Product image of Idarubicin Accord (Idarubicin Hydrochloride) supplied by GNH India

Idarubicin Accord

Active Ingredient:
Idarubicin Hydrochloride
Origin:
EU

Idarubicin Accord (Idarubicin Hydrochloride)

Idarubicin, the active ingredient in Idarubicin Accord, is an anthracycline antibiotic presented as an intravenous formulation for use in the treatment of acute myeloid leukemia in adult patients. It is manufactured to European Union standards and is indicated for induction and consolidation chemotherapy protocols.

GNH India supplies Idarubicin Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, ensuring quality, regulatory compliance and reliable sourcing for oncology treatment programs.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

  • Idarubicin Accord is an anthracycline chemotherapy agent used in the management of acute myeloid leukemia.
  • Acute Myeloid Leukemia (newly diagnosed): achieves remission by eradicating leukemic blasts during induction therapy.
  • Acute Myeloid Leukemia (relapsed or refractory): provides disease control when other regimens have failed.
  • Acute Myeloid Leukemia (consolidation): helps maintain remission by eliminating residual disease after induction.

How It Works

  • Idarubicin intercalates between DNA base pairs and strongly inhibits topoisomerase II, preventing the re‑ligation of DNA strands during replication. This results in permanent double‑strand breaks and the generation of free radicals, leading to apoptosis of rapidly dividing malignant cells, particularly leukemic blasts.

Side Effects

Idarubicin may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea and vomiting
  • Alopecia (hair loss)
  • Fatigue and weakness
  • Myelosuppression (neutropenia, anemia, thrombocytopenia)
  • Mucositis (inflammation of the mouth lining)
  • Diarrhea

Serious or Rare Side Effects

  • Cardiotoxicity (heart failure, reduced ejection fraction)
  • Severe infections due to profound neutropenia
  • Hemorrhage from thrombocytopenia
  • Secondary malignancies (e.g., therapy‑related leukemia)
  • Hepatic toxicity (elevated transaminases)
  • Pulmonary toxicity (interstitial pneumonitis)

Precautions & Warnings

  • When using Idarubicin Accord, clinicians should observe several precautionary measures to minimize risk.
  • Cardiac monitoring: perform baseline and periodic echocardiograms to detect cardiotoxicity.
  • Hematologic monitoring: conduct regular complete blood counts to manage myelosuppression.
  • Renal function assessment: evaluate kidney function before and during therapy.
  • Avoid in known hypersensitivity: discontinue if allergic reaction occurs.
  • Use caution in elderly patients: adjust monitoring due to increased susceptibility.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Idarubicin can interact with other medicines, affecting efficacy or toxicity.

Major Interactions (Avoid)

  • Concurrent use with other anthracyclines or trastuzumab: markedly increases risk of cardiotoxicity.
  • Co‑administration with high‑dose cyclophosphamide: amplifies bone‑marrow suppression.
  • Combination with live vaccines: may cause uncontrolled infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise idarubicin plasma levels.
  • CYP3A4 inducers (e.g., rifampin, phenytoin): may reduce drug exposure.
  • Anticoagulants (e.g., warfarin): increased bleeding risk from thrombocytopenia.
  • Nephrotoxic agents (e.g., cisplatin): heightened renal toxicity when combined.

Frequently Asked Questions

Idarubicin Accord is employed in the treatment of acute myeloid leukemia (AML). It is used as part of induction, consolidation, or salvage chemotherapy regimens to eradicate leukemic cells and achieve remission in adult patients.

Idarubicin intercalates into DNA and blocks topoisomerase II activity, causing irreversible double‑strand breaks. The drug also generates free radicals that damage cellular membranes, leading to apoptosis of rapidly dividing cancer cells, especially leukemic blasts.

The dose of Idarubicin Accord is individualized by the prescribing oncologist based on factors such as disease stage, patient weight, renal and hepatic function, and prior therapy. Specific dosing regimens are determined in the treatment protocol.

Idarubicin is classified as contraindicated during pregnancy and lactation because it can cross the placenta and is excreted in breast milk, posing a risk of fetal or infant toxicity. Women of child‑bearing potential should use effective contraception during treatment.

To request Idarubicin Accord, 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 (including cold‑chain where required) and import documentation.

Idarubicin is structurally related to daunorubicin but has a higher lipophilicity, allowing better cellular uptake and potentially greater antileukemic activity. Compared with doxorubicin, it is more potent against AML but shares a similar cardiotoxicity profile, requiring careful cardiac monitoring.

Idarubicin Accord should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. The product should be kept in its original packaging until ready for preparation and administration.

Idarubicin Accord is administered intravenously by a qualified healthcare professional. It is typically given as a short infusion over several minutes, according to the prescribing oncologist’s schedule and the specific chemotherapy protocol.

The most critical risks include cardiotoxicity (heart failure or reduced ejection fraction), severe myelosuppression leading to infection or bleeding, and secondary malignancies. Patients should be monitored regularly with cardiac imaging, blood counts, and clinical assessment for signs of infection or hemorrhage.

Idarubicin Accord should be avoided in patients with known hypersensitivity to idarubicin or other anthracyclines, those with severe pre‑existing cardiac dysfunction, uncontrolled infections, or pregnant and breastfeeding women. Caution is also advised for the elderly and patients with impaired hepatic or renal function.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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