Travogen 1% cream 20 g

$15.63

Travogen 1% cream 20 g

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SKU: 01684197185 Categories: , , Tag:

Description

Composition
Active substance:
100 g of cream contains: isoconazole nitrate – 1.0 g ;.
Excipients:
Polysorbate 60 – 3.5 g of sorbitan stearate – 1.0 g cetylstearyl alcohol (60% cetyl alcohol, stearyl alcohol 40%) – 5.0 g Liquid paraffin – 10.0 g White petrolatum – 10.0 g , purified water – 69.5 g
Description:
White or white with a yellowish tint, opaque, homogeneous cream.
Product form:
Cream for external application of 1% to 20 or 50 g of an aluminum tube, sealed with a membrane-closed screw cap, the tube together with instructions for use placed in a cardboard box.
Contraindications
Hypersensitivity to the active agent or any excipients.
Dosage
10 mg / g
Indications
Superficial fungal infections of the skin, including the localization in the skin folds, interdigital spaces, groin, vulva;
Erythrasma.
Interaction with other drugs
on interaction studies have not been conducted.
Overdose
Until now, data on overdose are available. Due to the low toxicity isoconazole no reason to expect the risk of acute toxicity after treatment at the high dose or inadvertent ingestion.
pharmachologic effect
Pharmacological group:
Antifungal agent.
Pharmacodynamics:
Isoconazole – synthetic derivative of imidazole. It has a broad antifungal and antibacterial spectrum of action. Acts fungicidal and bactericidal. Active against dermatophytes (Trychophyton spp, Microsporum spp, Epidermophyton spp…); molds, yeasts and yeast-like fungi of the genus Candida spp, and Corynebacterium minutissimum -. erythrasma pathogen and Gram-positive bacteria Staphylococcus spp,.
Streptococcus spp.
Pharmacokinetics:
Isoconazole nitrate penetrates quickly into the skin, the maximum concentration in the stratum corneum and in underlying layers of the epidermis is achieved 1 hour after application of the drug (high concentration was maintained for at least 7 hours).
The concentration in the deep layers of the epidermis is higher than the minimum inhibitory concentration for dermatophytes. When applied topically isoconazole nitrate concentration in the epidermis is greater than in the dermis and subcutaneous tissue. When applied to the skin is negligible systemic absorption.
Pregnancy and breast-feeding
Use of the drug during pregnancy is possible in cases where the potential benefit to the mother outweighs the risk to the fetus. Not determined whether isoconazole passes into breast milk, so the drug should not be applied to the breasts before feeding.
If necessary, use of the drug to resolve the issue with your doctor about the termination of breastfeeding.
Fertility.
These pre-clinical studies have not identified a risk in relation to fertility.
Conditions of supply of pharmacies
By prescription.
side effects
The most frequently observed in clinical trials, adverse reactions include irritation and burning in the area of ​​applying the cream on the skin Travogen®.
The frequency of adverse reactions is determined in accordance with the frequency estimation rules
WHO: often (by> 1/100 to 1/1000 to 1/10000 to
General reactions.
Often the irritation and burning at the site of application.
Uncommon: dryness and itching at the site of application.
Rare: swelling, and cracks in the site of application.
Frequency unknown: erythema, vesicles, and the site of application.
Violations of the skin and subcutaneous tissue
Uncommon: weeping eczema, pompholyx, contact dermatitis.
Frequency not known: allergic skin reaction.
If any of these instructions side effects are compounded, or if you notice any other side effects not mentioned in the instructions, tell your doctor.
special instructions
When applying Travogen® cream on the face to avoid getting the drug into the eye.
During treatment to observe good personal hygiene.
When applied to a cream Travogen® pudendal region and use during treatment barrier contraceptive condom or the risk of rupture of the diaphragm increases, as included in the formulation of liquid paraffin and petrolatum can cause damage contraceptive products of latex, thus reducing their effectiveness.
You must use reliable methods of contraception.
When allergic reactions or irritations at the site of drug treatment is stopped. Cetylstearyl alcohol, part of the drug may cause development of contact dermatitis. In the absence of the effect of the treatment should consult a doctor.
Effect of the drug on the ability to operate vehicles, machinery.
The drug does not affect the ability to drive vehicles or to engage in other potentially hazardous activities that require high concentration and psychomotor speed reactions.
Storage conditions
Store at a temperature not higher than 30 ° C.
Keep out of the reach of children.
Dosing and Administration
Outwardly. Travogen® cream is applied 1 time per day to the affected skin. The usual duration of topical treatment of fungal infections is 2-3 weeks, in the case of hard-to-therapy of infections (especially in the interdigital spaces) – 4 weeks. Perhaps a more prolonged course of treatment.
To prevent relapse, treatment should continue for a further 2 weeks after resolution of clinical manifestations.
Travogen® drug treatment in children is conducted under the supervision of a physician. Correction of dosage regimen is required.
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

LEO PHARMA

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