ИнноВет

GENERAL INFORMATION. 1.1 METAPHYSIOL is a feed additive for the regulation of metabolic and physiological processes in the liver of farm animals and poultry. 2.2 METAFIZIOL is a multicomponent mixture of fat and water-soluble vitamins and amino acids , antioxidant and stabilizer. As an active ingredient, 1000 ml contains: L-carnitine - 5000 mg, vitamin B6-500 mg, vitamin B12-15 mg, nicotinamide - 150 mg, calcium pantetonade (D-panthenol) -1000 mg. DL-methionine -10000 mg, sorbitol-100 mg L-lysine - 1000 mg, L-glycine 2000 mg, L-glutamic acid - 1500 mg, L-aspartic acid - 1500 mg. The feed additive is not contains genetically modified products. 1.3 In appearance, METAFIZIOL is a transparent liquid from light red to dark red, well soluble in water. 1.4 Feed additive is packaged in canisters made of polymeric materials, sealed with screw caps of 1 and 10 liters, as well as in glass bottles of 100 ml. Each package is marked in Russian, indicating: the manufacturer's organization, its address and trademark, the name of the feed additive, purpose, method of application, composition and guaranteed parameters, batch number, volume, date of manufacture, shelf life and storage conditions, marked "For animals ". Store in a closed container in a dry place, protected from direct sunlight, at temperatures from + 5C to + 25C. Shelf life in original packaging and subject to temperature conditions - 18 months. 1.5 Do not use METAFIZIOL after the expiration date. APPLICATION PROCEDURE. METAFIZIOL provides detoxifying effect in farm animals and poultry, increases energy capacity, eliminates the toxic effect of ammonia during the period of intensive growth, performs choleretic and vitaminizing actions. The feed additive is used orally with water for drinking daily for 5-7 days at the rate of: poultry: 50-100 ml per 100 liters of drinking water large animals: (cattle, pigs, horses) 30 ml per head small animals: (sheep, goats, piglets, calves and foals) 10 ml per head. Repeat if necessary after a week. < / p> The working solution is prepared immediately before use, taking into account the daily fluid intake and the required concentration. Complications and side effects during use no feed additive has been identified in accordance with this instruction. Do not use METAFIZIOL in the drinking system together with oral vaccines, organic acids. The feed additive contains vitamins and amino acids for which there is no period expectations, i.e. products from farm animals and poultry can be used for food purposes without restrictions. PERSONAL PREVENTION MEASURES. When working with a feed additive, you must follow the rules of personal hygiene and technology security. In case of accidental contact of the product on the skin or mucous membranes, wash them with plenty of water and, if necessary, consult a doctor. METAFIZIOL should be stored in places inaccessible to children. PROCEDURE FOR SUBMISSION OF CLAIMS. In case of non-compliance of the feed additive with the requirements of this instruction, as well as detection of complications, the use of the feed additive is discontinued and the State Enterprise "Belgostsvettsentr" "(Minsk, Krasnaya str. 19a, tel. 2904279), and it is also necessary to transfer 3 arrivals of the additive from the batch in which complications were detected. FULL NAME OF THE MANUFACTURER. Manufacturer: Chemifarma SpA, Italy, Forlì, st. Via Don Eugenio Servadei 16-4710011а1

1. GENERAL INFORMATION< / p> < p>1.1 "Lauritin-C" (Lauritinum C) < p>1.2 The drug is a sterile, transparent, colorless or light yellow liquid with a specific smell of camphor. < p>1.3 The main active ingredients are contained in 1.0 cm3 of the preparation: ascorbic acid-10.0 mg; camphor-1.0 mg; butaphosphane-32.0 mg and excipients-glucose monohydrate-110.0 mg; magnesium chloride-0.13 mg; calcium chloride-0.9 mg / ml; magnesium sulfate-0.08 mg; neutral ingredients: - stabilizers, preservatives and water for injection. < p>1.4 "Lauritin-C" is produced in glass or polypropylene transparent bottles of 100 cm3. < p>1.5 The drug is stored in its original packaging according to list B, in a dry, protected from light place at a temperature of + 8 to + 15 °C. It is allowed to transport "Lauritin-C" packed in an isothermal container for 7 days at an ambient temperature from -20 to + 30 °C. 1.6 The shelf life of the drug is 2 (two) years from the date of manufacture, subject to the storage rules.2. PHARMACOLOGICAL PROPERTIES< / strong>2.1. "Lauritin-C" has a pacemaker, analeptic, antihistamine, antiaggregate and antioxidant effects on the animal's body due to the presence of a balanced composition of biologically available ingredients in its composition. It stimulates the restoration of the general resistance of the body by stabilizing its hormonal background, correcting the functions of the endocrine glands, energy metabolism and metabolism in general. Ascorbic acid is an antioxidant, participates in the formation of collagen, the synthesis of corticosteroids, serotonin, interferon, in the process of immunomodulation, increasing the body's resistance to infections. Promotes phagocytosis, blood clotting, tissue regeneration, reduces vascular permeability, reduces the need for vitamins B, B2, A, E, folic acid, pantothenic acid. It has antiaggregate properties. Maintains the colloidal state of the intercellular substance, normalizing capillary permeability and blood microcirculation. Activates proteolytic enzymes, participates in the exchange of aromatic amino acids, pigments and cholesterol, promotes the accumulation of glycogen in the liver. It is mainly metabolized in the liver to deoxyascorbic acid and then to oxalic acid and diketogulonic acid. It is excreted through the kidneys, intestines, with sweat and milk, in the form of unchanged ascorbate and metabolites. Camphor, stimulating the central nervous system, has a stimulating effect on blood circulation, respiration and metabolic processes in the myocardium. With the weakening of the tissue respiration of the myocardium, it normalizes the oxidative processes, increasing the metabolism and increasing the sensitivity of the heart muscles to the influence of sympathetic nerves. Camphor tones the heart well: - during tachycardia, the heart rate slows down while increasing the contraction of a single push. The release of camphor from the body occurs by its diffusion into the blood of regional microcapillaries. It is excreted through the kidneys, lungs and with bile for 2-3 days in an unchanged form. Butaphosphane, which is part of the drug, has a