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

Metronidazole Biogaran

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazole Biogaran (Metronidazole)

Metronidazole, the active ingredient in Metronidazole Biogaran, is a nitroimidazole antibiotic presented as an oral tablet for systemic use. It treats bacterial vaginosis, trichomoniasis, amoebiasis, giardiasis and a range of anaerobic bacterial infections in adult patients.
GNH India supplies Metronidazole Biogaran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Biogaran

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Indications & Clinical Uses

Metronidazole is used to target anaerobic microorganisms and protozoa in several clinical settings.

  • Bacterial vaginosis: restores normal vaginal flora by eliminating anaerobic bacteria.
  • Trichomoniasis: eradicates Trichomonas vaginalis, relieving symptoms and preventing transmission.
  • Amoebiasis: clears intestinal Entamoeba histolytica infection and associated dysentery.
  • Giardiasis: eliminates Giardia lamblia, reducing diarrhea and malabsorption.
  • Anaerobic bacterial infections: treats intra‑abdominal, pelvic, skin and soft‑tissue infections caused by susceptible anaerobes.

How It Works

  • Metronidazole enters anaerobic cells and is reduced by ferredoxin proteins to reactive nitro radical anions. These radicals damage DNA, inhibit nucleic acid synthesis and disrupt essential metabolic pathways, leading to irreversible bacterial and protozoal cell death while sparing aerobic organisms.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Metallic taste: transient metallic sensation in the mouth.
  • Headache: occasional dull or throbbing pain.
  • Abdominal pain: cramping or discomfort.
  • Diarrhea: loose stools during therapy.
  • Loss of appetite: reduced desire to eat.

Serious or Rare Side Effects

  • Seizures: rare neurologic events.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Stevens‑Johnson syndrome: serious skin blistering.
  • Clostridioides difficile infection: colitis risk.
  • Hepatotoxicity: liver enzyme elevation or injury.

Precautions & Warnings

Before initiating Metronidazole therapy, consider the following safety measures.

  • Pregnancy: consult a prescriber; data are limited and risk‑benefit must be evaluated.
  • Alcohol: avoid consumption during treatment to prevent disulfiram‑like reactions.
  • Liver disease: use with caution; monitor hepatic function.
  • Renal impairment: dose adjustment may be required in severe dysfunction.
  • Drug interactions: review all concomitant medications for potential interactions.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Alcohol: may cause severe flushing, tachycardia and nausea.
  • Warfarin: can increase anticoagulant effect and bleeding risk.
  • Lithium: may raise lithium levels, leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: efficacy may be reduced; consider backup contraception.
  • Phenytoin: may lower metronidazole plasma concentrations, reducing effectiveness.

Frequently Asked Questions

Metronidazole Biogaran is indicated for bacterial vaginosis, trichomoniasis, amoebiasis, giardiasis and a variety of anaerobic bacterial infections such as intra‑abdominal or skin‑soft tissue infections. It targets the underlying anaerobic organisms to resolve infection and alleviate symptoms.

Metronidazole is taken up by anaerobic bacteria and protozoa, where intracellular reduction creates nitro radical anions. These reactive species damage DNA and inhibit nucleic acid synthesis, leading to irreversible cell death while sparing aerobic cells.

The specific dose and duration are determined by the prescribing clinician based on the infection type, severity, patient age, weight and renal or hepatic function. Patients should follow the prescriber’s instructions and the product label.

Safety data for Metronidazole in pregnancy are limited, and the drug is classified as pregnancy category unknown. It should only be used if the potential benefit justifies the risk. Breastfeeding mothers should consult a healthcare professional before use.

Enquiries are submitted via the product page on 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 and any required import documentation.

Metronidazole shares a similar mechanism with other nitroimidazoles such as tinidazole, but differences exist in pharmacokinetics, dosing frequency and side‑effect profiles. Clinicians choose based on infection type, patient tolerance, drug‑interaction potential and local resistance patterns.

Metronidazole Biogaran should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain potency.

Metronidazole Biogaran is administered orally, typically as a tablet taken with or without food as directed by the prescriber. The tablet should be swallowed whole with water; crushing or chewing may affect absorption.

Serious risks include seizures, peripheral neuropathy, severe allergic reactions such as Stevens‑Johnson syndrome, Clostridioides difficile‑associated colitis and hepatotoxicity. Patients should seek immediate medical attention if they experience neurological symptoms, severe rash or persistent abdominal pain.

Metronidazole is contraindicated in patients with known hypersensitivity to metronidazole or other nitroimidazoles. Caution is advised for individuals with severe hepatic impairment, those taking disulfiram, and patients with a history of neurologic disorders that could be exacerbated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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