Masticefum syringe dispenser 10g
DESCRIPTION
Masticef (Masticefum) is a veterinary drug used in large and small ruminants in clinical and subclinical forms of bacterial mastitis. In appearance, the drug is a slightly exfoliating suspension from white to light yellow.
COMPOSITION
One syringe (10.0 g) contains 350.0 mg of cephalexin, 35.0 mg of gentamicin, excipients, base up to 10.0 g.
PHARMACOLOGICAL PROPERTIES
Gentamicin sulfate is an antibiotic from the aminoglycoside group, has a wide spectrum of antimicrobial action, is active against most gram-negative (Escherichia coli, Enterobacter spp., Klebsiella pneumoniae, Salmonella spp., Campylobacter spp., Pseudomonas aeruginosa (Proteus Cpp.) And gram-positive microorganisms. spp., Staphylococcus aureus, Bacillus spp., Listeria monocytogenes). The antibiotic does not act on anaerobic bacteria, fungi, viruses, protozoa.
Cephalexin belongs to the group of ОІ-lactam antibiotics. The mechanism of action consists in inhibiting the biosynthesis of the cell wall, disrupting the permeability of the cytoplasmic membrane. The spectrum of action is similar to that of aminoglycoside antibiotics.
The antimicrobial components of the drug have a synergistic effect.
Gentamicin sulfate and cephalexin are not metabolized in the body and, when administered intracisternally, are excreted in milk.
The drug is low-toxic, does not irritate the breast tissue.
DOSAGE AND APPLICATION
The drug is used in large and small ruminants in clinical and subclinical forms of bacterial mastitis.
The contents of the syringe are injected intracisternally after delivery once a day for 3 to 5 days.
Before using the drug, the secret of the diseased lobe of the mammary gland must be carefully milked, the skin of the nipple sphincter must be treated with an antiseptic.
Subsequent milking of the secret of the diseased lobe of the mammary gland can be carried out no earlier than six hours after the administration of the drug, in a separate dish, followed by disposal of the secret by boiling or mixing with a disinfectant (glutex, bleach, etc.).
SPECIAL INSTRUCTIONS
The use of the drug does not exclude the use of pathogenetic and symptomatic therapy.
Slaughter of animals for meat is allowed no earlier than seven days after the last use of the drug. In the event of the forced slaughter of animals before the established date, the meat is used to feed carnivores. Milk is allowed to be used for food purposes not earlier than five days after the last use of the medicinal product.
CONTRAINDICATIONS
The use of the drug is contraindicated in animals with allergic reactions to antibiotics-aminoglycosides and antibiotics-cephalosporins.
SIDE EFFECTS
If allergic reactions occur, the drug should be canceled, antihistamines and calcium preparations (calcium gluconate or calcium chloride) should be prescribed.
SHELF LIFE AND STORAGE
The drug is stored according to list B in a dry, dark place at a temperature from 0 В° C to plus 25 В° C. The shelf life of the drug is 2 years from the date of manufacture, subject to the rules of storage and transportation.
PACKAGING
The drug is produced in disposable syringes made of polymeric material with a cannula for intracisternal administration with a nominal weight of 10 g.
Specifications
KolVUP
32
Manufacturer
Belarus
Temperature regime
from 0 to +25
Teaser
used in cattle and small ruminants in clinical and subclinical forms of mastitis of bacterial etiology