Product image of Metronidazol Noridem (Metronidazole) supplied by GNH India

Metronidazol Noridem

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazol Noridem (Metronidazole)

Metronidazole, the active ingredient in Metronidazol Noridem, is a nitroimidazole antibiotic presented as an intravenous solution for intravenous use. It is employed to treat anaerobic bacterial infections and specific protozoal diseases in both adult and pediatric patients when prescribed by a healthcare professional.

GNH India supplies Metronidazol Noridem as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with the product sourced from the European Union market. The product meets EU pharmacopeial specifications and undergoes rigorous quality control before distribution.

Manufacturer / TM Owner

Noridem Enterprises Ltd

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Indications & Clinical Uses

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

  • Bacterial vaginosis: restores normal vaginal flora by eliminating over‑growth of anaerobic bacteria.
  • Trichomoniasis: eradicates Trichomonas vaginalis, relieving symptoms and preventing recurrence.
  • Amoebiasis: kills Entamoeba histolytica trophozoites in intestinal and extra‑intestinal disease.
  • Anaerobic intra‑abdominal infections: controls mixed anaerobic flora in peritonitis and abscesses.
  • Clostridioides difficile infection: reduces toxin‑producing bacteria and aids clinical resolution.

How It Works

  • Metronidazole is taken up by anaerobic microorganisms and reduced by intracellular redox proteins to generate nitro‑radical intermediates. These reactive species damage DNA, inhibit nucleic acid synthesis, and disrupt essential metabolic pathways, leading to bacterial or protozoal cell death while having minimal effect on aerobic cells.

Side Effects

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

Common Side Effects

  • Nausea: transient upset stomach often occurring early in therapy.
  • Metallic taste: a characteristic metallic sensation in the mouth.
  • Headache: mild to moderate headache reported by some patients.
  • Diarrhea: loose stools that usually resolve after treatment completion.

Serious or Rare Side Effects

  • Seizures: rare neurologic events requiring immediate medical attention.
  • Severe allergic reaction: anaphylaxis with rash, swelling, and breathing difficulty.
  • Peripheral neuropathy: numbness or tingling in extremities, potentially irreversible if not recognized early.

Precautions & Warnings

Before using Metronidazol Noridem, consider the following safety measures.

  • Renal impairment: adjust dose or monitor plasma concentrations in patients with reduced kidney function.
  • Hepatic dysfunction: use with caution in patients with liver disease, as metabolism may be impaired.
  • Alcohol consumption: avoid during and for at least 48 hours after therapy to prevent a disulfiram‑like reaction.
  • Pregnancy: prescribe only when benefits outweigh potential risks to the fetus.
  • Concurrent warfarin therapy: monitor INR closely due to possible potentiation of anticoagulant effect.
  • Store at below 25°C: keep in the original container, protect from light and moisture.

Avoid Interactions

Metronidazol Noridem can interact with several medicines; some require avoidance while others need monitoring.

Major Interactions (Avoid)

  • Alcohol: may cause severe flushing, tachycardia, and hypotension.
  • Lithium: concurrent use can increase lithium toxicity.
  • Warfarin: potentiates anticoagulant effect, raising bleeding risk.

Moderate Interactions (Monitor Closely)

  • Phenobarbital: may reduce metronidazole plasma levels, decreasing efficacy.
  • Cimetidine: can increase metronidazole concentrations, enhancing side‑effect potential.
  • Phenytoin: may lower metronidazole effectiveness by increasing its metabolism.

Frequently Asked Questions

Metronidazol Noridem is indicated for bacterial vaginosis, trichomoniasis, amoebiasis, intra‑abdominal and other anaerobic bacterial infections, and Clostridioides difficile infection. It is prescribed by a qualified healthcare professional based on the specific diagnosis and patient characteristics.

Metronidazole enters anaerobic bacteria and protozoa and is reduced by cellular redox proteins to form nitro‑radical intermediates. These reactive species damage DNA and inhibit nucleic acid synthesis, leading to irreversible cell injury and death of the pathogen.

The dosage and duration of Metronidazol Noridem are determined by the prescribing clinician according to the infection type, severity, patient weight, renal and hepatic function, and other clinical factors. No fixed regimen is provided here.

Safety data in pregnancy are limited, and the product is classified as pregnancy category unknown. It should be used only if the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult their physician, as the drug is excreted in milk.

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

Metronidazol Noridem contains the same active ingredient, metronidazole, as other nitroimidazole products. Differences lie mainly in formulation, concentration, and regulatory status. The intravenous solution offers rapid systemic exposure, which can be advantageous in severe or hospitalized infections compared with oral tablets.

Store the product at or below 25 °C in its original packaging, protecting it from moisture and direct light. Do not freeze. Follow standard aseptic handling procedures for intravenous solutions and discard any product that appears discolored or cloudy.

Metronidazol Noridem is given by intravenous infusion under the supervision of qualified medical personnel. The infusion rate and dilution are determined by the prescriber based on the clinical situation and patient tolerance.

Serious adverse events include seizures, severe allergic reactions such as anaphylaxis, and peripheral neuropathy that may become irreversible. Patients should be monitored for neurological symptoms, rash, or breathing difficulties, and therapy should be stopped immediately if these occur.

Metronidazol Noridem is contraindicated in patients with known hypersensitivity to metronidazole or other nitroimidazole derivatives. Caution is also advised for individuals with severe hepatic impairment, early‑term pregnancy, or those receiving disulfiram, due to the risk of severe reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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