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 a sterile injectable solution for intravenous use. It is employed in the treatment of acute myeloid leukemia, targeting rapidly dividing malignant cells in adult patients, and is indicated for newly diagnosed or relapsed disease as part of combination chemotherapy protocols.

GNH India supplies Idarubicin Accord as a licensed, GDP‑compliant international pharmaceutical supplier, adhering to stringent quality standards and providing the product to hospitals, oncology centres, and pharmacies worldwide for cancer care programs.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Idarubicin is an anthracycline antibiotic used primarily in the management of acute myeloid leukemia, a malignant disorder of the blood and bone marrow.

  • Acute myeloid leukemia (AML): induces remission by killing leukemic blasts and is incorporated into induction or consolidation chemotherapy regimens.

How It Works

  • Idarubicin 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 double‑strand breaks and triggers apoptosis of rapidly proliferating cancer cells. The drug’s high lipophilicity facilitates cellular uptake, and its activity is not significantly reduced by common resistance mechanisms such as P‑glycoprotein efflux.

Side Effects

Idarubicin may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Nausea and vomiting: frequent gastrointestinal upset during infusion.
  • Myelosuppression: decreased blood cell counts leading to anemia, neutropenia, and thrombocytopenia.
  • Alopecia: hair loss occurring during treatment cycles.
  • Mucositis: inflammation of the mouth and gastrointestinal lining.
  • Fatigue: generalized tiredness and weakness.

Serious or Rare Side Effects

  • Cardiotoxicity: dose‑dependent heart muscle damage that may progress to heart failure.
  • Severe neutropenia: profound low neutrophil levels increasing infection risk.
  • Acute hypersensitivity reactions: rash, fever, or anaphylaxis during infusion.
  • Secondary malignancies: rare risk of therapy‑related leukemias or solid tumors.

Precautions & Warnings

When using Idarubicin, several precautions should be observed to minimize risks and ensure safe handling.

  • Cardiac monitoring: assess baseline and periodic cardiac function due to potential cardiotoxicity.
  • Hematologic surveillance: perform regular complete blood counts to detect myelosuppression.
  • Concomitant nephrotoxic drugs: avoid or adjust dosing when used with other kidney‑affecting agents.
  • Pregnancy and lactation: contraindicated unless benefits outweigh risks; discuss with specialist.
  • Handling precautions: use aseptic technique and protective equipment to prevent exposure.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Idarubicin can interact with other medicines, affecting its efficacy or safety profile.

Major Interactions (Avoid)

  • Anthracycline combination: concurrent use with other anthracyclines increases cardiotoxic risk.
  • CYP3A4 inhibitors: strong inhibitors (e.g., ketoconazole) may raise idarubicin plasma levels.
  • Live vaccines: immunosuppression may reduce vaccine efficacy and increase infection risk.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: enhanced bleeding risk due to thrombocytopenia.
  • Myelosuppressive agents: additive bone‑marrow suppression when combined with other cytotoxics.
  • Diuretics: may exacerbate fluid balance issues in patients with cardiac dysfunction.

Frequently Asked Questions

Idarubicin Accord contains the anthracycline idarubicin and is used in the treatment of acute myeloid leukemia (AML). It is administered as part of induction or consolidation chemotherapy regimens to eradicate leukemic cells in adult patients.

Idarubicin intercalates into DNA and stabilizes the topoisomerase II‑DNA complex, preventing the re‑ligation of DNA strands after cleavage. This creates permanent double‑strand breaks, leading to apoptosis of rapidly dividing cancer cells, particularly leukemic blasts.

The dosing regimen for Idarubicin Accord is determined by the prescribing oncologist based on the patient’s clinical condition, disease stage, and treatment protocol. Only a qualified healthcare professional should set the dose and schedule.

Idarubicin is classified as contraindicated in pregnancy and breastfeeding unless the potential therapeutic benefit justifies the risk. It can cross the placenta and is excreted in breast milk, so use should be avoided and discussed with a specialist.

To request Idarubicin 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 and import documentation.

Idarubicin belongs to the anthracycline class and offers higher lipophilicity than doxorubicin, potentially improving cellular uptake. Compared with other agents such as cytarabine, it provides a distinct mechanism of DNA damage, and is often combined with them for synergistic effect in AML protocols.

Idarubicin Accord should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Prior to administration, allow the product to reach room temperature if required, and handle using aseptic technique and appropriate protective equipment.

Idarubicin Accord is given by intravenous infusion under the supervision of a qualified healthcare professional. The infusion rate and duration are set by the treating physician, and patients are monitored for infusion‑related reactions and vital signs throughout the procedure.

The most serious risks include cardiotoxicity, which can lead to irreversible heart failure, severe myelosuppression causing life‑threatening infections or bleeding, and rare hypersensitivity reactions such as anaphylaxis. Continuous monitoring and supportive care are essential to manage these risks.

Idarubicin Accord should not be used in patients with known hypersensitivity to idarubicin or other anthracyclines, in those with uncontrolled cardiac disease, or in pregnant or breastfeeding women unless the benefits outweigh the risks. It is also contraindicated in individuals with severe hepatic impairment without dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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