Product image of Nodriga (Dasatinib) supplied by GNH India

Nodriga

Active Ingredient:
Dasatinib
Origin:
EU

Nodriga (Dasatinib)

Dasatinib, the active ingredient in Nodriga, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is indicated for the treatment of chronic myeloid leukemia and Philadelphia chromosome‑positive acute lymphoblastic leukemia in adult patients.

GNH India supplies Nodriga as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Alkaloid-Int D.O.O.

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Indications & Clinical Uses

Dasatinib is a targeted tyrosine‑kinase inhibitor used in hematologic malignancies that involve BCR‑ABL or SRC family kinases.

  • Chronic Myeloid Leukemia (CML): helps achieve cytogenetic and molecular remission by blocking proliferative signaling in BCR‑ABL‑positive cells.
  • Philadelphia chromosome‑positive Acute Lymphoblastic Leukemia (Ph+ ALL): contributes to disease control by inhibiting the same oncogenic kinase pathways, supporting remission induction and maintenance.

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 inhibition disrupts signaling cascades that drive malignant cell proliferation, survival, and migration, leading to apoptosis of leukemic cells and reduced tumor burden.

Side Effects

Dasatinib may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: watery stools often occurring early in therapy.
  • Fatigue: persistent tiredness affecting daily activities.
  • Rash: skin erythema or pruritus.

Serious or Rare Side Effects

  • Pleural effusion: accumulation of fluid around the lungs requiring medical evaluation.
  • Pulmonary hypertension: elevated pressure in pulmonary arteries, potentially life‑threatening.
  • Severe bleeding: hemorrhage due to platelet dysfunction or thrombocytopenia.

Precautions & Warnings

Patients receiving Dasatinib should be monitored closely for safety concerns.

  • Blood counts: perform regular CBC to detect myelosuppression.
  • Liver function: assess hepatic enzymes periodically.
  • Cardiac monitoring: evaluate for signs of pulmonary hypertension or heart failure.
  • Drug interactions: avoid strong CYP3A4 inhibitors that may increase exposure.
  • Storage: Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Dasatinib interacts with several medication classes that can alter its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise dasatinib plasma levels.
  • Proton pump inhibitors: can reduce absorption of the oral tablet.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin): may modestly increase exposure.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may lower drug concentrations.
  • QT‑prolonging agents (e.g., quinidine): monitor cardiac rhythm.

Frequently Asked Questions

Nodriga, whose active ingredient is dasatinib, is prescribed for adults with chronic myeloid leukemia (CML) and for patients with Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL). Both diseases involve abnormal tyrosine‑kinase activity that dasatinib specifically inhibits.

Dasatinib blocks the ATP‑binding sites of BCR‑ABL and SRC family tyrosine kinases. By preventing these enzymes from phosphorylating downstream proteins, the drug stops the signaling pathways that drive uncontrolled growth of malignant blood cells, leading to cell death and disease control.

The dose of Nodriga is individualized by the prescribing clinician based on disease phase, patient weight, renal and hepatic function, and other clinical factors. Only a qualified healthcare professional should determine the appropriate dosing regimen.

Safety data for dasatinib in pregnancy and lactation are limited, and the drug may pose risks to the fetus or infant. It is generally advised to avoid use during pregnancy and while nursing unless the potential benefit justifies the potential risk, as determined by a physician.

To request Nodriga, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. 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.

Nodriga (dasatinib) is a second‑generation BCR‑ABL inhibitor with activity against a broader range of SRC family kinases compared with first‑generation agents like imatinib. This broader spectrum can translate into efficacy in patients resistant to earlier drugs, though safety profiles differ and must be evaluated individually.

Nodriga should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain stability and potency.

Nodriga is taken orally, usually as a whole tablet with water. It may be taken with or without food, but patients should follow the specific instructions provided by their healthcare provider to ensure consistent absorption.

Serious risks include pleural effusion, pulmonary hypertension, severe bleeding, and profound myelosuppression that can lead to infection or anemia. Patients should be monitored regularly for respiratory symptoms, bleeding signs, and blood count changes.

Nodriga is contraindicated in patients with known hypersensitivity to dasatinib or any of its excipients. Caution is also advised for individuals with uncontrolled cardiac disease, severe hepatic impairment, or those taking strong CYP3A4 inhibitors without appropriate dose adjustments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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