GNH USA

Europe — EMA

Imurel

GNH USA supplies Imurel (Azathioprine), an immunosuppressant for organ transplantation, rheumatoid arthritis, IBD and lupus.

Azathioprine

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What is Azathioprine?

Azathioprine, the active ingredient in Imurel, is an immunosuppressant presented as an oral tablet for oral use. It is employed to reduce immune system activity in conditions such as organ transplantation, rheumatoid arthritis, inflammatory bowel disease, and systemic lupus erythematosus. GNH USA supplies Imurel as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, pharmacies and clinics worldwide.

What is Azathioprine used for?

Azathioprine is used to modulate immune activity in several chronic inflammatory and autoimmune conditions. - Organ transplantation: helps prevent graft rejection by suppressing lymphocyte proliferation. - Rheumatoid arthritis: reduces joint inflammation and disease progression. - Inflammatory bowel disease: controls symptoms of Crohn's disease and ulcerative colitis. - Systemic lupus erythematosus: diminishes systemic immune activation and organ damage.

What are the side effects of Azathioprine?

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

Common Side Effects: - Nausea or vomiting: gastrointestinal discomfort is frequently reported. - Leukopenia: reduced white blood cell count, increasing infection risk. - Elevated liver enzymes: mild hepatic irritation detectable in blood tests. - Rash or mild skin irritation: occasional dermatologic response.

Serious or Rare Side Effects: - Severe bone marrow suppression: pancytopenia requiring medical intervention. - Hepatotoxicity: significant liver injury manifesting as jaundice or hepatitis. - Increased risk of opportunistic infections: due to profound immunosuppression. - Possible malignancy risk: long‑term use may be associated with certain cancers.

What precautions apply to Azathioprine?

Before initiating therapy with Azathioprine, several safety considerations are recommended. - Baseline testing: obtain complete blood count and liver function tests prior to treatment. - Monitoring: perform regular CBC and hepatic panels to detect toxicity early. - Infection vigilance: advise patients to report signs of infection promptly. - Pregnancy and lactation: discuss potential risks with a healthcare professional before use. - Drug interactions: review concomitant medications for possible interactions. - Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

What does Azathioprine interact with?

Azathioprine can interact with other medicines, altering 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.

Moderate Interactions (Monitor Closely): - Warfarin: may enhance anticoagulant effect, requiring INR monitoring. - Live vaccines: increased risk of infection; avoid administration. - Antacids containing magnesium or aluminum: may reduce absorption. - Ribavirin: potential additive hematologic toxicity. - Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase renal risk when combined.

Frequently asked questions

What conditions is Imurel used to treat?+
Imurel, whose active ingredient is azathioprine, is prescribed to help prevent organ transplant rejection, manage rheumatoid arthritis, control inflammatory bowel disease such as Crohn's disease and ulcerative colitis, and treat systemic lupus erythematosus by suppressing overactive immune responses.
How does azathioprine work in the body?+
Azathioprine is converted inside cells to 6‑mercaptopurine, which blocks the synthesis of purine nucleotides needed for DNA replication. This action limits the proliferation of lymphocytes, thereby reducing immune system activity and inflammation in autoimmune and transplant settings.
What is the usual dose of Imurel?+
The appropriate dose of Imurel is individualized by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and response to therapy. Dosage adjustments are made according to laboratory monitoring and clinical judgment.
Is Imurel safe to use during pregnancy or while breastfeeding?+
The safety of azathioprine during pregnancy or lactation is not definitively established. Healthcare providers should evaluate potential benefits against possible risks, and women who are pregnant, planning pregnancy, or breastfeeding should discuss their situation with a qualified medical professional before using Imurel.
How do I order Imurel from GNH USA?+
To request Imurel, 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 Imurel compare with other immunosuppressants?+
Azathioprine is a purine analogue that offers oral administration and a well‑characterized safety profile, making it a common choice for long‑term immunosuppression. Compared with calcineurin inhibitors like cyclosporine, azathioprine generally has fewer nephrotoxic effects but may require more frequent blood monitoring for bone‑marrow suppression.
What are the storage requirements for Imurel?+
Imurel should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture, excessive heat and direct sunlight to maintain product stability throughout its shelf life.
How is Imurel administered to patients?+
Imurel is taken orally, usually with food or a glass of water to reduce gastrointestinal irritation. The exact timing and frequency are determined by the prescribing clinician, who will provide instructions tailored to the individual’s therapeutic needs.
What are the most serious risks associated with Imurel?+
The most serious risks include severe bone‑marrow suppression leading to pancytopenia, significant liver toxicity, heightened susceptibility to opportunistic infections, and a potential increased risk of certain malignancies with long‑term use. Regular laboratory monitoring helps detect these complications early.
Who should not use Imurel?+
Imurel is contraindicated in patients with known hypersensitivity to azathioprine or its metabolites, those with severe liver disease, active infections, or a history of bone‑marrow failure. It should also be avoided in individuals with markedly reduced TPMT activity unless dose‑adjusted under specialist 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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