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. Approved in the European Union, it is prescribed to treat dermatophyte skin infections such as athlete’s foot, ringworm and jock itch, as well as fungal nail infections (onychomycosis) in adult patients.

GNH India supplies Lamisil as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, transplant centres and clinics worldwide, providing reliable sourcing, regulatory support and consistent product quality. The company adheres to stringent Good Distribution Practice standards to ensure product integrity throughout the supply chain.

Manufacturer / TM Owner

Novartis Farmacéutica S.A.

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Indications & Clinical Uses

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

  • Tinea pedis (athlete’s foot): reduces itching and clears the infection of the foot skin.
  • Tinea corporis (ringworm): eliminates the fungal lesions on the body.
  • Tinea cruris (jock itch): resolves inflammation and scaling in the groin area.
  • Onychomycosis (fungal nail infection): improves nail appearance and eradicates the causative fungus.

How It Works

  • Terbinafine acts by inhibiting the fungal enzyme squalene epoxidase, a key step in ergosterol biosynthesis. Blockade of this enzyme leads to intracellular accumulation of squalene, which is toxic to the fungus, and a depletion of ergosterol, an essential component of the fungal cell membrane, ultimately causing cell death. The selective inhibition spares human cells because the target enzyme is absent in mammalian cholesterol pathways, providing a high therapeutic index for systemic treatment.

Side Effects

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

Common Side Effects

  • Gastrointestinal discomfort: nausea, abdominal pain or diarrhea.
  • Headache: mild to moderate intensity.
  • Skin rash: localized erythema or pruritus.
  • Taste disturbance: temporary loss or alteration of taste.
  • Elevated liver enzymes: mild, transient increase detected in lab tests.
  • Dizziness: occasional light‑headedness.

Serious or Rare Side Effects

  • Hepatotoxicity: severe liver injury or hepatitis.
  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Blood dyscrasias: agranulocytosis, aplastic anemia.
  • Persistent taste loss: prolonged dysgeusia affecting nutrition.
  • Peripheral neuropathy: rare nerve damage.

Precautions & Warnings

Before prescribing terbinafine, clinicians should consider several safety precautions.

  • Liver function monitoring: assess baseline hepatic enzymes and repeat during therapy.
  • Hypersensitivity caution: avoid in patients with known allergy to terbinafine or other allylamines.
  • Concomitant hepatotoxic drugs: use with caution when combined with other agents that affect liver.
  • Renal impairment: dose adjustment may be required in severe renal dysfunction.
  • Pregnancy and lactation: evaluate risk‑benefit; use only if clearly needed.
  • Store below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Terbinafine can interact with other medicines, altering its concentration or that of the co‑administered drug.

Major Interactions (Avoid)

  • Cimetidine: may increase terbinafine plasma levels, raising toxicity risk.
  • Itraconazole: combined use can lead to hepatic injury.
  • Ritonavir (and other strong CYP3A4 inhibitors): significantly raise terbinafine exposure.

Moderate Interactions (Monitor Closely)

  • Warfarin: terbinafine may enhance anticoagulant effect, requiring INR monitoring.
  • Oral contraceptives: efficacy may be reduced, consider alternative contraception.
  • Cyclosporine: increased risk of nephrotoxicity; monitor renal function.

Frequently Asked Questions

Lamisil (terbinafine) is prescribed for dermatophyte infections of the skin such as athlete’s foot (tinea pedis), ringworm (tinea corporis), jock itch (tinea cruris), and for fungal nail infections (onychomycosis). These conditions are caused by fungi that invade keratinized tissues.

Terbinafine inhibits the fungal enzyme squalene epoxidase, blocking a crucial step in ergosterol synthesis. This causes toxic squalene buildup and loss of ergosterol, disrupting the fungal cell membrane and 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 treatment duration. 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 the potential risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their clinician.

To order 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 required import documentation.

Lamisil belongs to the allylamine class, which differs from azoles and polyenes. Allylamines like terbinafine target squalene epoxidase, offering a rapid fungicidal effect and a lower potential for drug‑drug interactions compared with many azoles that inhibit CYP enzymes.

Lamisil tablets should be stored below 25 °C in their original packaging, protected from moisture and light. Do not store in bathrooms or near heat sources, and keep out of reach of children.

Lamisil is taken orally, usually with a glass of water. The tablet is swallowed whole and not required to be taken with food, although patients may follow any specific instructions given by their prescriber.

The most serious risks include severe liver injury (hepatotoxicity) and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis. Patients should report any signs of jaundice, dark urine, rash or fever promptly.

Lamisil should be avoided in individuals with known hypersensitivity to terbinafine or other allylamines, in patients with severe hepatic impairment, and in those taking contraindicated medications that may cause serious interactions. Pregnant or nursing women should use only if clearly indicated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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