Product image of Medofloran (Terbinafine) supplied by GNH India

Medofloran

Active Ingredient:
Terbinafine
Origin:
EU

Medofloran (Terbinafine)

Terbinafine, the active ingredient in Medofloran, is an allylamine antifungal presented as an oral dosage form for systemic use. It treats fungal infections of the skin, nails and related tissues in adult patients.

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

Manufacturer / TM Owner

Medochemie Ltd.

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Indications & Clinical Uses

Terbinafine is used to treat infections caused by dermatophytes and other fungi affecting the skin and nails.

  • Onychomycosis: eradicates fungal growth in toenails and fingernails, improving nail appearance and health.
  • Tinea corporis: clears ring‑shaped skin lesions caused by dermatophyte infection.
  • Tinea pedis: relieves athlete’s foot symptoms and eliminates the causative fungus.
  • Tinea cruris: treats fungal infection of the groin area, reducing itching and redness.

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, which is toxic to fungal cells, and depletes ergosterol, a vital component of the fungal cell membrane, leading to loss of membrane integrity and cell death.

Side Effects

Terbinafine may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal discomfort, or diarrhea.
  • Headache: mild to moderate intensity.
  • Skin rash or pruritus: localized itching or erythema.
  • Taste disturbance: altered taste perception or loss of taste.
  • Elevated liver enzymes: mild, transient increases in hepatic transaminases.

Serious or Rare Side Effects

  • Hepatotoxicity: signs of liver injury such as jaundice or dark urine.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hematologic abnormalities: neutropenia or agranulocytosis.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Anaphylaxis: rare systemic allergic response requiring immediate medical attention.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential risks.

  • Liver function assessment: obtain baseline hepatic enzymes and repeat if symptoms arise.
  • Hypersensitivity screening: avoid use in patients with known terbinafine allergy.
  • Renal impairment caution: adjust dosing in severe kidney disease.
  • Drug interaction vigilance: review concomitant medications that affect CYP pathways.
  • Pregnancy and lactation: safety data are limited; use only if benefit outweighs risk.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Terbinafine can alter the plasma levels of several co‑administered drugs.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): may increase terbinafine exposure.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic effectiveness.

Moderate Interactions (Monitor Closely)

  • Warfarin: monitor INR as terbinafine can enhance anticoagulant effect.
  • Oral contraceptives: efficacy may be decreased; advise additional contraceptive measures.
  • Alcohol: concurrent use may heighten risk of liver toxicity.
  • Cimetidine: may modestly raise terbinafine concentrations.
  • Antihistamines metabolized by CYP2C9: observe for altered response.

Frequently Asked Questions

Medofloran contains terbinafine and is prescribed for fungal infections such as onychomycosis (nail fungus), tinea corporis (ringworm of the body), tinea pedis (athlete’s foot), and tinea cruris (jock itch). It targets the fungi that cause these skin and nail disorders, helping to clear infection and relieve associated symptoms.

Terbinafine blocks the fungal enzyme squalene epoxidase, which is essential for producing ergosterol, a key component of fungal cell membranes. Inhibiting this step leads to toxic buildup of squalene and depletion of ergosterol, compromising membrane integrity and causing fungal cell death.

The specific dose of Medofloran is determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and local treatment guidelines. Patients should follow the exact regimen provided by their healthcare professional.

Safety data for terbinafine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant. Healthcare providers will assess individual circumstances before prescribing.

To request Medofloran, 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 (including any cold‑chain requirements) and necessary import documentation.

Compared with azole antifungals, terbinafine (Medofloran) has a different mechanism—blocking squalene epoxidase rather than inhibiting lanosterol 14α‑demethylase. This often results in a shorter treatment duration for nail infections and a lower potential for drug‑drug interactions with CYP3A4 substrates, though individual response varies.

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

Medofloran is taken orally, usually with a full glass of water. The tablet (or capsule) should be swallowed whole and not chewed or crushed, unless the prescribing information specifies otherwise.

The most serious adverse events include hepatotoxicity (liver injury), severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and rare blood disorders like neutropenia. Patients should report any signs of jaundice, rash, or unexplained bruising to their healthcare provider promptly.

Medofloran is contraindicated in individuals with known hypersensitivity to terbinafine or any component of the formulation. Caution is also advised for patients with severe liver disease, and it should be avoided in those where the risk outweighs benefit, as determined by a qualified clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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