Pharmavectin 1% (Farmavektinum 1%) injection 100ml
DESCRIPTION
Pharmavectin 1% for injection (Farmavektinum 1% pro injectionibus) is a veterinary drug prescribed for animals with arachnoentamosis and nematodes. In appearance, the drug is a clear, colorless or slightly yellowish liquid without mechanical impurities.
COMPOSITION
1.0 cm3 of the preparation contains 0.01 g of ivermectin.
PHARMACOLOGICAL PROPERTIES
Pharmavectin 1% for injection has a wide spectrum of antiparasitic action, has a detrimental effect on nematodes and gadfly larvae, causative agents of sarcoptoidosis and animal entomoses.
The mechanism of action of the drug is based on an increase in the production of a mediator of inhibition, ОІ-aminobutyric acid, a violation of the transmission of nerve impulses in parasites, which leads to their paralysis and death.
The drug in the recommended doses has no mutagenic, sensitizing, embryotoxic and teratogenic effects. The drug is excreted from the body with urine and bile, in lactating cows it is also excreted with milk. Toxic to fish and bees.
DOSAGE AND APPLICATION
Pharmavectin 1% for injection is prescribed to animals with arachno-entamosis and nematodes.
Cattle and sheep - with dictyocaulosis, ostertagiasis, haemonchosis, trichostrongylosis, cooperiosis, haberthiasis, esophagostomosis, nematodyrosis, bunostomiasis, strongyloidiasis, thelaziosis, siphunculus psoriasis, malignant psoriasis, malastosis.
Pigs - with ascariasis, esophagostomosis, trichocephalosis, strongyloidosis, metastrongylosis, hematopinosis and sarcoptic mange.
The drug is administered to animals once, in compliance with the rules of asepsis, subcutaneously in the shoulder, forearm (cattle) or the back third of the neck (sheep, goats and pigs) in doses: cattle, sheep, goats 1.0 cm3 of the drug per 50 kg of animal weight (0.0002 g / kg by ADV), pigs - 1.0 cm3 of the drug per 33 kg of animal weight (0.0003 g / kg by ADV).
In the treatment of scabies, demodicosis and sifunculosis, the drug is re-administered to animals with an interval of 7-10 days.
De-worming of animals is carried out in the fall before stalling and in the spring before pasture, with estrosis of sheep and hypodermosis of cattle, they are treated in October-November.
Before mass processing of animals, each batch of the drug is tested on a small group of animals (10 animals each) of different ages and fatness. In the absence of signs of side effects within three days after the administration of the drug, they begin to process the entire livestock.
SPECIAL INSTRUCTIONS
If allergic or other adverse reactions occur, cancel the drug, prescribe antihistamines and calcium preparations.
Slaughter of pigs and cattle for meat is allowed no earlier than 28 days, and sheep 21 days after the last use of the drug. In the event of the forced slaughter of animals earlier than the specified period, the meat is used as feed for carnivores or for the production of meat and bone meal.
After opening the bottle with the drug, it must be used within six months.
CONTRAINDICATIONS
The use of the drug is contraindicated in pregnant women four weeks before childbirth, lactating animals and animals with infectious diseases.
SIDE EFFECTS
In recommended doses, the drug does not cause side effects, however, toxicosis is possible in weakened and emaciated animals.
SHELF LIFE AND STORAGE
The drug is stored in the manufacturer's package according to list B in a dry, dark place at a temperature from 0 to plus 25 В° C.
Shelf life of the drug is 2 years from the date of manufacture, subject to storage rules.
PACKAGING
Produced in sterile form, in glass bottles of 100 ml.
Specifications
KolVUP
50
Manufacturer
Belarus
Temperature regime
from 0 to +25
Teaser
prescribed to animals with arachno-entamosis and nematodes