stimulating effect on most metabolic processes in the body, increases the tone of smooth muscles, myocardium, and improves bone regeneration. It stimulates and normalizes metabolic and energy metabolism, improves the utilization of glucose in the blood, accelerates the metabolic processes by stimulating the ADP-ATP cycle, and protein synthesis. It is not deposited in organs and tissues and does not penetrate into milk. It is excreted from the body through the kidneys.3. PROCEDURE FOR THE USE OF THE DRUG< / p> < p>3.1 "Lauritin-C" is used for all types of productive and non-productive animals. It is an effective tool in the intensive care of critical conditions (shock) with multiple organ failure. In the treatment of various diseases associated with the suppression of respiratory, cardiovascular and hepatic-renal activity of the body, acute and chronic intoxication, including infectious diseases accompanied by fever. Dilutes sputum, helping to improve ventilation in the pulmonary system. By stabilizing hormones and energy metabolism, effective in disorders of metabolism and activation of the General resistance of the organism to reduce the recovery time after an illness, a difficult birth, hyperresponsiveness, stress factors, etc. Used for sedation in the post anesthetic period. < p>3.2 "Lauritin-C" is administered intravenously, intramuscularly or subcutaneously 1-2 times a day. To Enter Slowly! < p>3.3 The dosage and duration of use is determined by the veterinarian individually, depending on the condition of the animal. Average doses: K R S, horses-10-20 ml per animal; foals, calves - 5-10 ml per animal; pigs, sheep, goats-2-5 ml; dogs, cats-1.0 -5.0 ml per animal; rabbits, minks-0.2 -0.5 ml per animal. The drug is not toxic. If necessary, the dose can be doubled. It is allowed to use it daily until the animal is fully recovered. < p>3.4 Side effects: with caution, it should be used in females during pregnancy and lactation. A single passing vomiting is possible with a jet intravenous injection. Intramuscular and subcutaneous jet injection causes a painful reaction. < p>3.5 Do not mix with other drugs in the same syringe. It is permissible to mix with neutral liquids during infusion therapy. 3.6 Slaughter of large, small cattle and pigs for meat is allowed no earlier than 3 days after the last use of the drug. Milk of dairy cows and sheep is allowed to be used no earlier than 3 days after the last application of the drug. The meat of animals forcibly killed before the expiration of the specified period can be used as food for fur-bearing animals.4. PERSONAL PREVENTION MEASURES < p>4.1 When working with the drug, it is necessary to observe generally accepted personal hygiene and safety measures5. THE PROCEDURE FOR FILING COMPLAINTS< / p>5.1 In the event of complications after the use of the drug, its use is discontinued, the consumer applies to the State Veterinary Institution in the territory where he is located. Veterinary specialists of this institution study compliance with all the rules for the use of this drug in accordance with the instructions. When confirming the detection of a negative effect of the drug on the animal's body, veterinary specialists take samples in the required amount for laboratory tests, write a sampling report and send it to the State Institution "Belarusian State Veterinary Center" of the Republic of Belarus, Minsk, Krasnaya str.19a for confirmation of compliance with regulatory documents.6. FULL NAME OF THE MANUFACTURER< / strong>6.1 " ImmKont GmbH "(Germany), Angermunder str. 45, Eberswalde D -16227, Germany. Telefax +49 3334 383075; e-mail: The manual was developed by the specialists of the company "ImmKont GmbH" (Germany)

GENERAL INFORMATION The drug is intended for the treatment of calves, pigs, chickens, turkeys, rabbits, laying hens INDICATIONS: Bacterial enteritis from gram-negative bacteria such as Salmonella, E. coli, Hemophilus influenzae, Pasteurella spp., Klebsiella spp., Shigella, Pseudomonas, Enterobacter spp. E Proteus spp. Dosage and method of administration In drinking water or liquid feed for all types of animals: 4.2 - 5.0 ml / 100 kg of animal weight (equal to 5.0 - 6.0 mg of colistin sulfate / kg of animal weight) depending on age, weight and water consumption of animals, 3-15 days. To ensure the correct dosage, the weight of the animal must be determined as accurately as possible to avoid treatment with insufficient doses. Use proper and appropriate dispensing equipment. Do not use in solid feed. For correct use, remove residual water or liquid feed from the drinking bowls and use Colisid according to your veterinarian's instructions. It is recommended to inject the product every 12 hours, dividing the daily dose into two applications. At the end of the treatment, restore drinking water without the drug. Ingestion of the drug can be changed depending on the disease. Repeated or prolonged use should be avoided by improving containment and disinfection practices. SPECIAL PRECAUTIONS The use of veterinary drug (colistin) in poultry must comply with Commission Regulation EC 1177/2006 and national regulations transposition. Due to possible variations (in place and time) in the sensitivity of the target species to colistin, a bacteriological examination and susceptibility test are recommended. Any use of the drug not in accordance with the instructions can increase the prevalence of bacteria resistant to colistin and can reduce the effectiveness of treatment with other antibiotics of the polymyxin group and develop cross-resistance. Do not leave water diluted with the preparation within reach of other animals. Special precautions must be taken by the person using the drug when treating animals: No special precautions are required when working with the drug. However, it is advisable to avoid direct skin contact and inhalation of the drug. The use of protective gloves is recommended when working with the drug. In case of accidental contact, wash thoroughly with soap and water. If irritation persists, seek medical attention. People with known hypersensitivity to colistin should avoid contact with veterinary medicinal products. CONTRAINDICATIONS Do not use in animals with known hypersensitivity to colistin. Do not use in animals with a polygastric digestive system with functioning scars. ADVERSE REACTIONS Prolonged use of the drug can cause intestinal dysbiosis and lead to the development of insensitive microorganisms. In case of any adverse reactions or other reactions not mentioned here, please notify your veterinarian.

