Product image of Lamisil (Terbinafine) supplied by GNH India

Lamisil

Active Ingredient:
Terbinafine
Origin:
EU

Lamisil (Terbinafine)

Terbinafine, the active ingredient in Lamisil, is an allylamine antifungal presented as an oral tablet for systemic use. It treats fungal infections of the skin, hair and nails, primarily in adult patients requiring prescription therapy.

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

Manufacturer / TM Owner

Novartis Ireland Limited

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Indications & Clinical Uses

  • Lamisil is an allylamine antifungal indicated for several dermatophyte infections.
  • Onychomycosis: eradicates fungal infection of the toenails and fingernails, improving nail appearance and preventing spread.
  • Tinea pedis: relieves athlete's foot symptoms and clears the infection of the feet.
  • Tinea corporis: treats ringworm of the body, reducing redness and scaling.
  • Tinea cruris: resolves jock itch caused by dermatophytes, alleviating itching and inflammation.

How It Works

  • Terbinafine inhibits the fungal enzyme squalene epoxidase, a key step in ergosterol biosynthesis. By blocking this pathway, intracellular squalene accumulates while ergosterol levels fall, disrupting fungal cell membrane integrity and leading to cell death. The selective inhibition targets fungal cells with minimal effect on human cholesterol synthesis.

Side Effects

Terbinafine may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Gastrointestinal discomfort such as nausea, abdominal pain or diarrhoea.
  • Headache or dizziness.
  • Skin rash or pruritus.
  • Altered taste sensation (dysgeusia).
  • Elevated liver enzymes detected on routine testing.
  • Mild fatigue.

Serious or Rare Side Effects

  • Severe liver injury or hepatitis.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Blood dyscrasias including neutropenia or agranulocytosis.
  • Anaphylactic reactions.
  • Severe skin reactions such as drug reaction with eosinophilia and systemic symptoms (DRESS).

Precautions & Warnings

  • Before initiating therapy, clinicians should consider several safety measures.
  • Assess liver function: obtain baseline hepatic enzymes and monitor periodically.
  • Monitor for skin reactions: advise patients to report rash, blistering or mucosal involvement promptly.
  • Review concomitant medications: check for drugs that share metabolic pathways.
  • Use caution in pregnancy: category B, weigh benefits against potential risks.
  • Avoid in patients with known hypersensitivity to terbinafine or other allylamines.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Terbinafine can interact with other medicines through shared metabolic pathways.

Major Interactions (Avoid)

  • Cimetidine: may increase terbinafine plasma levels, risking toxicity.
  • Itraconazole: combined use can lead to elevated hepatic burden.
  • Ritonavir (and other strong CYP3A4 inhibitors): may markedly raise terbinafine concentrations.

Moderate Interactions (Monitor Closely)

  • Warfarin: monitor INR as terbinafine may enhance anticoagulant effect.
  • Oral contraceptives: efficacy may be reduced; advise alternative contraception.
  • Statins metabolised by CYP3A4 (e.g., simvastatin): monitor for myopathy.
  • Antidepressants (e.g., fluoxetine): observe for increased side‑effect profile.

Frequently Asked Questions

Lamisil (terbinafine) is prescribed for fungal infections such as onychomycosis (nail fungus), athlete's foot (tinea pedis), ringworm of the body (tinea corporis) and jock itch (tinea cruris). It works systemically to eliminate the dermatophytes responsible for these conditions.

Terbinafine blocks the fungal enzyme squalene epoxidase, halting the conversion of squalene to ergosterol. This causes squalene to accumulate and ergosterol levels to fall, disrupting 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 specific infection, patient weight, renal and hepatic function, and local treatment guidelines. Patients should follow the exact regimen provided by their healthcare professional.

Terbinafine is classified as pregnancy category B, indicating no evidence of risk in animal studies but insufficient human data. It should be used only if the potential benefit justifies the potential risk. Breastfeeding mothers should consult their doctor, as limited data are available.

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 different target (squalene epoxidase) and often achieves higher cure rates for nail infections with a shorter treatment duration. It is generally well‑tolerated but requires liver function monitoring, whereas some azoles have more drug‑interaction potential.

Lamisil tablets should be stored below 25 °C in a dry place. Keep them in the original container, protect from moisture and direct sunlight, and keep out of reach of children.

Lamisil is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

The most serious risks include severe liver injury, life‑threatening skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and rare blood disorders like agranulocytosis. Patients should report any signs of jaundice, rash, fever or unusual bleeding promptly.

Lamisil should be avoided in individuals with known hypersensitivity to terbinafine or other allylamine antifungals. Caution is advised for patients with pre‑existing liver disease, and it is generally not recommended for children under the age specified in the prescribing information.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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