Expiration date: 01/2025

Kaforsen - a solution for injection is used in animals for the prevention and treatment of diseases accompanied by disorders of mineral metabolism. In appearance, the drug is a colorless transparent liquid.

Structure

As active substances, Kaforsen contains components of mineral origin (in 1000 ml): Acidum silicicun1 D4 trituration - 45.0 mg, Ca1cium carbonicum Halmen1anni D4 tritmation - 450.0 mg, Calciinm f1uoratum D4 trituration - 470,O mg, Calcium phosphogysp D4 trituration - 500.0 mg, Phosphorus 0=D3 - 250 pl and · excipients: methyl parahydroxybenzoate - 0.5g; sodium chloride - 5.8 r, sodium * acetate trihydrate - 2.0 g, hydrochloric acid to pH 5.4, ethyl alcohol 95% 5.26 g, water for injection up to 1000 ml.

PHARMACOLOGICAL PROPERTIES

Kaforsen refers to combined homeopathic medicines. Regulates the level of calcium, phosphorus and magnesium in the body of animals, corrects the metabolism of bone tissue, normalizes osteogenesis, and also helps to reduce the consolidation of bone fragments in traumatic bone injuries.

According to the degree of exposure to the body, the drug belongs to low-hazard substances (hazard class 4 according to GOST 12.1.007), does not have a locally irritating and sensitizing effect.

Purpose

Kaforsen is prescribed to dogs, cats, rabbits, cattle, horses in the complex therapy of diseases accompanied by a violation of mineral metabolism, including osteopathies, secondary hyperparathyroidism, osteoporosis, osteomalacia, rickets, fractures and cracks of bones, as well as during rehabilitation after surgery on the musculoskeletal system.

DOSAGE AND APPLICATION

Kaforsen is used intramuscularly or subcutaneously 1 time a day for 10-21 days in doses: dogs, cats - 0.1 ml / 1 kg of animal weight; rabbits - 1.0 ml / animal; cattle - 5.0 ml / animal; horses - 10.0 ml / animal; calves, foals - 2.0-3.0 ml / animal.

To prevent eclampsia, the drug is used 1 time a day, starting from the second week of lactation. The duration of the preventive course is 4-6 weeks.

SPECIAL INSTRUCTIONS

Omissions should be avoided when administering the next dose of the drug, as this can lead to a decrease in therapeutic and preventive effectiveness. If one dose is missed, the use of the drug should be resumed as soon as possible in the same dose and according to the same scheme.

The use of Kaforsen does not exclude the use of other drugs for etiotropic, pathogenetic and symptomatic therapy.

Products of animal origin during and after the application of Kaforsen can be used without restrictions.

Contraindications

Contraindication to the use of the drug is an individual hypersensitivity of the animal to its components.

SIDE EFFECTS

When using Kaforsen in accordance with this instruction, side effects and complications are usually not noted. With increased individual sensitivity of the animal to the components of the drug and the occurrence of allergic reactions, the use of the drug is discontinued and antihistamines and symptomatic therapy are prescribed to the animal.

SHELF LIFE AND STORAGE

Kaforsen is stored in the manufacturer's closed packaging, separately from food and feed, in a dry place protected from direct sunlight at a temperature from 0 to 30 ° C. The shelf life of the drug, subject to storage conditions in the manufacturer's closed packaging, is 3 years from the date of production, after the first opening of the bottle - 21 days.