Product image of Lenalidomida Generis (Lenalidomide) supplied by GNH India

Lenalidomida Generis

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomida Generis (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomida Generis, is an Immunomodulatory imide drug (IMiD) presented as an oral tablet for oral use. It is employed in the treatment of certain hematologic cancers, including multiple myeloma, myelodysplastic syndromes with del(5q), and mantle cell lymphoma.

GNH India supplies Lenalidomida Generis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU GMP standards and provides reliable logistics for bulk and kit‑size orders across multiple continents.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

  • Lenalidomide is used in hematologic malignancies that involve abnormal plasma or lymphoid cells.
  • Multiple Myeloma: improves progression‑free survival and overall response rates in patients with relapsed or refractory disease.
  • Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and induces cytogenetic remission.
  • Mantle Cell Lymphoma: contributes to disease control in patients receiving combination therapy.

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 transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), leading to reduced proliferation of malignant cells, enhanced immune‑mediated tumor cell killing, inhibition of angiogenesis, and modulation of cytokine production. It also affects the tumor microenvironment by decreasing stromal support and altering adhesion molecule expression.

Side Effects

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

Common Side Effects

  • Neutropenia: decreased neutrophil count leading to infection risk.
  • Thrombocytopenia: reduced platelet levels causing easy bruising.
  • Fatigue: persistent tiredness affecting daily activities.
  • Nausea: feeling of sickness often accompanied by vomiting.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Severe neutropenia: profound drop in neutrophils with febrile episodes.
  • Secondary primary malignancies: emergence of new cancers unrelated to original disease.

Precautions & Warnings

  • When prescribing Lenalidomida Generis, clinicians should observe several safety measures.
  • Monitor blood counts: perform regular CBC to detect neutropenia or thrombocytopenia.
  • Assess thrombotic risk: consider prophylactic anticoagulation in high‑risk patients.
  • Contraindicated in pregnancy: avoid use due to potential teratogenicity; ensure effective contraception.
  • Infection vigilance: monitor for signs of infection and manage promptly.
  • Drug interaction awareness: review concomitant medications that affect CYP3A4 or increase clot risk.
  • Store at ambient temperature: keep below 25 °C in original container, protect from moisture and light.

Avoid Interactions

Lenalidomida Generis can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase lenalidomide exposure.
  • Anticoagulants combined with high thrombotic risk: may exacerbate clot formation.
  • Teratogenic agents used concurrently: additive risk of birth defects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy.
  • P‑gp inhibitors (e.g., amiodarone): could modestly raise plasma levels.
  • Live vaccines: immunomodulation may diminish vaccine effectiveness.

Frequently Asked Questions

Lenalidomida Generis is the generic form of lenalidomide, an oral immunomodulatory agent indicated for treatment of certain hematologic cancers such as multiple myeloma, myelodysplastic syndromes with deletion 5q, and mantle‑cell lymphoma, usually as part of combination therapy prescribed by a hematologist or oncologist.

Lenalidomide binds to the cereblon component of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This leads to ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos, which reduces malignant cell proliferation, enhances immune‑mediated tumor cell killing, inhibits angiogenesis, and modulates cytokine production.

The dosage of Lenalidomida Generis is individualized by the prescribing physician based on the specific indication, disease stage, renal function, and concomitant therapies. The prescriber determines the appropriate strength, schedule and any necessary dose adjustments, and patients should follow the written prescription exactly.

Lenalidomida Generis is classified as having unknown pregnancy and lactation categories, and animal studies suggest a risk of fetal harm. It is generally contraindicated in pregnancy; women of child‑bearing potential must use effective contraception and undergo regular pregnancy testing. Breastfeeding is not recommended while receiving the drug.

To place an order, 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 (including any cold‑chain requirements) and the necessary import documentation.

The primary alternative to lenalidomide is thalidomide, another immunomodulatory imide drug. Lenalidomide generally offers greater potency with a more favorable safety profile, particularly lower rates of peripheral neuropathy, but both share risks of thrombosis and teratogenicity. Choice of therapy depends on disease characteristics, prior treatment history and individual patient tolerance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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