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 immunosuppressant (antimetabolite) presented as an oral tablet for oral use. It is employed to reduce immune system activity in patients requiring long‑term suppression, such as organ transplant recipients and individuals with certain autoimmune disorders.

GNH India supplies Imurel as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support import and clinical use.

Manufacturer / TM Owner

Aspen Pharma Trading Limited

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Indications & Clinical Uses

  • Azathioprine is used to modulate immune activity in several chronic inflammatory and transplant‑related conditions.
  • Organ transplant rejection prevention: reduces the risk of acute and chronic graft rejection by suppressing lymphocyte proliferation.
  • Rheumatoid arthritis: alleviates joint inflammation and slows disease progression in patients with moderate to severe disease.
  • Inflammatory bowel disease (Crohn's disease, ulcerative colitis): induces and maintains remission by dampening intestinal immune responses.
  • Systemic lupus erythematosus: helps control systemic autoimmune activity and prevent organ damage.

How It Works

  • Azathioprine is a purine analog that is converted intracellularly to 6‑mercaptopurine, which interferes with de novo purine synthesis. By inhibiting the formation of DNA and RNA precursors, it blocks the proliferation of rapidly dividing T and B lymphocytes, thereby reducing cellular immune responses and cytokine production. The drug also induces apoptosis of activated immune cells and modulates the expression of adhesion molecules, contributing to its overall immunosuppressive effect.

Side Effects

Azathioprine may cause a range of adverse reactions, varying from mild to potentially life‑threatening.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset occurring early in therapy.
  • Loss of appetite: reduced desire to eat.
  • Mild leukopenia: slight decrease in white blood cell count.
  • Elevated liver enzymes: transient increase in hepatic transaminases.
  • Hair thinning: mild alopecia.

Serious or Rare Side Effects

  • Severe bone marrow suppression: profound pancytopenia requiring medical intervention.
  • Hepatotoxicity: significant liver injury with jaundice or hepatitis.
  • Increased infection risk: opportunistic infections due to immunosuppression.
  • Pancreatitis: acute inflammation of the pancreas.
  • Malignancy: heightened long‑term risk of lymphomas and skin cancers.

Precautions & Warnings

  • Before initiating azathioprine therapy, several safety considerations should be reviewed.
  • Baseline blood tests: obtain complete blood count and liver function tests to assess eligibility.
  • Monitor regularly: schedule periodic CBC and liver enzymes to detect toxicity early.
  • Infection vigilance: advise patients to report signs of infection promptly.
  • Avoid live vaccines: immunosuppression can reduce vaccine efficacy and increase risk.
  • Pregnancy and lactation: discuss potential risks with a specialist before use.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Allopurinol and febuxostat: potentiate azathioprine toxicity, may cause severe bone marrow suppression.
  • Warfarin: increased anticoagulant effect, risk of bleeding.
  • Live vaccines: may lead to uncontrolled infection.

Moderate Interactions (Monitor Closely)

  • Rituximab: additive immunosuppression, monitor infection signs.
  • Sulfasalazine: may enhance myelosuppression, check blood counts.
  • Antibiotics (e.g., trimethoprim‑sulfamethoxazole): can increase myelosuppressive risk, require monitoring.

Frequently Asked Questions

Imurel contains azathioprine, an immunosuppressant that is prescribed to prevent organ transplant rejection and to treat several autoimmune disorders such as rheumatoid arthritis, inflammatory bowel disease (including Crohn's disease and ulcerative colitis) and systemic lupus erythematosus.

Azathioprine is a purine analog that is metabolised to 6‑mercaptopurine inside cells. This metabolite interferes with the synthesis of DNA and RNA, thereby inhibiting the proliferation of activated T‑ and B‑lymphocytes and reducing the overall immune response.

The dosage of Imurel is individualized. A qualified prescriber determines the appropriate amount based on the patient’s condition, weight, renal and hepatic function, and response to therapy. No fixed dosing regimen is provided here.

The safety of azathioprine in pregnancy and lactation is not fully established. Use is generally considered only when the potential benefit outweighs the risk, and it should be discussed with a specialist obstetrician or rheumatologist before starting therapy.

To order 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 most common alternative to azathioprine is mycophenolate mofetil, another antimetabolite immunosuppressant. Both agents suppress lymphocyte proliferation, but mycophenolate often has a different side‑effect profile, with less bone‑marrow suppression but more gastrointestinal upset. Choice depends on the clinical scenario, tolerance and physician preference.

Imurel tablets should be stored at ambient temperature, below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and store out of reach of children.

Imurel is taken orally. The tablets are swallowed whole with a glass of water, usually with or without food as directed by the prescriber. Patients should follow the dosing schedule provided by their healthcare professional.

Serious risks include severe bone‑marrow suppression (pancytopenia), hepatotoxicity, opportunistic infections, pancreatitis and an increased long‑term risk of certain cancers such as lymphomas and skin malignancies. Prompt medical attention is required if symptoms such as fever, persistent fatigue, jaundice or unusual bruising occur.

Imurel should be avoided in individuals with known hypersensitivity to azathioprine or its metabolites, those with severe bone‑marrow suppression, active uncontrolled infections, or significant liver disease. Caution is also advised for pregnant or nursing women and patients with compromised renal function, unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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