Product image of Lenalidomid Alkaloid-Int (Lenalidomide) supplied by GNH India

Lenalidomid Alkaloid-Int

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomid Alkaloid-Int (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomid Alkaloid-Int, is an immunomodulatory imide drug (IMiD) presented as an oral formulation for oral use. It treats multiple myeloma, mantle cell lymphoma, and myelodysplastic syndromes with 5q deletion in adult patients.

GNH India supplies Lenalidomid Alkaloid-Int as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, ensuring consistent quality, regulatory compliance, and reliable logistics for oncology therapeutics. The company adheres to stringent Good Distribution Practice standards and provides comprehensive support for product registration, customs clearance, and cold‑chain management where required.

Manufacturer / TM Owner

Alkaloid-Int D.O.O.

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Indications & Clinical Uses

Lenalidomide is employed in hematologic malignancies and related myelodysplastic conditions.

  • Multiple myeloma: improves progression‑free survival and overall response rates in relapsed or refractory disease.
  • Mantle cell lymphoma: induces tumor regression and prolongs remission when combined with standard chemotherapy.
  • Myelodysplastic syndromes with 5q deletion: corrects ineffective hematopoiesis and reduces transfusion dependence.

How It Works

  • Lenalidomide binds to the cereblon subunit of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This interaction promotes ubiquitination and proteasomal degradation of the transcription factors Ikaros (IKZF1) and Aiolos (IKZF3). The resulting loss of these factors leads to anti‑angiogenic activity, modulation of cytokine production, enhanced natural‑killer‑cell‑mediated cytotoxicity, direct inhibition of malignant plasma‑cell proliferation, and tumor microenvironment remodeling.

Side Effects

Lenalidomide may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Fatigue
  • Diarrhea
  • Rash
  • Constipation

Serious or Rare Side Effects

  • Thromboembolic events such as deep‑vein thrombosis or pulmonary embolism
  • Severe neutropenia or leukopenia
  • Teratogenic effects leading to fetal harm

Precautions & Warnings

Key precautions should be observed when prescribing lenalidomide to minimize risks.

  • Pregnancy: contraindicated; category X, avoid use in pregnant women.
  • Thrombosis risk: assess patient history and consider prophylactic anticoagulation.
  • Hematologic monitoring: perform regular CBC to detect neutropenia or anemia.
  • Renal impairment: adjust therapy and monitor renal function.
  • Drug interactions: avoid concomitant use with strong CYP3A4 inducers without supervision.
  • Store at ambient temperature: keep below 25°C in original container, protect from moisture.

Avoid Interactions

Lenalidomide can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce lenalidomide exposure.
  • Anticoagulants (warfarin): increased risk of bleeding when combined with lenalidomide.
  • Immunosuppressants (e.g., cyclosporine): heightened risk of severe cytopenias.

Moderate Interactions (Monitor Closely)

  • P‑glycoprotein inhibitors (e.g., verapamil): may increase plasma levels.
  • NSAIDs: may exacerbate thrombocytopenia.
  • Hormonal contraceptives: reduced efficacy, advise alternative non‑hormonal methods.

Frequently Asked Questions

Lenalidomid Alkaloid-Int contains the active ingredient lenalidomide and is indicated for the treatment of adult patients with multiple myeloma, mantle cell lymphoma, and myelodysplastic syndromes that carry a deletion of chromosome 5q. These indications reflect its role as an antineoplastic agent in hematologic cancers.

Lenalidomide exerts its effect by binding to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex. This binding changes the complex’s target profile, leading to the ubiquitination and degradation of transcription factors Ikaros and Aiolos. The loss of these proteins produces anti‑angiogenic, immunomodulatory, and direct anti‑tumor actions.

The specific dose of Lenalidomid Alkaloid-Int is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Healthcare professionals follow approved labeling and local guidelines to set the appropriate regimen.

Lenalidomid Alkaloid-Int is classified as pregnancy category X, meaning it is contraindicated in pregnancy because of known teratogenic risk. It is also not recommended for breastfeeding mothers, as the drug may be excreted in milk and could harm the infant.

To place an order, visit the product page on gnhindia.com and submit an enquiry with the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide. The sales

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GNH India Pharmaceuticals Limited

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Last updated:

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