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 a sterile injection for intravenous use. It is employed to treat a range of anaerobic bacterial infections and certain protozoal diseases in both adult and pediatric patients when administered under medical supervision.

GNH India supplies Metronidazole B. Braun as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide through regulated procurement channels. The company adheres to stringent quality standards and ensures traceability throughout the supply chain.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

  • Metronidazole is a nitroimidazole antibiotic used to treat infections caused by anaerobic bacteria and certain protozoa.
  • Anaerobic bacterial infections: eliminates susceptible anaerobic organisms, helping resolve intra‑abdominal, skin, and pelvic infections.
  • Bacterial vaginosis: reduces Gardnerella vaginalis and associated flora, restoring normal vaginal microbiota.
  • Trichomoniasis: eradicates Trichomonas vaginalis, relieving symptoms and preventing transmission.
  • Amebic liver abscess: destroys Entamoeba histolytica trophozoites, aiding resolution of hepatic lesions.
  • Clostridioides difficile infection: targets toxin‑producing C. difficile, helping control severe colitis.

How It Works

  • Metronidazole is reduced within anaerobic microorganisms to reactive nitro radicals that damage DNA and inhibit nucleic acid synthesis, leading to bacterial and protozoal cell death while sparing aerobic cells.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate nausea that may improve with continued dosing.
  • Metallic taste: a transient metallic sensation in the mouth during treatment.
  • Headache: occasional headache, generally low intensity.
  • Diarrhea: mild gastrointestinal upset, usually self‑limiting.
  • Dizziness: feeling light‑headed or unsteady, often resolves after therapy.

Serious or Rare Side Effects

  • Seizures: rare neurologic events, more likely with high cumulative doses.
  • Peripheral neuropathy: tingling, numbness, or burning sensations in hands or feet.
  • Severe allergic reactions: rash, swelling, or anaphylaxis requiring immediate medical attention.
  • Stevens‑Johnson syndrome: serious skin and mucous membrane disorder with blistering and detachment.

Precautions & Warnings

When prescribing Metronidazole, clinicians should consider several safety precautions to minimize risks.

  • Pregnancy: Category B – use only if clearly needed after risk‑benefit assessment.
  • Alcohol consumption: avoid concurrent alcohol to prevent a disulfiram‑like reaction.
  • Renal impairment: dose adjustment may be required; monitor renal function.
  • Hepatic impairment: use with caution; monitor liver enzymes during therapy.
  • Neurologic effects: discontinue if signs of peripheral neuropathy or seizures develop.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Metronidazole can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Alcohol: may cause severe flushing, tachycardia, and hypotension.
  • Warfarin: increased anticoagulant effect, raising bleeding risk.
  • Lithium: elevated lithium levels, increasing toxicity potential.

Moderate Interactions (Monitor Closely)

  • Cimetidine: may raise metronidazole plasma concentrations.
  • Oral contraceptives: reduced effectiveness, consider alternative contraception.
  • Phenytoin: may lower metronidazole levels, decreasing therapeutic effect.

Frequently Asked Questions

Metronidazole B. Braun is indicated for the treatment of anaerobic bacterial infections, bacterial vaginosis, trichomoniasis, amebic liver abscess, and Clostridioides difficile infection. It is administered intravenously under the direction of a qualified 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 cell death of susceptible bacteria and protozoa while sparing aerobic cells.

The dosage of Metronidazole B. Braun is determined by the prescribing clinician based on the specific infection, patient weight, renal and hepatic function, and other clinical factors. The product is supplied for intravenous administration only.

Metronidazole is classified as Pregnancy Category B, indicating that animal studies have not shown risk but there are limited human data. It should be used during pregnancy only if clearly needed. Caution is advised during breastfeeding, and the prescriber should assess the risk‑benefit ratio.

To order, submit an enquiry on the product page at gnhindia.com with 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 cold‑chain if required) and import documentation.

Metronidazole is a nitroimidazole that specifically targets anaerobic organisms and certain protozoa, offering a broad spectrum for these pathogens. Compared with beta‑lactam antibiotics, it provides effective coverage for anaerobes without the need for beta‑lactamase inhibitors, but choice of therapy depends on the infection site and susceptibility patterns.

Metronidazole B. Braun should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until ready for use to maintain stability.

The product is supplied as a sterile solution for intravenous injection. It is administered by a healthcare professional using aseptic technique, typically diluted in compatible IV fluids and infused over the prescribed period.

Serious risks include seizures, peripheral neuropathy, severe allergic reactions such as anaphylaxis, and rare skin disorders like Stevens‑Johnson syndrome. Patients should be monitored for neurologic symptoms or hypersensitivity, and therapy should be discontinued if these events occur.

Metronidazole should be avoided in patients with known hypersensitivity to the drug or other nitroimidazoles. Caution is required in individuals with severe hepatic or renal impairment, and it should not be used concurrently with alcohol due to a disulfiram‑like reaction.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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