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 a 100 mg oral tablet for oral use. It treats 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 used to target BCR‑ABL–driven leukemias, providing disease‑specific therapy for several phases of chronic myeloid leukemia and for Ph+ acute lymphoblastic leukemia.

  • Chronic Myeloid Leukemia (chronic phase): improves hematologic, cytogenetic and molecular response in adult patients.
  • Chronic Myeloid Leukemia (accelerated phase): achieves disease control when used as first‑line or subsequent therapy.
  • Philadelphia chromosome‑positive Acute Lymphoblastic Leukemia: provides targeted inhibition of BCR‑ABL as part of combination regimens.

How It Works

  • Dasatinib binds to the ATP‑binding site of BCR‑ABL and Src family tyrosine kinases, preventing phosphorylation of downstream substrates. This blockade halts signaling pathways that drive malignant cell proliferation and survival, leading to apoptosis of leukemic cells while sparing most normal tissues.

Side Effects

Dasatinib may cause a range of adverse reactions, varying from mild to potentially serious.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Nausea: upset stomach often accompanied by loss of appetite.
  • Diarrhea: loose stools that may lead to dehydration.
  • Rash: skin irritation or redness.
  • Myelosuppression: reduced white blood cells, platelets or red cells.
  • Headache: mild to moderate head pain.

Serious or Rare Side Effects

  • Pleural effusion: fluid accumulation around the lungs causing breathing difficulty.
  • Pulmonary hypertension: elevated blood pressure in lung arteries, potentially life‑threatening.
  • Severe bleeding: uncontrolled hemorrhage due to platelet dysfunction.
  • Cardiac dysfunction: reduced heart contractility or arrhythmias.
  • Severe infections: opportunistic infections requiring hospitalization.
  • Liver toxicity: significant elevation of liver enzymes or hepatic failure.

Precautions & Warnings

When prescribing Dasatinib, clinicians should observe several safety measures to minimize risks.

  • Monitor blood counts: perform regular complete blood counts to detect cytopenias.
  • Assess cardiac function: obtain baseline echocardiogram and repeat if symptoms arise.
  • Evaluate liver function: check transaminases before treatment and periodically thereafter.
  • Avoid strong CYP3A4 inhibitors: concurrent use may increase dasatinib exposure.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light.

Avoid Interactions

Dasatinib interacts with several medicines that can alter its plasma concentration or increase toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): raise dasatinib levels and risk of adverse effects.
  • Antacids containing aluminum or magnesium: reduce oral absorption of dasatinib.
  • Co‑administration with other BCR‑ABL inhibitors: may lead to additive toxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): lower dasatinib exposure, reducing efficacy.
  • Proton pump inhibitors (e.g., omeprazole): may modestly affect gastric pH and absorption.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): increase bleeding risk when combined with dasatinib.

Frequently Asked Questions

Nodriga, whose active ingredient is dasatinib, is indicated for adult patients with chronic myeloid leukemia in the chronic or accelerated phase and for Philadelphia chromosome‑positive acute lymphoblastic leukemia. In each case the drug targets the BCR‑ABL fusion protein that drives malignant cell growth.

Dasatinib inhibits the ATP‑binding pocket of BCR‑ABL and Src family tyrosine kinases, blocking phosphorylation of downstream signaling proteins. This interruption stops the proliferative and survival signals in leukemic cells, leading to apoptosis while sparing most normal cells.

The prescribed dose of Nodriga is individualized by the treating physician based on the patient’s disease phase, prior therapy, renal and hepatic function, and tolerance. Only a qualified healthcare professional can set the appropriate dosing regimen.

The safety of dasatinib in pregnancy and lactation has not been established. It is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant, and decisions should be made in consultation with a specialist.

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.

Dasatinib is a second‑generation BCR‑ABL inhibitor that binds both active and inactive kinase conformations, offering greater potency and activity against many imatinib‑resistant mutations. Imatinib, a first‑generation inhibitor, has a narrower mutation coverage but a longer safety record. Choice of therapy depends on disease characteristics and prior treatment response.

Nodriga tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Do not store in areas of high humidity or direct sunlight, and keep out of reach of children.

Nodriga is taken orally, usually once daily, with or without food as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Clinicians and patients should be alert for pleural effusion, pulmonary hypertension, severe bleeding, significant drops in blood cell counts, and liver toxicity. Prompt medical evaluation is required if symptoms such as shortness of breath, unexplained bruising, jaundice or severe fatigue develop.

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, active severe infections, or those taking strong CYP3A4 inhibitors without appropriate dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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