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 a Allylamine antifungal presented as a tablet for oral use. It treats fungal infections of the skin, hair and nails, particularly in adults and adolescents who require systemic therapy.
GNH India supplies Lamisil as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Novartis Farma S.P.A.

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Indications & Clinical Uses

Lamisil is an oral allylamine antifungal indicated for infections caused by dermatophytes and related fungi.

  • Onychomycosis: eradicates the fungal pathogen within the nail plate, promoting normal nail growth.
  • Tinea pedis (athlete's foot): relieves itching and clears the infection on the feet.
  • Tinea corporis (ringworm): eliminates the fungal lesion on the body’s skin.
  • Tinea cruris (jock itch): resolves the infection in the groin area and reduces discomfort.

How It Works

  • Terbinafine inhibits the fungal enzyme squalene epoxidase, a key step in ergosterol synthesis. By blocking this pathway, the drug causes accumulation of squalene and depletion of ergosterol, disrupting fungal cell membrane integrity and leading to cell death without affecting human cholesterol synthesis.

Side Effects

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal pain or dyspepsia.
  • Headache: mild to moderate intensity.
  • Skin reactions: rash, pruritus or mild erythema.
  • Altered taste: dysgeusia or loss of taste sensation.
  • Elevated liver enzymes: mild, transient increases.

Serious or Rare Side Effects

  • Hepatotoxicity: hepatitis, jaundice or liver failure.
  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hematologic abnormalities: neutropenia, agranulocytosis or eosinophilia.
  • Peripheral neuropathy: numbness or tingling in extremities.
  • Anaphylaxis: rare, potentially life‑threatening allergic response.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Assess liver function: obtain baseline hepatic enzymes and monitor periodically.
  • Monitor for skin reactions: discontinue if severe rash or blistering develops.
  • Avoid use in known hypersensitivity: do not prescribe to patients with documented allergy to terbinafine or other allylamines.
  • Review concomitant medications: evaluate for potential drug‑drug interactions.
  • Use with caution in renal impairment: adjust dosing if required.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Terbinafine may interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Itraconazole: combined use can increase risk of hepatotoxicity.
  • Cimetidine: may raise terbinafine plasma levels.
  • CYP2D6 inhibitors (e.g., quinidine): can elevate terbinafine concentrations.

Moderate Interactions (Monitor Closely)

  • Alcohol: may exacerbate liver enzyme elevations.
  • Warfarin: monitor INR for potential anticoagulant effect changes.
  • Rifampin: may reduce terbinafine efficacy by inducing metabolism.

Frequently Asked Questions

Lamisil is prescribed for fungal infections such as onychomycosis (nail fungus), tinea pedis (athlete's foot), tinea corporis (ringworm) and tinea cruris (jock itch). It targets dermatophyte and some yeast infections that affect skin, hair and nails.

Terbinafine blocks the fungal enzyme squalene epoxidase, halting ergosterol synthesis. This causes toxic squalene buildup and loss of ergosterol, weakening the fungal cell membrane and leading to cell death while sparing human cells.

The dosage of Lamisil is determined by the prescribing clinician based on the infection type, severity and patient characteristics. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for terbinafine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the Lamisil 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 such as itraconazole or fluconazole, terbinafine often achieves higher cure rates for dermatophyte infections and requires a shorter treatment duration. However, drug‑interaction profiles differ, and individual patient factors guide the choice of therapy.

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 away from excessive heat.

Lamisil is taken orally as a tablet, swallowed whole with a glass of water. It can be taken with or without food, but patients should follow any specific instructions provided by their healthcare provider.

The most serious adverse events include liver toxicity (hepatitis, jaundice), severe skin reactions such as Stevens‑Johnson syndrome, and blood disorders like neutropenia. Patients should report any signs of liver dysfunction, rash or unusual bleeding to their clinician promptly.

Lamisil should be avoided in individuals with known hypersensitivity to terbinafine or other allylamine antifungals, in patients with severe liver disease, and in those taking medications that have a major interaction risk unless closely supervised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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