Mastisan A (20 doses) 100ml
DESCRIPTION
Mastisan - the drug is used to treat mastitis in lactating cows.
COMPOSITION
Mastisan in 1 ml contains 20 mg of streptomycin sulfate, 20,000 IU of benzylpenicillin sodium or potassium salt, 70 mg of sulfadimezin as active ingredients, and refined sunflower oil up to 1 ml as auxiliary components.
PHARMACOLOGICAL PROPERTIES
Mastisan belongs to the pharmacotherapeutic group of systemic antimicrobials.
It has a wide range of antibacterial action due to the components that make up the drug, which exhibit synergy with respect to individual microorganisms.
The drug is active against gram-positive and gram-negative microorganisms (staphylococci, streptococci, proteus, E. coli, salmonella, etc.).
The drug in recommended doses does not have a sensitizing, local irritating, embryotoxic, teratogenic and mutagenic effect. It is excreted from the body with milk.
According to the degree of impact on the body, it belongs to low-hazard substances (hazard class 4 according to GOST 12.1.007-76).
DOSAGE AND APPLICATION
Before using the drug, milk is removed from the diseased quarter of the udder and disposed of, the nipple is disinfected.
Before use, the contents of the vial are heated to 36-39 В° C, shaken thoroughly until a uniform suspension is obtained. The drug is taken from the vial with a sterile syringe in the amount of 5-20 ml, the cannula of the syringe is tightly pressed against the opening of the nipple canal and injected by gently pressing the syringe plunger into the teat tank of the udder. After the introduction, a light massage of the nipple of the affected quarter of the udder is performed from the bottom up. Depending on the severity of the inflammatory process, Mastisan is administered in a dose of 5-20 ml with an interval of 24 hours for 5-8 days, and for purulent and catarrhal-purulent mastitis up to 10 days.
If one or more doses of the drug are missed, it is necessary to resume use in the prescribed dosage and regimen. Do not enter double doses to compensate for missed doses.
SPECIAL INSTRUCTIONS
When using the drug according to the instructions, overdose symptoms were not established. In case of an overdose, the animal must be prescribed detoxification and symptomatic therapy.
The meat of animals killed during treatment with Mastisan is used on a general basis, with the exception of the udder, which is rejected. If it is impossible to cull the udder, in case of forced slaughter of animals during therapy with Mastisan and before the expiration of 3 days after the last application of the drug, the meat can be used as feed for carnivores.
Milk obtained from the affected lobes of the udder of an animal during treatment and within 3 days after the last injection of the drug is taken into a separate bowl, disinfected and disposed of, and fed from healthy lobes of the udder to the animals after boiling. The use of milk for human consumption is allowed 3 days after the last injection of the drug, provided that the clinical signs of mastitis, confirmed by bacteriological and other laboratory studies, completely disappear.
CONTRAINDICATIONS
There are no contraindications to the use of Mastisan according to this instruction.
SIDE EFFECTS
When used in recommended doses, side effects and complications are usually not observed.
SHELF LIFE AND STORAGE
Store the medicinal product in the manufacturer's sealed packaging in a place protected from direct sunlight, at a temperature from 0 В° C to 20 В° C.
The shelf life of the medicinal product, subject to storage conditions in a sealed package, is 18 months from the date of production, after opening the bottle - 60 days.
PACKAGING
Glass bottle 100 ml.
Specifications
KolVUP
50
Manufacturer
Nita-Farm
Temperature regime
from 0 to +25
Teaser
for the treatment of cows with mastitis