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

Lamisil

Active Ingredient:
Terbinafine Hydrochloride
Origin:
EU

Lamisil (Terbinafine Hydrochloride)

Terbinafine, the active ingredient in Lamisil, is an allylamine antifungal presented as an oral tablet for systemic use. It is prescribed for the treatment of dermatophyte infections of the skin and nails, such as onychomycosis, athlete’s foot and ringworm, in adult patients.

GNH India supplies Lamisil as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, transplant centres and oncology centres worldwide. Our quality‑assured batches meet EU regulatory standards and are shipped with full documentation to support import requirements through reliable logistics partners.

Manufacturer / TM Owner

Novartis Pharma N.V.

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Indications & Clinical Uses

Lamisil (terbinafine) is used to treat fungal infections caused by dermatophytes affecting skin and nails.

  • Onychomycosis: eradicates the fungal infection of the toenail or fingernail, promoting normal nail growth.
  • Tinea pedis (athlete’s foot): clears the fungal infection of the foot skin, relieving itching and scaling.
  • Tinea corporis (ringworm): eliminates the dermatophyte infection of the body skin, restoring healthy appearance.

How It Works

  • Terbinafine inhibits fungal squalene epoxidase, a key enzyme in ergosterol synthesis. This inhibition leads to accumulation of squalene and depletion of ergosterol, disrupting the fungal cell membrane structure and causing cell death. The selective action targets dermatophyte organisms while sparing human cells, providing effective systemic antifungal therapy.

Side Effects

Terbinafine is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal discomfort or diarrhea.
  • Headache: mild to moderate intensity.
  • Altered taste sensation: temporary dysgeusia or loss of taste.
  • Skin rash: mild erythema or pruritus.
  • Elevated liver enzymes: mild, transient increases in hepatic transaminases.

Serious or Rare Side Effects

  • Hepatotoxicity: signs of liver injury such as jaundice or dark urine.
  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hematologic abnormalities: neutropenia or eosinophilia.
  • Peripheral neuropathy: numbness or tingling in extremities.
  • Anaphylaxis: rare systemic allergic response.

Precautions & Warnings

Before initiating therapy, consider the following precautions.

  • Assess liver function: obtain baseline hepatic enzymes and monitor periodically.
  • Review medication history: avoid concomitant use with strong CYP inducers or inhibitors.
  • Evaluate renal status: dose adjustment may be needed in severe impairment.
  • Monitor for skin reactions: discontinue if severe rash or hypersensitivity develops.
  • Counsel on alcohol use: limit intake as it may increase hepatic risk.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Terbinafine may interact with other medicines; awareness of interaction severity is essential.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): can raise terbinafine plasma levels.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce terbinafine efficacy.

Moderate Interactions (Monitor Closely)

  • Cimetidine: may increase terbinafine concentrations.
  • Warfarin: potential for altered anticoagulant effect; monitor INR.
  • Antiretrovirals metabolized by CYP enzymes: adjust therapy based on clinical response.
  • Oral contraceptives: rare reports of reduced effectiveness; advise additional contraceptive measures.

Frequently Asked Questions

Lamisil (terbinafine) is prescribed for dermatophyte infections such as onychomycosis of the nails, tinea pedis (athlete’s foot), and tinea corporis (ringworm of the body). It targets the fungi that cause these skin and nail disorders, helping to clear the infection and restore normal tissue.

Terbinafine blocks the fungal enzyme squalene epoxidase, which is essential for producing ergosterol, a key component of fungal cell membranes. By preventing ergosterol synthesis, the drug causes squalene to accumulate and the membrane to become defective, leading to fungal cell death while sparing human cells.

The dosage of Lamisil is determined by the prescribing healthcare professional based on the specific infection, patient weight, renal and hepatic function, and local guidelines. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of terbinafine in pregnancy and lactation has not been definitively established. It is classified as pregnancy category unknown, and clinicians usually weigh potential benefits against risks. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To request Lamisil, 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 any necessary import documentation.

Compared with azole antifungals, terbinafine has a shorter treatment duration for nail infections and a favorable safety profile for many patients. Its mechanism targets squalene epoxidase, which differs from the azoles that inhibit lanosterol 14α‑demethylase, offering an alternative when resistance or intolerance to azoles occurs.

Lamisil tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the medication out of reach of children and do not use it after the expiry date printed on the packaging.

Lamisil is taken orally, usually with a full glass of water. The tablet is swallowed whole and may be taken with or without food, unless the prescriber advises otherwise. Patients should follow the dosing schedule provided by their healthcare professional.

Serious adverse events, though rare, include hepatotoxicity (liver injury), severe skin reactions such as Stevens‑Johnson syndrome, and hematologic abnormalities like neutropenia. Patients should promptly report symptoms such as jaundice, rash, fever, or unexplained bruising to their clinician.

Lamisil is contraindicated in individuals with known hypersensitivity to terbinafine or any component of the formulation. Caution is advised for patients with pre‑existing liver disease, severe renal impairment, or those taking medications that strongly interact with terbinafine metabolism.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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