Product image of Metronidazol-Human Teva Gyógyszergyár (Metronidazole) supplied by GNH India

Metronidazol-Human Teva Gyógyszergyár

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazol-Human Teva Gyógyszergyár (Metronidazole)

Metronidazole, the active ingredient in Metronidazol-Human Teva Gyógyszergyár, is a nitroimidazole antibiotic presented as an intravenous solution for parenteral use. It treats anaerobic bacterial infections and selected protozoal diseases in adult patients, offering broad-spectrum activity against susceptible organisms.
GNH India supplies Metronidazol-Human Teva Gyógyszergyár as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Teva Gyógyszergyár Zrt

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Indications & Clinical Uses

Metronidazole acts on anaerobic bacteria and certain protozoa, making it useful for a range of infections.

  • Anaerobic bacterial infections: effective against infections caused by anaerobic organisms, reducing bacterial load.
  • Clostridioides difficile‑associated colitis: helps resolve toxin‑mediated diarrhea and colitis.
  • Bacterial vaginosis: restores normal vaginal flora by eliminating pathogenic anaerobes.
  • Trichomoniasis: eradicates Trichomonas vaginalis, relieving symptoms.
  • Amoebic liver abscess: targets Entamoeba histolytica in hepatic tissue.
  • Pelvic inflammatory disease: assists in controlling mixed anaerobic pelvic infections.

How It Works

  • Metronidazole is reduced by electron‑transport proteins of anaerobic microorganisms, generating reactive nitro radicals that damage DNA and inhibit nucleic acid synthesis. This leads to strand breakage and cell death, selectively affecting anaerobic bacteria and susceptible protozoa while sparing aerobic cells.

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 alteration of taste perception.
  • Diarrhea: loose stools, usually self‑limiting.
  • Abdominal pain: cramping or discomfort in the abdomen.
  • Headache: mild to moderate headache episodes.
  • Dizziness: occasional light‑headedness.

Serious or Rare Side Effects

  • Severe allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Seizures: rare neurologic events, especially with high doses.
  • Neutropenia: reduced white blood cell count, increasing infection risk.
  • Stevens‑Johnson syndrome: severe skin and mucous membrane disorder.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Peripheral neuropathy: tingling or numbness in extremities.

Precautions & Warnings

Metronidazole requires careful use in specific clinical situations.

  • Renal impairment: adjust dosing and monitor renal function.
  • Hepatic disease: monitor liver enzymes and consider dose modification.
  • Alcohol consumption: avoid alcohol to prevent disulfiram‑like reactions.
  • Pregnancy: use only when benefits outweigh potential risks.
  • Concurrent warfarin therapy: monitor INR closely for increased anticoagulation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Metronidazole can interact with several medicines, requiring vigilance.

Major Interactions (Avoid)

  • Alcohol: may cause severe disulfiram‑like reaction.
  • Warfarin: increased anticoagulant effect, risk of bleeding.
  • Lithium: elevated lithium levels, potential toxicity.

Moderate Interactions (Monitor Closely)

  • Phenytoin: may reduce metronidazole plasma concentrations.
  • Cimetidine: can increase metronidazole levels, enhancing effects.
  • Theophylline: possible increased theophylline toxicity.

Frequently Asked Questions

Metronidazol-Human is employed to treat infections caused by anaerobic bacteria and certain protozoa, including Clostridioides difficile‑associated colitis, bacterial vaginosis, trichomoniasis, amoebic liver abscess, and pelvic inflammatory disease. It is administered intravenously in hospital settings for these indications.

Metronidazole is taken up by anaerobic organisms and reduced to reactive nitro radicals. These radicals interact with DNA, causing strand breakage and inhibiting nucleic acid synthesis, which leads to cell death. The mechanism selectively targets anaerobic bacteria and susceptible protozoa while sparing aerobic cells.

The dosage of Metronidazol-Human is determined by the prescribing clinician based on the specific infection, patient weight, renal and hepatic function, and severity of disease. Healthcare professionals tailor the regimen to each individual case.

Safety data for Metronidazol-Human in pregnancy are limited. It should be used only if the potential benefits justify any potential risk to the fetus. Breastfeeding mothers should consult their physician, as the drug can be excreted in breast milk.

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, and any necessary import documentation.

Metronidazol-Human shares the same class and mechanism as other nitroimidazoles such as tinidazole. Compared with oral formulations, the intravenous version offers rapid systemic exposure, which is advantageous for severe infections or when oral intake is not feasible. Efficacy and safety profiles are generally comparable when used appropriately.

Metronidazol-Human should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze the product, and keep it in the original packaging to maintain stability until it is prepared for intravenous administration.

The product is supplied as an intravenous solution and is administered by a healthcare professional through a vein using aseptic technique. The infusion rate and duration are set by the prescriber according to the indication and patient-specific factors.

Serious risks include severe allergic reactions (anaphylaxis), seizures, neutropenia, Stevens‑Johnson syndrome, hepatic dysfunction, and peripheral neuropathy. Patients should be monitored for any signs of these events, and treatment should be discontinued if they occur.

Metronidazol-Human is contraindicated in patients with a known hypersensitivity to metronidazole or other nitroimidazole derivatives. Caution is also advised for individuals with severe hepatic impairment, and it should be avoided in patients who are unable to abstain from alcohol due to the risk of disulfiram‑like reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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