Composition and form of releaseInotyl 200 contains 200 mg of tylosin tartrate as the active ingredient in 1 ml, and benzyl alcohol, dimethylacetamide, propylene glycol, and water for injection as excipients.Inotil 200 is produced packaged in 100 ml glass bottles of the appropriate capacity, capped with rubber stoppers, reinforced with aluminum caps. The vials are packed in individual cardboard boxes. The drug in appearance is a transparent, colorless, oily liquid.Pharmacological propertiesIntel 200 (200 Inotyl) - an antibacterial drug in the form of a solution for injection, intended for the treatment of animals with diseases of bacterial etiology.Tylosin tartrate, which is part of the drug, belongs to the macrolide group of antibiotics, is active against most Gram-positive and some Gram-negative microorganisms, including Stapylococcus spp., Streptococcus spp., Clostridium spp., Corynebacterium spp., Pasteurella spp., Treponema hyodysenteriae, Chlamydia spp., Spirocheta spp. and Mycoplasma spp. Microorganisms of the Enterobacteriaceae family are resistant to the antibiotic. The mechanism of bacteriostatic action of tylosin tartrate is to block protein synthesis in the microbial cell. When administered intramuscularly, the antibiotic is well absorbed from the injection site into the blood and penetrates almost all organs and tissues of the body. The highest levels of tylosin are found in the lungs, liver, mammary glands, and kidneys. After a single injection, the therapeutic concentration of the antibiotic remains in the body for at least 20 hours.Tylosin is released from the body of animals mainly with bile, in smaller amounts - with urine and milk.According to the degree of exposure to the body, Inotil 200 is a moderately dangerous substance (hazard class 3 according to GOST 12.1.007-76).Indications for useInotil 200 is used for the treatment of bronchopneumonia, infectious agalactia of large and small cattle, enzootic pneumonia, arthritis, dysentery, atrophic rhinitis and erysipelas of pigs, mastitis of cattle, as well as for therapeutic and prophylactic purposes in secondary infections. < h3>DosageThe drug is used intramuscularly in animals, 1 time a day for 3 days in the following doses: cattle-0.5-1 ml/20 kg of animal weight; sheep and pigs-1 ml/20 kg of animal weight.When using the drug to pigs, in rare cases, allergic reactions are possible, which quickly pass after stopping the administration of the drug. In connection with a possible pain reaction, do not inject more than 10 ml in one place to cattle, pigs and sheep more than 5 ml, and also mix it in one syringe with other medicines.Special instructionsSlaughter of animals for meat is allowed no earlier than 8 days after the last use of the drug. The meat of animals forcibly killed before the expiration of the specified period can be used for feeding fur-bearing animals.Milk of dairy animals during the treatment period within 4 days after the last administration of the drug is prohibited to be used for food purposes. Such milk after boiling can be used for feeding fur-bearing animals.Storage conditions and terms< / h3> < p>Store the drug in a closed package, in a dry place, protected from direct sunlight, at a temperature from 5 0C to 25 0C.The shelf life of the drug, subject to storage conditions, is 2 years from the date of manufacture.Inotil 200 should not be used after the expiration date.Intel 200 should be stored in places inaccessible to children.Manufacturer< / h3> "CEVA Sante Animale" / "CEVA Sante Animale" (France)

InoxelFor the treatment of diseases of bacterial etiology in cattle and pigs, prevention of bacterial infections in chickens < h3>General informationTrade name of the medicinal product: Inoxel.International nonproprietary name: ceftiofur.Dosage form: powder for the preparation of a solution for injection. Inoxel as an active substance in 1 bottle contains ceftiofur sodium-1.06 g (equivalent to 1 g of ceftiofur) or 4.2 g (equivalent to 4 g of ceftiofur).In appearance, the drug is an amorphous powder of white or light beige color.Inoxel is produced in the form of a sterile powder, packaged in 1.06 g or 4.2 g in glass vials with a capacity of 20 ml or 80 ml, respectively. The powder bottles are packed in individual cardboard boxes.Store Inoxel in the closed packaging of the manufacturer, separately from food and feed, in a dry place, protected from direct sunlight, at a temperature of 5 0C to 20 0C. The shelf life of the drug under the conditions of storage in a closed package is 2 years from the date of production, after opening the bottle – 28 days < br>It is forbidden to use Inoxel after the expiration date. Inoxel should be stored out of the reach of children.Unused medicinal product is disposed of in accordance with the requirements of the legislation. Pharmacological propertiesInoxel belongs to the antibacterial drugs of the cephalosporin group.Ceftiofur sodium, which is part of the drug, has a wide spectrum of antibacterial action on Gram-negative and gram-positive bacteria, including strains that produce beta-lactamase, and some anaerobic bacteria, including: Escherichia coli, Pasteurella (Mannheimia) haemolytica, Pasteurella multocida, Haemophilus somnus, Actinobacillus pleuropneumoniae, Haemophilus parasuis, Salmonella cholerasuis, Salmonells typhimurium, Streptococcus suis, Streptococcus zooepidemicus, Streptococcus equi, Streptococcus agalactiae, Streptococcus dysgalactiae, Streptococcus bovis, Pasteurella spp., Staphilococcus spp., Actynomyces pyogenes, Klebsiela, Citrobacter, Enterobacter, Bacillus spp., Proteus spp., Fusobacterium necrophorum and Porphiromonas assacharolytica (Bacteroides melaninogenicus). The mechanism of the bactericidal action of the antibiotic is to inhibit the synthesis of the cell wall of the bacterium. After parenteral administration, ceftiofur enters the systemic bloodstream, is rapidly metabolized, reversibly binds to plasma proteins, and is concentrated at the sites of inflammation.The maximum concentration of the antibiotic in the blood plasma after intramuscular administration of the drug is reached in 0.5-2 hours and remains at the therapeutic level for up to 24 hours. The antibiotic is excreted from the body mainly in the urine and partially with feces, the half-life, depending on the type, age of the animal and the method of administration, is 10-19 hours.