Product image of Imurel (Azathioprine) supplied by GNH India

Imurel

Active Ingredient:
Azathioprine
Origin:
EU

Imurel (Azathioprine)

Azathioprine, the active ingredient in Imurel, is an antimetabolite presented as an oral tablet for oral use. It is employed to suppress the immune response in organ transplantation, rheumatoid arthritis, and inflammatory bowel disease, helping to reduce tissue rejection and disease activity.

GNH India supplies Imurel as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, and pharmacies worldwide, ensuring consistent quality and regulatory compliance across markets. The company leverages a robust distribution network to meet the needs of clinical and procurement teams in diverse regions.

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

Azathioprine is an immunosuppressive agent used in several chronic immune‑mediated conditions.

  • Organ transplantation: reduces risk of graft rejection by inhibiting lymphocyte proliferation.
  • Rheumatoid arthritis: decreases joint inflammation and slows disease progression.
  • Inflammatory bowel disease: helps maintain remission in Crohn’s disease and ulcerative colitis.

How It Works

  • Azathioprine is a purine analog that is converted intracellularly to 6‑mercaptopurine, which interferes with de novo purine synthesis. By incorporating into DNA and RNA, it blocks the proliferation of rapidly dividing cells, particularly activated T and B lymphocytes, thereby dampening the immune response. The metabolite also inhibits the activity of enzymes involved in nucleotide salvage pathways, further reducing lymphocyte activation and cytokine production.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset that may affect appetite.
  • Fatigue: persistent tiredness that can interfere with daily activities.
  • Elevated liver enzymes: mild hepatic changes detectable in routine blood tests.

Serious or Rare Side Effects

  • Bone marrow suppression: anemia, leukopenia, or thrombocytopenia leading to increased infection risk.
  • Severe infections: opportunistic bacterial, viral or fungal infections requiring prompt medical attention.
  • Hepatotoxicity: significant liver injury that may present with jaundice or elevated transaminases.

Precautions & Warnings

When prescribing azathioprine, clinicians should consider several safety precautions to minimize risks.

  • Baseline testing: obtain complete blood count and liver function tests before initiation.
  • Monitoring: perform regular CBC and liver enzymes during therapy.
  • Infection risk: avoid use in patients with active infections or immunodeficiency.
  • Vaccination: ensure required vaccines are administered prior to starting treatment.
  • Pregnancy and lactation: assess risks and discuss alternatives with women of childbearing potential.
  • Store at ambient temperature: keep tablets in original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Allopurinol: can increase azathioprine toxicity; dose reduction or avoidance required.
  • Warfarin: may enhance anticoagulant effect, increasing bleeding risk.
  • Live vaccines: concurrent use may cause severe infection.

Moderate Interactions (Monitor Closely)

  • Ribavirin: may augment bone marrow suppression.
  • Mycophenolate mofetil: additive immunosuppression increasing infection risk.
  • ACE inhibitors: possible increase in renal toxicity.

Frequently Asked Questions

Imurel, which contains azathioprine, is prescribed to prevent rejection after organ transplantation and to manage chronic autoimmune disorders such as rheumatoid arthritis. It is also used to maintain remission in inflammatory bowel diseases, including Crohn’s disease and ulcerative colitis.

Azathioprine is a purine analog that is metabolized to 6‑mercaptopurine inside cells. This metabolite interferes with DNA and RNA synthesis, limiting the proliferation of activated T and B lymphocytes, which reduces the overall immune response and inflammation.

The prescribed dose of Imurel is individualized by the treating physician based on the specific indication, the patient’s body weight or surface area, baseline laboratory values, and the presence of any comorbid conditions. Dose adjustments are made according to clinical response and safety monitoring.

Data on azathioprine use in pregnancy and lactation are limited. The drug crosses the placenta and is excreted in breast milk, so clinicians weigh potential fetal or infant risks against therapeutic benefits. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To request Imurel, 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.

The primary alternative to azathioprine is mycophenolate mofetil, another antimetabolite. While both suppress lymphocyte proliferation, mycophenolate often has a more rapid onset and a different side‑effect profile, such as higher rates of gastrointestinal upset. Choice between them depends on the clinical scenario, tolerability, and physician preference.

Imurel tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Protect them from moisture, excessive heat, and direct light to maintain stability throughout the shelf life.

Imurel is taken orally, usually as a tablet swallowed whole with water. The exact timing (e.g., with or without food) is determined by the prescribing physician based on individual tolerance and therapeutic goals.

The most serious risks include bone‑marrow suppression leading to anemia, leukopenia, or thrombocytopenia; severe infections due to immunosuppression; and hepatotoxicity that can progress to liver failure. Regular laboratory monitoring is essential to detect these complications early.

Imurel is contraindicated in patients with known hypersensitivity to azathioprine or its metabolites, those with active severe infections, and individuals with significant bone‑marrow failure. Caution is also advised for patients with pre‑existing liver disease or severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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