GNH USA

Europe — EMA

Idarubicine Accord

GNH USA supplies Idarubicine Accord (Idarubicin), a anthracycline antibiotic for acute myeloid leukemia and acute lymphoblastic leukemia.

Idarubicin Hydrochloride

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What is Idarubicin Hydrochloride?

Idarubicin, the active ingredient in Idarubicine Accord, is an anthracycline antibiotic presented as an injection for intravenous use. It treats acute myeloid leukemia and acute lymphoblastic leukemia in adult and pediatric patients.

GNH USA supplies Idarubicine Accord as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Idarubicin Hydrochloride used for?

Idarubicin is an anthracycline antineoplastic agent used in the treatment of hematologic malignancies.

- Acute myeloid leukemia (AML): induces remission by targeting rapidly dividing leukemic blasts. - Relapsed or refractory AML: provides an alternative therapeutic option when standard regimens fail. - Acute lymphoblastic leukemia (ALL): contributes to disease control through DNA damage in lymphoid blasts.

What are the side effects of Idarubicin Hydrochloride?

Idarubicine Accord may cause a range of adverse reactions.

Common Side Effects: - Nausea and vomiting: gastrointestinal upset common during infusion. - Myelosuppression: reduced white blood cells, platelets, and red cells. - Alopecia: hair loss that may be temporary. - Fatigue: generalized tiredness during treatment. - Mucositis: inflammation of the mouth and gastrointestinal lining.

Serious or Rare Side Effects: - Cardiotoxicity: irreversible heart damage, especially at high cumulative doses. - Severe neutropenia or febrile neutropenia: increased infection risk. - Secondary malignancies: rare development of new cancers. - Hepatic toxicity: elevated liver enzymes or liver dysfunction. - Severe infusion reactions: hypotension, dyspnea, or anaphylaxis.

What precautions apply to Idarubicin Hydrochloride?

Before initiating therapy, clinicians should assess patient‑specific risk factors and monitor organ function.

- Cardiac monitoring: baseline and periodic ejection fraction assessment due to risk of cardiotoxicity. - Hematologic monitoring: regular complete blood counts to detect myelosuppression. - Renal and hepatic function: evaluate and adjust therapy in patients with impairment. - Concomitant cardiotoxic agents: avoid or use with caution to limit additive heart damage. - Pregnancy and lactation: use only if potential benefits justify potential risks; data are limited. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Idarubicin Hydrochloride interact with?

Idarubicine Accord can interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Other anthracyclines: additive cardiotoxicity. - Live vaccines: heightened infection risk due to immunosuppression. - Strong CYP3A4 inhibitors: may increase idarubicin exposure. - Chest radiation therapy: synergistic cardiac toxicity.

Moderate Interactions (Monitor Closely): - Azole antifungals (e.g., fluconazole): may alter metabolism. - Cyclophosphamide: overlapping myelosuppressive effects. - Granulocyte‑colony stimulating factors: may affect blood count recovery.

Frequently asked questions

What is Idarubicine Accord used for?+
Idarubicine Accord is an intravenous formulation of idarubicin used primarily to treat acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). It is administered in hospital or oncology centre settings as part of a chemotherapy regimen designed to eradicate malignant blood cells.
How does Idarubicin work?+
Idarubicin intercalates into DNA and blocks topoisomerase II, preventing the resealing of DNA strands during replication. This creates double‑strand breaks and generates free radicals, leading to apoptosis of rapidly dividing cancer cells, especially leukemic blasts.
What is the usual dose of Idarubicine Accord?+
The exact dose of Idarubicine Accord is determined by the prescribing oncologist based on the patient’s age, disease status, prior therapies, and organ function. Dosing regimens are individualized and should follow established clinical protocols.
Is Idarubicine Accord safe during pregnancy or breastfeeding?+
Safety data for idarubicin in pregnancy and lactation are limited. The drug should only be used when the potential therapeutic benefit justifies the potential risk to the fetus or infant, and it is generally avoided unless no safer alternatives exist.
How do I order Idarubicine Accord from GNH USA?+
To order Idarubicine Accord, 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 cold‑chain if needed), and import documentation.
How does Idarubicine Accord compare with other anthracyclines?+
Idarubicin is structurally related to daunorubicin but is more lipophilic, allowing better cellular uptake and potentially greater potency. Compared with other anthracyclines, it may have a slightly different toxicity profile, but cardiotoxicity and myelosuppression remain common concerns across the class.
What are the recommended storage conditions for Idarubicine Accord?+
Idarubicine Accord should be stored refrigerated between 2 °C and 8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution, as these actions can degrade the product.
How is Idarubicine Accord administered?+
Idarubicine Accord is given by intravenous infusion, typically over a period of 30 to 60 minutes, under the supervision of qualified healthcare professionals. Infusion rates and schedules are defined by the treating physician and may be adjusted based on patient tolerance and response.
What are the most serious risks to watch for with Idarubicine Accord?+
The most serious risks include cardiotoxicity (which can be irreversible), severe myelosuppression leading to infection or bleeding, and rare but life‑threatening infusion reactions. Patients should be monitored closely for cardiac function, blood counts, and any signs of hypersensitivity during treatment.
Who should not use Idarubicine Accord?+
Idarubicine Accord is contraindicated in patients with known hypersensitivity to idarubicin or other anthracyclines, and in those with severe pre‑existing cardiac dysfunction (e.g., low ejection fraction). Caution is also advised for individuals with uncontrolled infections or significant hepatic impairment.
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
Idarubicin Hydrochloride
Route
Intravenous Use
Manufacturer
Accord Healthcare France Sas
Origin
EU

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