GNH USA

Europe — EMA

Imuran

GNH USA supplies Imuran (Azathioprine), a immunosuppressant for organ 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 manage autoimmune disorders such as rheumatoid arthritis, inflammatory bowel disease, 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, providing consistent quality and regulatory compliance across EU and global markets through reliable logistics and dedicated support to customers.

What is Azathioprine used for?

Azathioprine is used in several immune‑mediated conditions to reduce pathological immune activity. - Organ transplant rejection prophylaxis: prevents acute and chronic rejection episodes by suppressing lymphocyte activation. - Rheumatoid arthritis: reduces joint inflammation, pain and disease progression. - Inflammatory bowel disease (Crohn's disease, ulcerative colitis): maintains remission and decreases flare frequency. - Systemic lupus erythematosus: controls disease activity and organ involvement.

What are the side effects of Azathioprine?

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

Common Side Effects: - Nausea or vomiting - Loss of appetite - Mild leukopenia - Elevated liver enzymes

Serious or Rare Side Effects: - Severe bone‑marrow suppression (pancytopenia) - Hepatotoxicity (clinically significant liver injury) - Opportunistic infections

What precautions apply to Azathioprine?

When prescribing azathioprine, clinicians should observe several safety precautions to minimize toxicity. - Monitor blood counts: perform regular complete blood count (CBC) testing. - Assess liver function: schedule periodic liver‑function tests (LFTs). - Screen for infections: test for latent tuberculosis, hepatitis B/C before initiation. - Adjust dose in renal/hepatic impairment: follow clinical guidelines for dose reduction. - Store at room temperature: keep tablets in original packaging, protect from moisture.

What does Azathioprine interact with?

Azathioprine interacts with several medicines that can alter its efficacy or increase toxicity.

Major Interactions (Avoid): - Allopurinol: potentiates azathioprine toxicity, may require dose reduction. - Warfarin: enhances anticoagulant effect, increasing bleeding risk. - Ribavirin: combined use raises risk of severe myelosuppression.

Moderate Interactions (Monitor Closely): - ACE inhibitors: may affect renal function, requiring monitoring. - NSAIDs: additive bone‑marrow suppression potential. - Live vaccines: reduced efficacy and possible infection risk.

Frequently asked questions

What is Imuran used for?+
Imuran contains azathioprine, an immunosuppressant used to prevent organ transplant rejection and to manage autoimmune conditions such as rheumatoid arthritis, inflammatory bowel disease (Crohn’s disease and ulcerative colitis) and systemic lupus erythematosus. It works by reducing the activity of the immune system.
How does azathioprine work?+
Azathioprine is a pro‑drug that is converted in the body to 6‑mercaptopurine. This metabolite interferes with the synthesis of purine nucleotides, which are essential for DNA, RNA and protein production in rapidly dividing lymphocytes. By limiting lymphocyte proliferation, azathioprine suppresses immune responses.
What is the usual dose of Imuran?+
The dose of Imuran is individualized by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and laboratory monitoring results. Dosage adjustments are made to achieve therapeutic effect while minimizing toxicity, and patients should follow the prescriber’s written instructions.
Is Imuran safe during pregnancy or breastfeeding?+
Imuran is classified as Pregnancy Category D, indicating evidence of risk to the fetus; it should only be used when the potential benefit justifies the risk. Limited data are available for breastfeeding, and the drug may pass into breast milk, so continuation should be decided by the treating physician.
How do I order Imuran from GNH USA?+
To place an order, submit an enquiry on the Imuran product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.
How does Imuran compare with mycophenolate mofetil?+
Both azathioprine (Imuran) and mycophenolate mofetil are antimetabolite immunosuppressants that inhibit lymphocyte proliferation, but they act on different enzymes in the purine pathway. Mycophenolate generally has a more rapid onset and may be associated with higher rates of gastrointestinal side effects, while azathioprine is often chosen for its longer clinical experience and lower cost in many transplant protocols.
How should Imuran be stored?+
Imuran tablets should be stored at room temperature, below 25 °C (77 °F). Keep them in the original blister pack or container, protect from moisture and direct sunlight, and store out of reach of children. Do not refrigerate or freeze the tablets.
How is Imuran administered?+
Imuran is taken orally as a tablet, usually with food or a glass of water to reduce gastrointestinal irritation. The tablet should be swallowed whole; it should not be crushed, chewed, or split unless specifically instructed by a healthcare professional. Dosing frequency and timing are determined by the prescribing clinician.
What are the most serious risks associated with Imuran?+
The most serious risks include severe bone‑marrow suppression leading to pancytopenia, hepatotoxicity, pancreatitis, opportunistic infections, and an increased long‑term risk of certain malignancies such as lymphoma or skin cancer. Patients should undergo regular blood count and liver‑function monitoring to detect these complications early.
Who should not use Imuran?+
Imuran is contraindicated in patients with known hypersensitivity to azathioprine or its metabolites, in those with active severe infections, and in pregnant women unless the therapeutic benefit outweighs fetal risk. It should also be avoided in individuals with severe hepatic impairment or in patients receiving live vaccines without appropriate medical supervision.
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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