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

Metronidazol Labesfal

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazol Labesfal (Metronidazole)

Metronidazole, the active ingredient in Metronidazol Labesfal, is a Nitroimidazole antibiotic presented as an intravenous solution for intravenous use. It treats anaerobic bacterial infections and certain protozoal infections in adults and children as prescribed.

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

Manufacturer / TM Owner

Labesfal Laboratorios Almiro, S.A.

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Indications & Clinical Uses

Metronidazole is employed to manage infections caused by anaerobic bacteria and susceptible protozoa.

  • Anaerobic bacterial infections: effective against mixed aerobic‑anaerobic infections, reducing bacterial load.
  • Intra‑abdominal infections: helps resolve peritonitis and abscesses originating in the abdomen.
  • Pelvic inflammatory disease: targets the anaerobic organisms contributing to PID.
  • Bacterial vaginosis: restores normal vaginal flora by eliminating over‑growth of anaerobes.
  • Trichomoniasis: eradicates Trichomonas vaginalis in affected patients.
  • Clostridioides difficile colitis: reduces toxin‑producing C. difficile bacteria in the colon.

How It Works

  • Metronidazole enters susceptible anaerobic microorganisms and is reduced by intracellular ferredoxin proteins, generating nitro radicals. These reactive intermediates damage DNA and other critical macromolecules, inhibiting nucleic acid synthesis and leading to cell death of the targeted bacteria or protozoa.

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 alteration of taste perception.
  • Headache: occasional mild to moderate headache.
  • Diarrhea: loose stools that may be self‑limiting.

Serious or Rare Side Effects

  • Seizures: rare neurologic events, especially with high doses.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Severe allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Stevens‑Johnson syndrome: rare severe skin reaction.
  • Liver toxicity: elevated liver enzymes or hepatitis.
  • Blood dyscrasias: neutropenia, thrombocytopenia, or anemia.

Precautions & Warnings

Metronidazole requires careful consideration of patient‑specific factors before use.

  • Pregnancy: Category B – use only if clinical benefit justifies potential risk.
  • Renal impairment: dose adjustment may be necessary in severe renal dysfunction.
  • Hepatic impairment: monitor liver function tests during therapy.
  • Alcohol consumption: avoid alcohol to prevent a disulfiram‑like reaction.
  • Drug interactions: review concomitant medications for potential interactions.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Metronidazole can interact with several drugs, requiring vigilance.

Major Interactions (Avoid)

  • Alcohol: may cause severe disulfiram‑like reaction.
  • Warfarin: potentiates anticoagulant effect, increasing bleeding risk.
  • Lithium: may increase lithium serum concentrations and toxicity.
  • Live vaccines: reduced efficacy and increased infection risk.

Moderate Interactions (Monitor Closely)

  • Phenytoin: may lower metronidazole plasma levels.
  • Cimetidine: can increase metronidazole concentrations.
  • Carbamazepine: may reduce metronidazole effectiveness.

Frequently Asked Questions

Metronidazol Labesfal contains metronidazole, an antibiotic indicated for treating anaerobic bacterial infections, intra‑abdominal infections, pelvic inflammatory disease, bacterial vaginosis, trichomoniasis, and Clostridioides difficile colitis when administered intravenously.

Metronidazole is reduced inside anaerobic microorganisms, forming nitro radicals that damage DNA and other essential macromolecules, thereby inhibiting nucleic acid synthesis and leading to cell death of the targeted bacteria or protozoa.

The specific 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.

Metronidazole is classified as Pregnancy Category B, indicating no evidence of risk in animal studies but limited human data. It should be used only if the potential benefit justifies any possible risk to the fetus, and breastfeeding mothers should consult their healthcare provider.

Enquiries are submitted via the product page at gnhindia.com, where you specify 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 needed), and import documentation.

Metronidazole is unique among antibiotics for its potent activity against anaerobic bacteria and certain protozoa, whereas many other classes (e.g., beta‑lactams) target aerobic organisms. Its nitro‑radical mechanism provides coverage not offered by most broad‑spectrum agents.

The product should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the solution. Before administration, allow the solution to reach room temperature if required by the clinical protocol.

Metronidazol Labesfal is given as an intravenous infusion. The infusion rate and duration are set by the prescriber, typically over 30‑60 minutes, and the solution is diluted according to institutional guidelines.

Serious risks include seizures, peripheral neuropathy, severe allergic reactions such as anaphylaxis or Stevens‑Johnson syndrome, liver toxicity, and hematologic abnormalities like neutropenia or thrombocytopenia. Prompt medical attention is required if these occur.

Patients with known hypersensitivity to metronidazole or other nitroimidazoles should avoid the product. Caution is also advised for individuals with severe hepatic or renal impairment, and those taking interacting medications such as warfarin, lithium, or alcohol.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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