Lamisil DermGel

Lamisil DermGel

terbinafine

Manufacturer:

GlaxoSmithKline Consumer

Distributor:

DKSH
Full Prescribing Info
Contents
Terbinafine.
Description
One gram contains 10 mg terbinafine base.
Excipients/Inactive Ingredients: Ethanol; isopropyl polysorbate 20; carbomer 974 P; sorbitan monolaurate; benzyl alcohol; sodium hydroxide; butylhydroxytoluene; purified water.
Action
Pharmacotherapeutic group: Antifungal for topical use. ATC Code: D01AE15.
Pharmacology: Pharmacodynamics: Mechanism of Action: Terbinafine interferes specifically with fungal sterol biosynthesis at an early step. This leads to a deficiency in ergosterol and to an intracellular accumulation of squalene, resulting in fungal cell death. Terbinafine acts by inhibition of squalene epoxidase in the fungal cell membrane. The enzyme squalene epoxidase is not linked to the cytochrome P-450 system. Terbinafine does not influence the metabolism of hormones or other drugs.
Terbinafine is an allylamine which has a broad spectrum of antifungal activity in the fungal infections of the skin caused by dermatophytes such as Trichophyton (e.g. T. rubrum, T. mentagrophytes, T. verrucosum, T. violaceum), Microsporum canis and Epidermophyton floccosum. At low concentrations terbinafine is fungicidal against dermatophytes, moulds and certain dimorphic fungi. The activity against yeast is fungicidal (e.g. Malassezia furfur) or fungistatic, depending on the species.
Pharmacokinetics: Absorption: Less than 5% of the dose is absorbed after topical application to humans; systemic bioavailability is therefore very low.
Distribution: Following application for 7 days, concentration of terbinafine in excess of those required for fungicidal activity are available in the affected stratum corneum for at least 7 days after treatment cessation.
Indications/Uses
Fungal infections of the skin caused by dermatophytes such as Trichophyton (e.g. T. rubrum, T. mentagrophytes, T. verrucosum, T. violaceum), Microsporum canis and Epidermophyton floccosum e.g. interdigital type tinea pedis (athlete's foot), tinea cruris (dhobie (jock) itch) and tinea corporis (ringworm).
Pityriasis (tinea) versicolor caused by Pityrosporum orbiculare (also known as Malassezia furfur).
Dosage/Direction for Use
For cutaneous use only.
Elderly: There is no evidence to suggest that elderly patients require different dosages or experience side effects different to those in younger patients.
Adults and adolescent aged 12 years and over: Duration and frequency of treatment: Interdigital type tinea pedis: Once a day for one week.
Tinea corporis, tinea cruris: Once a day for one week.
Pityriasis versicolor: Once or twice a day for one week.
Clinical symptoms usually start to improve within a few days. Irregular use or premature discontinuation of treatment carries the risk of recurrence.
If there are no signs of improvement within 2 weeks of first starting treatment, patients should see a doctor or pharmacist to verify diagnosis.
Method of administration: Before first use, the sealing membrane of the tube must be pierced using the point incorporated into the screw cap.
The affected area should be cleaned and dried thoroughly before application. The gel should be applied to the affected skin and surrounding area in a thin layer and rubbed it lightly. In the case of intertriginous infections (submammary, interdigital, intergluteal, inguinal), the application may be covered with a gauze, especially at night.
Children: Not recommended for use in children below 12 years of age due to insufficient data on safety and efficacy.
Overdosage
Signs and symptoms: The low systemic absorption of topical terbinafine renders overdosage extremely unlikely during cutaneous use.
Accidental ingestion of one 30 g tube of gel, which contains 300 mg terbinafine base, is comparable to ingestion of one Terbinafine 250 mg tablet (adult oral unit dose).
Symptoms/signs of overdose following ingestion of terbinafine may include headache, nausea, epigastric pain and dizziness.
Further management should be as clinically indicated.
In case of accidental oral ingestion, the alcohol content (9.4% w/w) of Lamisil DermGel has to be considered.
Contraindications
Contraindicated in patients with a prior hypersensitivity reaction to terbinafine or any other ingredient of the preparation.
Special Precautions
May be irritating to the eyes. In case of accidental contact with the eyes, rinse eyes thoroughly with running water.
Keep out of the sight and reach of children.
Infants must not be allowed to come into contact with any treated skin, including the breast.
For external use only.
Should be used with caution in patients with lesions where alcohol could be irritating (e.g. after sun exposure or in case of severe skin scaling).
Should not be used on the face.
Contains butylhydroxytoluene (E321), which may cause local skin reactions (e.g. contact dermatitis), or irritation to the eyes and mucuous membranes.
Ability to perform tasks that require judgement, motor or cognitive skills: Cutaneous application of terbinafine has no influence on the ability to drive and use machines.
Use In Pregnancy & Lactation
Pregnancy: For terbinafine, no clinical data on exposed pregnancies are available. Animal studies do not indicate any harmful effects with respect to pregnancy or the health of the foetus. It is not appropriate for the consumer to use the product during pregnancy unless clearly necessary.
Lactation: Terbinafine is excreted into breast-milk. After topical use, only a low systemic exposure is expected. Terbinafine should only be used in a nursing mother if the expected benefit justifies the risk to the infant. In addition, infants must not be allowed to come into contact with any treated skin, including the breast.
Adverse Reactions
Adverse reactions are listed below by system organ class and frequency. Frequencies are defined as: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to 1/1,000); very rare (<1/10,000), or not known (cannot be estimated from available data). Adverse reactions indentified during post-marketing use are reported voluntarily from a population of uncertain size, the frequency of these reactions is not known but likely to be rare or very rare. Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. (See table.)

Click on icon to see table/diagram/image
Drug Interactions
There are no clinically relevant drug interactions.
Storage
Store below 30°C.
ATC Classification
D01AE15 - terbinafine ; Belongs to the class of other antifungals for topical use.
Presentation/Packing
Topical gel 1% x 15 g.
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