Terbinorm spray dermal solution 10.08 mg/ml 20ml — Made in Romania — Free Delivery

Skin spray "Terbinorm" is used for the following indications:

The active substance is terbinafine (1 ml of the preparation  contains terbinafine hydrochloride 10.08 mg).

Excipients: propylene glycol, macrogol 300, ethanol 96%, purified water.

Hypersensitivity to the active substance or other components of the preparation.

The preparation is intended for external use only.

Before using it, thoroughly clean and dry the affected skin. Spray on the affected areas in an amount sufficient to thoroughly moisturize them, and, in addition, apply to nearby areas of both affected and intact skin.

The duration of treatment and the frequency of use depends on the indications:

epidermophytosis of the feet and trachophytosis of smooth skin - 1 time per day for a week;

versicolor versicolor - 2 times a day for a week.

Clinical experience with pregnant women is limited, so the preparation can be used during pregnancy only if the expected benefit to the mother outweighs the potential risk to the fetus.

Terbinafine in a small amount penetrates into breast milk, so the preparation should not be used during breastfeeding. Contact of infants with any area of ​​the skin to which the preparation was applied should be avoided.

Elderly patients do not require dose adjustment.

Relief of the symptoms of the disease is usually expected within a few days. Unsystematic use or premature termination of treatment leads to the occurrence of relapses of the disease.

If there are no signs of improvement after a week of treatment, you should consult a doctor.

The safety and efficacy of terbinafine in children have not been established, therefore it is not recommended to use the preparation  in children under the age of 18 years.

The preparation does not affect the reaction rate when driving vehicles or using other mechanisms.

The low systemic absorption of terbinafine when applied topically causes an extremely low likelihood of overdose.

In case of accidental ingestion, the content of ethyl alcohol in the medicinal product (4032.8 mg / vial) should be taken into account.

In case of accidental ingestion of the contents of more than one vial, manifestations of such adverse reactions as headache, nausea, pain in the epigastric region, dizziness are possible.

Treatment of overdose consists in the removal of the active substance, primarily by the use of activated charcoal and symptomatic therapy, if necessary.

Local symptoms such as itching, peeling or burning of the skin, pain and irritation at the site of application, pigmentation disorders, erythema, crusting and others may be observed at the site of application. These minor symptoms must be distinguished from hypersensitivity reactions, including rashes, which have been reported in rare cases and require discontinuation of treatment. In case of accidental contact with the eyes, the preparation may cause eye irritation. In rare cases, an exacerbation of a latent fungal infection is possible.

Store at a temperature not exceeding 25 ° C, out of the reach of children.

Shelf life - 3 years.