GNH USA

Europe — EMA

Imuran

GNH USA supplies Imuran (Azathioprine), an immunosuppressant for transplant rejection, rheumatoid arthritis, inflammatory bowel disease and lupus.

Azathioprine

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What is Azathioprine?

Azathioprine, the active ingredient in Imuran, is an immunosuppressant presented as a tablet for oral use. It is employed to prevent organ transplant rejection and to treat several autoimmune disorders, including rheumatoid arthritis, inflammatory bowel disease (Crohn’s disease and ulcerative colitis), and systemic lupus erythematosus.

GNH USA supplies Imuran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The product complies with EU regulatory standards and is distributed across multiple markets, ensuring consistent quality and availability.

What is Azathioprine used for?

Azathioprine is used to modulate immune activity in several chronic inflammatory and transplant‑related conditions. - Organ transplant rejection: helps prevent the immune system from attacking the transplanted organ. - Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Inflammatory bowel disease: induces and maintains remission in Crohn’s disease and ulcerative colitis. - Systemic lupus erythematosus: decreases disease activity and flares.

What are the side effects of Azathioprine?

Azathioprine may cause a range of adverse reactions, from mild to potentially serious.

Common Side Effects: - Nausea: mild gastrointestinal upset. - Fatigue: general tiredness. - Elevated liver enzymes: mild hepatic enzyme rise. - Decreased white blood cell count: mild leukopenia.

Serious or Rare Side Effects: - Bone marrow suppression: severe leukopenia, anemia, or thrombocytopenia. - Hepatotoxicity: significant liver injury. - Increased risk of malignancy: especially lymphomas and skin cancers.

What precautions apply to Azathioprine?

Before initiating azathioprine therapy, several precautions should be considered to minimize risks. - Baseline testing: obtain complete blood count and liver function tests prior to treatment. - Monitoring: perform regular CBC and liver enzyme assessments during therapy. - Infection risk: avoid use in patients with active infections or uncontrolled viral illnesses. - Pregnancy: drug is classified as Category D; discuss risks with a healthcare professional. - Drug interactions: assess concomitant medications that affect thiopurine metabolism. - Store at ambient temperature: keep tablets below 25 °C in the original container, protected from moisture.

What does Azathioprine interact with?

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

Major Interactions (Avoid): - Allopurinol or febuxostat: may cause severe bone marrow suppression. - Thiopurine methyltransferase (TPMT) inhibitors: increase risk of toxicity. - Live vaccines: heightened risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - Warfarin: azathioprine may enhance anticoagulant effect. - Mycophenolate mofetil: additive immunosuppressive effect. - Corticosteroids: may increase risk of infection when combined.

Frequently asked questions

What conditions is Imuran used to treat?+
Imuran, whose active ingredient is azathioprine, is prescribed to prevent organ transplant rejection and to manage autoimmune diseases such as rheumatoid arthritis, inflammatory bowel disease (including Crohn’s disease and ulcerative colitis), and systemic lupus erythematosus. It works by suppressing the immune system to reduce inflammation and tissue damage.
How does azathioprine work in the body?+
Azathioprine is a prodrug that is converted inside cells to 6‑mercaptopurine, which interferes with purine synthesis. This disruption hampers DNA and RNA production, limiting the proliferation of activated T and B lymphocytes. The resulting reduction in immune cell activity provides the immunosuppressive effect needed for transplant and autoimmune disease management.
What is the usual dose of Imuran?+
The dosage of Imuran is individualized and set by the prescribing healthcare professional based on the specific indication, patient weight, renal and hepatic function, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose without medical guidance.
Is Imuran safe to use during pregnancy or breastfeeding?+
Imuran is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should only be used during pregnancy if the potential benefit justifies the risk, and under close medical supervision. Limited data are available for breastfeeding; the decision to continue should be made by a healthcare provider weighing infant exposure against maternal benefit.
How do I order Imuran from GNH USA?+
To request Imuran, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, and will ask for trade or institutional credentials. The sales team then provides pricing, availability, shipping details (including any temperature requirements) and assists with import documentation.
How does Imuran compare with other immunosuppressants?+
Compared with alternatives such as mycophenolate mofetil or cyclosporine, azathioprine offers a well‑established efficacy profile for transplant and autoimmune indications but may have a slower onset of action. Its side‑effect spectrum differs, with notable risks of bone‑marrow suppression and hepatotoxicity, while other agents may have distinct renal or cardiovascular concerns. Choice depends on patient factors and physician judgment.
What are the recommended storage conditions for Imuran?+
Imuran tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original packaging to protect from moisture and light. Do not store in bathrooms or near heat sources, and keep out of reach of children.
How is Imuran administered?+
Imuran is taken orally as a tablet, usually with food or a glass of water to reduce gastrointestinal irritation. The exact timing (e.g., morning or evening) and whether it is taken with or without food should follow the prescribing clinician’s directions.
What are the most serious risks associated with Imuran?+
The most serious risks include bone‑marrow suppression leading to severe leukopenia, anemia or thrombocytopenia; hepatotoxicity that can progress to liver failure; opportunistic infections due to immunosuppression; and an increased long‑term risk of certain malignancies such as lymphomas and skin cancers. Regular laboratory monitoring is essential to detect these complications early.
Who should not use Imuran?+
Imuran is contraindicated in patients with known hypersensitivity to azathioprine or any of its components, those with active severe infections, and individuals with significant bone‑marrow failure or severe liver disease. Caution is also advised for patients with thiopurine methyltransferase (TPMT) deficiency, as they are at higher risk for toxicity.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Azathioprine
Route
Oral Use
Manufacturer
Aspen Pharma Trading Limited
Origin
EU

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