Ivermec injection 20ml

DESCRIPTION

Ivermek is an injection solution for the treatment and prevention of parasitic diseases in ruminants, camels, pigs and poultry. In appearance, the preparation is a transparent opalescent colorless or light yellow liquid.

ADVANTAGES

A new unique water-dispersed (micellar) form of ivermectin with a broad spectrum of antiparasitic action.

An effective agent for combating endo- and ectoparasites

Intramuscular injection possible

Permanent parasiticidal action for 10-14 days

A wide range of nematicidal, ovocidal and arachnoentomocidal action

High therapeutic efficacy at low dosages

Lower degree of toxicity in comparison with analogues

COMPOSITION

1 ml contains ivermectin - 10 mg and tocopherol acetate (vitamin E) - 40 mg as active ingredients, as well as auxiliary substances dimethylacetamide - 400 mg, polyethylene glycol-660, hydroceystearate - 150 mg, benzyl alcohol - 10 mg and water for injection - up to 1 ml.

PHARMACOLOGICAL PROPERTIES

Ivermectin, which is part of the drug, has a pronounced antiparasitic effect on larval and sexually mature phases of development of gastrointestinal and lung nematodes, larvae of subcutaneous, nasopharyngeal, gastric gadflies, lice, bloodsuckers and sarcoptoid ticks.

After parenteral administration of the drug, ivermectin is rapidly absorbed from the injection site and is distributed in the organs and tissues of the animal, providing a parasiticidal effect for 10-14 days. It is excreted from the body of animals with urine and bile, in lactating animals also with milk.

After oral administration to birds, ivermectin is well absorbed in the gastrointestinal tract, enters the systemic circulation, reaching a maximum concentration in the blood after 1 hour, and is evenly distributed in organs and tissues. Ivermectin is excreted from the body of poultry with droppings.

According to the degree of impact on the body, according to GOST 12.1.007-76, Ivermek is classified as a “moderately hazardous” substance (hazard class 3), the active substance, ivermectin, is a “extremely hazardous” substance (hazard class 1).

DOSAGE AND APPLICATION

Ivermek is prescribed to animals with a therapeutic and prophylactic purpose for arachno-entomoses and nematodes

cattle with strongilatosis, trichocephalosis, strongyloidosis, telaziosis, sifunculatoses, hypodermatosis, psoroptosis, sarcoptic mange and chorioptosis

sheep and goats with dictyocaulosis, protostrongylosis, mulleriosis, hemonchosis, ostertagiosa, nematodyrosis, marshallagiosa, cooperative disease, habertiosis, esophagostomiasis, bunostomosis, trichocephalosis, estrogenic psoriasis, ichyloidosis

deer with dictyocaulosis, ostertagiasis, nematodyrosis, strongyloidiasis, trichocephalosis, edemagenosis, cephenomyosis and sarcoptic mange

camels with dictyocaulosis, ostertagiasis, nematodyrosis, strongyloidiasis, trichocephalosis and sarcoptic mange

pigs with trichocephalosis, ascariasis, metastrongylosis, esophagostomosis, strongyloidosis, stefanurosis, hematopinosis and sarcoptic mange

chickens (broiler chickens, breeding poultry, replacement chickens and poultry during the molting period) with ascariasis, heterakydosis, capillariasis, entomoses caused by Dermatoryktes mutans, Aphaniptera spp., Menacanthus stramineus, Cerato, acphyllus gallaxina, gallinae

Ivermek is injected once intramuscularly in compliance with the rules of asepsis: to pigs in the neck or inner thigh, to ruminants - in the croup or neck in the following doses:

cattle and small ruminants, deer and camels - 1.0 ml per 50 kg of animal weight (200 Ојg of ivermectin per 1 kg of weight)

pigs - 1.0 ml per 33 kg of animal weight (300 Ојg of ivermectin per 1 kg of weight)

In severe cases of animal disease with sarcoptoidosis, treatment is carried out twice with an interval of 8-10 days.

If the volume of the injected solution is more than 10 ml, it should be administered to the animal in several places.

Treatment of animals against nematodes is carried out in the fall before being placed in stalls and in the spring before being taken to pasture, against gadfly infestations - immediately after the end of gadfly flight, against pathogens of arachno-entomoses - according to indications.

Each batch of the drug is preliminarily tested on a small group (7-10 animals) of animals. In the absence of complications, the entire livestock is processed within 3 days.

For chickens (broiler chickens, breeding birds, replacement chickens and poultry during the molting period) Ivermek is used orally in a group way with water for drinking in a daily dose of 400 Ојg of ivermectin per 1 kg of bird weight, which corresponds to 0.4 ml / l of drinking water.

To prepare a medical solution, Ivermek in a single dose, calculated for the treated livestock of birds, is diluted in 1/4 of the daily intake of drinking water.

The prepared medical solution is drunk once for nematodes, three times for arachno-entomoses: twice with an interval of 24 hours, and then once every 14 days.

To ensure that the bird receives a therapeutic dose of the drug, 2 hours before drinking the solution, the supply of drinking water is stopped.

SPECIAL INSTRUCTIONS

In case of an overdose of the drug, the animal may experience a depression, tremor, increased salivation, refusal to feed, loose stools.

Ivermec should not be used concurrently with medicinal products containing macrocyclic lactones, due to the possible mutual enhancement of the toxic effect.

Slaughter of ruminants, camels and pigs for meat is allowed no earlier than 28 days, birds - no earlier than 9 days after the last application of Ivermec. In the event of the forced slaughter of animals and poultry before the established deadlines, the meat can be used as feed for fur animals.

Milk of dairy animals may be used for food purposes not earlier than 28 days after the last injection of Ivermek. Milk obtained earlier than the specified period can be used after boiling in animal feed.

CONTRAINDICATIONS

A contraindication to the use of Ivermek is the individual hypersensitivity of the animal to the components of the drug (including a history).

It is not allowed to use the drug in dairy animals, patients with infectious diseases and malnourished animals, pregnant females whose milk will be used for food purposes, less than 28 days before the start of lactation.

It is not allowed to use the drug in laying hens, replacement chickens less than 14 days before the start of egg-laying, due to the accumulation of ivermectin in the eggs.

SIDE EFFECTS

As a rule, side effects and complications are not observed when using Ivermec in accordance with this instruction. In some animals, increased salivation, increased frequency of bowel movements and urination, ataxia are possible. These symptoms usually go away spontaneously without the use of therapeutic agents. With increased individual sensitivity of the animal to the components of the drug and the appearance of allergic reactions, the animal is prescribed antihistamines and symptomatic therapy.

SHELF LIFE AND STORAGE

Store Ivermek in the manufacturer's closed packaging, separately from food and feed, in a dry, dark place at a temperature from 0 В° C to 25 В° C. The shelf life of the medicinal product, subject to storage conditions in a sealed package, is 2 years from the date of production, after the first opening of the bottle - no more than 42 days.

PACKAGING

Ivermek is available packaged in 50 ml glass bottles, sealed with rubber stoppers, reinforced with aluminum caps.

Specifications

Product subcategory

Injection

KolVUP

60

Manufacturer

Nita-Farm

Temperature regime

from 0 to +25

Teaser

for the treatment and prevention of parasitic diseases in ruminants, camels, pigs and poultry