Product image of Myleran (Busulfan) supplied by GNH India

Myleran

Active Ingredient:
Busulfan
Origin:
EU

Myleran (Busulfan)

Busulfan, the active ingredient in Myleran, is an alkylating agent presented as a tablet for oral use. It is approved in the European Union for the treatment of chronic myeloid leukemia and as part of conditioning regimens prior to bone marrow transplantation, where it provides myeloablation to enable donor stem‑cell engraftment.

GNH India supplies Myleran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance and reliable global logistics.

Manufacturer / TM Owner

Aspen Pharma Trading Limited

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Indications & Clinical Uses

Busulfan is an alkylating antineoplastic agent used in hematologic malignancies and transplant conditioning.

  • Chronic myeloid leukemia: reduces leukemic cell proliferation and helps achieve disease control.
  • Acute myeloid leukemia (pre‑transplant conditioning): eradicates residual malignant cells before hematopoietic stem cell transplantation.
  • Bone marrow transplantation conditioning: provides myeloablation to facilitate engraftment of donor stem cells.

How It Works

  • Busulfan exerts its antineoplastic effect by alkylating DNA bases, creating interstrand cross‑links that block DNA replication and transcription. The resulting DNA damage triggers apoptosis in rapidly dividing hematopoietic cells, leading to myeloablation and suppression of malignant clones.

Side Effects

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

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset commonly reported during therapy.
  • Oral mucositis: painful inflammation of the mouth lining.
  • Fever and chills: may indicate early infection or cytokine release.
  • Alopecia: temporary hair loss during treatment.
  • Skin rash: mild erythematous eruptions.

Serious or Rare Side Effects

  • Pulmonary fibrosis: progressive scarring of lung tissue that can impair breathing.
  • Hepatic veno‑occlusive disease: blockage of small hepatic veins leading to liver dysfunction.
  • Seizures: central nervous system events, especially at high plasma concentrations.
  • Severe bone marrow suppression: pancytopenia with heightened infection and bleeding risk.
  • Secondary malignancies: rare development of new cancers after prolonged exposure.
  • Life‑threatening infections: opportunistic infections due to profound immunosuppression.

Precautions & Warnings

Before initiating Busulfan therapy, several safety measures should be observed.

  • Monitor blood counts: perform regular complete blood count assessments to detect myelosuppression.
  • Assess liver function: check hepatic enzymes and bilirubin prior to and during treatment.
  • Evaluate pulmonary status: obtain baseline lung function tests, especially in patients with prior lung disease.
  • Avoid use in known hypersensitivity: discontinue if allergic reactions occur.
  • Use effective contraception: advise patients to employ reliable birth control during treatment and for a defined period afterward.
  • Store at ambient temperature: keep below 25°C in the original packaging, protect from moisture.

Avoid Interactions

Busulfan interacts with several medicines that can alter its efficacy or toxicity.

Major Interactions (Avoid)

  • Concomitant thiotepa: combined myeloablation increases risk of severe toxicity.
  • Azathioprine: additive myelosuppressive effect may lead to profound pancytopenia.
  • Phenytoin: enzyme induction reduces Busulfan plasma levels, compromising efficacy.
  • High‑dose cyclophosphamide: overlapping toxicities heighten organ damage risk.

Moderate Interactions (Monitor Closely)

  • Antifungal azoles (e.g., fluconazole): may raise Busulfan concentrations, requiring level monitoring.
  • Anticonvulsants such as carbamazepine: can modify Busulfan metabolism.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may affect platelet function and increase bleeding tendency.

Frequently Asked Questions

Myleran contains Busulfan, an alkylating chemotherapy drug indicated for the treatment of chronic myeloid leukemia and as part of conditioning regimens before bone marrow or stem‑cell transplantation. In these settings it helps eradicate malignant cells and prepares the patient’s marrow for donor cell engraftment.

Busulfan alkylates DNA bases, forming cross‑links that prevent DNA replication and transcription. This DNA damage triggers apoptosis in rapidly dividing cells, especially hematopoietic progenitors, resulting in myeloablation and suppression of leukemic clones.

The exact dose of Myleran is individualized by the prescribing physician based on factors such as the patient’s body surface area, disease indication, treatment protocol, organ function and concurrent therapies. No fixed regimen is provided here; dosing decisions are made by qualified healthcare professionals.

Safety data for Busulfan in pregnancy and lactation are limited, and the drug is generally considered contraindicated because of potential teratogenic and embryotoxic effects. Women of child‑bearing potential should use effective contraception during treatment and for a period recommended by their clinician. Breastfeeding is not advised while on Busulfan.

To request Myleran, visit the product page on gnhindia.com, enter the required quantity, and submit the enquiry form. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Busulfan is often compared with cyclophosphamide or total body irradiation as part of conditioning regimens. Busulfan provides potent myeloablation with a relatively predictable pharmacokinetic profile, but it carries specific risks such as pulmonary fibrosis and hepatic veno‑occlusive disease. Choice of agent depends on disease protocol, patient comorbidities and institutional experience.

Myleran tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the product out of reach of children and avoid storing in bathrooms or other humid environments.

Myleran is supplied as oral tablets that are taken with a full glass of water. The prescribing physician determines the dosing schedule, which may involve single or divided doses over several days. Patients should follow the exact instructions provided by their healthcare team.

The most critical adverse events include pulmonary fibrosis, hepatic veno‑occlusive disease, severe bone‑marrow suppression leading to pancytopenia, seizures at high plasma levels, and opportunistic infections. Early recognition of respiratory symptoms, liver dysfunction or unexplained fever is essential, and patients should seek immediate medical attention if these occur.

Myleran is contraindicated in individuals with known hypersensitivity to Busulfan or any tablet excipients, in patients with severe hepatic or pulmonary impairment, and in those with uncontrolled infections. It should also be avoided in pregnant or nursing women unless the benefits clearly outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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