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Trade name of the drug: EIMESTAT 5% (EIMESTAT 5%).

International nonproprietary name: toltrazuril.

EIMESTAT 5% contains in 1 g as an active ingredient: toltrazuril - 50 mg, as well as auxiliary components: sodium docusate - 2.5 mg, semiticone emulsion - 0.5 mg (defoamer), sodium benzoate - 2.1 mg, sodium propionate 2.1 mg, propylene glycol - 105 mg, bentonite - 3.5 mg, xanthan gum - 3 mg, citric acid - 6 mg and distilled water - up to 1 ml.

EYESTAT 5% is produced packaged by 10, 50, 100, 250, 500, 1000, 2500, 5000 ml in glass or plastic vials, capped with screw-on lids with a first opening control ring and provided with instructions for use.

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Price on request
Dosage form
Suspension for oral use
Suspension from white to yellowish color
250ml; 1l; 5l
Pharmacological properties

EYMESTAT 5% is an anticoccidial drug for the treatment and prevention of coccidiosis in piglets, young cattle and rabbits. Toltrazuril, which is part of the drug, is a synthetic substance that belongs to the triazintrione group, has a wide spectrum of anticoccidial action and a high degree of safety. Toltrazuril is effective against all types of parasitic coccidia, in pigs and cattle, at the stages of intracellular development of parasites, including Isospora suis, E. arloingi, Eimeria scabra, E. guevarai. E. bovis, E. zuernii, E. alabamensis, as well as eimeria rabbits E. stiedae, E.intestinalis, E.magna, E. media, E. calcicola, E. irresidua, E. perforans, E.piriformis, including strains resistant to other anticoccidial drugs.

Toltrazuril, blocking respiratory enzymes of coccidia, has a damaging effect on mitochondria and the processes of division of the coccidia nucleus, disrupting the formation of macrogametocytes. After oral administration, toltrazuril is slowly absorbed and has a coccidiocidal effect on the mucous and submucosal membranes of the gastrointestinal tract.

Toltrazuril is excreted from the body mainly unchanged, as well as in the form of metabolites (sulfones) and partially with urine.

EYMESTAT 5% by the degree of exposure to the body refers to low-hazard substances of the 4th hazard class according to GOST 12.1.007, in recommended doses does not cause side effects and complications in animals, does not interfere with the formation of immunity to coccidiosis.

The order of application:

EIMESTAT 5% is prescribed to piglets and young cattle up to 9 months of age for therapeutic and prophylactic purposes in coccidiosis.

EYMESTAT 5% is applied to piglets and young cattle up to 9 months of age orally individually once using a special dispenser in the following doses:

Before use, the suspension in the container should be thoroughly shaken In farms with coccidiosis in order to achieve maximum preventive effect and reduce the number of oocysts released into the external environment, EIMESTAT suspension of 5% should be prescribed to animals before the first clinical signs of the disease appear in the herd.

The drug is used once.


Contraindication to the use of EIMESTAT 5% is an increased individual sensitivity of the animal to the components of the drug. It is forbidden to use EIMESTAT 5% in dairy cows, due to its excretion with milk; the drug should not be used in ruminants with developed cicatricial digestion.


In case of overdose in animals, there may be a decrease in appetite, a decrease in water consumption and weight loss.

The peculiarities of the action of the drug at the first intake or at its cancellation were not revealed.


Side effects and complications in piglets and calves when using EIMESTAT 5% in accordance with this instruction, as a rule, are not observed.

With increased individual sensitivity to the drug and the appearance of allergic reactions, antihistamines and symptomatic medications are prescribed to the animal.

Drug interactions have not been identified.

EYMESTAT 5% suspension is compatible with vitamins, known feed additives and medicines used in animal husbandry.

Slaughter of piglets for meat is allowed no earlier than 91 days, young cattle and rabbits no earlier than 70 days after the application of 5% Eymestat. The meat of animals forcibly killed earlier than the deadline can be used to feed carnivorous animals.

Personal prevention measures:

When working with EIMESTAT 5%, the general rules of personal hygiene and safety provided for when working with medicines should be observed. Smoking, drinking and eating are prohibited during work. At the end of the work, hands should be washed with warm water and soap.

In case of accidental contact of the drug with the skin or mucous membranes of the eyes, they must be rinsed with plenty of water. People with hypersensitivity to the components of the drug should avoid direct contact with EIMESTATom5%. In case of allergic reactions or accidental ingestion of the drug into the human body, you should immediately contact a medical institution (have instructions for the use of the drug or a medical label with you).

Empty bottles from under the drug are prohibited from being used for household purposes, they are subject to disposal with household waste.

Shelf life and storage conditions

EIMESTAT 5% is stored in the manufacturer's closed packaging, separately from food and feed, in a dry, light-protected place, at a temperature from 5 ° C to 25 ° C.

The shelf life of the drug, subject to storage conditions in a closed package, is 3 years from the date of production, after opening the package - no more than 3 months.

It is forbidden to use the drug after the expiration date.

EYMESTAT 5% should be stored in places inaccessible to children.

Unused medicinal product is disposed of in accordance with the requirements of the legislation.

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