shelf life after first opening the immediate packaging : 12 months
Carton box containing 12 polypropylene tubes of 8 tablets, sufficient to treat 800 kg of bodyweight, closed by a child proof cap.
No known interaction with other equine medicaments.
A tolerance study performed in foals with doses up to 5 times the recommended dosage did not show any adverse reactions.
Safety studies conducted with a similar veterinary medicinal product (EQUIMAX oral gel) administered to mares at 3 times the recommended dosage at 14-day intervals during the whole gestation and lactation periods did not result in any abortions, nor any adverse effects during gestation, at parturition or on the mares general health, nor any abnormalities in the foals.
Safety studies conducted with a similar veterinary medicinal product (EQUIMAX® oral gel) administered to stallions at 3 times the recommended dosage did not show any adverse effects in particular on the reproductive performances.
All prices include VAT where applicable.
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