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 oral use. It treats fungal infections of the nails and skin, such as onychomycosis and various tinea conditions, in adult patients. Approved in the European Union, the product meets stringent quality standards and works by targeting the fungal cell membrane synthesis pathway, offering a systemic option for infections that are difficult to resolve with topical agents.

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

Manufacturer / TM Owner

Novartis Europharm Limited

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Indications & Clinical Uses

Lamisil (terbinafine) is used to treat fungal infections of the skin and nails.

  • Onychomycosis: eradicates dermatophyte infection of the toenail or fingernail, improving nail appearance and preventing spread.
  • Tinea pedis: relieves athlete’s foot symptoms by eliminating the causative fungi on the feet.
  • Tinea corporis: clears ringworm lesions on the body by targeting the fungal organisms.
  • Tinea cruris: treats jock itch by resolving fungal overgrowth in the groin area.
  • Tinea capitis: combats scalp fungal infection, promoting hair regrowth and reducing inflammation.

How It Works

  • Terbinafine exerts its antifungal activity by inhibiting the enzyme squalene epoxidase, a key step in the ergosterol biosynthesis pathway of fungi. Blockade of this enzyme leads to accumulation of squalene, which is toxic to fungal cells, and a depletion of ergosterol, an essential component of the fungal cell membrane, resulting in cell death. The selective inhibition spares human cells because the target pathway is absent in mammals.

Side Effects

Terbinafine may cause adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Gastrointestinal discomfort: nausea, abdominal pain or dyspepsia.
  • Headache: mild to moderate intensity.
  • Skin rash: pruritic or erythematous eruptions.
  • Taste disturbance: altered taste perception or loss of taste.

Serious or Rare Side Effects

  • Hepatotoxicity: elevated liver enzymes or hepatitis.
  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hematologic abnormalities: neutropenia, thrombocytopenia or anemia.

Precautions & Warnings

Before prescribing terbinafine, clinicians should consider several safety precautions.

  • Assess liver function: obtain baseline hepatic enzymes and monitor periodically.
  • Evaluate hypersensitivity: avoid use in patients with known allergy to terbinafine or related compounds.
  • Monitor renal function: adjust therapy in severe renal impairment.
  • Review concomitant medications: consider potential drug interactions that may affect terbinafine levels.
  • Counsel women of childbearing potential: pregnancy safety is not established; discuss risks.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Terbinafine interacts with several medicines; awareness of the interaction level guides clinical management.

Major Interactions (Avoid)

  • Rifampin: strong enzyme inducer that may markedly reduce terbinafine plasma concentrations.
  • Ketoconazole: potent CYP inhibitor that can increase terbinafine exposure and risk of toxicity.
  • Cimetidine: may raise terbinafine levels by inhibiting hepatic metabolism.

Moderate Interactions (Monitor Closely)

  • Warfarin: terbinafine can enhance anticoagulant effect; monitor INR.
  • Oral contraceptives: possible reduction in efficacy; advise additional contraceptive measures.
  • Cyclosporine: increased risk of liver enzyme elevation; monitor hepatic function.

Frequently Asked Questions

Lamisil (terbinafine) is prescribed for fungal infections of the nails and skin, including onychomycosis, athlete’s foot (tinea pedis), body ringworm (tinea corporis), jock itch (tinea cruris) and scalp ringworm (tinea capitis). It provides a systemic option when topical agents are insufficient.

Terbinafine inhibits the fungal enzyme squalene epoxidase, disrupting the synthesis of ergosterol, a vital component of the fungal cell membrane. This blockage causes toxic squalene buildup and loss of membrane integrity, leading to fungal cell death while sparing human cells.

The appropriate dose of Lamisil is determined by the prescribing healthcare professional based on the specific infection, patient weight, renal and hepatic function, and other clinical factors. Patients should follow the prescriber’s instructions and not alter the regimen on their own.

The safety of terbinafine in pregnancy and lactation has not been definitively established. It is generally classified as contraindicated or used only when the potential benefit justifies the potential risk. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their clinician.

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

Compared with azole antifungals, terbinafine offers a shorter treatment duration for many nail infections and a distinct mechanism targeting squalene epoxidase. It is often preferred for onychomycosis due to higher cure rates, but drug‑interaction profiles differ, so clinicians choose based on infection type, patient comorbidities and concomitant medicines.

Lamisil should be stored at room temperature, below 25 °C, in its original packaging. Keep the tablets away from moisture, excessive heat and direct sunlight to maintain stability and potency throughout the shelf life.

Lamisil is taken orally, usually as a tablet swallowed with water. The exact dosing schedule, frequency and length of therapy are set by the prescriber and should be followed precisely to achieve optimal outcomes.

Serious adverse events include liver toxicity (hepatitis, elevated transaminases), severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and blood disorders like neutropenia or thrombocytopenia. Patients should report any signs of jaundice, rash, or unusual bleeding promptly.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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