VETKO

COLIVET ORAL is a veterinary oral solution containing colistin sulphate at 2,000,000 IU per ml according to the manufacturer’s product information. Colistin belongs to the polymyxin group of antibiotics and has bactericidal activity against selected Gram-negative bacteria. It acts primarily by interacting with the outer membrane of susceptible organisms, disrupting membrane integrity and ultimately causing bacterial cell damage and lysis. A key practical characteristic of colistin after oral administration is its very limited absorption from the gastrointestinal tract, so its antibacterial activity remains concentrated mainly within the intestinal lumen.
The product information identifies susceptible Gram-negative organisms such as Escherichia coli, Salmonella, Haemophilus, Pasteurella and selected Pseudomonas species among its target spectrum. COLIVET ORAL is therefore intended for the treatment of selected gastrointestinal infections caused by colistin-sensitive bacteria, particularly colibacillosis and salmonellosis in calves, lambs, kids and poultry when the attending veterinarian considers colistin appropriate.
The solution is freely mixable with water, allowing practical administration through drinking-water systems. Correct preparation is essential. The amount of product added should follow the approved label, and actual water consumption should be monitored to help ensure that animals receive the intended dose. Drinking-water lines should remain clean, and medicated water should not be stored or used beyond the period recommended by the manufacturer. Clinical progress should also be monitored, because diarrhea and enteric disease can have viral, parasitic, nutritional or management causes for which an antibacterial drug would not be appropriate.
Responsible use of colistin is especially important because antimicrobial resistance to polymyxins is a significant concern in both animal and human health. COLIVET ORAL should therefore be reserved for cases in which a clear bacterial indication exists and where susceptibility is expected or confirmed. Culture and susceptibility testing are recommended whenever feasible, particularly in recurrent herd or flock problems. Approved species, indications, contraindications and withdrawal periods must be followed strictly.
COLIVET ORAL is for veterinary use only. This website description is intended to provide a clear product overview and does not replace the official package leaflet, local regulations or veterinary advice. Always follow the manufacturer’s approved dosage, treatment duration, withdrawal period, storage conditions and handling precautions.

GENTA-DOX 20/20 WSP is a concentrated water-soluble veterinary antibacterial powder combining gentamicin and doxycycline at equal strength. Each gram contains 200 mg gentamicin sulphate and 200 mg doxycycline hyclate. The formulation is designed to provide complementary antibacterial activity through two different mechanisms. Gentamicin is an aminoglycoside antibiotic with bactericidal activity, particularly against many Gram-negative organisms, while doxycycline is a tetracycline antibiotic that inhibits bacterial protein synthesis and is active against a broad range of Gram-positive and Gram-negative bacteria as well as selected atypical pathogens such as Mycoplasma, Chlamydia and Rickettsia species.
GENTA-DOX 20/20 WSP is intended for the treatment of infections caused by microorganisms susceptible to gentamicin and/or doxycycline. According to the product information, it is particularly suitable for gastrointestinal and respiratory tract infections in calves, lambs, kids, pigs and poultry when the causative organisms fall within the susceptible spectrum. The two active ingredients have useful complementary distribution characteristics. Gentamicin is poorly absorbed from the gastrointestinal tract following oral administration and therefore remains active locally in the intestinal lumen, while doxycycline is absorbed and distributes effectively into tissues, including lung tissue. This makes the combination relevant in clinical situations where intestinal and respiratory bacterial infections may occur within the same production group.
The product may be administered through drinking water or feed in accordance with the approved product label. Correct preparation and accurate dosing are essential, especially in group medication programs where variations in water or feed intake can influence the actual amount received by each animal. The medicated mixture should be prepared using the instructions supplied by the manufacturer, used within the specified period after mixing, and accompanied by careful monitoring of the animals during treatment.
Antimicrobial stewardship is an important part of using GENTA-DOX 20/20 WSP responsibly. Treatment should ideally be based on a veterinary diagnosis and, whenever practical, supported by culture and susceptibility testing. Unnecessary or prolonged use of antibiotics may contribute to bacterial resistance and should be avoided. The product should not be administered to animals with known hypersensitivity to aminoglycosides or tetracyclines, and special consideration is required in animals with significant renal or hepatic impairment. Potential drug incompatibilities and the official withdrawal periods must also be respected.
GENTA-DOX 20/20 WSP is for veterinary use only. This website description is intended as a general overview and does not replace the official package leaflet, local registration conditions, or professional veterinary advice. Always follow the approved dosage, duration, contraindications, withdrawal times and storage requirements printed on the product documentation.

