Product image of Mycomax (Fluconazole) supplied by GNH India

Mycomax

Active Ingredient:
Fluconazole
Origin:
EU

Mycomax (Fluconazole)

Fluconazole, the active ingredient in Mycomax, is an azole antifungal presented as an oral tablet for systemic use. It treats a range of fungal infections, including candidiasis, cryptococcal meningitis and dermatophyte infections, and is prescribed for adult and pediatric patients under medical supervision. The drug is absorbed well after oral administration and achieves therapeutic concentrations in blood and tissues.

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

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

Fluconazole is an azole antifungal that targets systemic and mucosal fungal infections.

  • Candidiasis: effective for oral, esophageal and vaginal infections, reducing fungal load and alleviating symptoms.
  • Cryptococcal meningitis: used in combination therapy to eradicate Cryptococcus neoformans from the central nervous system.
  • Dermatophyte infections: treats skin and nail infections caused by Trichophyton, Microsporum and Epidermophyton species.
  • Invasive candidiasis: administered intravenously (when formulated) to treat bloodstream infections and deep‑tissue candidiasis.

How It Works

  • Fluconazole inhibits the fungal cytochrome P450 enzyme 14α‑demethylase, a key step in ergosterol synthesis. By blocking this enzyme, the drug disrupts the formation of ergosterol, an essential component of the fungal cell membrane, leading to increased membrane permeability and inhibition of fungal growth. The selective inhibition results in high potency against susceptible yeasts and molds while sparing human cells in vivo.

Side Effects

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

Common Side Effects

  • Nausea: mild stomach upset often reported.
  • Headache: transient cranial discomfort.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Diarrhea: loose stools without blood.
  • Rash: mild skin erythema or itching.
  • Elevated liver enzymes: transient increase in hepatic transaminases.
  • Dizziness: feeling of lightheadedness or unsteadiness.
  • Taste disturbance: altered perception of flavors.

Serious or Rare Side Effects

  • Hepatotoxicity: severe liver injury, jaundice or hepatitis.
  • Stevens‑Johnson syndrome: severe skin blistering and mucosal involvement.
  • Anaphylaxis: acute allergic reaction with airway compromise.
  • Severe neutropenia: marked reduction in white blood cells.
  • Cardiac arrhythmias: QT prolongation leading to irregular heartbeat.

Precautions & Warnings

Before prescribing fluconazole, clinicians should consider several precautionary measures to ensure patient safety.

  • Assess liver function: obtain baseline hepatic enzyme tests and monitor periodically.
  • Evaluate renal function: adjust dose in patients with severe renal impairment.
  • Review concomitant medications: avoid or monitor drugs that may interact adversely.
  • Screen for hypersensitivity: discontinue if rash or anaphylaxis occurs.
  • Pregnancy and lactation: weigh potential risks as safety data are limited.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture.

Avoid Interactions

Fluconazole interacts with several medicines; some combinations require avoidance while others need careful monitoring.

Major Interactions (Avoid)

  • Rifampin: induces metabolism, markedly reducing fluconazole levels.
  • Terbinafine: combined use increases risk of hepatotoxicity.
  • Phenytoin: accelerates clearance, lowering antifungal efficacy.
  • Azole‑azole combinations: additive toxicity, especially hepatic.

Moderate Interactions (Monitor Closely)

  • Warfarin: fluconazole may increase INR, requiring dose adjustment.
  • Oral contraceptives: reduced estrogen levels may diminish contraceptive effectiveness.
  • Cyclosporine: increased blood concentrations may lead to nephrotoxicity.
  • Statins (e.g., simvastatin): higher risk of myopathy, monitor muscle symptoms.

Frequently Asked Questions

Mycomax contains fluconazole, an azole antifungal indicated for the treatment of candidiasis, cryptococcal meningitis, and dermatophyte infections. It is prescribed to manage both mucosal and systemic fungal infections in patients where a systemic antifungal agent is required.

Fluconazole works by inhibiting the fungal cytochrome P450 enzyme 14α‑demethylase, which is essential for converting lanosterol to ergosterol. This blockade disrupts the synthesis of ergosterol, a key component of the fungal cell membrane, leading to increased membrane permeability and inhibition of fungal growth.

The dosage of Mycomax is determined by the prescribing clinician based on the type and severity of the infection, patient age, weight, renal and hepatic function, and other clinical factors. No standard dose is provided here; the prescriber will set the appropriate regimen.

Safety data for fluconazole in pregnancy are limited and the pregnancy category is not definitively established. It should be used only if the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult their healthcare provider, as fluconazole can be excreted in breast milk.

To order Mycomax, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Compared with other azoles such as itraconazole, fluconazole (Mycomax) generally has a more favorable safety profile and fewer drug‑food interactions, but it may be less potent against certain molds. Unlike amphotericin B, fluconazole is oral, has lower nephrotoxicity, and is easier to administer, though it may be less effective for severe invasive infections.

Mycomax should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged or the tablets appear discoloured.

Mycomax is supplied as an oral tablet and should be swallowed whole with a glass of water. It may be taken with or without food, unless the prescriber advises otherwise. The tablet should not be crushed, chewed, or dissolved unless specifically instructed by a healthcare professional.

The most serious risks include hepatotoxicity, which can present as jaundice or elevated liver enzymes, and severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis. Rare but critical events also include anaphylaxis and significant cardiac arrhythmias, particularly QT prolongation.

Mycomax should be avoided in patients with known hypersensitivity to fluconazole or other azole antifungals. It is also contraindicated in individuals with severe liver impairment or those taking medications that have a major interaction leading to potentially life‑threatening toxicity, unless close monitoring and dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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