| - | - | - |
|---|---|---|
| Product Group | : | Vitamins and Minerals |
| Pharmaceutical Form | : | Solution for Injection |
| Active Ingredient | : | Toldimfos sodium |
| Target Animal | : | Cattle, Horse, Sheep, Goat, Dog, Cat |
| Package Form | : | 20 ml, 50 ml and 100 ml Amber Colored Glass Flacons |
COMPOSITION
Fosfovet solution for Injection is a colorless, clear, sterile solution containing 200 mg of Toldimphos sodium per ml. The organic phosphorus content of the active substance is 14%.
PHARMACOLOGICAL PROPERTIES
Pharmacodynamic Properties
Toldimphos belongs to the group of aromatic phosphorus compounds and has a stimulating and regulatory effect on metabolism. Phosphorus is an important element that participates in most vital processes. Toldimphos stimulates metabolism. In this way, it increases blood calcium levels without the need for calcium administration, normalizes GOT values, and has beneficial effects on serum cholesterol levels.
Pharmacokinetics Properties
Elimination in dogs shows that approximately 90% of the substance is recovered in the urine 4 hours after intravenous injection and 8 hours after intramuscular injection. After 24 hours, 97% to 93% of the substance is eliminated. Toldimphos is excreted unchanged in dogs.
It is rapidly absorbed and distributed in the body. In cattle, maximum plasma concentrations are observed within 10 to 20 minutes after intramuscular administration. Elimination primarily occurs via the urinary tract. Repeated dosing does not lead to biological accumulation of the product.
AREA OF USE/INDICATIONS
It is used for the prevention and treatment of phosphorus deficiency in cattle, sheep, goats, horses, cats, and dogs.
USAGE AND DOSAGE
It is administered via intravenous, intramuscular, or subcutaneous injection. The dosage should be determined by the veterinarian based on the animal's phosphorus needs and condition. The recommended doses are as follows:
In cattle, sheep, goats, and horses, 10 mg/kg (practically 1 ml per 20 kg of body weight)
In cats and dogs, 20 mg/kg (practically 0.5 ml per 5 kg of body weight).
Generally, 3-5 administrations with a 3-day interval are sufficient. In emergency situations, half of the dose can be given intravenously, and the remaining amount can be administered intramuscularly or subcutaneously.
In cases of chronic deficiency, 5-10 administrations (intramuscular or subcutaneous) with 48-hour intervals may be applied.
SPECIAL CLINICAL INFORMATION AND SPECIAL WARNINGS FOR TARGET SPECIES
It should be used with caution in animals with renal dysfunction. In horses, when administered subcutaneously or intramuscularly, it is recommended that the dose be applied to more than one site.
Use during pregnancy: It depends on the veterinarian’s benefit/risk assessment.
ADVERSE EFFECTS
Unknown.
DRUG INTERACTIONS
It should not be used in combination with other products.
SYMPTOMS OF OVERDOSE, PRECAUTIONS AND ANTIDOTE
An overdose may cause electrolyte imbalance.
WITHDRAWAL PERIODS
Milk and Meat: 0 (zero) days.
CONTRAINDICATIONS
It should not be used in animals known to be sensitive to the components contained in the product.
GENERAL WARNINGS
Consult a veterinarian before use and if any unexpected effects occur. Keep out of reach of children.
PRECAUTIONS TO BE TAKEN BY THE ADMINISTRATOR AND WARNINGS FOR VETERINARY SURGEON
Avoid contact with the medication and wash your hands after use.
STORAGE CONDITIONS AND SHELF LIFE
The product should be stored in the original packages, below 25°C, without freezing or refrigeration. Protect from sunlight. Shelf life is 36 months.
DISPOSAL AFTER USE AND WARNINGS FOR NON-TARGET SPECIES
Used or leftover product must be disposed of according to the relevant legislation.
COMMERCIAL PRESENTATION FORM
20 ml, 50 ml, and 100 ml amber colored flacons with box.
PLACE AND CONDITIONS OF SALE
Sold with a veterinarian’s prescription; available at pharmacies, veterinary clinics, and animal hospitals. (VSP)
APPROVAL DATE OF LEAFLET: 21.12.2022
MARKETING AUTHORIZATION DATE AND NO: 18.02.2002-011/1011
MARKETING AUTHORIZATION HOLDER
VİLSAN Veteriner İlaçları Tic. ve San. A.Ş.
Balıkhisar Mah, Balıkhisar Köy İçi Küme Evleri No:765A Akyurt/Ankara-Türkiye
MANUFACTURER COMPANY
VİLSAN Veteriner İlaçları Tic. ve San. A.Ş.
Balıkhisar Mah, Balıkhisar Köy İçi Küme Evleri No:765A Akyurt/Ankara-Türkiye
Made in Turkiye
