Product image of Isozid (Isoniazid) supplied by GNH India

Isozid

Active Ingredient:
Isoniazid
Origin:
EU

Isozid (Isoniazid)

Isoniazid, the active ingredient in Isozid, is an antitubercular agent presented as an injectable solution for intravenous use. It is employed in the treatment of active tuberculosis and in the prophylaxis of latent tuberculosis infection across adult and pediatric populations.

GNH India supplies Isozid as a licensed, GDP‑compliant international pharmaceutical product serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory documentation to support import and clinical use. Isozid is manufactured under strict GMP conditions and packaged to maintain sterility throughout distribution.

Manufacturer / TM Owner

Esteve Pharmaceuticals Gmbh

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Indications & Clinical Uses

  • Isoniazid is used in the antitubercular drug class to manage Mycobacterium tuberculosis infections.
  • Active tuberculosis: contributes to bacterial eradication and clinical cure when combined with standard multidrug regimens.
  • Latent tuberculosis infection: reduces the risk of progression to active disease when given as prophylaxis.

How It Works

  • Isoniazid is a pro‑drug that requires activation by the Mycobacterium tuberculosis catalase‑peroxidase enzyme KatG. Once activated, it forms a radical that inhibits the synthesis of mycolic acids, essential components of the mycobacterial cell wall, leading to loss of cell wall integrity and bacterial death. The inhibition is irreversible and selective for mycobacteria, which explains its high efficacy in combination therapy.

Side Effects

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

Common Side Effects

  • Nausea or vomiting
  • Peripheral neuropathy (tingling or numbness)
  • Skin rash or mild fever
  • Elevated liver enzymes (transaminases)

Serious or Rare Side Effects

  • Hepatotoxicity, including severe hepatitis
  • Severe hypersensitivity reactions such as Stevens‑Johnson syndrome
  • Drug‑induced lupus erythematosus
  • Anaphylactic shock or severe allergic reaction

Precautions & Warnings

When prescribing Isozid, clinicians should observe several safety measures to minimize risk.

  • Pregnancy: Category C – use only if potential benefit justifies the risk to the fetus.
  • Liver function: obtain baseline hepatic enzymes and monitor periodically during therapy.
  • Neuropathy: consider pyridoxine (vitamin B6) supplementation to prevent peripheral nerve damage.
  • Concomitant hepatotoxic drugs: avoid or monitor closely when combined with other agents that affect liver.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Isoniazid interacts with several medicines; the nature of the interaction determines the required clinical action.

Major Interactions (Avoid)

  • Rifampicin: combined use increases hepatotoxic risk and may reduce isoniazid efficacy.
  • Certain antiretrovirals (e.g., efavirenz): may lead to increased neurotoxicity.

Moderate Interactions (Monitor Closely)

  • Phenytoin: may enhance hepatic enzyme induction, affecting isoniazid metabolism.
  • Alcohol: concurrent use raises risk of liver injury.
  • Pyrazinamide: co‑administration can amplify hepatotoxic potential.

Frequently Asked Questions

Isozid contains isoniazid, an antitubercular agent indicated for the treatment of active tuberculosis and for prophylaxis of latent tuberculosis infection. It is administered intravenously as part of a multidrug regimen to eradicate Mycobacterium tuberculosis.

Isoniazid is a pro‑drug that is activated by the bacterial KatG enzyme. The activated form blocks the synthesis of mycolic acids, which are essential components of the mycobacterial cell wall, leading to cell‑wall disruption and bacterial death.

The dose of Isozid is determined by the prescribing clinician based on the patient’s weight, age, disease severity, and renal or hepatic function. No fixed regimen is provided here; the prescriber sets the appropriate dosing schedule.

Isoniazid is classified as Pregnancy Category C, meaning it should be used only if the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding; the decision should be made by a healthcare professional.

Enquiries for Isozid can be submitted via the product page on gnhindia.com. Provide the required quantity and institutional credentials; GNH India will verify trade or procurement eligibility, then respond with pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Isoniazid is a first‑line agent with a unique mechanism targeting mycolic‑acid synthesis, whereas drugs like rifampicin inhibit RNA synthesis. Isoniazid is generally well‑tolerated but carries a higher risk of hepatotoxicity and neuropathy, which can be mitigated with pyridoxine supplementation.

Isozid injectable solution should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use to maintain sterility and potency.

Isozid is given intravenously by a healthcare professional. The solution is typically diluted in an appropriate compatible fluid and infused over a prescribed period, following aseptic technique and institutional protocols.

The most serious adverse reactions include severe hepatotoxicity, hypersensitivity reactions such as Stevens‑Johnson syndrome, drug‑induced lupus, and rare cases of anaphylaxis. Prompt monitoring of liver function and early recognition of skin or systemic reactions are essential.

Isozid is contraindicated in patients with known hypersensitivity to isoniazid or any component of the formulation. Caution is advised in individuals with pre‑existing liver disease, severe peripheral neuropathy, or those taking other hepatotoxic medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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