Expiration date: 01/2026

Detail info about the product: 

Packing: 5 Bottles (10ml)

Gamavit is an immunomodulatory supplement to enhance the natural resistance, immune and reduce the effects of intoxication in animals and birds 

Structure and ingredients

Gamavit is a complex drug, the main active ingredients which are emulsified denatured placenta (PDE) and nukleinat sodium; manufactured drug in liquid form, based on a growth nutrient medium containing a balanced salt solution, amino acids and vitamins. 

In appearance the product is a clear, red liquid. The drug is packaged by10 ml sterile vials of neutral glass, sealed with rubber stoppers and aluminum caps break in. It could have the different packing due to the treatment course. 

PHARMACOLOGICAL PROPERTIES 

Gamavit contains a complex of biologically active substances, to help optimize the metabolic processes in the organism (in particular, protein, vitamins and minerals), and normalizes blood formula increases the serum bactericidal activity, and provides a general tonic immunomodulatory effect. Is a biogenic stimulant and adaptogen, reduces postnatal mortality, improves the viability of offspring, increases muscle performance and resistance of animals to high loads and stress. A source of substrate metabolism, growth increases. 

Prescription

The drug is used for the prevention and treatment of various diseases such us: : with anemia, hypovitaminosis, infectious and parasitic diseases, pyometra, in case of poisoning, in the postoperative period, with toxemia of pregnancy, childbirth, the preparation of animals for exhibitions, competitions and transportation. 

DOSAGE AND METHOD OF UISAGE

The drug is administered subcutaneously, intramuscularly, intravenously, may desoldering. 

In order to prevent Gamavit administered 0.1 ml / kg of animal body weight (prophylactic dose). 

With the purpose of treatment - at 0.3-0.5 ml / kg (therapeutic dose). 

Use Gamavit to prevent anemia, hypovitaminosis, debilitated old animals in the recovery period after illness and drug operations intramuscularly administered 1-3 times per week. Duration of the course is on average 2-4 weeks or more. At higher loads, to increase the resistance of animals to technological stresses, the drug is prescript prior to exposure to stress once or over the course of 8, 6, 4 days before and immediately prior to exposure to stressors. 

To improve fertility Gamavit should be administered at a dose of 0.025-0.05 ml / kg per day of fertilization, to facilitate a birth and prevention of obstetric complications the Gamavit should be used in the same dose for 1 week before birth and during labor. 

To prevent early mortality, malnutrition, to increase resistance to disease and weight gain the Gamavit is administered to newborns at 1, 3, 5 or 7 days of life in a dose of 0.1 ml / kg. 

For the treatment purpose : for treatment of infectious and parasitic diseases (including piroplasmosis) the Gamavit is administered as part of the complex of standard therapy 2-3 times a day for 3-5 days. 

When poisoning Gamavit is administered subcutaneously, intravenously or 1 drop every 3 to 5 times the therapeutic dose of the composition of the complex of the standard therapy. When violations of feeding, growth retardation and intoxications Gamavit injected 1 time per day for 5-7 days. 

When deworming Gamavit is used in conjunction with anthelmintics. The drug is administered intramuscularly in the day and again after deworming day. For the treatment of obstetric and gynecological diseases Gamavit is used as part of the complex of standard therapy: 1 time per day for 5-7 days, with a pathological birth Gamavit is used once a curative dose twice. Gamavit well with other pharmacological agents. Combination with Fosprenilom enhances the effect of the drug. 

SIDE EFFECTS 

Side effects and complications after applying Gamavita not established. 

CONTRAINDICATIONS 

Not established. 

SPECIAL INSTRUCTIONS 

No. 

STORAGE 

Drug store at 4 ° C to 25 ° C, avoiding freezing. Shelf life - 1 year from date of manufacture. Drug vials with impaired integrity in turbidity or color change, the presence of impurities, when expired or inappropriate storage and transportation conditions are not suitable for use.