Product image of Metronidazole Mercury Pharmaceuticals Limited (Metronidazole) supplied by GNH India

Metronidazole Mercury Pharmaceuticals Limited

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazole Mercury Pharmaceuticals Limited (Metronidazole)

Metronidazole, the active ingredient in Metronidazole Mercury Pharmaceuticals Limited, is a nitroimidazole antibiotic presented as an injectable solution for intravenous use. It treats infections caused by anaerobic bacteria and protozoa in adult patients and is commonly employed for bacterial vaginosis, trichomoniasis, amoebiasis, Clostridioides difficile infection, and other anaerobic infections.

GNH India supplies Metronidazole Mercury Pharmaceuticals Limited as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Mercury Pharmaceuticals Ltd.

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Indications & Clinical Uses

Metronidazole is a nitroimidazole antibiotic indicated for several anaerobic and protozoal infections.

  • Bacterial vaginosis: restores normal vaginal flora and relieves discharge.
  • Trichomoniasis: eradicates Trichomonas vaginalis and resolves genital irritation.
  • Amoebiasis: eliminates intestinal Entamoeba histolytica and prevents tissue invasion.
  • Clostridioides difficile infection: reduces toxin‑producing bacterial load in the colon.
  • Anaerobic bacterial infections: targets a broad range of anaerobes in intra‑abdominal, pelvic, and soft‑tissue sites.

How It Works

  • Metronidazole enters susceptible anaerobic cells and is reduced by intracellular electron transport proteins, generating nitro radicals. These reactive intermediates damage DNA, inhibit nucleic acid synthesis, and disrupt bacterial and protozoal replication, leading to cell death without affecting most 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: dull or throbbing head pain.
  • Diarrhea: loose stools, sometimes watery.
  • Skin rash: mild erythema or itching.
  • Dark urine: harmless discoloration of urine.

Serious or Rare Side Effects

  • Peripheral neuropathy: tingling or numbness in extremities.
  • Seizures: rare convulsive episodes.
  • Severe allergic reaction: hives, swelling, or difficulty breathing.
  • Hepatotoxicity: elevated liver enzymes or jaundice.
  • Stevens‑Johnson syndrome: severe skin blistering.
  • Hematologic abnormalities: low white blood cell or platelet counts.

Precautions & Warnings

Metronidazole should be used with caution in specific clinical situations.

  • Renal impairment: monitor renal function and adjust therapy if needed.
  • Hepatic disease: use carefully; liver function tests may be required.
  • Alcohol consumption: avoid alcohol during treatment and for 48 hours after to prevent disulfiram‑like reaction.
  • Pregnancy: safety not established; weigh benefits against potential risks.
  • Breastfeeding: consider infant exposure; consult a healthcare professional.
  • Storage: Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

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

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Cimetidine: may raise metronidazole plasma concentrations.
  • Phenytoin: may reduce phenytoin levels, decreasing seizure control.
  • Alcoholic beverages: can intensify disulfiram‑like reaction.

Frequently Asked Questions

Metronidazole is prescribed for infections caused by anaerobic bacteria and certain protozoa, including bacterial vaginosis, trichomoniasis, amoebiasis, Clostridioides difficile infection, and a variety of anaerobic bacterial infections in the abdomen, pelvis, and soft tissues.

The drug is taken up by susceptible anaerobic organisms and reduced by their internal electron transport proteins, forming nitro radicals that damage DNA and inhibit nucleic acid synthesis, ultimately leading to microbial cell death.

The dosage and duration of Metronidazole therapy are determined by the prescribing clinician based on the specific infection, patient characteristics, and local treatment guidelines.

Safety data for Metronidazole in pregnancy are limited, and the drug is generally used only when the potential benefit justifies any possible risk. Breastfeeding mothers should consult a healthcare professional, as the medication can be excreted in breast milk.

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 protozoa, offering a broad spectrum against these pathogens. Alternatives such as clindamycin or carbapenems may be used, but Metronidazole often provides a more focused approach with a well‑established safety profile for many anaerobic infections.

Metronidazole injectable solution should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen. Follow the manufacturer’s packaging instructions to maintain product stability.

The medication is given intravenously by a healthcare professional. The infusion rate and duration are set by the prescriber, and the solution is administered through a suitable IV line under aseptic conditions.

Serious adverse events include peripheral neuropathy, seizures, severe allergic reactions such as Stevens‑Johnson syndrome, hepatotoxicity, and hematologic abnormalities like thrombocytopenia. Patients should be monitored for any of these signs during treatment.

Metronidazole is contraindicated in individuals with a known hypersensitivity to the drug or other nitroimidazoles. Caution is also advised for patients with severe hepatic impairment, and it should be avoided in those taking disulfiram.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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