< br> Inoxel by the degree of exposure to the animal body belongs to the moderately dangerous substances (hazard class 3 according to GOST 12.1.007). Application procedureInoxel is prescribed for the treatment of bacterial respiratory infections in cattle caused by Pasteurella haemolytica, Pasteurella multocida, Haemophillus somnus, Actinobacillus pleuropneumoniae, and pigs caused by Pasteurella haemolytica, Pasteurella multocida, Haemophillus somnus, Actinobacillus pleuropneumoniae, Salmonella cholerasuis, Streptococcus suis; for the treatment of necrobacteriosis associated with Fusobacterium necrophorum and Porphiromonas assacharolytica (Bacteroides melaninogenicus in cattle, and for the prevention of early death of one-day-old chickens caused by Escherichia coli and Staphylococcus aureus. Contraindication to the use of Inoxel is an increased individual sensitivity of the animal to antibiotics of the cephalosporin group.Inoksel used for animals parenterally in a sterile solution, making the vial 1.06 g sterile powder make 20 ml of solvent (water for injection, saline diluent for vaccines Marek (if the drug is used to treat birds)), in a bottle from 4.02 g of sterile powder 80 ml of solvent. Dissolution Inoksela should be carried out as quickly as possible, water for injection (water for injection, saline diluent for vaccines Marek (if the drug is used to treat birds)), type in a sterile syringe with a large amount of needle with a large diameter and contribute to the vial with powder, then shake the vial immediately until the powder is completely dissolved. The resulting therapeutic solution contains 50 mg of ceftiofur /ml. The term of use of the therapeutic solution is: when stored in a dark place at a temperature of 5°C to 20°C – 12 hours, when stored in the refrigerator at a temperature of 2°C to 8°C-7 days, when stored in frozen form at a temperature of minus 4 ° C to minus 18°C-8 weeks.The therapeutic solution is administered to the animal once a day in the following doses: - to cattle-intramuscularly 1 ml per 50 kg of weight (1 mg of ceftiofur per 1 kg of animal weight). The course of treatment for respiratory diseases caused by Mannheimia haemolytica, Pasteurella multocida and Histophilus somni – 3-5 days; for acute interdigital necrobacillosis (panaritium, hoof rot) caused by Fusobacterium necrophorum and Bacteroides melaninogenicus – 3 days; - pigs – intramuscularly 1 ml per 16 kg of weight (3 mg ceftiofura per 1 kg of animal weight). The course of treatment for respiratory diseases caused by Pasteurella multocida, Actinobacillus pleuropneumonia and Streptococcus suis is 3-5 days; - one-day-old chickens-subcutaneously in the neck at a dose of 0.2 ml. Before administration to chickens, the standard solution (50 mg of ceftiofur/ml) is diluted with water for injection in accordance with the table, so that 0.2 ml of the administered solution contains 0.08 – 0.2 mg of ceftiofur (3 column of the table).TableDose of ceftiofur/chicken Volume of standard Inoxel solution (50 mg / ml) Volume of added solvent1 2 30.08 mg 1 ml 124 ml < br>0.10 mg 1 ml 99 ml < br>0.12 mg 1 ml 82 ml0.14 mg 1 ml 70 ml0.16 mg 1 ml 61 ml0.18 mg 1 ml 54 ml0.20 mg 1 ml 49 mlWith an overdose of the drug, the animal may experience a decrease in appetite, inflammatory reaction at the injection site.Features of the action at the first administration of the drug and at its cancellation were not revealed.Skipping the next dose of the drug should be avoided, as this can lead to a decrease in therapeutic effectiveness. In case of missing one dose, it is necessary to introduce it as soon as possible, then the interval between injections of the drug does not change.Side effects and complications when using Inoxel in accordance with this instruction, as a rule, are not observed. In some animals, a local reaction may occur at the injection site in the form of edema, which resolves spontaneously within a few days. With increased individual sensitivity to the drug and the manifestation of allergic reactions, the use of the drug is discontinued and the animal is prescribed antihistamines and symptomatic therapy.Inoxel should not be prescribed simultaneously with drugs of bacteriostatic action, due to a decrease in its bactericidal activity, as well as mixed in one syringe with other drugs.Slaughter of cattle for meat is allowed no earlier than 24 hours, pigs-no earlier than 48 hours after the last application of Inoxel. The meat of animals that were forcibly killed before the expiration of these terms can be used as food for fur-bearing animals. Milk of dairy cows during and after the use of Inoxel is allowed to be used for food purposes without restrictions. Personal prevention measuresWhen working with Inoxel, you should follow the general rules of personal hygiene and safety, provided for when working with medicines. At the end of the work, wash your hands with warm water and soap.In case of accidental contact of the drug with the skin or mucous membranes of the eye, they should be washed with plenty of water. People with hypersensitivity to the components of the drug should avoid direct contact with Inoxel. In case of allergic reactions or accidental ingestion of the drug in the human body, you should immediately contact a medical institution (you should have the instructions for using the drug or the label). Empty vials from under the drug may not be used for household purposes, they are subject to disposal with household waste.Manufacturer:< / h3> < p>VETANCO S. A.; Chile 33 B 1603 CMA Vicinte Lopez, Buenos Aires, Argentina.