HYDRATE ORAL is a veterinary oral rehydration product developed to support fluid, electrolyte and energy balance in animals affected by dehydration, diarrhea, stress or reduced water intake. The formulation combines readily available energy with key electrolytes and supportive nutrients in a form that can be administered conveniently through drinking water. According to the product label, its composition includes dextrose monohydrate, glycine, potassium chloride, sodium salts, phosphate and sodium propionate. Together, these components are intended to help replace fluids and electrolytes lost during digestive disturbances and other stressful conditions.
Dextrose provides a rapidly available energy source and can support the intestinal co-transport of sodium and water, an important mechanism in oral rehydration. Sodium, potassium and chloride contribute to normal electrolyte balance, cellular function and maintenance of hydration, while phosphate and related salts help support the broader mineral balance of the body. Glycine provides an additional nutritional component and may contribute to intestinal absorption processes. For these reasons, HYDRATE ORAL can be useful as supportive care during episodes of diarrhea, dehydration, transportation stress, heat stress, reduced feed and water intake, or recovery from illnesses associated with fluid loss.
The product is administered orally, usually through drinking water, allowing practical use in individual animals or groups depending on the species and management system. Oral rehydration is most effective when introduced early, before dehydration becomes severe. Animals should be monitored for water intake, general activity, hydration status and persistence of digestive signs. When dehydration is advanced, when an animal is unable to drink, or when diarrhea or weakness persists, veterinary assessment is essential because intravenous fluid therapy, diagnostics or treatment of the underlying disease may be required.
HYDRATE ORAL is a supportive nutritional and electrolyte product rather than an antimicrobial treatment. It does not replace treatment of an underlying bacterial, viral, parasitic or metabolic disorder. Instead, it can be incorporated into a broader veterinary management plan to help maintain hydration and support recovery while the primary cause is addressed. Medicated or supplemented drinking water should be prepared according to the label, kept clean, and replaced within the recommended time after mixing.
HYDRATE ORAL is intended for veterinary use only. The information on this page is a general product overview and does not replace the official product leaflet or professional veterinary advice. Always follow the approved directions for use, species-specific dosing, preparation, storage and any warnings printed on the product packaging.

SULTRIM ORAL is a veterinary oral antibacterial solution combining trimethoprim and sulfamethoxazole. According to the manufacturer, each milliliter contains 20 mg trimethoprim and 100 mg sulfamethoxazole. The formulation is designed to take advantage of the well-known synergistic action between these two active ingredients. They inhibit two sequential steps in the bacterial folate pathway, creating a stronger combined antibacterial effect against susceptible organisms than either component would generally provide alone.
The susceptible spectrum includes a variety of Gram-positive and Gram-negative bacteria such as Staphylococcus, Streptococcus, Escherichia coli, Klebsiella, Salmonella, Proteus, Pasteurella, Haemophilus and Corynebacterium species. SULTRIM ORAL is therefore intended for the treatment of gastrointestinal, respiratory and urinary tract infections caused by susceptible bacteria in calves, sheep, goats, pigs and poultry, subject to veterinary diagnosis and the conditions of the local product authorization.
The product is administered through drinking water, allowing practical treatment of individual animals or groups depending on the production system. Correct mixing and accurate calculation of the required amount are essential. Water intake should be monitored because disease, age and environmental temperature can affect consumption and therefore the actual dose received by each animal. Medicated drinking water should be prepared as directed and used within the period stated by the manufacturer. Clinical response should also be assessed during treatment; lack of improvement or deterioration should prompt veterinary re-evaluation rather than simply extending therapy.
Trimethoprim-sulfonamide combinations should be used responsibly. SULTRIM ORAL should not be administered to animals with known hypersensitivity to trimethoprim or sulfonamides, and significant liver or kidney dysfunction, certain hematopoietic disorders, oliguria or anuria may be contraindications according to the product information. Restrictions relating to laying birds producing eggs for human consumption must also be respected. Hypersensitivity reactions and cross-resistance within the sulfonamide class can occur, so treatment should be limited to clinically justified cases and the approved duration.
SULTRIM ORAL is intended for veterinary use only. This description is suitable as a general website overview but does not replace the official package leaflet, local regulatory requirements or professional veterinary advice. Always follow the approved dosage, treatment duration, contraindications, withdrawal periods, handling precautions and storage instructions supplied with the product.

