Product image of Imurek I.V. (Azathioprine) supplied by GNH India

Imurek I.V.

Active Ingredient:
Azathioprine
Origin:
EU

Imurek I.V. (Azathioprine)

Azathioprine, the active ingredient in Imurek I.V., is a immunosuppressant (antimetabolite) presented as a sterile injectable solution for intravenous use. It is employed to prevent organ transplant rejection and to manage certain autoimmune diseases in adult patients.
GNH India supplies Imurek I.V. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Aspen Pharma Trading Limited

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Indications & Clinical Uses

Azathioprine is used as an immunosuppressive agent in conditions where modulation of the immune response is required.

  • Organ transplant rejection: helps prevent acute and chronic rejection of transplanted organs.
  • Rheumatoid arthritis: reduces joint inflammation and slows disease progression.
  • Inflammatory bowel disease: maintains remission in Crohn's disease and ulcerative colitis.

How It Works

  • Azathioprine is metabolized to 6‑mercaptopurine, which inhibits purine nucleotide synthesis. This blockade reduces DNA replication in rapidly dividing cells, particularly T and B lymphocytes, leading to suppressed proliferation and diminished immune responses essential for transplant tolerance and autoimmune disease control.

Side Effects

Azathioprine may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea or vomiting: gastrointestinal discomfort occurring shortly after infusion.
  • Decreased appetite: reduced desire to eat, potentially leading to weight loss.
  • Mild leukopenia: slight reduction in white blood cell count, monitored with routine labs.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Severe bone marrow suppression: profound leukopenia or pancytopenia requiring medical intervention.
  • Hepatotoxicity: significant liver injury presenting with jaundice or elevated bilirubin.
  • Pancreatitis: acute inflammation of the pancreas with abdominal pain and elevated enzymes.

Precautions & Warnings

Before initiating therapy, several safety measures should be observed.

  • Monitor blood counts: perform regular CBC to detect leukopenia early.
  • Assess liver function: schedule periodic LFTs to identify hepatotoxicity.
  • Screen for viral infections: test for hepatitis B, C and HIV prior to treatment.
  • Avoid in known hypersensitivity: discontinue if allergic reactions occur.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • Allopurinol: markedly increases azathioprine toxicity; concurrent use is contraindicated.
  • Warfarin: may enhance anticoagulant effect, increasing bleeding risk.
  • Ribavirin: can potentiate bone marrow suppression.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: may increase risk of renal impairment.
  • NSAIDs: can exacerbate gastrointestinal irritation and affect renal function.
  • Live vaccines: reduced vaccine efficacy and potential for infection.

Frequently Asked Questions

Imurek I.V. contains azathioprine and is used as an immunosuppressive therapy to prevent organ transplant rejection and to treat autoimmune conditions such as rheumatoid arthritis and inflammatory bowel disease.

Azathioprine is converted to 6‑mercaptopurine, which interferes with purine synthesis. This inhibition reduces DNA replication in rapidly dividing T and B lymphocytes, thereby suppressing the immune response needed for transplant tolerance and autoimmune disease control.

The dosage of Imurek I.V. is individualized. The prescribing clinician determines the appropriate dose based on the patient’s condition, weight, renal and hepatic function, and response to therapy.

Azathioprine crosses the placenta and is excreted in breast milk. Its safety in pregnancy and lactation has not been fully established, so use is generally avoided unless the potential benefit justifies the potential risk to the fetus or infant.

To place an order, 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 necessary import documentation.

Compared with calcineurin inhibitors such as cyclosporine, azathioprine offers a different mechanism by targeting purine synthesis. It may have a lower risk of nephrotoxicity but can cause bone marrow suppression, requiring regular blood monitoring.

Imurek I.V. should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Follow the packaging label for any additional handling instructions.

Imurek I.V. is given by intravenous infusion under medical supervision. The infusion rate and duration are determined by the prescribing physician, and patients are monitored for any adverse reactions during and after administration.

The most serious risks include severe bone marrow suppression leading to pancytopenia, hepatotoxicity with potential liver failure, and rare cases of pancreatitis. Prompt recognition and monitoring are essential to mitigate these risks.

Imurek I.V. is contraindicated in patients with known hypersensitivity to azathioprine or its components, those with severe bone marrow depression, active infections, or significant liver disease. It should also be avoided in pregnant women unless clearly needed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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