1. GENERAL INFORMATION 1.1. Ingaflor 10% solution (INGAFLOR 10% LIQUID) 1.2. Ingaflor 10% solution is an antibacterial drug in the form of a solution for oral administration, containing 100 mg / ml florfenicol as an active ingredient, as well as an auxiliary component - polyethylene glycol 400 to 1000 ml. 1.3. In appearance, the drug is a yellowish transparent viscous liquid, odorless, for the preparation of solutions with drinking water for animals. 1.4. The drug is produced packaged in high density polyethylene bottles with a capacity of 250 ml, 1L and 5L. 1.5. Store the medicinal product with precautions (list B), in a cool and dry place, protected from direct sunlight, at temperatures from + 5 ° C to + 25 ° C, avoiding freezing. Keep out of reach of children. 1.6. Shelf life of the veterinary medicinal product, in its original packaging: 2 years. Shelf life after opening the original packaging: 3 weeks. 2. PHARMACOLOGICAL PROPERTIES 2.1. Ingaflor 10% solution contains the active ingredient: florfenicol. The drug is used in veterinary medicine as an antibacterial agent. Florfenicol is a thiamphenicol derivative in which the hydroxyl group is replaced by a fluorine atom. Florfenicol has a bacteriostatic effect on sensitive microorganisms. In the protoplasm of a bacterial cell, it binds to the 70S ribosomal subunit, where it blocks the enzyme peptidyl transferase, which leads to inhibition of protein synthesis in sensitive bacteria at the ribosome level. Florfenicol is active against bacteria that produce acetyltransferase and are resistant to chloramphenicol. 3. ORDER OF APPLICATION OF THE PREPARATION 3.1. The drug is intended for the treatment of infections in poultry caused by microorganisms sensitive to florfenicol, such as Chlamydia, E. coli, Pasteurella, and Mycoplasma (for chlamydia, mycoplasmosis, CRD, necrotizing enteritis, colibacillosis, cholera), in pigs for the treatment of infections caused by Actinobacillus plepneumonia , Pasteurella species (P. multocida, P. haemolytica) and for the treatment of respiratory diseases caused by Haemophylus species. 3.2. The drug is used in birds and pigs. Ingaflor 10% solution is administered to birds orally with drinking water in a daily dose of 20 mg per 1 kg of body weight, which corresponds to: chickens under 4 weeks of age 150 ml of the drug per 100 liters of drinking water. For birds older than 4 weeks, 200 ml of the preparation per 100 l of water. Within 5 days. Ingaflor 10% solution is administered to pigs orally with drinking water in a daily dose of 10 mg florfenicol per 1 kg of body weight. (The average amount is equivalent to 100 ml "Ingaflor 10% solution" per 100 liters of drinking water). Within: 7 days. 4. PRECAUTIONS 4.1. When working with the drug, you should follow the general rules of personal hygiene and safety measures provided for when working with drugs. 5. PROCEDURE FOR SUBMISSION OF CLAIMS 5.1. In case of complications after using the drug, its use is stopped, and the consumer applies to the State Veterinary Institution in the territory in which he is located. Veterinary specialists of this institution conduct a study of compliance with all rules for the use of the drug in accordance with the instructions ... Upon confirmation of the detection of a negative effect of the drug on the animal's body, veterinary specialists take samples in the required amount for laboratory tests, write a sampling act and send it to the State Institution "Belarusian State Veterinary Center" for confirmation of compliance with regulatory documents. 6. MANUFACTURER 6.1. United Pharma, Hungary Instructions for the use of Ingaflor 10% solution prepared by the applicant Inga Pharm LLC, (Russia, 236016 Kaliningrad, Grazhdanskaya st., 28, building 11) < / p>

1. GENERAL INFORMATION 1.1. Ingaflor 10% oral powder (INGAFLOR 10% ORAL POWDER) 1.2. Ingaflor 10% oral powder is an antibacterial drug for oral administration, containing florfenicol 100 g as an active ingredient, and two excipients tixosil 1.0 g and dextrose monohydrate up to 1000 g. 1.3. In appearance, the drug is a white or almost white crystalline powder, odorless, for inclusion in animal feed. 1.4. The drug is produced packaged in multilayer polyethylene bags of 1 kg and 10 kg. 1.5. Store the drug with caution (list B), in a cool and dry place, protected from direct sunlight, at a temperature not lower than + 25 ° C. Keep out of reach of children. 1.6. Shelf life of the veterinary medicinal product, in its original packaging: 2 years. 