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Peni powder for *inj (5pcs. bottle)
Powder for injectionDescriptionWhite or white powder with a yellowish tinge, which forms a stable fine suspension with water.Storage1 vial of the drug contains the active substance:benzylpenicillin sodium salt - 1,000,000 IU.Pharmacological propertiesATC vet classification code QJ01- antibacterial veterinary drugs for systemic use. QJ 01 CE 01 - Benzylpenicillin.Benzylpenicillin sodium is a bactericidal antibiotic of the penicillin series, which has a detrimental effect on gram-positive and some gram-negative microorganisms: Streptococcus spp . Staphylococcus spp., Bacillus spp., Neisseria spp., Pasteurella spp. and other.The mechanism of action of the drug is to inhibit the activity of enzymes for the synthesis of peptidoglycan, which is the basis of the cell wall of microorganisms, which leads to delayed reproduction and growth of bacteria.Penicillin when administered intramuscularly is rapidly absorbed into the blood and distributed in body fluids and tissues; penetrates into the cerebrospinal fluid in small quantities. The maximum concentration of benzylpenicillin in the blood is observed after 30-60 minutes. introduction. In 3-4 hours only traces of an antibiotic are found in blood. To maintain a concentration high enough for a therapeutic effect, injections should be given every 3-4 hours. When administered intravenously, the concentration of penicillin in the blood decreases rapidly. Benzylpenicillin sodium is practically not metabolized in the liver and is excreted unchanged through the kidneys.Oxytoc 10 I.U. units Solution *inj – 300ml (100ml*3pcs)
Oxytocin 10 I.U. injectable
hormone of the hypothalamus, which consists of pentapeptydnoho cycle and side chain residues of three amino acids that accumulate in the posterior pituitary. It increases the permeability of sodium myofibrils uterus, stimulating its contraction. Threshold oxytocin induced contractions of the uterus decreases during pregnancy, high estrogen or if the animal has already begun delivery.
Oxytocin is decomposed in the gastrointestinal tract, so it should be administered parenterally. After intramuscular administration of the drug effect observed after 3-5 minutes.
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