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

Lamisil

Active Ingredient:
Terbinafine Hydrochloride
Origin:
EU

Lamisil (Terbinafine Hydrochloride)

Terbinafine Hydrochloride, the active ingredient in Lamisil, is an allylamine antifungal presented as a topical formulation for cutaneous use. It is employed to treat superficial fungal infections of the skin, such as ringworm, athlete’s foot, and jock itch, in adult and pediatric patients as directed by a healthcare professional.

GNH India supplies Lamisil as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides full regulatory documentation to support global distribution and import requirements.

Manufacturer / TM Owner

Karo Healthcare Ab

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Indications & Clinical Uses

Lamisil is used to treat dermatophyte infections of the skin and superficial structures.

  • Tinea corporis (ringworm): eliminates the fungal infection on the body, reducing redness and scaling.
  • Tinea pedis (athlete’s foot): clears the infection between the toes and on the soles, relieving itching and burning.
  • Tinea cruris (jock itch): resolves the fungal rash in the groin area, improving comfort and preventing spread.
  • Other superficial dermatophyte infections: treats infections such as onychomycosis of the nail surface and other cutaneous fungal conditions.

How It Works

  • Terbinafine Hydrochloride acts by inhibiting the fungal enzyme squalene epoxidase, a key step in the biosynthesis of ergosterol, an essential component of fungal cell membranes. Blockade of this pathway leads to accumulation of toxic squalene and depletion of ergosterol, disrupting membrane integrity and causing fungal cell death. This mechanism provides a fungicidal effect that is effective with short treatment courses.

Side Effects

Topical terbinafine may cause local and systemic adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Skin irritation: mild redness, itching, or burning at the application site.
  • Pruritus: transient itching unrelated to infection.
  • Erythema: localized redness of the treated skin.
  • Dryness: occasional peeling or flaking of the skin.

Serious or Rare Side Effects

  • Allergic contact dermatitis: severe rash, swelling, or blistering requiring medical attention.
  • Hepatotoxicity: rare systemic absorption leading to liver enzyme elevation.
  • Stevens‑Johnson syndrome: extremely rare but life‑threatening skin reaction.
  • Anaphylaxis: rare systemic allergic response with respiratory distress.

Precautions & Warnings

When using Lamisil, certain precautions should be observed to ensure safety and effectiveness.

  • Application area: apply a thin layer only to affected skin and avoid healthy surrounding tissue.
  • Duration of therapy: follow the prescriber’s recommended treatment length and do not exceed it.
  • Age restrictions: use in children only as directed by a healthcare professional; avoid use in infants without guidance.
  • Concomitant skin conditions: avoid application on eczematous, ulcerated, or infected skin not caused by dermatophytes.
  • Pregnancy and lactation: discuss use with a physician; terbinafine is generally avoided unless benefits outweigh risks.
  • Store at room temperature: keep the product in its original container, protect from moisture and direct sunlight.

Avoid Interactions

Terbinafine can interact with other medicines, altering its efficacy or increasing the risk of adverse effects.

Major Interactions (Avoid)

  • Cytochrome P450 2D6 inhibitors: may increase systemic exposure to terbinafine, raising toxicity risk.
  • Antifungal agents with overlapping toxicity: concurrent use with itraconazole or ketoconazole can enhance hepatotoxic potential.
  • Warfarin: terbinafine may potentiate anticoagulant effect, requiring close monitoring of INR.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: terbinafine may reduce hormonal efficacy, consider alternative contraception.
  • Rifampin: may decrease terbinafine levels, reducing antifungal effectiveness.
  • Alcohol: excessive intake can increase liver strain when combined with terbinafine.

Frequently Asked Questions

Lamisil contains terbinafine hydrochloride and is indicated for the topical treatment of superficial fungal infections such as tinea corporis (ringworm), tinea pedis (athlete’s foot), tinea cruris (jock itch) and other dermatophyte infections of the skin.

Terbinafine inhibits the fungal enzyme squalene epoxidase, blocking ergosterol synthesis. This causes toxic squalene to accumulate and disrupts the fungal cell membrane, leading to rapid fungal cell death.

The prescribed dose of Lamisil is determined by the treating clinician based on the infection type, severity, patient age and other factors. The prescriber will specify the amount to apply and the duration of therapy.

Safety data for topical terbinafine in pregnancy and lactation are limited. Healthcare providers usually avoid routine use unless the potential benefit outweighs any possible risk. Patients should discuss their situation with a qualified professional before starting treatment.

To request Lamisil, submit an enquiry on the product page at gnhindia.com, indicating 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 any required import documentation.

Lamisil belongs to the allylamine class, which acts by inhibiting squalene epoxidase, whereas azole antifungals block lanosterol 14‑α‑demethylase. Allylamines often achieve faster fungicidal activity and are effective against dermatophytes, while azoles have a broader spectrum but may require longer treatment periods.

Lamisil should be stored at room temperature, below 25 °C, in its original packaging. Keep the container tightly closed, protect it from moisture and direct sunlight, and keep it out of reach of children.

Apply a thin layer of the cream or solution to the affected skin area once or twice daily, as directed by the prescriber. Gently rub it in, avoid covering with occlusive dressings unless instructed, and wash hands after application.

Although rare, serious adverse reactions can include severe allergic contact dermatitis, Stevens‑Johnson syndrome, anaphylaxis and hepatotoxicity. Patients should seek immediate medical attention if they notice widespread rash, blistering, swelling, difficulty breathing or signs of liver dysfunction.

Lamisil should not be used by individuals with known hypersensitivity to terbinafine or any component of the formulation. It is also contraindicated in patients with extensive ulcerated or infected skin not caused by dermatophytes, and caution is advised in pregnant or nursing women unless advised otherwise by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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