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Sodium chloride solution – 250 ml (8.45 fl. oz) – BF
DESCRIPTION
Structure
1 ml of the drug contains: sodium chloride - 9 mgDescription
The liquid is colorless, transparent.Pharmacological properties
Sodium chloride is involved in water-salt metabolism, maintains and regulates osmotic pressure, has detoxification, rehydration effect, replenishes sodium deficiency in various pathological conditions of the body, temporarily increases the volume of fluid circulating through the vessels. Sodium ions penetrate the cell membrane through various transport mechanisms, in particular the sodium-potassium pump (Na-K-ATPase).Β Sodium contributes to the transmission of signals in neurons, electrophysiological processes of the heart, metabolic processes in the kidneys.Β It is excreted from the body after renal reabsorption in the urine, a small amount in the feces and sweat.Indications
Treatment of animals with significant losses of organic fluid (dehydration) - intoxication, diarrhea, burn disease, toxic dyspepsia, decreased blood pressure, shock, after surgery. For washing wounds, mouth, nose, mucous membranes of the eyes, as a solvent for veterinary and biological products.APPLICATIONMethod of administration and dosage
Before use, the drug is heated to the body temperature of the animal and injected intravenously, intramuscularly, or subcutaneously in the following doses per animal:- cattleΒ - 500-3000 ml;
- horsesΒ - 300-2500 ml;
- sheep, goatsΒ - 100-500 ml;
- pigsΒ - 10-150 ml;
- dogsΒ - 20-100 ml.
Kafors inj* 100ml (3.38oz)
Kaforsen injection 100ml Eliminates violation of mineral metabolism Description Guidance on the use of Caporsen as a homeopathic remedy for the regulation of mineral metabolism in animals. I. General information. 1. Caporsen is a homeopathic medicine intended for the regulation of mineral metabolism in animals. 2. Caforsen contains as active ingredients Calcium carbonicum, Calcium phosphoricum, Calcium fluoricum, Silicea, Phosphorus, as well as auxiliary components: sodium chloride and water for injection (injection solutions) or sugar crumbs, calcium stearate (tablets). 3. Caforsen is produced in 10 and 100 cm3 in glass vials of appropriate capacity, sealed with rubber stoppers, reinforced with aluminum caps, or in tablets - 50 tablets each in polymer jars for medicines closed with polyethylene lids or on orange glass jars of appropriate capacity. Store Kaforsen in a dry, dark place at temperatures from 00C to 250C. The shelf life of the medicinal product, subject to storage conditions, is 3 years from the date of manufacture (solution for injection), 5 years (tablets). The drug in vials with impaired integrity, in the presence of turbidity or discoloration, foreign impurities, with an expired shelf life or violation of storage conditions is not suitable for use.
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