Expiration date: 01/2025

Travmatin is a complex homeopathic drug that, thanks to a unique combination of components, has the ability to favorably affect the focus of inflammation, significantly accelerating the recovery of damaged tissues in the animal's body. Dosage form: solution for injection. In appearance, the drug is a colorless transparent liquid.

Structure

As active substances, Travmatin contains matrix tinctures of plant origin, mineral and organic components (in 1000 ml): Echinacea purpurea Ø 4.5 ml; Matricaria recutita Ø 4.5 ml; Calendula officinalis Ø 3 ml; Arnica montana Ø= D1 15 ml; Hypericum perforatum Ø 0.03 ml; Atropa belladonna Ø 2 ml; Hepar sulfuris D4 0.1g; ASD-2 15 pcl and excipients: methyl parahydroxybenzoate - 0.5 g, sodium chloride - 5.8 g sodium acetate trihydrate - 2.0 g, hydrochloric acid to pH 5.4, ethyl alcohol 95% - 5.26 g, water for injection up to 1000 ml.

PHARMACOLOGICAL PROPERTIES

Travmatin refers to combined homeopathic medicines.

It has an anti-inflammatory and anti-exudative effect, restores microcirculation in the damaged area, reduces capillary bleeding, promotes rapid regeneration of damaged tissues and full-fledged epithelization.

According to the degree of exposure to the body, the drug belongs to low-hazard substances (hazard class 4 according to GOST 12.1.007), does not have a locally irritating and sensitizing effect.

INDICATIONS

Travmatin is prescribed to dogs, cats and farm animals in the complex therapy of traumatic injuries, including birth injuries, as well as in the treatment of accidental and surgical wounds.

DOSAGE AND APPLICATION

Travmatin is used intramuscularly or subcutaneously 1-2 times a day for 1-5 days in single doses: dogs, cats - 0.1 ml / 1 kg of animal weight; cattle - 5.0-7.0 ml / animal; horses - 5.0-8.0 ml / animal; pigs - 5.0 ml / animal.

SPECIAL INSTRUCTIONS

Symptoms of overdose in animals have not been established.

The peculiarities of the drug's action during its first use and cancellation have not been established.

Omissions should be avoided when administering the next dose of the drug, as this can lead to a decrease in therapeutic and preventive effectiveness. If one dose is missed, the use of the drug should be resumed as soon as possible in the same dose and according to the same scheme.

The use of Travmatin does not exclude the use of other drugs for etiotropic, pathogenetic and symptomatic therapy.

Products of animal origin during and after the use of Travmatin can be used without restrictions.

Contraindications

Contraindication to the use of the drug is an individual hypersensitivity of the animal to its components.

SIDE EFFECTS

When using Travmatin in accordance with this instruction, side effects and complications are usually not noted.

SHELF LIFE AND STORAGE

Travmatin is stored in the manufacturer's closed packaging, separately from food and feed, in a dry place protected from direct sunlight at a temperature from 0 to 30 ° C.

The shelf life of the drug, subject to storage conditions in the manufacturer's closed packaging, is 3 years from the date of production, after the first opening of the bottle - 21 days.

Travmatin is prohibited to be used after the expiration date. It should be kept out of the reach of children.

Travmatin