Description                                            

Powder is white or almost white.

Compound

1 vial contains:

streptomycin sulfate – 1,0 g

Pharmacological properties

Streptomycin sulfate – an aminoglycoside antibiotic, which has a wide spectrum of antimicrobial (bactericidal) action. The drug is active against Mycobacterium tuberculosis, most of the gram-negative bacteria (Escherichia coli, Salmonella spp., Shigella spp., Yersinia spp., Klebsiella spp., Including Klebsiella pneumoniae, Haemophilus influenzae, Neisseria gonorrhoeae, Neisseria meningitidis, Yersinia pestis, Francisella tularensis, Brucella spp.) and some gram-positive microorganisms (Staphylococcus spp., Corynebacterium diphtheriae). Less active drug against Streptococcus spp. (including Streptococcus pneumoniae), Enterobacter spp. Streptomycin is inactive relative to anaerobic bacteria, Spirochaetaceae, Rickettsia spp., Proteus spp., Pseudomonas aeroginosa. The bactericidal action of the drug is detected as a result of binding to the 30S subunit of the bacterial ribosome, which in the future leads to suppression of protein synthesis in microorganisms.

Application

Treatment of diseases of the digestive tract, respiratory and urogenital system, skin and soft tissue caused by microorganisms susceptible to streptomycin in cattle, sheep, goats, pigs and horses.

Dosage

Intramuscularly 2 times a day with an interval of 12 hours in the following doses:

Intramuscular injections make deep muscle. The course of treatment is 4-7 days.

For intramuscular administration, the drug is dissolved in water for injection, 0.9% solution of sodium chloride or 0.25-0.5% solution of novocaine from the calculation of 4 ml of solvent per 1 g of preparation. The solution is prepared immediately before use.

Contraindication

Hypersensitivity to streptomycin. Do not use at the same time as aminoglycoside antibiotics.

Contraindicated in the treatment of diseases of the auditory and vestibular apparatus associated with Neuritis VIII pair of cranial nerves, in severe forms of cardiovascular and renal failure.

Warning

The slaughter of animals for meat and the consumption of milk for human consumption is allowed, respectively, 7 and 2 days after the last application of the drug. Obtained before the specified date, meat and milk are disposed of or fed to unproductive animals, depending on the conclusion of the veterinary medicine physician.

Form of release

Glass vials closed with a rubber stopper under an aluminum rim of 1,0 оr 5,0 g.

Storage

A dry, dark, inaccessible place for children at a temperature from 15 ° С to 25 ° С.

The expiration date – 3 years since manufacturing date.

 For applying in veterinary medicine!