Product image of Metronidazol Artesan-Drossapharm (Metronidazole) supplied by GNH India

Metronidazol Artesan-Drossapharm

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazol Artesan-Drossapharm (Metronidazole)

Metronidazole, the active ingredient in Metronidazol Artesan-Drossapharm, is a nitroimidazole antibiotic presented as an oral dosage form for systemic use. It treats a range of anaerobic bacterial and protozoal infections in adults and children as prescribed by a healthcare professional.

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

Manufacturer / TM Owner

Drossapharm Gmbh

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Indications & Clinical Uses

Metronidazole is indicated for infections caused by anaerobic bacteria and susceptible protozoa. It is employed across several clinical pathways:

  • Bacterial vaginosis: eliminates the anaerobic flora responsible for the condition.
  • Trichomoniasis: eradicates Trichomonas vaginalis, relieving symptoms.
  • Amoebiasis: treats intestinal infection caused by Entamoeba histolytica.
  • Giardiasis: clears Giardia lamblia from the gastrointestinal tract.
  • Anaerobic bacterial infections: manages intra‑abdominal, pelvic, skin and soft‑tissue infections caused by anaerobes.
  • Clostridioides difficile‑associated diarrhea (adjunct): reduces toxin‑producing bacterial load when used with standard therapy.

How It Works

  • Metronidazole is taken up by anaerobic microorganisms and reduced by intracellular electron‑transport proteins to reactive nitro radicals. These radicals damage DNA, inhibit nucleic acid synthesis and disrupt vital metabolic pathways, ultimately leading to cell death of susceptible bacteria and protozoa.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Metallic taste: transient metallic sensation in the mouth.
  • Headache: occasional mild headache.
  • Diarrhea: loose stools during therapy.
  • Abdominal pain: cramping or discomfort.
  • Loss of appetite: reduced desire to eat.

Serious or Rare Side Effects

  • Seizures: rare neurologic events.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Severe allergic reactions: anaphylaxis, rash, or swelling.
  • Stevens‑Johnson syndrome: severe skin reactions.
  • Hepatic toxicity: elevated liver enzymes or hepatitis.
  • Neutropenia: reduced white blood cell count.

Precautions & Warnings

Before initiating therapy, consider the following safety measures:

  • Assess renal function: adjust use in patients with impaired kidney function.
  • Avoid alcohol: risk of disulfiram‑like reaction.
  • Monitor for allergic reactions: discontinue if severe rash or swelling occurs.
  • Use caution in pregnancy: discuss risks with a healthcare provider.
  • Contraindicated in known hypersensitivity: do not administer to patients with documented allergy to metronidazole.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

Metronidazole can interact with several medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Alcohol: may cause severe flushing, tachycardia, and hypotension.
  • Warfarin: potentiates anticoagulant effect, increasing bleeding risk.
  • Lithium: may raise lithium serum concentrations, risking toxicity.

Moderate Interactions (Monitor Closely)

  • Carbamazepine: may lower metronidazole levels, reducing effectiveness.
  • Cimetidine: can increase metronidazole plasma concentration.
  • Phenytoin: may decrease metronidazole exposure, requiring monitoring.

Frequently Asked Questions

Metronidazol Artesan-Drossapharm contains metronidazole and is used to treat infections caused by anaerobic bacteria and certain protozoa, including bacterial vaginosis, trichomoniasis, amoebiasis, giardiasis, intra‑abdominal anaerobic infections, and as an adjunct in Clostridioides difficile‑associated diarrhea.

Metronidazole enters susceptible microorganisms and is reduced to reactive nitro radicals. These radicals damage DNA and inhibit nucleic acid synthesis, leading to cell death of anaerobic bacteria and protozoa.

The appropriate dose and duration are set by the prescribing clinician based on the specific infection, patient age, weight, renal function and other clinical factors. No fixed regimen is provided here.

Metronidazole’s pregnancy category is listed as unknown. Use only if clearly needed and after discussion with a healthcare professional. Caution is advised during breastfeeding, and the prescriber should evaluate potential risks and benefits.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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.

Metronidazole is a nitroimidazole with broad activity against anaerobic bacteria and protozoa, offering oral convenience and a well‑established safety profile. Alternatives such as tinidazole have similar mechanisms but differ in dosing frequency and side‑effect spectra, while newer agents may target specific parasites with narrower activity.

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

The medication is taken orally, usually with water. It may be taken with or without food, but taking it with meals can reduce gastrointestinal upset. Follow the prescriber’s instructions regarding timing and any required fasting.

Serious adverse events include seizures, peripheral neuropathy, severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, hepatic toxicity, and neutropenia. Patients should seek immediate medical attention if they experience neurological symptoms, rash, or signs of liver injury.

Metronidazole is contraindicated in individuals with a known hypersensitivity to metronidazole or other nitroimidazoles. Caution is also advised for patients with severe hepatic impairment, those receiving disulfiram, and patients with a history of seizures or neuropathy unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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