Vitamin E + Sodium Selenite Injection

1. Name of the medicinal product for veterinary use:

trade name of the medicinal product: Vit E-Selenite injection

2. Dosage form – solution for injection.

Vit E-Selenite injection in 1 ml contains as active ingredients: selenium (in the form of sodium selenite) – 0.5 mg and vitamin E – 50 mg, and as excipients: polyethylene-35-ricinol, benzyl alcohol and water for injections.

3. In appearance, the drug is a colorless or slightly yellow liquid opalescent in transmitted light.

Shelf life, subject to storage conditions in the manufacturer’s closed packaging, is 3 years from the date of production, after opening the bottle – 14 days.

It is forbidden to use the drug Vit E-Selenite injection after the expiration date.

4. Store the medicinal product in the manufacturer’s closed packaging, separately from food and feed, in a place protected from direct sunlight at a temperature of 4°C to 25°C.

5.Vit E-Selenite injection should be stored out of the reach of children.

6.Vit E-Selenite injection is dispensed without a veterinarian’s prescription.

II. Pharmacological properties

1.Vit E-Selenite injection refers to complex vitamin-microelement preparations. Compensates for the lack of vitamin E and selenium in the body of animals.

Selenium is excreted from the body by 75% in the urine and 25% in the feces, vitamin E is excreted in the bile and in the form of metabolites in the urine.

2. Vit E-Selenite injection, according to the degree of impact on the body, belongs to low-hazard substances. In the recommended doses, it is well tolerated by animals, does not have a local irritating and sensitizing effect

III. Application procedure

1.Vit E-Selenite injection is used for the prevention and treatment of diseases caused by a lack of vitamin E and selenium (white muscle disease, traumatic myositis and cardiopathy, toxic liver dystrophy), as well as in stress and stressful situations, impaired reproduction and fetal development, growth retardation and insufficient weight gain, infectious and parasitic diseases, preventive vaccinations and deworming, poisoning with nitrates, heavy metals and mycotoxins.

2. Contraindications for use are individual hypersensitivity of animals to selenium, or excessive selenium content in feed and body (alkaline disease).

3. When working with the drug Vit E-Selenite injection, you should follow the general rules of personal hygiene and safety precautions provided for when working with drugs.

4. For pregnant and lactating animals, the drug is used with caution under the supervision of a veterinarian. For young animals, the drug is used according to indications, with caution, under the supervision of a veterinarian.

5. The drug is administered to animals intramuscularly or subcutaneously (horses only intramuscularly) for prophylactic purposes 1 time in 2-4 months, for therapeutic purposes 1 time in 7-10 days 2-3 times in a dose: adult animals: 1 ml per 50 kg of body weight ; young farm animals 0.2 ml per 10 kg of body weight; dogs, cats, fur animals: 0.04 ml per 1 kg of body weight.

6. For ease of administration of small volumes of the drug, it can be diluted with sterile water or saline and mixed thoroughly.

7. When using the drug Vit E-Selenite injection in accordance with the instructions for use, side effects and complications have not been established.

8. In case of an overdose of Vit E-Selenite injection, toxic effects may occur, so the dose to one animal should not exceed: for horses – 20 ml; cows -15 ml; sheep, goats, pigs – 5 ml.

9. In case of an overdose in animals, ataxia, dyspnea, anorexia, abdominal pain (gnashing of teeth), salivation, cyanosis of visible mucous membranes, and sometimes skin, tachycardia, sweating increases, body temperature decreases. Exhaled air of garlic smell and the same smell of skin. In ruminants, hypotension and atony of the pre-stomachs. In pigs, dogs and cats – vomiting, pulmonary edema.

10.If you miss taking one or more doses of the drug, the application is carried out according to the same scheme in accordance with this instruction.

11. Slaughter of animals for meat is allowed for pigs and small cattle no earlier than 14 days later, and for cattle no earlier than

12. 30 days after intramuscular or subcutaneous administration of the drug. The meat of animals forcedly killed before the expiration of the specified periods is used for feeding carnivorous animals.

Hebei Veyong pharmaceutical Co., Ltd, was established in 2002, located in Shijiazhuang City, Hebei Province, China, next to the Capital Beijing. She is a large GMP-certified veterinary drug enterprise, with R&D, production and sales of veterinary APIs, preparations, premixed feeds and feed additives. As Provincial Technical Center, Veyong has established an innovated R&D system for new veterinary drug, and is the nationally known technological innovation based veterinary enterprise, there are 65 technical professionals. Veyong has two production bases: Shijiazhuang and Ordos, of which the Shijiazhuang base covers an area of 78,706 m2, with 13 API products including Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, and 11 preparation production lines including injection, oral solution, powder, premix, bolus, pesticides and disinfectant, ects. Veyong provides APIs, more than 100 own- label preparations, and OEM & ODM service.

Veyong attaches great importance to the management of EHS(Environment, Health& Safety) system, and obtained the ISO14001 and OHSAS18001 certificates. Veyong has been listed in the strategic emerging industrial enterprises in Hebei Province and can ensure the continuous supply of products.

Veyong established the complete quality management system, obtained the ISO9001 certificate, China GMP certificate, Australia APVMA GMP certificate, Ethiopia GMP certificate, Ivermectin CEP certificate, and passed US FDA inspection. Veyong has professional team of registeration, sales and technical service, our company has gained reliance and support from numerous customers by excellent product quality, high-quality pre-sales and after-sales service, serious and scientific management. Veyong has made long term cooperation with many internationally known animal pharmaceutical enterprises with products exported to the Europe, South America, Middle East, Africa, Asia, etc. more than 60 countries and regions.