Product image of Metronidazole B Braun (Metronidazole) supplied by GNH India

Metronidazole B Braun

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazole B Braun (Metronidazole)

Metronidazole, the active ingredient in Metronidazole B Braun, is a nitroimidazole antibiotic presented as an injectable solution for intravenous use. It treats anaerobic bacterial infections and selected protozoal infections in adults and children as prescribed.

GNH India supplies Metronidazole B Braun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

B.Braun Medical Sas

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Indications & Clinical Uses

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

  • Anaerobic bacterial infections: reduces bacterial load and improves clinical symptoms in mixed anaerobic infections.
  • Clostridioides difficile infection: eradicates toxin‑producing C. difficile, aiding resolution of colitis.
  • Bacterial vaginosis: restores normal vaginal flora by eliminating anaerobic overgrowth.
  • Trichomoniasis: eliminates Trichomonas vaginalis, relieving genital symptoms.
  • Amebic liver abscess: destroys Entamoeba histolytica trophozoites, facilitating abscess resolution.

How It Works

  • Metronidazole enters anaerobic cells and is reduced by ferredoxin‑type proteins to reactive nitro radicals. These radicals interact with DNA, causing strand breakage and loss of helical structure, and also inhibit nucleic acid synthesis. The resulting damage leads to bacterial or protozoal cell death, while aerobic cells are largely unaffected due to lack of reduction.

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: occasional throbbing headache.
  • Diarrhea: loose stools during therapy.
  • Abdominal pain: cramping or discomfort.
  • Dizziness: light‑headed feeling.

Serious or Rare Side Effects

  • Seizures: rare neurologic events requiring immediate care.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Severe allergic reactions: anaphylaxis, rash, or swelling.
  • Stevens‑Johnson syndrome: serious skin eruption.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Neutropenia: reduced white blood cell count increasing infection risk.

Precautions & Warnings

Metronidazole requires careful use in specific patient groups and conditions.

  • Renal impairment: adjust dosing and monitor renal function.
  • Hepatic impairment: use with caution; monitor liver enzymes.
  • Alcohol consumption: avoid during and 48 hours after therapy to prevent disulfiram‑like reaction.
  • Pregnancy and lactation: assess risk–benefit; limited safety data available.
  • Concurrent anticoagulants: monitor coagulation parameters for enhanced effect.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Metronidazole can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Alcohol: may cause severe disulfiram‑like reaction.
  • Warfarin: increased anticoagulant effect; monitor INR closely.
  • Lithium: elevated lithium levels; monitor for toxicity.

Moderate Interactions (Monitor Closely)

  • Phenytoin: may reduce metronidazole plasma concentrations.
  • Cimetidine: may increase metronidazole levels, enhancing side effects.
  • Phenobarbital: may decrease metronidazole efficacy through enzyme induction.

Frequently Asked Questions

Metronidazole B Braun is indicated for the treatment of anaerobic bacterial infections, Clostridioides difficile‑associated colitis, bacterial vaginosis, trichomoniasis, and amebic liver abscess. It is administered intravenously to target these infections in both adult and pediatric patients as determined by a healthcare professional.

Metronidazole is taken up by anaerobic microorganisms and reduced to reactive nitro radicals. These radicals damage DNA and inhibit nucleic acid synthesis, leading to loss of cellular integrity and death of the bacteria or protozoa while sparing aerobic cells.

The specific dose and infusion rate of Metronidazole B Braun are set by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and local treatment guidelines. No standard dose is provided here.

Safety data for Metronidazole B Braun in pregnancy and lactation are limited. Prescribers should weigh potential benefits against possible risks and consider alternative therapies when appropriate. Breastfeeding mothers should discuss continuation with their healthcare provider.

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 cold‑chain if needed), and import documentation.

Metronidazole is a nitroimidazole that specifically targets anaerobic organisms and certain protozoa, offering rapid bactericidal activity. Compared with broad‑spectrum beta‑lactams, it has a narrower spectrum but is often preferred for its efficacy against anaerobes and lower risk of resistance in those pathogens.

Metronidazole B Braun should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Before use, inspect the solution for particulate matter or discoloration and use within the manufacturer’s recommended time after reconstitution.

Metronidazole B Braun is given as an intravenous infusion. The infusion rate and duration are determined by the prescriber, typically over 30‑60 minutes, and may be adjusted for renal or hepatic impairment. Administration should follow aseptic technique and institutional IV‑therapy protocols.

Serious risks include seizures, peripheral neuropathy, severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, hepatic dysfunction, and neutropenia. Patients should be monitored for neurological symptoms, skin changes, liver function abnormalities, and blood count alterations during therapy.

Metronidazole B Braun is contraindicated in patients with a known hypersensitivity to metronidazole or other nitroimidazoles. Caution is advised for individuals with severe hepatic disease, those receiving disulfiram, and patients with a history of seizures or peripheral neuropathy until evaluated by a clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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