VETKOFLOR 20% ORAL is a veterinary oral solution containing florfenicol at 200 mg per ml. It is formulated to provide broad-spectrum antibacterial treatment for infections caused by organisms that are susceptible to florfenicol. The active ingredient works by binding to bacterial ribosomal subunits and inhibiting protein synthesis, thereby interfering with essential processes needed for bacterial growth and survival. Its activity extends across a number of Gram-positive and Gram-negative bacteria as well as selected atypical organisms.
Florfenicol is highly lipophilic, which supports effective tissue distribution and useful concentrations at sites of infection. Product information lists clinically important organisms such as Pasteurella, Actinobacillus, Salmonella and Streptococcus species among those that may fall within its susceptible spectrum. VETKOFLOR 20% ORAL is consequently indicated for the prevention and treatment of selected respiratory and gastrointestinal bacterial infections in pigs and poultry when the attending veterinarian determines that florfenicol is appropriate.
The product is administered through drinking water and is suitable for group medication programs. Accurate preparation is essential. The amount of product used should follow the approved label and should be adjusted only in accordance with veterinary guidance and the actual water consumption of the treated animals. Water intake can vary significantly with disease, environmental temperature and age, so it should be monitored to help ensure an appropriate dose. Medicated drinking water should be prepared freshly, used within the stated time after mixing and supplied in suitable equipment that is compatible with the product.
VETKOFLOR 20% ORAL should be used within a responsible antimicrobial program. Whenever practical, bacterial culture and susceptibility testing should support treatment decisions, particularly in recurrent disease. Avoid unnecessary antimicrobial exposure and do not use the product when a bacterial indication is not established. Animals with known hypersensitivity to florfenicol should not receive the product, and label restrictions regarding breeding pigs, laying birds, pregnancy and lactation must be followed according to the local authorization. Temporary changes in appetite, water consumption, fecal consistency or perianal tissues may occur in some pigs and should be monitored.
This product is intended for veterinary use only. The information on this page is a concise commercial and technical overview and does not replace the official package leaflet or the advice of a licensed veterinarian. Always follow the approved indications, dosage, treatment duration, withdrawal periods, contraindications, handling precautions and storage conditions supplied by the manufacturer.

VETKOVIT AD3E 100/20/20 ORAL is a balanced veterinary oral vitamin supplement combining vitamins A, D3 and E in one formulation to support growth, reproduction, immunity, muscle function and skeletal health in production animals. According to the manufacturer, each milliliter contains 100,000 IU vitamin A, 20,000 IU vitamin D3 and 20 mg vitamin E. These three fat-soluble vitamins perform distinct but complementary roles in normal physiology, and deficiencies can have a significant effect on growth, fertility, immunity and production performance.
Vitamin A supports epithelial integrity, vision, immune function, growth and reproduction. Vitamin D3 is essential for the regulation and utilization of calcium and phosphorus and therefore contributes directly to normal bone development and skeletal strength. Vitamin E acts as an important antioxidant, helping to protect cell membranes from oxidative damage while also supporting muscle function, reproduction and immune responses. Together, the three vitamins provide useful nutritional support during periods of rapid growth, high production demand or increased physiological stress.
VETKOVIT AD3E 100/20/20 ORAL is indicated for the treatment and prevention of deficiencies of vitamins A, D3 and/or E. Product information also identifies situations such as muscular dystrophy, rickets, reduced fertility, lower hatchability in poultry and stressful conditions during transportation, high environmental temperatures or recovery after viral and bacterial infections as circumstances in which additional vitamin support may be beneficial. It may also be used after certain disease episodes when veterinary assessment indicates an increased nutritional requirement.
The product can be administered through drinking water and is suitable for poultry, cattle, horses, camels, pigs, sheep and goats in accordance with the approved label. Because vitamins A and D are fat-soluble and can accumulate when supplied excessively, correct dosing is important. Unplanned combination with other concentrated vitamin supplements should be avoided unless total dietary intake has been considered by a veterinarian or nutrition professional.
VETKOVIT AD3E 100/20/20 ORAL is intended for veterinary use only. Store the product in its closed container under the dry and dark conditions recommended by the manufacturer. This website description provides a professional overview of the formulation and its nutritional role but does not replace the official package leaflet or veterinary advice. Always follow the approved species directions, dosage, duration of use and storage instructions supplied with the product.