LEVAVERM 10% - Oral Solution for Cattle, Sheep, Pigs & Chickens - 1L

LEVAVERM 10% 1L

LEVAVERM 10%, oral solution for cattle, sheep, pigs, and chickens.
Levamisole HCl

DECLARATION OF ACTIVE SUBSTANCES AND OTHER INGREDIENTS:
1 ml of the product contains:
Active Substance:
Levamisole (as HCl) 100 mg
Excipients:
Methyl parahydroxybenzoate 1 mg
Sodium metabisulfite 1.5 mg

INDICATIONS:
Levaverm 10% is indicated for cattle, sheep, and pigs in the treatment of infections caused by the following parasites sensitive to the action of levamisole:
– Pulmonary parasites: Dictyocaulus spp, Metastrongylus spp, and Protostrongylus spp;
– Gastrointestinal nematodes: Haemonchus spp, Trichostrongylus spp, Ostertagia spp, Cooperia spp, Bunostomum spp, Nematodirus spp, Oesophagostomum spp, Strongyloides spp, Chabertia spp, Toxocara vitellorum, Hyostrongylus spp, Trichuris spp, and Ascaris spp.
For chickens, the product is indicated in the treatment of infections caused by the larval and adult stages of Amidostomum anserus, Ascaridia spp, Heterakis gallinarium, Capillaria spp, and Syngamus trachea, sensitive to the action of levamisole.

CONTRAINDICATIONS:
Do not use in animals with severe liver or kidney conditions. Do not use in animals with pre-existing blood disorders. Not to be used in case of hypersensitivity to the active substance or any of the excipients.

ADVERSE REACTIONS:
If you observe serious reactions or other effects not mentioned in this leaflet, please inform your veterinarian.

TARGET SPECIES:
Cattle, sheep, pigs, and chickens.

DOSAGE FOR EACH SPECIES, ROUTE(S) OF ADMINISTRATION AND METHOD OF ADMINISTRATION:
The product is administered orally, in drinking water, as follows:
Cattle, sheep, and pigs: 1 ml of product/10 kg body weight or 1 liter of product/1000 liters of drinking water, administered once.
Chickens: 1–1.5 liters of product/1000 liters of drinking water, administered once.

RECOMMENDATIONS FOR CORRECT ADMINISTRATION:
The intake of medicated water depends on the clinical conditions of the animals. During treatment, animals should only be given medicated drinking water. To ensure accurate dosing, the body weight of the animals should be determined as precisely as possible.

WITHDRAWAL TIME:
Cattle and sheep: 15 days.
Pigs: 11 days.
Chickens: 3 days.
Do not use in animals producing milk for human consumption. Do not use in birds producing eggs for human consumption.

SPECIAL STORAGE PRECAUTIONS:
Keep out of the reach and sight of children. Store below 25 °C. Do not freeze. Keep the bottle tightly closed. Do not use after the expiration date marked on the label. Shelf life after first opening the primary packaging: 3 months. Shelf life after reconstitution in drinking water: 24 hours.

SPECIAL WARNINGS:
The following practices should be avoided, as they increase the risk of developing resistance and ultimately lead to treatment ineffectiveness:
– Frequent and repeated use of antiparasitics from the same class over a long period;
– Underdosing that may result from underestimating the body weight of the animals.
Suspected clinical cases of resistance to anthelmintics should be investigated using appropriate methods (fecal egg count, etc.). If test results clearly indicate the establishment of resistance to a certain anthelmintic, another anthelmintic from a different pharmacological class with a different mode of action should be used.

Special precautions for use in animals:
Not applicable.

Special precautions to be taken by the person administering the veterinary medicinal product to animals:
In case of accidental ingestion, seek medical advice immediately and present the leaflet or label of the product. Individuals with known hypersensitivity to the active substance should avoid contact with the product. Personal protective equipment should be worn when handling the veterinary medicinal product. In case of accidental contact with the eyes, rinse thoroughly with water and seek medical advice immediately, presenting the product leaflet or label. After administering the product, handwashing is recommended.

Use during pregnancy, lactation or laying period:
No adverse reactions have been reported with the use of Levaverm 10% during pregnancy and lactation.

Interactions with other medicinal products or other forms of interaction:
The concurrent administration of levamisole with organophosphorus insecticides may occasionally lead to toxic reactions.

Overdose (symptoms, emergency procedures, antidotes):
The therapeutic index of levamisole is 2.5 to 12 times the prescribed dose.

Incompatibilities:
In the absence of compatibility studies, this veterinary medicinal product should not be mixed with other veterinary medicinal products.

SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCT OR WASTES, WHERE APPLICABLE:
Medicines should not be disposed of in wastewater or household waste. Please ask your veterinarian for information regarding the disposal of medicines that are no longer required. These measures contribute to environmental protection.

SIZE:
Bottle x 1 liter.