Termikon spray 30ml 1%

$10.79

Termikon spray 30ml 1%

Quantity:

SKU: 089004899 Categories: , , Tag:

Description

Composition
Active substance:
1 vial contains: terbinafine hydrochloride – 0.15 g or 0.30 g ;.
Excipients:
Ethanol (ethyl alcohol rectified) – 5.625 g or 11.25 g of propylene glycol – 0.30 g or 0.60 g, poloxamer – 0.15 g or 0.30 g, purified water – 8.775 g or 17.55 g
Description:
Transparent colorless or pale yellow liquid with a characteristic smell of ethyl alcohol.
Product form:
Spray for external application of 1%. 15 g or 30 g of an aluminum cylinder or polypropylene vial fitted with a metering pump, the nozzle and the protective cap or vial of polyethylene, provided with a pump sprayer and a protective cap. A container (vial), along with instructions for use in a stack of cardboard.
Contraindications
Hypersensitivity to terbinafine or to the excipients included in the composition of the drug, children under 18 years.
Precautions: hepatic and / or renal failure, alcoholism, depression of bone marrow hematopoiesis, tumors, metabolic disease, limb occlusive vascular disease.
Dosage
1 %
Indications
Prevention and treatment of fungal infections of the skin, including: – foot mycoses ( “mushroom” of the foot) – jock itch – fungal lesions of the smooth skin of the body, caused by dermatophytes (Trichophyton, Microsporum, athlete, rubrofitii).
Pityriasis versicolor, caused by the dimorphic fungi.
Diaper rash caused by fungi.
Interaction with other drugs
Any drug interactions for spray Termikon® not known.
Overdose
No cases of overdose have been reported. If accidentally Termikon® spray is ingested, it is possible to expect development of the same side effects as an overdose of pills Termikon® (headache, nausea, epigastric pain and dizziness). It should also take into account the content of the preparation of ethyl alcohol.
Treatment: activated charcoal, if necessary – symptomatic supportive therapy.
pharmachologic effect
Pharmacological group:
Antifungal agent.
Pharmacological properties:
Antifungal agent for topical application, with a broad spectrum of antifungal activity. At low concentrations of terbinafine has fungicidal activity against dermatophytes (Trychophyton rubrum, T. mentagrophytes, T. verrucosum, T. violaceum, T. tonsurans, Microsporum canis, Epidermophyton floccosum), mold defined dimorphic (Pityrosporum orbiculare) and yeasts (in mainly Candida albicans). Activity against yeast fungi, depending on their type, may be a fungicidal or fungistatic.
Terbinafine specifically alters the early stage of the biosynthesis of sterols, occurring in fungi. This leads to a deficiency of ergosterol and to an intracellular accumulation of squalene, which causes death of fungal cells. Action terbinafine accomplished by inhibition of the enzyme squalene epoxidase located on the cell membrane of the fungus.
Terbinafine has no effect on tsitohroma P450 system in humans and, accordingly, the metabolism of hormones or other drugs.
Pharmacokinetics:
When applied topically absorption – less than 5% has little systemic effect.
Pregnancy and breast-feeding
teratogenic properties of terbinafine have been identified in experimental studies. To date, no reports of any malformation when applying Termikona®. However, as clinical experience with Termikona® in pregnant women is very limited, it should be used only on strict conditions.
Terbinafine is excreted in breast milk. However, in the case of nursing mother Termikona® spray through the skin is absorbed a small quantity of active substance, however the adverse effect on the infant is unlikely.
Conditions of supply of pharmacies
Without recipe.
side effects
In the field application of the drug redness, itching or a burning sensation. Allergic reactions.
special instructions
Reducing the severity of the clinical manifestations usually noted in the first days of treatment. In the case of irregular or premature treatment termination are at risk of recurrent infection. In the event that after a week of treatment shows no sign of improving, you should verify the diagnosis.
Caution must be exercised when applying spray Termikon® on damaged skin because the alcohol can cause irritation.
Termikon® spray intended for external use only. Avoid contact with eyes, as it may cause irritation. In case of accidental spraying into the eyes, they should immediately wash with running water, and in the case of persistent phenomena of irritation consult a doctor.
If the drug was accidentally introduced into the respiratory tract by inhalation, that in case of any symptoms, and especially when they are persistent preservation, it is necessary to consult a doctor.
With the development of allergic reactions need to remove the drug.
The effect on the ability to operate vehicles, machinery
Data on the effect of the drug on the ability to drive vehicles or operating other machines do not.
Storage conditions
At a temperature of not higher than 30 ° C. Do not freeze. Keep out of the reach of children.
Dosing and Administration
Outwardly. Adults. Termikon® spray can be applied 1 or 2 times a day, depending on indications. Before using the product, thoroughly clean and dry the affected areas of skin. To ensure uniform spray content pre produce several short strokes at the spray nozzle. The drug is applied to the affected and surrounding skin areas of healthy skin in a sufficient amount for wetting them.
Multiplicity of the drug and duration of treatment: – ringworm of the body, legs: 1 times a day for 1 week; – tinea pedis: 1 times a day for 1 week; – pityriasis versicolor: 2 times a day for 1 week; – jock itch, diaper rash caused by fungi: 1 times a day for 1 week.
Information
Appearance may differ from that depicted in the picture. There are contraindications. You need to read the manual or consult with a specialist

Additional information

Weight0.100 kg
Manufacturer

OTISIFARM

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