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

Idarubicine Accord

Active Ingredient:
Idarubicin Hydrochloride
Origin:
EU

Idarubicine Accord (Idarubicin Hydrochloride)

Idarubicin Hydrochloride, the active ingredient in Idarubicine Accord, is an anthracycline antibiotic presented as an injection solution for intravenous use. It is employed in the treatment of acute myeloid leukemia and acute lymphoblastic leukemia in adult and pediatric patients. The drug is formulated for sterile infusion and is indicated for patients with newly diagnosed or relapsed disease.

GNH India supplies Idarubicine Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, ensuring quality and regulatory compliance across EU and global markets.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Idarubicine Accord, an anthracycline chemotherapy, is used in the treatment of acute leukemias.

  • Acute Myeloid Leukemia (AML): induces remission and reduces leukemic burden in newly diagnosed or relapsed AML patients.
  • Acute Lymphoblastic Leukemia (ALL): contributes to disease control and improves survival outcomes in ALL patients.

How It Works

  • Idarubicin hydrochloride intercalates between DNA base pairs, disrupting the double‑helix structure and preventing replication. It also stabilizes the DNA‑topoisomerase II complex, inhibiting the enzyme’s ability to reseal DNA strands after cleavage, which results in permanent DNA breaks and triggers apoptosis in rapidly proliferating malignant cells. The drug accumulates preferentially in tumor tissue due to its high affinity for nucleic acids and is metabolized primarily by hepatic pathways.

Side Effects

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

Common Side Effects

  • Nausea and vomiting
  • Alopecia (hair loss)
  • Fatigue
  • Myelosuppression (neutropenia, anemia, thrombocytopenia)
  • Mucositis
  • Diarrhea

Serious or Rare Side Effects

  • Cardiotoxicity leading to heart failure
  • Severe infections secondary to neutropenia
  • Hemorrhage due to thrombocytopenia
  • Secondary malignancies
  • Severe infusion‑related reactions
  • Hepatic toxicity

Precautions & Warnings

When using Idarubicine Accord, careful monitoring and risk mitigation are essential.

  • Cardiac monitoring: baseline and periodic assessment of left ventricular function is recommended.
  • Hematologic monitoring: regular complete blood counts to detect neutropenia, anemia, and thrombocytopenia.
  • Liver function monitoring: evaluate transaminases and bilirubin before and during therapy.
  • Renal function monitoring: assess creatinine clearance as dosage may require adjustment.
  • Pregnancy and breastfeeding: use only if the potential benefit justifies the potential risk; safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Idarubicine Accord can interact with several medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Concurrent use with other anthracyclines (e.g., daunorubicin) may increase cardiotoxic risk.
  • Combination with known cardiotoxic agents such as trastuzumab should be avoided.

Moderate Interactions (Monitor Closely)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole) may raise idarubicin exposure.
  • Anticoagulants (e.g., warfarin) can heighten bleeding risk.
  • Other myelosuppressive chemotherapy agents may exacerbate bone‑marrow suppression.

Frequently Asked Questions

Idarubicine Accord is an injectable anthracycline chemotherapy indicated for the treatment of acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). It is used in adult and pediatric patients to achieve remission or disease control in newly diagnosed or relapsed cases.

Idarubicin Hydrochloride intercalates into DNA, disrupting its structure, and stabilizes the DNA‑topoisomerase II complex. This prevents the enzyme from resealing DNA strands after cleavage, leading to permanent DNA breaks and triggering apoptosis of rapidly dividing cancer cells.

The dose of Idarubicine Accord is determined by the prescribing oncologist based on factors such as the patient’s age, weight, disease status, renal and hepatic function, and prior treatment history. No fixed regimen is provided here; dosing is individualized.

Safety data for Idarubicine Accord in pregnancy and lactation are limited. It should be used only when the potential therapeutic benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To order Idarubicine Accord, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Idarubicine Accord contains idarubicin, which is more lipophilic than older anthracyclines such as daunorubicin, allowing better cellular uptake and potentially higher anti‑leukemic activity. However, the safety profile, especially cardiotoxicity, remains similar across the class, and choice of agent depends on clinical judgment and patient factors.

Idarubicine Accord should be stored at 2‑8 °C (refrigerated). Keep the vials in their original packaging, protect from light, and avoid freezing or shaking the solution to maintain stability.

Idarubicine Accord is administered as a sterile intravenous infusion. The infusion is given under controlled clinical conditions, typically over a period of 30–60 minutes, with appropriate monitoring of vital signs and cardiac function.

The most serious risks include cardiotoxicity (which can lead to heart failure), severe myelosuppression resulting in life‑threatening infections or bleeding, and rare but serious infusion reactions. Continuous cardiac monitoring and regular blood counts are essential to detect these complications early.

Patients with known hypersensitivity to idarubicin or any component of the formulation, those with severe pre‑existing cardiac dysfunction, uncontrolled infections, or significant hepatic impairment should not receive Idarubicine Accord unless a risk‑benefit assessment justifies its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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