2. PHARMACOLOGICAL PROPERTIES 2.1. Ingaflor 10% oral powder contains the active ingredient: florfenicol. The drug is used in veterinary medicine as an antibacterial agent. Effective in the treatment of infections caused by gram-positive and gram-negative bacteria. It is used to treat infections of pigs caused by microorganisms sensitive to the drug, such as Actinobacillus pleuropneumoniae, E. coli, Salmonella cholerae-suis, Pasteurella, Streptococcus suis, Mycoplasma, as well as some types of anaerobic microorganisms; and in fish for the treatment of furunculosis (peptic ulcer disease), as well as yersiniosis. 3. ORDER OF APPLICATION OF THE PREPARATION 3.1. Target animals: Pigs. Indications for use: pneumonia, enteritis and microorganisms sensitive to the drug. 3.2. Method of application and dosage: pigs 10 mg / kg body weight / day for 5 consecutive days with feed. For the treatment of enzootic pneumonia in pigs: Ingaflor 10% oral powder should be added to the feed add 10 mg of florfenicol per kg of body weight daily. The dose is 200-400 mg / kg of florfenicol in feed - the equivalent of 2 to 4 kg. Ingaflor 10% oral powder per ton of feed administered over 5 consecutive days. 4. PRECAUTIONS 4.1. When working with the drug, you should follow the general rules of personal hygiene and safety measures provided for when working with drugs. 5. PROCEDURE FOR SUBMISSION OF CLAIMS 5.1. In case of complications after using the drug, its use is stopped, and the consumer applies to the State Veterinary Institution in the territory in which he is located. Veterinary specialists of this institution conduct a study of compliance with all rules for the use of the drug in accordance with the instructions ... Upon confirmation of the detection of a negative effect of the drug on the animal's body, veterinary specialists take samples in the required amount for laboratory tests, write a sampling act and send it to the State Institution "Belarusian State Veterinary Center" for confirmation of compliance with regulatory documents. 6. MANUFACTURER 6.1. United Pharma, Hungary Instructions for the use of Ingaflor 10% oral powder were prepared by the applicant Inga Pharm LLC, (Russia, 236016 Kaliningrad, Grazhdanskaya st., 28, building 11)

GENERAL INFORMATION In appearance, the drug is a flowing yellow powder. The shelf life of the drug, subject to storage conditions in a sealed package, is 36 months from the date of production. The shelf life of liquid feed with the preparation is 12 hours. After opening the package, it is recommended to completely use up the product during therapy. It is forbidden to use after the expiration date. The medicinal product is produced in the form of a sterile powder packaged in 1 kg each in white polyethylene jars with a safety stopper, complete with a bottom lid and an insert, each packing unit is supplied with instructions for use. PHARMACOLOGICAL (BIOLOGICAL) PROPERTIES DOXIPHARM 50% - antibiotic, tetracycline group, ATC code Vet: QJ01AA02, intended for the treatment of broilers and pigs with diseases of bacterial and mycoplasma etiology. Tetracyclines are bacteriostatic antibiotics that inhibit protein synthesis necessary for the life of bacterial cells. Tetracyclines act by binding to the 30-S ribosome of bacteria through chelating bonds with the phosphate groups of messenger RNA. They also prevent the connection of transport RNA with messenger RNA ORDER OF APPLICATION DOXIPHARM 50% are used in pigs for the treatment of chronic respiratory diseases and other respiratory diseases, mainly caused by Pasteurella spp., Mycoplasma spp. ., Haemophilus gallinarum., Bordetella avium and Chlamydia psittaci. It is also used in pigs for the treatment of atrophic rhinitis and respiratory diseases, mainly caused by Actinobacillus spp. Bordetella bronchiseptica, Mycoplasma spp., Pasteurella multocida, Streptococcus suis. It is forbidden to use DOXIPHARMA 50% in animals with severe liver and kidney damage, with significant disorders in the development of cartilage tissue, with lesions of the nervous system, accompanied by convulsions; with hypersensitivity to doxycycline and tetracyclines. DOXIFARM 50% is used: for broilers - 4.0 g of the drug per 100 kg of animal weight (equivalent to 20 mg of doxycycline per 1 kg of animal weight), which corresponds to approximately 15-30 g of the drug per 100 liters of water for 3-5 days. pigs - 2.0 g of the drug per 100 kg of animal weight (equivalent to 10 mg of doxycycline per 1 kg of animal weight) for 3-5 days. It is recommended to divide the dose into two doses a day. PERSONAL PREVENTION MEASURES When working in DOXYFARM 50%, you should follow the general rules of personal hygiene and safety measures provided for when working with medicines ... When working with the drug, it is prohibited to drink, smoke and eat. After handling the medicine, wash your hands with soap and water. FULL NAME OF MANUFACTURER CHEMIFARMA S.p.A., Italy, Forlì, st. Via Don Eugenio Servadei, 16- 47100.

