Product image of Mubucho (Dasatinib) supplied by GNH India

Mubucho

Active Ingredient:
Dasatinib
Origin:
EU

Mubucho (Dasatinib)

Dasatinib, the active ingredient in Mubucho, is a tyrosine kinase inhibitor presented as an oral formulation for oral administration. It targets BCR‑ABL and Src family kinases, providing therapeutic benefit in chronic myeloid leukemia and Philadelphia‑positive acute lymphoblastic leukemia in adult patients.

GNH India supplies Mubucho as a licensed, GDP‑compliant international pharmaceutical supplier, delivering the product to hospitals, oncology centres, transplant units and pharmacies worldwide with consistent quality and regulatory compliance.

Manufacturer / TM Owner

Zentiva Pharma Gmbh

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Indications & Clinical Uses

Dasatinib is indicated for hematologic malignancies driven by the BCR‑ABL fusion protein and related tyrosine‑kinase pathways.

  • Chronic myeloid leukemia (chronic phase): achieves cytogenetic and molecular remission by inhibiting leukemic cell proliferation.
  • Chronic myeloid leukemia (accelerated phase): reduces disease progression and improves hematologic response.
  • Chronic myeloid leukemia (blast phase): provides disease control when combined with other therapies.
  • Philadelphia‑positive acute lymphoblastic leukemia: induces remission by targeting BCR‑ABL‑positive blasts.

How It Works

  • Dasatinib binds competitively to the ATP‑binding site of BCR‑ABL and Src family tyrosine kinases, preventing phosphorylation of downstream substrates. This blockade halts proliferative signaling, induces apoptosis of malignant cells, and impairs leukemic cell migration and adhesion, leading to disease control in BCR‑ABL‑driven cancers.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Myelosuppression (neutropenia, thrombocytopenia)
  • Fluid retention or peripheral edema
  • Nausea
  • Diarrhea

Serious or Rare Side Effects

  • Pulmonary arterial hypertension
  • Severe hemorrhage
  • Cardiac dysfunction (e.g., left‑ventricular failure)

Precautions & Warnings

Careful monitoring is required before and during therapy.

  • Blood counts: perform regular complete blood count monitoring.
  • Fluid status: assess for signs of edema or pleural effusion.
  • Cardiac function: evaluate baseline and periodic cardiac assessment.
  • Hepatic impairment: use with caution in patients with severe liver dysfunction.
  • Pregnancy: avoid use unless potential benefit justifies the risk; safety data are limited.
  • Store at room temperature: keep in the original container, protect from moisture.

Avoid Interactions

Dasatinib may interact with several concomitant medications.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole)
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine)
  • QT‑prolonging agents (e.g., sotalol, quinidine)

Moderate Interactions (Monitor Closely)

  • Proton pump inhibitors (may reduce absorption)
  • Warfarin (potential alteration of INR)

Frequently Asked Questions

Mubucho contains dasatinib, which is prescribed for adults with chronic myeloid leukemia (any phase) and for Philadelphia‑positive acute lymphoblastic leukemia. The drug targets the BCR‑ABL fusion protein that drives these cancers, helping to achieve remission and control disease progression.

Dasatinib inhibits the ATP‑binding sites of BCR‑ABL and Src family tyrosine kinases. By blocking these enzymes, it stops downstream signaling that promotes malignant cell growth, survival, and migration, leading to apoptosis of leukemic cells and clinical disease control.

The dose of dasatinib is individualized by the prescribing clinician based on the specific indication, disease phase, patient weight, renal and hepatic function, and concomitant therapies. Only a qualified health‑care professional should determine the appropriate regimen.

Safety data for dasatinib in pregnancy and lactation are limited. The product is classified as pregnancy category unknown, and it is generally avoided unless the potential therapeutic benefit outweighs the possible risk to the fetus. Breastfeeding is not recommended while receiving treatment.

To place an enquiry, visit the product page on gnhindia.com, enter the required quantity, and submit the request. 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.

The primary alternative to dasatinib is imatinib, a first‑generation BCR‑ABL inhibitor. Dasatinib has a broader kinase inhibition profile, including Src family kinases, and often achieves faster and deeper molecular responses, especially in patients resistant or intolerant to imatinib. Choice of therapy depends on individual patient factors and physician judgment.

Mubucho should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and avoid exposure to high humidity or extreme temperatures.

Mubucho is taken orally, usually with a glass of water. It may be taken with or without food, but patients should follow the specific instructions provided by their prescriber to maintain consistent absorption.

The most serious adverse events include pulmonary arterial hypertension, severe bleeding, and cardiac dysfunction such as left‑ventricular failure. Patients should promptly report symptoms like shortness of breath, chest pain, unexplained bruising or bleeding, and swelling of the legs or ankles.

Mubucho is contraindicated in patients with known hypersensitivity to dasatinib or any of its excipients. It should be used with caution in individuals with severe hepatic impairment, uncontrolled cardiac disease, or those who are pregnant or breastfeeding unless the benefit clearly outweighs the risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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