Product image of Metroderme (Metronidazole) supplied by GNH India

Metroderme

Active Ingredient:
Metronidazole
Origin:
EU

Metroderme (Metronidazole)

Metronidazole, the active ingredient in Metroderme, is a nitroimidazole antibiotic presented as a topical formulation for topical use. It treats anaerobic bacterial and protozoal skin infections in adults and children. The product meets EU quality standards and is manufactured under GMP conditions. It is intended for external application on affected skin areas. Healthcare professionals select Metroderme for its targeted antimicrobial activity and favorable tolerability profile.

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

Manufacturer / TM Owner

Laboratorios Galderma S.A. - Sucursal Em Portugal

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Indications & Clinical Uses

Metronidazole is used topically to manage infections caused by anaerobic bacteria and certain protozoa.

  • Rosacea: reduces inflammatory papules, pustules and persistent erythema.
  • Bacterial vaginosis: eradicates anaerobic bacterial overgrowth in the vaginal flora.
  • Perioral dermatitis: controls the bacterial component and improves skin appearance.

How It Works

  • Metronidazole penetrates microbial cells and undergoes reduction of its nitro group under anaerobic conditions. The reduced metabolites interact with DNA, causing strand breakage and loss of helical stability, which inhibits nucleic acid synthesis and leads to cell death of susceptible anaerobic bacteria and protozoa.

Side Effects

Topical application of Metroderme may cause local reactions, while systemic absorption can rarely produce serious events.

Common Side Effects

  • Skin irritation: mild redness or discomfort at the application site.
  • Burning or stinging sensation during or after use.
  • Dryness or peeling of the treated skin.
  • Itching or mild pruritus.
  • Erythema: transient redness.
  • Sensation of warmth.

Serious or Rare Side Effects

  • Allergic reaction: hives, swelling, or difficulty breathing.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Severe skin rash or bullous dermatitis.
  • Photosensitivity leading to exaggerated sunburn.
  • Anaphylaxis: rapid onset of systemic allergic response.
  • Systemic toxicity: nausea, headache, or seizures (rare with extensive use).

Precautions & Warnings

When using Metroderme, consider the following safety measures.

  • Hypersensitivity: avoid if the patient has known allergy to metronidazole or nitroimidazoles.
  • Extensive skin damage: do not apply on large open wounds, burns, or ulcerated areas.
  • Pregnancy and lactation: use only if the prescriber determines benefit outweighs risk.
  • Alcohol consumption: advise patients to limit alcohol to reduce disulfiram‑like reactions.
  • Concomitant medications: review for potential interactions before initiating therapy.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Metronidazole can interact with several systemic agents; monitoring is advised.

Major Interactions (Avoid)

  • Alcohol: may cause severe flushing, nausea, and tachycardia.
  • Warfarin: increased anticoagulant effect, risk of bleeding.
  • Lithium: heightened lithium toxicity.
  • Phenytoin: reduced efficacy of metronidazole.
  • Cimetidine: elevated metronidazole plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: possible reduction in contraceptive effectiveness.
  • Other antiepileptics (e.g., carbamazepine): enzyme induction may lower metronidazole levels.
  • Rifampin: may decrease metronidazole exposure, reducing therapeutic effect.

Frequently Asked Questions

Metroderme is a topical formulation of metronidazole indicated for the treatment of rosacea, bacterial vaginosis and certain skin infections caused by anaerobic bacteria or protozoa. It helps reduce inflammation, erythema and bacterial load on the skin or mucosal surfaces.

Metronidazole penetrates anaerobic microorganisms and is reduced to reactive metabolites that bind to DNA, causing strand breakage and loss of helical structure. This inhibits nucleic acid synthesis, leading to cell death of the targeted bacteria or protozoa.

The dosage and frequency of Metroderme are determined by the prescribing healthcare professional based on the specific indication, severity of the condition and patient characteristics. Patients should follow the prescriber’s instructions and the product label.

Safety data for topical metronidazole in pregnancy and lactation are limited. Use is generally reserved for situations where the potential benefit justifies any possible risk. The prescriber should evaluate the individual case and discuss options with the patient.

To request Metroderme, 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.

Metroderme (metronidazole) offers a unique mechanism targeting anaerobic organisms and protozoa, which differs from many other topical antibiotics that primarily act on aerobic bacteria. It is especially effective for rosacea and bacterial vaginosis, where its anti‑inflammatory properties provide added benefit.

Store Metroderme at room temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Metroderme is applied externally to the affected skin or mucosal area as a thin layer, usually once or twice daily, or as directed by the prescriber. The area should be cleaned and gently patted dry before application.

Serious risks include severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, toxic epidermal necrolysis, and photosensitivity. Patients should seek immediate medical attention if they experience widespread rash, blistering, swelling, or breathing difficulties.

Metroderme should not be used by individuals with a known hypersensitivity to metronidazole or other nitroimidazole compounds, nor on extensive open wounds, burns or severely damaged skin. Patients with certain medical conditions should consult their prescriber before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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