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, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Alkaloid-Int D.O.O.

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Indications & Clinical Uses

  • Dasatinib targets BCR‑ABL‑positive leukemias and related tyrosine‑kinase driven disease pathways.
  • Chronic myeloid leukemia (CML): reduces disease progression and achieves cytogenetic responses in chronic phase patients.
  • Accelerated phase CML: provides hematologic and cytogenetic improvement in advanced disease.
  • Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL): enhances remission rates when used in combination regimens.

How It Works

  • Dasatinib binds to the ATP‑binding site of BCR‑ABL and Src family tyrosine kinases, inhibiting their enzymatic activity. This blockade prevents downstream signaling that drives malignant cell proliferation and survival, leading to apoptosis of leukemic cells and interruption of disease progression.

Side Effects

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

Common Side Effects

  • Myelosuppression: decreased white blood cells, neutrophils, or platelets.
  • Gastrointestinal upset: nausea, diarrhea, or abdominal pain.
  • Fluid retention: peripheral edema or pleural effusion.
  • Fatigue or generalized weakness.

Serious or Rare Side Effects

  • Pulmonary arterial hypertension.
  • Severe bleeding or hemorrhage.
  • Cardiac dysfunction, including left ventricular failure.
  • Severe infections such as sepsis.
  • Liver toxicity with elevated transaminases.

Precautions & Warnings

  • Patients should be monitored regularly for hematologic and organ‑specific toxicities.
  • Baseline assessment: obtain complete blood count and liver function tests before initiating therapy.
  • Infection risk: monitor for signs of infection and manage promptly.
  • Bleeding tendency: avoid concomitant anticoagulants unless medically necessary.
  • Cardiac monitoring: assess for symptoms of pulmonary hypertension or heart failure.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Dasatinib metabolism and transport can be affected by other medicines, requiring careful review.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce dasatinib exposure.
  • Antacids containing aluminum or magnesium: can decrease oral absorption.
  • Proton‑pump inhibitors: may lower bioavailability.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin, fluconazole): may increase plasma levels.
  • P‑glycoprotein inhibitors (e.g., verapamil): can raise dasatinib concentrations.
  • Concomitant anticoagulants: heightened bleeding risk warrants close observation.

Frequently Asked Questions

Nodriga, whose active ingredient is dasatinib, is prescribed for chronic myeloid leukemia (CML) and Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL). It targets the BCR‑ABL tyrosine‑kinase that drives these cancers, helping to control disease progression.

Dasatinib inhibits BCR‑ABL and Src family tyrosine kinases by binding to their ATP‑binding pockets. This blocks downstream signaling pathways that promote malignant cell growth and survival, leading to apoptosis of leukemic cells and reduction of disease activity.

The dose of Nodriga is individualized by the prescribing clinician based on the patient’s disease phase, prior therapy, and tolerance. Only a qualified healthcare professional can determine the appropriate regimen and any necessary adjustments.

Safety data for dasatinib in pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant. Women of child‑bearing potential should use effective contraception during treatment.

To request Nodriga, submit an enquiry on the product page at gnhindia.com with 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 tyrosine‑kinase inhibitor offering broader kinase inhibition than first‑generation agents like imatinib. It is often selected for patients with resistance or intolerance to earlier drugs, providing deeper and faster molecular responses in many cases.

Nodriga should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture and direct sunlight, and store out of reach of children.

Nodriga is taken orally, usually once daily with a low‑fat meal or a light snack to improve absorption. The tablet should be swallowed whole with water and not crushed or chewed.

Serious risks include pulmonary arterial hypertension, severe bleeding, cardiac dysfunction, and significant infections. Patients should be monitored regularly for signs of these events, and therapy should be adjusted or discontinued if they occur.

Nodriga is contraindicated in patients with known hypersensitivity to dasatinib or any component of the formulation. Caution is also advised for individuals with uncontrolled infections, severe cardiac disease, or pre‑existing pulmonary hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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