E-Selen

МРС - Домашние животные - изображение NITA FARM

Sodium selenite, vitamin E

A water-soluble complex of vitamin E and selenium in the form of solution for injections used for treatment and prevention of diseases caused by vitamin E and selenium deficiency in animals.

Significant antioxidant effect

Promoted growth and weight gain in young animals

Immunostimulating, antistress, and antitoxic effects

Very effective even at low doses

Administration once every 2 to 4 months

Hepatoprotective effect.

Description
A water-soluble complex of vitamin E and selenium in the form of solution for injections used for treatment and prevention of diseases caused by vitamin E and selenium deficiency in animals.

E-selen is a clear colourless to light yellow liquid, opalescent at diffuse light.

Packing: 50 and 100 mL glass bottles sealed with rubber stoppers and flip-off caps.
Composition
Composition

1 ml
E-Selen

0,5 mg selenium (in form of sodium selenite)

50 mg vitamin E
Pharmacological properties
Pharmacological properties

E-Selen compensates for vitamin E and selenium deficiency in the animal body. Vitamin E regulates redox processes and influences carbohydrate-lipid metabolism, enhances effects of vitamins A and D₃, improves the function of the immune system and general resistance. Biological role of selenium is connected with its antioxidant characteristics. It promotes excretion of toxicological agents out of body and improves immunity in animals. Injection of the veterinary drug into organism causes quick increase of vitamin E and selenium level in the animal body, metabolic processes recovery.
Indications
Indications

E-Selen is prescribed for cattle, small ruminants, horses, pigs to prevent and treat diseases developed against the background of vitamin E and selenium deficiency in:
- reproductive dysfunctions
- fetal development disorders;white-muscle disease, traumatic myositis, and cardiopathy
- growth inhibition and insufficient weight gain
- contagious and invasive diseases
- preventive vaccinations and deworming
- nitrite, heavy metal, and mycotoxin poisonings
- stressful situations
- toxic dystrophy of the liver
Dosage and route of administration

Dosage and route of administration

The veterinary drug is administered to animals intramuscularly or subcutaneously (to horses only intramuscularly) for prevention - once with a 2- to 4-month interval; for treatment—once, 2 to 3 times, with a 7- to 10-day interval, in the following doses:

adult animals: 1 mL/50 kg of animal body weight
growing stock: 0.2 mL/10 kg of animal body weight.

To administer small volumes of the drug in a convenient way, it is possible to dilute it with sterile water or normal saline and mix thoroughly.

Curative dose may be increased by 1.5, and in regions with selenium deficiency - increased fivefold.

A dose per one animal should not exceed: for horses - 20 mL; cows - 15 mL; and sheep, goats - 5 mL, for pigs - 5 mL.

E-Selen treatment regimen to prevent white-muscle disease 1 in selenium-geodeficient zones¹

Animals	Dose, mL per 10 kg of body weight	Interval, days	Number of injections
Calves and lambs, 3 months and younger	0.5	14	6
Young animals, 3 months old and older	0.2	30	Once a month
Calves and lambs in groups with ill animals	1.0	7	3
Cows, 60 days left before calving	15 mL per animal	10-14	3-4
Ewes, 30 before lambing	0.5	10	2

¹ - E-Selen applied according to this regimen is permissible only in farms where selenium deficiency in the animal body is confirmed by clinical and biochemical studies.

Restrictions
Restrictions

Small ruminants and pigs can be slaughtered for human consumption no earlier than 14 days (and cattle - no earlier than 30 days) after the last administration of E-selen. In the case of forced slaughter of animals before the established deadlines, the meat can be used for feeding carnivores.

CONTRAINDICATIONS
Contraindications include high intra-patient animal sensitivity to selenium, or surplus contents of selenium in feed and animal body (alkali disease). Combined administration with vitamin C reduces bioavailability of E-selen. Avoid combining the drug with arsenic medication, as chemical antagonism occurs. E-selen disintegrates when interacting with heavy metals (hydrargyrum, cuprum, lead, and stanum).
SHELF LIFE

2 years from the date of manufacture; after first opening - 14 days

Description
Composition
Pharmacological properties
Indications
Dosage and route of administration
Restrictions

A water-soluble complex of vitamin E and selenium in the form of solution for injections used for treatment and prevention of diseases caused by vitamin E and selenium deficiency in animals.

E-selen is a clear colourless to light yellow liquid, opalescent at diffuse light.

Packing: 50 and 100 mL glass bottles sealed with rubber stoppers and flip-off caps.

Composition

1 ml

E-Selen

0,5 mg selenium (in form of sodium selenite)

50 mg vitamin E

Pharmacological properties

E-Selen compensates for vitamin E and selenium deficiency in the animal body. Vitamin E regulates redox processes and influences carbohydrate-lipid metabolism, enhances effects of vitamins A and D₃, improves the function of the immune system and general resistance. Biological role of selenium is connected with its antioxidant characteristics. It promotes excretion of toxicological agents out of body and improves immunity in animals. Injection of the veterinary drug into organism causes quick increase of vitamin E and selenium level in the animal body, metabolic processes recovery.

Indications

E-Selen is prescribed for cattle, small ruminants, horses, pigs to prevent and treat diseases developed against the background of vitamin E and selenium deficiency in:

reproductive dysfunctions
fetal development disorders;white-muscle disease, traumatic myositis, and cardiopathy
growth inhibition and insufficient weight gain
contagious and invasive diseases
preventive vaccinations and deworming
nitrite, heavy metal, and mycotoxin poisonings
stressful situations
toxic dystrophy of the liver

Video

Dosage and route of administration

adult animals: 1 mL/50 kg of animal body weight
growing stock: 0.2 mL/10 kg of animal body weight.

To administer small volumes of the drug in a convenient way, it is possible to dilute it with sterile water or normal saline and mix thoroughly.

Curative dose may be increased by 1.5, and in regions with selenium deficiency - increased fivefold.

A dose per one animal should not exceed: for horses - 20 mL; cows - 15 mL; and sheep, goats - 5 mL, for pigs - 5 mL.

E-Selen treatment regimen to prevent white-muscle disease 1 in selenium-geodeficient zones¹

Animals	Dose, mL per 10 kg of body weight	Interval, days	Number of injections
Calves and lambs, 3 months and younger	0.5	14	6
Young animals, 3 months old and older	0.2	30	Once a month
Calves and lambs in groups with ill animals	1.0	7	3
Cows, 60 days left before calving	15 mL per animal	10-14	3-4
Ewes, 30 before lambing	0.5	10	2

¹ - E-Selen applied according to this regimen is permissible only in farms where selenium deficiency in the animal body is confirmed by clinical and biochemical studies.

Restrictions

Small ruminants and pigs can be slaughtered for human consumption no earlier than 14 days (and cattle - no earlier than 30 days) after the last administration of E-selen. In the case of forced slaughter of animals before the established deadlines, the meat can be used for feeding carnivores.

CONTRAINDICATIONS

Contraindications include high intra-patient animal sensitivity to selenium, or surplus contents of selenium in feed and animal body (alkali disease). Combined administration with vitamin C reduces bioavailability of E-selen. Avoid combining the drug with arsenic medication, as chemical antagonism occurs. E-selen disintegrates when interacting with heavy metals (hydrargyrum, cuprum, lead, and stanum).