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DESCRIPTION

Vetom 1 - the drug is used for the prevention and treatment of gastrointestinal diseases. In appearance, Vetom 1 is a finely dispersed white powder, odorless, soluble in water, with the formation of a white precipitate.

ADVANTAGES

The duration of treatment is reduced by 4-5 days (maximum)

Average daily weight gain increases

The metabolism is restored

Immunity rises

COMPOSITION

Vetom 1 contains dry bacterial mass of live spore-forming bacteria of the Bacillus subtilis DSM 32424 strain, as well as auxiliary substances - powdered sugar and starch. 1 g of the preparation contains: live microbial cells of bacteria Bacillus subtilis - at least 1 xl 06 CFU (colony-forming units).

PHARMACOLOGICAL PROPERTIES

Pharmacotherapeutic group of the medicinal product for veterinary use: probiotic.

Bacillus subtilis DSM 32424 bacteria secrete antibiotic-like substances, enzymes, and other biologically active substances in the intestines of animals, under the influence of which the following are normalized: intestinal biocenosis; acidity of the environment; digestion; absorption and metabolism of iron, calcium, fats, proteins, carbohydrates, triglycerides, amino acids, dipeptides, sugars, bile salts. Vetam 1 stimulates cellular and humoral immunity factors, increases the resistance of animals and poultry to infection with viral and bacterial agents.

PURPOSE

Vetom 1 is used in cattle, pigs, horses, small pets to restore the natural resistance of the body, prevent and treat dysbacteriosis, with intestinal disorders after prolonged antibiotic treatment, when changing diets or when the quality of feed raw materials deteriorates. in violation of normal digestion processes associated with enzyme deficiency, increasing the safety and productivity of animals, stimulating the growth and development of young animals.

DOSAGE AND APPLICATION

For prophylactic purposes, Vetom 1 is used as a group method with water, feed, premixes, mineral and vitamin supplements and other feed mixtures at the rate of 1.5 kg per 1 ton or individually with water or feed at a dose of 50 mg / kg of live weight once a day within 15-20 days.

Rectal administration of Vetom 1 at a dose of 50 mg / kg of live weight is allowed once a day for 15-20 days. The drug is diluted with warm boiled water and administered to the animal after a cleansing enema.

For therapeutic purposes, the drug is prescribed individually at a dose of 50 mg / kg of live weight 2 times a day with an interval of 8-1O hours until the clinical signs of the disease disappear. In severe cases of the disease, it is allowed to increase the frequency of administration up to 4 times a day with an interval of 6 hours.

In order to correct immunodeficiency states, Vetom 1 is prescribed 1 to 2 times a day at a dose of 50 mg / kg body weight for 5 to 10 days.

When used as a solution, a drinking system must be used.

SPECIAL INSTRUCTIONS

Can be used in pregnant animals, in animals during lactation, in the offspring of animals (young animals in the early postnatal period).

It is forbidden to prescribe Vetom 1 simultaneously with antibiotics and sulfonamides. When used in dry loose compound feed, mixing is carried out in accordance with the regulations established for the lines for the production of compound feed. Do not expose the drug to temperatures above 100 В° C for more than 1 O minutes.

The peculiarities of the drug's action at the first administration or its cancellation have not been established.

Special measures for missing one or more doses of the drug are not provided, the course of treatment and prevention continues.

Slaughter products after the use of Vetom 1 are sold without restrictions.

CONTRAINDICATIONS

There were no contraindications to the use of the drug.

SIDE EFFECTS

Side effects were not identified, there are no adverse reactions when using the drug for veterinary use Vetom 1.

There were no symptoms of toxicosis or other adverse reactions in case of an overdose of Vetom 1. Overdose assistance is not required.

SHELF LIFE AND STORAGE

Vetom 1 is stored and transported in the manufacturer's packaging in a dry, dark place at a temperature of 0 В° C to 30 В° C.

The shelf life of the drug is 4 years from the date of release, subject to storage and transportation conditions. After the expiration date, the drug is not suitable for use. After opening the primary package, the drug is stored at room temperature for 15 days.

PACKAGING

The drug is packaged in 0.5 kg polymer bottles.

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