🐾 Vetom 1.2 powder, 5 g

Bacillus subtilis bacteria VKPM I-10641 secrete in the intestines of animals antibiotic-like substances, enzymes and other biologically active substances, which normalize: intestinal biocenosis, acidity, digestion, absorption and metabolism of iron, calcium, fats, proteins, carbohydrates, triglycerides, amino acids, dipeptides, sugars, bile acids salts.
Bacillus amyloliquefaciens VKPM B-10642 and Bacillus amyloliquefaciens VKPM B-10643 used for the preparation production are characterized by high resistance to digestive juices and gastrointestinal enzymes and ability to rapidly colonize it. In intestines of animals bacterial spores transform into vegetative forms and excrete antibiotic-like substances, enzymes and other bioactive substances, thus normalizing intestinal biocenosis, acidity, digestion, absorption and metabolism of iron, calcium, fat, proteins, carbohydrates, triglycerides, amino acids, dipeptides, sugars, bile acids salts.
Vetom 1.2 stimulates cellular and humoral immunity factors, increases resistance of animals and poultry to infection by viral and bacterial agents.

Special instructions

It is prohibited to prescribe Vetom 1.2 simultaneously with antibiotics and sulfonamides.
Possible use in pregnant animals, in animals during lactation, in the offspring of animals (young animals in the early postnatal period).
Animal slaughter products after using Vetom 1.2 are sold without restrictions.
Personal prevention measures
No special precautions are required when working with the drug.

Recommendations for use

For preventive purposes, Vetom 1.2 is used in a group method with water, feed, premixes, mineral-vitamin additives 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 1 time/day for 15-20 days.
The rectal route of administration of Vetom 1.2 is allowed at a dose of 50 mg/kg of live weight 1 time/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 8-10 hours until the clinical signs of the disease disappear. In severe cases of the disease, it is allowed to increase the frequency of administration to 4 times a day with an interval of 6 hours.
In order to correct immunodeficiency states, Vetom 1.2 is prescribed 1-2 times a day at a dose of 50 mg/kg live weight for 5-10 days.
When used as a solution, a drinking system must be used.
When used in dry bulk feed, mixing is carried out in accordance with the regulations established for feed production lines.
Do not expose the drug to temperatures above 100°C for more than 10 minutes.
The specific effects of the drug upon first use or its withdrawal have not been established.
Special measures are not provided for skipping one or more doses of the drug; the course of treatment and prevention is continued.

Side Effects

No side effects were identified, there are no adverse reactions when using the drug Vetom 1.2.
There were no symptoms of toxicosis or other adverse reactions with an overdose of Vetom 1.2. No assistance is required in case of overdose.

Manufacturer

NPF Research Center, Russia