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

Metronidazole Substipharm

Active Ingredient:
Metronidazole
Origin:
EU

Metronidazole Substipharm (Metronidazole)

Metronidazole, the active ingredient in Metronidazole Substipharm, is a nitroimidazole antibiotic presented as an oral dosage form for systemic use. It is indicated for infections caused by susceptible anaerobic bacteria and certain protozoa, and is commonly prescribed in both inpatient and outpatient settings.

GNH India supplies Metronidazole Substipharm as a licensed, GDP‑compliant international pharmaceutical supplier, providing quality‑assured medication to hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Substipharm

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Indications & Clinical Uses

Metronidazole is a nitroimidazole antibiotic used to treat infections caused by anaerobic bacteria and susceptible protozoa.

  • Bacterial vaginosis: restores normal vaginal flora by eliminating anaerobic overgrowth.
  • Trichomoniasis: eradicates Trichomonas vaginalis, relieving symptoms and preventing recurrence.
  • Amoebiasis: destroys intestinal Entamoeba histolytica trophozoites, aiding cure of dysentery.
  • Giardiasis: eliminates Giardia lamblia, reducing diarrhea and malabsorption.
  • Anaerobic bacterial infections: targets a broad range of anaerobes in intra‑abdominal, skin and dental infections.
  • Clostridioides difficile infection: suppresses toxin‑producing C. difficile, helping resolve colitis.

How It Works

  • Metronidazole is taken up by anaerobic microorganisms and reduced by intracellular electron transport proteins to generate reactive nitro radical anions. These anions covalently bind to DNA, causing strand breakage and inhibition of nucleic acid synthesis, which leads 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 upset stomach.
  • Metallic taste: persistent metallic sensation in the mouth.
  • Headache: transient cranial discomfort.
  • Diarrhea: loose stools, usually self‑limiting.
  • Abdominal pain: cramping or discomfort in the abdomen.
  • Loss of appetite: reduced desire to eat.

Serious or Rare Side Effects

  • Seizures: convulsive episodes, especially with high plasma levels.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Severe allergic reaction: anaphylaxis with rash, swelling, and breathing difficulty.
  • Stevens‑Johnson syndrome: severe skin and mucous membrane eruption.
  • Liver toxicity: elevated transaminases or hepatitis.
  • Pancytopenia: reduction of red cells, white cells, and platelets.

Precautions & Warnings

When prescribing Metronidazole, several safety considerations should be observed.

  • Pregnancy: safety not established; use only if benefits outweigh potential risks.
  • Alcohol: avoid concurrent consumption to prevent a disulfiram‑like reaction.
  • Renal impairment: dose adjustment may be required in severe dysfunction.
  • Hepatic disease: monitor liver function tests during therapy.
  • Drug interactions: review 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 other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Alcohol: may cause severe flushing, tachycardia, and hypotension.
  • Warfarin: increased anticoagulant effect, raising bleeding risk.
  • Lithium: heightened lithium toxicity due to reduced clearance.
  • Cimetidine: may raise metronidazole plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Phenytoin: may reduce metronidazole levels, decreasing efficacy.
  • Phenobarbital: may lower metronidazole concentrations.
  • Carbamazepine: may accelerate metronidazole metabolism.

Frequently Asked Questions

Metronidazole Substipharm is employed to treat infections caused by susceptible anaerobic bacteria and certain protozoa, including bacterial vaginosis, trichomoniasis, amoebiasis, giardiasis, intra‑abdominal anaerobic infections, and Clostridioides difficile‑associated colitis.

Metronidazole enters anaerobic microorganisms and is reduced to reactive nitro radical anions. These anions bind to DNA, causing strand breakage and inhibition of nucleic acid synthesis, which leads to cell death of the targeted bacteria or protozoa while sparing aerobic cells.

The prescribed dose of Metronidazole is determined by the treating clinician based on the specific infection, its severity, patient weight, renal and hepatic function, and local treatment guidelines. No universal dosing regimen is provided here.

Safety data for Metronidazole in pregnancy are limited and the pregnancy category is unknown. It should be used only when the potential benefit justifies the potential risk to the fetus. Caution is also advised during breastfeeding, and a healthcare professional should evaluate the risk‑benefit balance.

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 (including any cold‑chain requirements) and the necessary import documentation.

Metronidazole is distinct from many conventional antibiotics because it targets anaerobic organisms and certain protozoa through DNA damage. Compared with agents like clindamycin, it often has a narrower spectrum but is effective for specific infections such as bacterial vaginosis and C. difficile, and it does not typically cause the same degree of Clostridium difficile overgrowth.

Store Metronidazole at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed to maintain stability.

Metronidazole is administered orally, usually as tablets that are swallowed whole with or without food. The exact administration instructions, including whether to take it with meals, are provided by the prescribing healthcare professional.

Serious adverse events include seizures, peripheral neuropathy, severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, liver toxicity, and pancytopenia. Patients should seek immediate medical attention if they experience neurological symptoms, rash, jaundice, or signs of bleeding.

Metronidazole should be avoided in individuals with a known hypersensitivity to metronidazole or other nitroimidazole compounds, in patients with severe hepatic impairment, and in those for whom the risk of a disulfiram‑like reaction with alcohol is unacceptable. Clinicians must assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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