Viatoss adsorbent of mycotoxins in raw materials and feed for farm animals and poultry General information. Viatoss contains: ammonium salt, gelling agent (polyvinylpyrrolidone), colloidal aluminosilicates tri HSCAS with different charges and cation exchange capacity, micronized excipient. Release form - fine powder from brown to dark brown color. Biological properties. < p> Viatoss inactivates mycotoxins in contact with feed and in the intestines of animals and poultry. The process of inactivation of feed mycotoxins occurs in three different ways: silicate is aimed at the physical binding of polar mycotoxins - aflatoxin, zearalenone, T2 toxin, fumanisin; physical gelation of the gelling substance (3D lattice is formed) in the intestinal lumen; the process of chemical inactivation as a result of structural changes in the mycotoxin molecule, which is converted into net molecule (toxout). How to use it. Viatoss is added to the feed using the existing feed preparation technology. Recommended rates for the introduction of the Viatoss mycotoxin adsorbent ": for prophylaxis - from 500 g to 1.0 kg. per 1 ton of feed; with a low risk of contamination - from 1.0 kg to 1.5 kg per 1 ton of feed; with a high risk of contamination - up to 2.0 kg per 1 ton feed; Benefits of Viatoss The adsorbent does not cause side effects even at high rates of introduction. Products of farm animals and poultry after application of Viatoss can be used for food purposes without restrictions. Retains the activity of vitamins, minerals and other ingredients used for feeding in the feed itself and the small intestine. Manufacturer CHEMIFARMA SpA, Italy, Forli, Via Don Eugenio Servadei, 16-47100

General provisions In 1 ml. the drug contains 50 mg as an active ingredient. enrofloxacin. Excipients: propylene glycol-50 mg, potassium hydroxide-10 mg, benzyl alcohol-10 mg, methylparaben-1 mg, water for injection up to 1 ml. Bactyl 5 % injection is available in 100 ml vials. Pharmacological properties Enrofloxacin-quinolcarboxylic acid derivative belongs to fluoroquinols of the 3rd generation, has a wide spectrum of antibacterial action against gram-positive and gram-negative bacteria, in including Escherichia coli, Haemophilus spp., Pasteurella spp., Salmonella spp. Staphylococcus spp., Streptococcus spp., Clostridium perfmges, Bordetella bronchi- chiceptica, Campylobacter spp., Corinebacterium pyogenes, Pseudomonas spp. ... Cattle: slaughter of animals for meat is allowed no earlier than 14 days after the last use of the drug. The meat of animals that were forcedly killed before the expiration of the established period can be used to feed fur-bearing animals. How to use the drug Bactyl 5% injection is prescribed for medicinal purposes in cattle, pigs, dogs and cats for the treatment of bronchopneumonia, enzootic pneumonia, colibacillosis, salmonellosis, streptococcosis, septicemia, genitourinary and other diseases caused by microorganisms sensitive to fluoroquinolones, as well as mixed and secondary infections in viral diseases. Pigs are used for the treatment of enzymes. pneumonia, atopic rhinitis, mastitis-metritis-agalactia syndrome. The drug is used once a day in calves, dogs and cats subcutaneously, intramuscularly in pigs. For calves and pigs: 1 ml per 10 kg of animal weight (5 mg of enrofloxacin per 1 kg of animal weight) for 3-5 days. Dogs and cats: 1 ml per 10 kg of animal weight (5 mg of enrofloxacin per 1 kg of animal weight) for 5 days. At x ronic and severe diseases - up to 10 days. Contraindications Do not use Bactyl 5% for dogs under 1 year old, because of the possibility of damage to the articular cartilage during the period of rapid growth, especially in dogs large breeds. Use Bactil 5% with caution in very large breeds up to 18 months of age due to their longer growth period. Do not use in cats under 8 weeks of age. Bactyl 5% is not recommended for disease prevention. Cats: In case of overdose, damage to the retina, including blindness, is possible. In case of accidental overdose, there are no antidotes, and treatment should be symptomatic. When conducting a study of target groups of animals, daily administration of the drug at a dose of 15 mg / kg for 21 days led to a recoverable visual impairment in cats. With a single daily administration of the drug for 21 days at a dose of 30 mg / kg, an irreparable impairment of visual function was observed. With a single daily administration of the drug at a dose of 50 mg / kg for 21 days, blindness is possible. Dogs: Sometimes skin reactions may occur, especially when using the drug for hunting greyhounds. Do not exceed the recommended dose. Do not enter drug to the same site when repeated injections. Use of the drug must comply with local veterinary legislation. Fluoroquinolones should be used when the effectiveness of other antibiotics is in doubt and should remain stock antibiotics. < br> Fluoroquinolones should be used only after an antibiogram for sensitivity. Do not use lactating animals whose milk is used as food for humans. Do not use Bactyl 5% injection together with bacteriostatic antibiotics (levomycytin, macrolides and tetracyclines), theophylline and non-steroidal anti-inflammatory drugs. Manufacturer VETANCO S.A. company; Chile 33 B 1603 CMA Vicinte Lopez, Buenos Aires, Argentina.

