GNH USA

Europe — EMA

Imuran

GNH USA supplies Imuran (Azathioprine), a immunosuppressant for organ transplantation, rheumatoid arthritis and inflammatory bowel disease.

Azathioprine

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What is Azathioprine?

Azathioprine, the active ingredient in Imuran, is an immunosuppressant (antimetabolite) presented as an oral tablet for oral use. It is employed to reduce immune activity in patients undergoing organ transplantation, as well as in chronic inflammatory conditions such as rheumatoid arthritis and inflammatory bowel disease. GNH USA supplies Imuran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide.

What is Azathioprine used for?

Imuran is an immunosuppressive agent used in several autoimmune and transplant‑related disease pathways. - Organ transplantation prophylaxis: helps prevent rejection by suppressing T‑cell activation. - Rheumatoid arthritis: reduces joint inflammation and slows disease progression in moderate to severe cases. - Inflammatory bowel disease (Crohn's disease, ulcerative colitis): diminishes intestinal inflammation and maintains remission in patients unresponsive to first‑line therapies.

What are the side effects of Azathioprine?

Adverse reactions to Imuran vary in frequency and severity.

Common Side Effects: - Nausea or vomiting: gastrointestinal discomfort occurring shortly after dosing. - Decreased white blood cell count: mild leukopenia that may increase infection risk. - Elevated liver enzymes: transient hepatic enzyme changes detectable on routine labs. - Fatigue or malaise: general feeling of tiredness without specific cause.

Serious or Rare Side Effects: - Severe bone marrow suppression: pancytopenia requiring immediate medical attention. - Hepatotoxicity: significant liver injury presenting with jaundice or abnormal labs. - Increased risk of opportunistic infections: due to profound immunosuppression.

What precautions apply to Azathioprine?

Imuran requires careful monitoring and patient education before initiation. - Baseline testing: obtain complete blood count and liver function tests prior to therapy. - Regular monitoring: schedule periodic CBC and hepatic panels to detect toxicity early. - Infection vigilance: advise patients to report fever, sore throat, or unexplained infections promptly. - Drug interactions: review concomitant medications for potential synergistic myelosuppression. - Store at ambient temperature: keep tablets below 25 °C in the original container, protected from moisture and direct sunlight.

What does Azathioprine interact with?

Imuran may interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid): - Allopurinol or febuxostat: can markedly increase azathioprine toxicity; concurrent use is contraindicated. - Mycophenolate mofetil: combined immunosuppression may cause severe bone marrow suppression.

Moderate Interactions (Monitor Closely): - Warfarin: azathioprine may enhance anticoagulant effect; monitor INR closely. - Ribavirin: potential additive hematologic toxicity; regular blood counts recommended. - Live vaccines: immunosuppression may reduce vaccine efficacy and increase infection risk; avoid administration while on therapy.

Frequently asked questions

What conditions is Imuran used to treat?+
Imuran (azathioprine) is prescribed to prevent organ transplant rejection, to manage moderate to severe rheumatoid arthritis, and to maintain remission in inflammatory bowel diseases such as Crohn's disease and ulcerative colitis. It works by suppressing the immune system, thereby reducing inflammation and immune‑mediated tissue damage.
How does azathioprine work in the body?+
Azathioprine is a prodrug that is metabolized to 6‑mercaptopurine, which blocks the synthesis of purine nucleotides. This inhibition limits DNA replication in rapidly dividing lymphocytes, leading to decreased proliferation of T and B cells and a consequent reduction in immune‑driven inflammation.
What is the usual dose of Imuran?+
The appropriate dose of Imuran is individualized and determined by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and laboratory monitoring results. Patients should follow the dosage instructions provided by their healthcare professional and not adjust the dose on their own.
Is Imuran safe to use during pregnancy or while breastfeeding?+
The safety of Imuran during pregnancy and lactation has not been definitively established. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential risks and benefits with their physician, as the drug may cross the placenta and be present in breast milk.
How do I order Imuran from GNH USA?+
To order Imuran, submit an enquiry on the 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 Imuran (azathioprine) and mycophenolate mofetil are antimetabolite immunosuppressants, but they inhibit different enzymes in the purine synthesis pathway. Azathioprine is often used when cost considerations are paramount or when a clinician prefers its longer clinical experience, while mycophenolate may offer a more favorable side‑effect profile for some patients. Choice depends on individual patient factors and physician judgment.
What are the recommended storage conditions for Imuran?+
Imuran tablets should be stored at ambient temperature, below 25 °C, in their original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.
How is Imuran administered?+
Imuran is taken orally as a tablet, usually with a glass of water. It can be taken with or without food, but patients should follow any specific instructions from their prescriber regarding timing relative to meals.
What are the most serious risks associated with Imuran?+
The most serious risks include severe bone‑marrow suppression leading to pancytopenia, hepatotoxicity with potential liver failure, and an increased susceptibility to serious infections, including opportunistic pathogens. Patients should be monitored regularly with blood counts and liver function tests to detect these complications early.
Who should not use Imuran?+
Imuran is contraindicated in individuals with known hypersensitivity to azathioprine or any of its components, in patients with active severe infections, and in those with significant bone‑marrow failure or severe hepatic impairment. Caution is also advised for patients with a history of malignancy.
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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