Expiration date: 01/2025
Fospasim is a homeopathic drug for the prevention and treatment of stress, hyperexcitability and correction of behavioral disorders. Dosage form: oral solution (drops). In appearance, the preparations are a colorless transparent liquid.
Structure
Fospasim drops for oral use contain matrix tinctures of vegetable, organic origin and mineral components (in 1000 ml): Phosphorus Ø=D3 0.5 nl; Aconitum napellus Ø 1 pcl; Hyoscyamus niger Ø 1 nl; Passiflora incarnata Ø 1.5 nl; Moshus moschuferus Ø=D1 0.5 ml; Strychnos ignatii Ø 5 ml; Platinum metallicum Ø=D4 5 mg and excipients: glycerin up to 35% by weight, and purified water up to 1000 ml.
PHARMACOLOGICAL PROPERTIES
Fospasim refers to combined homeopathic medicines. It has a pronounced anxiolytic effect, prevents the development of hyperkinesis, locomotor stereotypy, increased emotional reactivity, normalizes the emotional and mental state, improves orientation reactions and learning.
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.
DOSAGE AND APPLICATION
Fospasim is prescribed to dogs, cats, rabbits, decorative rodents, horses, cattle with neurosis, increased excitability, behavioral disorders, phobias (fear of noises and explosions - fireworks, fireworks, thunderstorms, shots, etc.), stress (parting with the owner, early weaning of young animals from the mother, regrouping, transportation), for adaptation, optimization of the training process, with chronic fatigue syndrome in service dogs , as a premedication component.
Fospasim drops are administered orally to animals individually forcibly in the following single doses (per animal): dogs - 2 drops / 1 kg of animal weight; cats - 3 drops / 1 kg of animal weight; decorative rodents - 2-3 drops / animal.
Drops are applied orally 1-2 times a day for 7-14 days.
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 Fospasim does not exclude the use of other drugs for etiotropic, pathogenetic and symptomatic therapy.
Products of animal origin during and after the application of Fospasim 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 Fospasim in accordance with this instruction, side effects and complications are usually not noted. With increased individual sensitivity and the occurrence of allergic reactions, the use of the drug is discontinued and antihistamines and symptomatic therapy are prescribed to the animal.
SHELF LIFE AND STORAGE
Fospasim 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.
