Product image of Mykosert Bei Haut- Und Fußpilz (Sertaconazole Nitrate) supplied by GNH India

Mykosert Bei Haut- Und Fußpilz

Active Ingredient:
Sertaconazole Nitrate
Origin:
EU

Mykosert Bei Haut- Und Fußpilz (Sertaconazole Nitrate)

Sertaconazole nitrate, the active ingredient in Mykosert Bei Haut- Und Fußpilz, is an imidazole antifungal presented as a topical formulation for skin use. It treats fungal infections such as athlete’s foot, ringworm and jock itch in adults and children.

GNH India supplies Mykosert Bei Haut- Und Fußpilz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Dr. Pfleger Arzneimittel Gmbh

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Indications & Clinical Uses

Sertaconazole nitrate is used to treat superficial fungal infections of the skin and nails.

  • Tinea corporis (ringworm): reduces lesion size and eliminates the causative dermatophytes.
  • Tinea pedis (athlete's foot): relieves itching and clears the infection on the feet.
  • Tinea cruris (jock itch): improves redness and scaling in the groin area.
  • Cutaneous candidiasis: eradicates Candida species from affected skin sites.

How It Works

  • Sertaconazole nitrate inhibits the fungal enzyme lanosterol 14α‑demethylase (CYP51), a key step in ergosterol synthesis. By blocking ergosterol production, the drug disrupts fungal cell membrane formation, leading to increased membrane permeability and ultimately cell death of susceptible dermatophytes and yeasts.

Side Effects

Adverse reactions are generally mild and localized to the application site.

Common Side Effects

  • Burning sensation: transient warmth at the site of application.
  • Pruritus: mild itching that usually resolves with continued use.
  • Erythema: slight redness of the skin.
  • Dryness: occasional flaking or scaling.
  • Contact dermatitis: irritation in sensitive individuals.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, hives, or difficulty breathing.
  • Extensive skin irritation: blistering or ulceration.
  • Secondary bacterial infection: pus formation or worsening redness.
  • Systemic absorption effects: rare hepatic enzyme alterations.
  • Persistent pigmentation changes: darkening of treated skin.

Precautions & Warnings

Before using Mykosert, consider the following safety measures.

  • Assess skin integrity: avoid application on broken or inflamed skin.
  • Allergy check: discontinue if signs of hypersensitivity appear.
  • Concomitant topical products: avoid using other irritant creams simultaneously.
  • Pediatric use: follow prescriber guidance for children under 12.
  • Pregnancy and lactation: consult a healthcare professional before use.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Topical sertaconazole may interact with other agents applied to the same area.

Major Interactions (Avoid)

  • Systemic azole antifungals: concurrent use can increase systemic exposure when large skin areas are treated.
  • Corticosteroid creams: may mask signs of infection and reduce antifungal efficacy.

Moderate Interactions (Monitor Closely)

  • Other topical irritants (e.g., retinoids): may increase local irritation.
  • Occlusive dressings: can enhance absorption and raise risk of systemic effects.

Frequently Asked Questions

Mykosert Bei Haut- Und Fußpilz is a topical antifungal indicated for superficial fungal infections such as athlete’s foot (tinea pedis), ringworm (tinea corporis), jock itch (tinea cruris) and cutaneous candidiasis. It works by eliminating the fungi that cause these skin conditions.

Sertaconazole nitrate blocks the fungal enzyme lanosterol 14α‑demethylase, which is essential for producing ergosterol, a key component of the fungal cell membrane. Inhibiting this pathway disrupts membrane integrity, leading to fungal cell death and clearance of the infection.

The specific dose and frequency are determined by the prescribing healthcare professional based on the infection’s location, severity, and patient factors. Patients should follow the prescriber’s instructions and the product label for optimal results.

Safety data for sertaconazole nitrate in pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using the product.

To place an order, 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.

Mykosert contains sertaconazole nitrate, an imidazole with a broad spectrum against dermatophytes and yeasts. Compared with allylamine agents such as terbinafine, sertaconazole may offer a slightly different safety profile, with fewer systemic effects but similar efficacy for common skin fungal infections.

Store Mykosert at temperatures below 25 °C in its original packaging. Keep the product away from moisture, direct sunlight and extreme heat to maintain its stability and potency.

Apply a thin layer of the cream or solution to the affected skin area once or twice daily, as directed by the prescriber. Gently rub it in until fully absorbed, and wash hands before and after application to avoid spreading the infection.

Serious adverse events are rare but may include severe allergic reactions such as swelling, hives, or difficulty breathing, and extensive skin irritation or secondary bacterial infection. Immediate medical attention is required if any of these symptoms develop.

Individuals with a known hypersensitivity to sertaconazole nitrate or any component of the formulation should avoid using Mykosert. It is also contraindicated on severely damaged or inflamed skin until the underlying condition is treated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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