Product image of Metronidazole Biosedra (Metronidazole) supplied by GNH India

Metronidazole Biosedra

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazole Biosedra (Metronidazole)

Metronidazole, the active ingredient in Metronidazole Biosedra, is a Nitroimidazole presented as an injectable solution for Intravenous use. It treats anaerobic bacterial infections and related conditions in adult patients.

GNH India supplies Metronidazole Biosedra as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi France S.A.S.

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Indications & Clinical Uses

Metronidazole Biosedra is a nitroimidazole antibiotic that targets anaerobic bacteria and protozoa.

  • Anaerobic bacterial infections: eradicates susceptible anaerobes and resolves infection.
  • Bacterial vaginosis: restores normal vaginal flora by eliminating pathogenic anaerobes.
  • Trichomoniasis: eliminates Trichomonas vaginalis, relieving symptoms.
  • Amebic liver abscess: destroys Entamoeba histolytica trophozoites in hepatic tissue.
  • Clostridioides difficile infection: reduces toxin‑producing C. difficile and aids clinical recovery.

How It Works

  • Metronidazole is taken up by anaerobic microorganisms and reduced by intracellular electron transport proteins to reactive nitro radicals. These radicals interact with DNA, causing strand breaks and loss of helical structure, and they also inhibit nucleic acid synthesis, ultimately leading to microbial cell death.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Metallic taste: transient metallic sensation in the mouth.
  • Headache: mild to moderate headache.
  • Diarrhea: loose stools, often self‑limited.
  • Abdominal pain: cramping or discomfort.
  • Dizziness: occasional light‑headedness.

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 and mucous membrane reaction.
  • Liver toxicity: elevated transaminases or hepatitis.
  • Neutropenia: marked reduction in white blood cells.

Precautions & Warnings

Before using Metronidazole Biosedra, consider the following safety measures.

  • Renal impairment: adjust therapy and monitor renal function.
  • Hepatic disease: use with caution and monitor liver enzymes.
  • Alcohol consumption: avoid to prevent disulfiram‑like reaction.
  • Pregnancy: prescribe only if benefit outweighs potential risk.
  • Concurrent warfarin therapy: monitor INR closely for increased anticoagulation.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Alcohol: may cause severe disulfiram‑like reaction.
  • Warfarin: increased anticoagulant effect, risk of bleeding.
  • Lithium: heightened lithium toxicity.

Moderate Interactions (Monitor Closely)

  • Cimetidine: may raise metronidazole plasma levels.
  • Phenobarbital: may reduce metronidazole efficacy.
  • Phenytoin: may lower metronidazole concentrations.

Frequently Asked Questions

Metronidazole Biosedra is an intravenous nitroimidazole antibiotic indicated for the treatment of anaerobic bacterial infections, bacterial vaginosis, trichomoniasis, amebic liver abscess, and Clostridioides difficile infection. It is used in adult patients when a systemic, rapid‑acting antimicrobial is required.

Metronidazole enters anaerobic microorganisms and is reduced to reactive nitro radicals. These radicals damage DNA and inhibit nucleic acid synthesis, leading to loss of cellular function and death of the pathogen.

The exact dose and infusion rate are determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and other clinical factors. Dosing regimens can vary widely, so the prescriber sets the appropriate schedule.

Metronidazole’s pregnancy category is not definitively established. It should be used during pregnancy only when the potential benefit justifies any potential risk to the fetus. Breastfeeding mothers should consult their healthcare provider, as the drug is excreted in breast 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.

Metronidazole is often preferred for anaerobic infections because of its rapid bactericidal activity, excellent tissue penetration, and oral‑to‑IV switch capability. Compared with clindamycin, it has a lower risk of Clostridioides difficile overgrowth, while offering similar efficacy against many anaerobes.

Store the product at ambient temperature, preferably below 25 °C. Keep the vial in its original packaging, protect it from light and moisture, and ensure the container is tightly sealed until use.

Metronidazole Biosedra is given by intravenous infusion. The infusion rate and duration are set by the prescriber, typically over 30–60 minutes, and the solution should be administered using aseptic technique in a clinical setting.

Serious adverse events include seizures, peripheral neuropathy, severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, liver toxicity, and neutropenia. Patients should be monitored for neurological symptoms, skin reactions, and signs of hepatic dysfunction.

Metronidazole is contraindicated in individuals with a known hypersensitivity to metronidazole or other nitroimidazoles. It should be avoided in early pregnancy unless absolutely necessary, and used with caution in patients with severe hepatic impairment or those receiving concurrent alcohol.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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