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 oral use. It treats fungal infections of the skin, nails and related tissues in adult patients, targeting organisms such as dermatophytes that cause onychomycosis, athlete's foot, ringworm and jock itch.

GNH India supplies Lamisil as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing, regulatory documentation and logistics support for global healthcare providers, including both private and public sector institutions.

Manufacturer / TM Owner

Novartis Pharma N.V.

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Indications & Clinical Uses

  • Lamisil (terbinafine) is indicated for fungal skin and nail infections caused by dermatophytes and related organisms.
  • Onychomycosis: eliminates the dermatophyte infection of the nail plate and matrix, leading to gradual restoration of normal nail appearance.
  • Tinea pedis: treats athlete's foot by eradicating the causative fungus, reducing scaling, itching and redness on the feet.
  • Tinea corporis: resolves ringworm lesions on the body, decreasing erythema, scaling and preventing further spread.
  • Tinea cruris: clears jock itch infection in the groin area, relieving intense itching, redness and maceration.

How It Works

  • Terbinafine inhibits the fungal enzyme squalene epoxidase, a key step in ergosterol biosynthesis. By blocking this enzyme, the drug causes accumulation of squalene, which is toxic to fungal cells, and depletes ergosterol, an essential component of the fungal cell membrane. The resulting disruption of membrane integrity leads to fungal cell death, providing a fungicidal effect against dermatophytes, yeasts and some molds.

Side Effects

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

Common Side Effects

  • Taste disturbance: altered taste or loss of taste.
  • Gastrointestinal upset: nausea, abdominal discomfort or diarrhea.
  • Headache: mild to moderate headache.
  • Skin rash: mild erythematous rash.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Severe hepatic injury: hepatitis, jaundice or liver failure.
  • Stevens‑Johnson syndrome: life‑threatening skin detachment and mucosal involvement.
  • Eosinophilic pneumonia: respiratory symptoms with eosinophil accumulation in lungs.
  • Anaphylaxis: acute allergic reaction with airway compromise.
  • Blood dyscrasias: agranulocytosis or pancytopenia.

Precautions & Warnings

Before prescribing terbinafine, clinicians should consider several safety precautions to minimize risk.

  • Liver function monitoring: assess baseline transaminases and repeat if symptoms of hepatitis appear.
  • Renal impairment: adjust dose or avoid in severe renal dysfunction.
  • Hypersensitivity: discontinue immediately if rash, pruritus or systemic allergic reactions develop.
  • Pregnancy and lactation: use only if benefit outweighs potential risk; category B.
  • Drug interactions: review concomitant medications that affect CYP2D6 metabolism.
  • Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine, quinidine): may increase terbinafine plasma concentrations and risk of toxicity.
  • Concurrent use with itraconazole or ketoconazole: additive hepatotoxicity risk.

Moderate Interactions (Monitor Closely)

  • Warfarin: terbinafine may enhance anticoagulant effect, requiring INR monitoring.
  • Oral contraceptives: efficacy may be reduced, consider alternative contraception.
  • Sulfonylurea antidiabetics: possible increased hypoglycemia, monitor blood glucose.

Frequently Asked Questions

Lamisil (terbinafine) is prescribed for fungal infections such as onychomycosis, athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris). It works by eliminating the dermatophyte organisms that cause these skin and nail infections, helping to restore normal tissue.

Terbinafine exerts its antifungal effect by inhibiting the enzyme squalene epoxidase, which is essential for ergosterol synthesis in fungal cell membranes. This inhibition leads to toxic accumulation of squalene and depletion of ergosterol, disrupting membrane integrity and causing fungal cell death.

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 written on their prescription and not adjust the dose without medical advice.

Terbinafine is classified as Pregnancy Category B, indicating that animal studies have not shown risk to the fetus, but adequate human data are lacking. It should be used in pregnancy only if the potential benefit justifies the potential risk, and nursing mothers should consult a healthcare professional before use.

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 offers a fungicidal mechanism and a shorter treatment duration for many dermatophyte infections. It is metabolized primarily by CYP2D6, which can result in fewer drug‑drug interactions than some azoles, but clinicians must still assess individual patient factors when selecting 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 do not use it after the expiration date.

Lamisil is taken orally, usually with a full glass of water. The tablet should be swallowed whole and can be taken with or without food, unless the prescribing information advises otherwise. Patients should adhere to the prescribed schedule for the full course of therapy.

The most serious adverse events linked to terbinafine include severe hepatic injury, such as hepatitis or liver failure, and rare but life‑threatening skin reactions like Stevens‑Johnson syndrome or toxic epidermal necrolysis. Prompt medical attention is required if signs of liver dysfunction or severe rash develop.

Lamisil is contraindicated in individuals with known hypersensitivity to terbinafine or any of its excipients. Caution is also advised for patients with pre‑existing liver disease, severe renal impairment, or those taking medications that strongly inhibit CYP2D6, as these conditions may increase the risk of toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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