Product image of Ozathuia (Azathioprine) supplied by GNH India

Ozathuia

Active Ingredient:
Azathioprine
Origin:
EU

Ozathuia (Azathioprine)

Azathioprine, the active ingredient in Ozathuia, is an immunosuppressant presented as a tablet for oral use. It is used to prevent organ rejection and to manage certain autoimmune conditions in adults and children.

GNH India supplies Ozathuia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Resolution Chemicals Limited

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Indications & Clinical Uses

Ozathuia is an immunosuppressive agent indicated for several disease pathways that involve abnormal immune activation.

  • Organ transplantation: helps maintain graft survival by suppressing immune‑mediated rejection.
  • Rheumatoid arthritis: reduces joint inflammation and slows disease progression.
  • Inflammatory bowel disease (Crohn’s disease and ulcerative colitis): assists in achieving and maintaining remission.

How It Works

  • Azathioprine is a pro‑drug that is converted intracellularly to 6‑mercaptopurine, which interferes with purine synthesis and thereby inhibits DNA, RNA and protein production in rapidly proliferating lymphocytes. This reduces the clonal expansion of T and B cells, leading to broad immunosuppression and decreased inflammatory responses.

Side Effects

Adverse reactions to azathioprine can vary from mild to severe and should be monitored throughout therapy.

Common Side Effects

  • Nausea and vomiting: gastrointestinal discomfort that may improve with food.
  • Leukopenia: reduced white‑blood‑cell count, increasing infection risk.
  • Elevated liver enzymes: mild hepatic irritation detectable on routine labs.
  • Rash or mild skin irritation: occasional dermatologic response.
  • Fatigue: general sense of tiredness reported by some patients.

Serious or Rare Side Effects

  • Pancytopenia: profound suppression of all blood cell lines, requiring immediate medical attention.
  • Severe hepatotoxicity: marked liver injury that may present with jaundice.
  • Opportunistic infections: including viral, fungal or bacterial infections due to immune suppression.
  • Malignancy risk: potential increased incidence of lymphomas and skin cancers with long‑term use.
  • Hypersensitivity reactions: such as Stevens‑Johnson syndrome or drug‑induced fever.

Precautions & Warnings

When prescribing azathioprine, clinicians should consider several safety measures to minimise risk.

  • Baseline testing: obtain complete blood count and liver function tests before initiation.
  • Monitoring: perform regular CBC and LFT assessments during treatment.
  • Infection vigilance: advise patients to report signs of infection promptly.
  • Pregnancy and lactation: use only if benefits outweigh risks; discuss with a specialist.
  • Drug-specific contraindications: avoid in patients with known hypersensitivity to azathioprine.
  • Store at below 25°C: keep tablets in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Azathioprine interacts with several medicines that can alter its efficacy or safety profile.

Major Interactions (Avoid)

  • Allopurinol and febuxostat: may markedly increase azathioprine toxicity.
  • Antithymocyte globulin: additive immunosuppressive effect increasing infection risk.

Moderate Interactions (Monitor Closely)

  • Warfarin: azathioprine can enhance anticoagulant effect, requiring INR monitoring.
  • Mycophenolate mofetil: combined use may intensify bone‑marrow suppression.
  • Ribavirin: may increase risk of hematologic abnormalities.
  • Trimethoprim‑sulfamethoxazole: can potentiate myelosuppression, necessitating blood‑count checks.

Frequently Asked Questions

Ozathuia contains azathioprine, an immunosuppressant that is prescribed to help prevent organ rejection after transplantation and to manage autoimmune disorders such as rheumatoid arthritis and inflammatory bowel disease, including Crohn’s disease and ulcerative colitis.

Azathioprine is a pro‑drug that is converted inside cells to 6‑mercaptopurine, which blocks purine synthesis. This limits DNA and RNA production in rapidly dividing lymphocytes, reducing their proliferation and dampening the overall immune response.

The dosage of Ozathuia is individualized by the prescribing clinician based on the patient’s condition, weight, age, and laboratory monitoring results. Physicians determine the appropriate dose and any necessary adjustments.

Azathioprine crosses the placenta and is excreted in breast milk, so its use during pregnancy or lactation is only recommended when the potential benefits outweigh the risks. Treatment decisions should be made in consultation with a specialist obstetrician or neonatologist.

To request Ozathuia, 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 required import documentation.

Compared with calcineurin inhibitors such as cyclosporine, azathioprine offers oral administration and a different toxicity profile, with less nephrotoxicity but a higher risk of bone‑marrow suppression. Choice of therapy depends on the clinical scenario, patient tolerance and physician preference.

Store Ozathuia tablets at temperatures below 25 °C in their original packaging. Protect them from moisture, excessive heat and direct sunlight to maintain potency throughout the shelf‑life.

Ozathuia is supplied as oral tablets that are taken with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with water and not crushed or chewed unless specifically instructed.

The most serious risks include severe bone‑marrow suppression leading to pancytopenia, significant liver injury, opportunistic infections and an increased long‑term risk of certain cancers. Patients should be monitored regularly for blood‑count changes and liver‑function abnormalities.

Individuals with known hypersensitivity to azathioprine or any of its components, patients with severe liver disease, and those with existing bone‑marrow failure should avoid using Ozathuia. It is also contraindicated in pregnant women unless the therapeutic benefit justifies potential fetal risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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