General provisions "Antitox" - "Antitoxum". The drug is a sterile, transparent liquid with a specific smell of sulfur. 1.0 cm3 of the drug contains sodium thiosulfate pentahydrate 0, 2 g; sodium glutamate 0.022 g; chlorocresol 0.001 g; sodium bisulfite 0.0005 g; water for injection up to 1.0 cm3. The drug is produced packaged at 50.0; 100.0; 250.0 cm3 in glass vials. The drug is stored in the manufacturer's packaging according to the list in a dry, dark place at a temperature from + 5 ° C to + 25 ° C. Shelf life of the drug) years from the date of manufacture, subject to compliance rules for transportation and storage. Pharmacological properties The drug "Antitox" is intended for detoxification of the body by binding toxic products with the formation of non-toxic sulfites in case of poisoning with arsenic, mercury, lead and low-toxic rhodanic substances poisoning with hydrocyanic acid and its salts, iodine and bromine salts, ammonia utilization to urea. The resulting non-toxic compounds are excreted in the urine. The drug has a stabilizing effect on the membranes of hepatocytes, improves their energy supply, normalizes protein, carbohydrate and fat metabolism, increases the body's resistance to hypoxia. The drug helps to optimize the transport and use of oxygen in tissues, normalize the acid-base state of the blood, stimulate the transmission of excitation in the synapses of the central nervous system, increase the synthesis of protein and RNA in the liver tissue, preventing the development of hepatic coma in case of poisoning with hepatotropic poisons. Antitox "Improves the endocrine, immune and metabolic functions of the body, which play a major role in the prevention of multiple organ failure in critical conditions, which is an important condition for the treatment of this condition. How to use the drug The drug is used in as an antidote and hepatoprotector in case of poisoning with compounds of heavy metals, arsenic, cyanides, nitrates, nitrites, iodine and broma salts, as well as in mycotoxicosis and toxicosis of pregnant women. The drug is used in complex therapy In the treatment of metabolic disorders, liver dysfunction (hepatic coma), uremic syndrome, allergic dermatitis, eczema, acetonuria, acidosis, agalactia, anorexia, pododermatitis, neuritis, The drug is administered slowly, intravenously, intramuscularly, subcutaneously or intraperitoneally, once a day, until recovery in doses (per animal, ml): horses, cattle 40.0; pigs, sheep and goats 20 , 0-30.0; dogs 5.0-15.0; cats, rabbits, minks 3.0-5.0; guinea pigs, chinchillas, hamsters 1.5. If necessary, in severe cases of the disease) the dose of the drug should be doubled. The temperature of the drug at the time of administration should not be lower. There are no contraindications to the use of the drug. During pregnancy and lactation, the use of the drug does not wash away the negative effect on the condition of the animal and the fetus. As a result of individual intolerance, during the jet intravenous administration of dogs and cats are vomiting, Slaughter of animals for meat is allowed without a waiting period. Personal precautions When working, you should follow the rules of personal hygiene and safety measures provided for working with medicines ... Does not pose a Danger for the environment. Manufacturer ImmCont ImmCont GmbH), (Address: Angermunder Str16227 Eberswalde, Germany)

General information ANPROSOL AMINOBETA (ANPROSOL AMINOBETA is a feed additive for normalizing metabolism in all types of animals and poultry (regulator of liver function). It is a multicomponent mixture of water-soluble vitamins and amino acids, does not contain. As an active ingredient in 1 liter contains vitamin 110,000 mg, vitamin 24,000 mg, vitamin 64,000 mg, vitamin 1220 mg, vitamin 10 mg, pantothenic acid 22,000 mg, vitamin PP 45,000 mg, inositol ( vitamin 85 500 mg, chloride 200 000 mg and essential amino acids 8 530 mg in total. In appearance it is a transparent liquid from brown to brown, highly soluble in water. Biological properties < / strong> Vitamin 1- takes part in water, carbohydrate, protein and phosphorus metabolism.Participates in the transmission of nerve impulses and nervous excitement.Prevents oxidation of vitamins C and 6 participates in the synthesis of glycogen, fats, protein, nuc leic acids, stimulates the consumption of feed, creating conditions for the normal growth and development of farm animals and poultry. Vitamin 2- is part of 30 recovery processes, participates in the process of absorption and use of fats, the construction of hemoglobin molecules. Affects the correct metabolism of proteins and carbohydrates. Vitamin D-pantothenic acid (B3) - is an active part of many enzymes, is closely related to the metabolism of many B vitamins. Choline chloride is a carrier of mobile methyl groups. It is a constituent element of phospholipids. Choline is essential for the normal maturation of cartilage tissue and prevention of pecking, participates in fat metabolism of the liver, preventing fatty degeneration. Vitamin PP (B5) - in the body is converted into pantothenic acid and acquires its function. Stimulates the secretory function of the digestive glands, plays an important role in lipid metabolism, the metabolism of certain amino acids, participates in the Krebs cycle. Vitamin B6 - participates in the synthesis and breakdown of amino acids, fat, protein and energy metabolism, collagen synthesis. Inositol - is an integral part of lipoproteins, changes the concentration of calcium in the cytoplasm of the cell, activating calcium channels. Vitamin B12 - regulates the process of hematopoiesis, has a methionine-saving effect, is necessary for the normal activity of the mucous membrane of the gastrointestinal tract. Vitamin H - is part of the series enzymes, is involved in carbohydrate metabolism, the metabolism of cholesterol and nucleic acids, the development of immunity against infectious diseases. Amino acids are non-hydrolyzable proteids containing functional acidogroups - COOH and functional groups of primary amines - NH2 in their structure, participate in the formation of neurotransmitters, have antidepressant activity, participating comfort in the formation and accumulation of glycogen in muscles and liver, are part of proteins and contribute to muscle building. They stimulate the work of the pituitary gland, increase the production of growth hormone, take part in hematopoiesis, and above all in the production of hemoglobin. How to use ANPROSOL AMINOBETA is used to normalize work liver, metabolism and an increase in natural resistance in farm animals and poultry during the period of intensive growth, as well as an antistress agent during vaccination, restoration of intestinal microflora. Applied orally with water for drinking daily for 5-10 days at the rate of: poultry: 100-200 ml per 100 liters of drinking water per day; large animals (cattle, pigs, horses): 20-30 ml per head per day; small animals (sheep, goats, pigs, calves and foals): 5 ml per head per day. If necessary, the course can be extended up to 15 days. The working solution is prepared immediately before use, taking into account the daily consumption of liquid and the required concentration. Do not use cor new supplement ANPROSOL AMINOBETA in the drinking system together with oral vaccines and organic acids. Advantages ANPROSOL AMINOBETA contains vitamins and amino acids for which there is no period expectations, that is, products from farm animals and poultry can be used for food purposes without restrictions. The synergism of the action of vitamins and amino acids normalizes the functions of various enzyme systems of the body, which has a positive effect on metabolism and increases the natural resistance of the body, improves the average daily weight gain and safety of livestock. Manufacturer CHEMIFARMA SpA, Italy, Forli, Via Don Eugenio Servadei street, 16-47100