Auridexan ear drops 0.5 mg/ml bottle 5 ml

Instructions for use Auridexan ear drops 0.5 mg/ml bottle 5 ml

Composition

active ingredient: decamethoxine;

1 ml of solution contains decamethoxine in terms of 100% substance 0.5 mg;

excipient: ethanol (70%).

Dosage form

Ear drops.

Main physicochemical properties: colorless transparent liquid with an alcohol odor.

Pharmacotherapeutic group

Means for use in otology. Antimicrobial agents. ATX code S02A A.

Pharmacological properties

Pharmacodynamics

The drug has an antiseptic effect and a wide spectrum of antimicrobial action against gram-positive and gram-negative microorganisms (pyogenic cocci, including staphylococci with multiple antibiotic resistance, enterobacteria, corynebacteria diphtheria), protozoa, yeast-like fungi of the genus Candida, dermatomycetes and viruses. The drug has a bactericidal, sporicidal, fungicidal effect on microorganisms. Auridexan increases the sensitivity of bacteria to antibiotics, potentiates the effect of traditional antimicrobial agents in complex treatment.

Pharmacokinetics

Not researched.

Indication

Treatment of bacterial and fungal acute and chronic non-perforating otitis externa and otitis media.

Contraindication

Hypersensitivity to decamethoxine or ethanol.

Interaction with other medicinal products and other types of interactions

Not researched.

Application features

In case of individual hypersensitivity, the drug should not be used.

Ability to influence reaction speed when driving vehicles or other mechanisms

No effect.

Use during pregnancy or breastfeeding

The use of the drug during pregnancy or breastfeeding is possible only when the expected benefit to the mother outweighs the potential risk to the fetus or child.

Method of administration and doses

After opening, close the bottle with the dropper cap.

Adults and children over 12 years of age should instill 2-3 drops of Auridexan in each ear in a warm form 3-4 times a day. The duration of the treatment course depends on the severity of the disease and the achieved effect and is determined by the doctor individually.

Children

There is no experience with the use of decamethoxine in children under 12 years of age, so the drug should not be prescribed to this age group of patients.

Overdose

No cases of overdose were noted.

Adverse reactions

A transient burning sensation is possible when using the drug, as well as a reaction of local irritation of the skin of the ear (external auditory canal, auricle) with increased individual sensitivity to decamethoxin.

Expiration date

4 years.

Storage conditions

Store at a temperature not exceeding 25 °C in the original packaging.

Keep out of reach of children.

Packaging

5 ml in a bottle with a dropper cap in a pack.

Vacation category

According to the recipe.

Producer

Limited Liability Company "Research Plant "GNTSLS". Limited Liability Company "PHARMEX GROUP".

Location of the manufacturer and its business address

Ukraine, 61057, Kharkiv region, Kharkiv city, Vorobyovy street, building 8. Ukraine, 08301, Kyiv region, Boryspil city, Shevchenko street, building 100.