Product image of Lamisil Derma (Terbinafine Hydrochloride) supplied by GNH India

Lamisil Derma

Active Ingredient:
Terbinafine Hydrochloride
Origin:
EU

Lamisil Derma (Terbinafine Hydrochloride)

Terbinafine, the active ingredient in Lamisil Derma, is an allylamine antifungal presented as a topical formulation for skin use. It is used to treat fungal infections of the skin such as athlete’s foot, ringworm and jock itch in adults and children.

GNH India supplies Lamisil Derma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Karo Healthcare Ab

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Indications & Clinical Uses

Lamisil Derma (terbinafine) is indicated for superficial fungal infections of the skin caused by dermatophytes.

  • Tinea corporis: reduces redness, scaling and itching associated with body ringworm.
  • Tinea cruris: alleviates inflammation and itching of the groin area caused by jock itch.
  • Tinea pedis: clears the fungal infection of the feet, improving skin integrity and comfort.
  • Dermatophytosis: treats a broad range of dermatophyte infections of the skin surface.

How It Works

  • Terbinafine inhibits the fungal enzyme squalene epoxidase, which blocks the conversion of squalene to ergosterol, an essential component of fungal cell membranes. The resulting accumulation of squalene and depletion of ergosterol disrupts membrane integrity, leading to fungal cell death. This mechanism is selective for fungi, allowing topical application to target skin infections with minimal systemic absorption.

Side Effects

Topical terbinafine may cause local skin reactions, ranging from mild irritation to rare severe events.

Common Side Effects

  • Burning sensation: mild burning at the application site.
  • Itching: transient pruritus around the treated area.
  • Redness: localized erythema.
  • Dryness: skin dryness or flaking.
  • Peeling: mild desquamation of the skin.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, rash, or hives indicating possible hypersensitivity.
  • Contact dermatitis: intense inflammation and blistering.
  • Stevens‑Johnson syndrome: rare but life‑threatening skin eruption.
  • Systemic toxicity: unlikely but possible if large areas are applied, leading to liver enzyme elevation.

Precautions & Warnings

When using Lamisil Derma, follow these precautionary measures to ensure safe and effective treatment.

  • Apply only to intact skin: avoid broken or inflamed areas to reduce irritation.
  • Limit treatment area: do not exceed the recommended surface area without medical advice.
  • Avoid occlusion: do not cover the treated skin with airtight dressings unless directed.
  • Monitor for allergic response: discontinue use and seek medical attention if rash or swelling develops.
  • Use as directed by healthcare professional: follow prescribed frequency and duration.
  • Store at room temperature: keep below 25 °C, protect from moisture and direct sunlight in the original container.

Avoid Interactions

Topical terbinafine has a low potential for systemic drug interactions, but certain substances may affect its safety or efficacy.

Major Interactions (Avoid)

  • Systemic antifungals (e.g., itraconazole, fluconazole): concurrent systemic use may increase risk of hepatotoxicity.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): may raise systemic terbinafine levels if large skin areas are treated.
  • Alcoholic beverages: excessive intake can exacerbate potential liver effects.

Moderate Interactions (Monitor Closely)

  • Topical corticosteroids: may reduce antifungal effectiveness when used on the same site.
  • Warfarin: monitor INR if extensive skin areas are treated, as terbinafine can affect metabolism.
  • Hormonal contraceptives: observe for reduced efficacy when large areas are applied over prolonged periods.

Frequently Asked Questions

Lamisil Derma contains terbinafine and is applied topically to treat superficial fungal infections of the skin, including athlete’s foot (tinea pedis), body ringworm (tinea corporis), jock itch (tinea cruris) and other dermatophytosis caused by dermatophyte fungi.

Terbinafine blocks the fungal enzyme squalene epoxidase, preventing the synthesis of ergosterol, a key component of fungal cell membranes. The resulting buildup of squalene and loss of ergosterol destabilize the membrane, leading to fungal cell death and resolution of the infection.

The prescribed amount of Lamisil Derma is determined by the treating healthcare professional based on the infection type, severity and the area of skin involved. Patients should follow the exact instructions provided on the label or by their prescriber.

Safety data for topical terbinafine in pregnancy and lactation are limited. Healthcare providers generally weigh the benefits against potential risks before prescribing. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternative options with their clinician.

To request Lamisil Derma, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and necessary import documentation.

Compared with azole creams, terbinafine has a fungicidal action and often requires a shorter treatment duration. It is effective against many dermatophytes that may be resistant to azoles, making it a preferred option for tinea pedis and tinea corporis in many clinical guidelines.

Lamisil Derma should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and heat sources to maintain stability and potency.

Apply a thin layer of the cream or gel to the affected skin area once or twice daily, as directed by the prescriber. Gently rub it in until it disappears, and wash hands before and after application to avoid spreading the medication.

Although rare, serious adverse reactions can include severe allergic responses such as swelling, rash, or Stevens‑Johnson syndrome. If any signs of a systemic allergic reaction or extensive skin irritation appear, discontinue use and seek immediate medical attention.

Individuals with known hypersensitivity to terbinafine or any component of the formulation should avoid using Lamisil Derma. It is also contraindicated on severely damaged or infected skin without medical supervision, and caution is advised for patients with liver disease when large skin areas are treated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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