Amoxivet LA (Amoxivet LA) injection 100ml
DESCRIPTION
Amoxivet LA (Amoxivet LA) is a veterinary drug used in large and small ruminants, pigs with bacterial infections. In appearance, the drug is a suspension from white to light yellow, resuspended with shaking.
COMPOSITION
1.0 ml of the drug contains 0.15 g of amoxicillin (in the form of amoxicillin trihydrate), excipients, filler up to 1.0 ml.
PHARMACOLOGICAL PROPERTIES
Amoxicillin, which is part of the drug, belongs to the semi-synthetic antibiotics of the penicillin series.
The mechanism of action of the drug is based on the violation of the synthesis of the bacterial cell wall by inhibiting the enzymes transpeptidase and carboxypeptidase, which leads to disruption of the osmotic balance and destruction of the cell.
The drug has a wide spectrum of bactericidal action against gram-positive and gram-negative microorganisms, such as Actynomyces spp., Bacillus antacis, Clost ,, idium spp., Chupebacterium spp., E1 В· -ysipeloth ,, ix rhusiopathiae, Listegia spp. Monocytogen 'eptococcus spp., Escherichia coli, Salmonella spp., Fusobactegium spp., Haemophilus spp., Pasteiu '' ella spp., p ,, oteus spp., Leptospira spp. other. Has no effect on viruses, chlamydia, mycoplasma, rickettsia.
After parenteral administration of the drug, the maximum concentration of amoxicillin trihydrate in the blood serum is reached after 1 to 2 hours and is maintained at a therapeutic level for 48 hours. The antibiotic is excreted from the body with urine and feces, mainly in unchanged form.
DOSAGE AND APPLICATION
Amoxivet LA is used in cattle and small ruminants, pigs for bacterial infections of the respiratory and genitourinary systems, diseases of the skin and soft tissues caused by microorganisms sensitive to amoxicillin.
The drug is administered intramuscularly at a dose of 1.0 ml per 10.0 kg of animal weight once every two days at equal intervals until recovery, but no more than three injections.
The maximum volume of the drug for administration in one place should not exceed 20 ml for cattle, 10 ml for pigs, 5 ml for small ruminants and calves, and 2 ml for piglets.
Before use, the vial with the drug must be shaken thoroughly until a homogeneous suspension is obtained.
SPECIAL INSTRUCTIONS
If allergic and other adverse reactions occur, the drug is canceled and antihistamines and calcium preparations (calcium chloride, calcium gluconate, calcium borgluconate) are prescribed.
Slaughter of animals for meat is allowed no earlier than 28 days after the last injection 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 4 days after the last administration of the drug. Milk obtained earlier than the established date can be used for feeding animals after heat treatment.
CONTRAINDICATIONS
The use of the drug is contraindicated in small herbivores and rodents (rabbits, guinea pigs, hamsters). Do not use the drug in conjunction with tetracyclines, amphenicols, sulfonamides.
SIDE EFFECTS
When using the drug in recommended doses in accordance with the instructions, side reactions and complications are not observed, however, in animals with hypersensitivity to - lactam antibiotics (penicillins, cephalosporins), various allergic reactions are possible.
SHELF LIFE AND STORAGE
The drug is stored according to list B in a dry, dark place at a temperature from + 5 В° C to + 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 glass bottles with a volume of 100 ml.
Specifications
KolVUP
50
Manufacturer
Belarus
Temperature regime
from +5 to +25
Teaser
used in large and small ruminants, pigs for bacterial infections