Product image of Lenalidomide Eugia (Uk) (Lenalidomide) supplied by GNH India

Lenalidomide Eugia (Uk)

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Eugia (Uk) (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Eugia (Uk), is an immunomodulatory imide drug (IMiD) presented as an oral formulation for oral use. It treats multiple myeloma and myelodysplastic syndromes with del(5q) in adult patients.

GNH India supplies Lenalidomide Eugia (Uk) as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Eugia (Uk) Ltd

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Indications & Clinical Uses

Lenalidomide is used in hematologic malignancies that respond to immunomodulatory therapy.

  • Multiple Myeloma: improves progression‑free and overall survival when combined with dexamethasone.
  • Relapsed/Refractory Multiple Myeloma: restores disease control after prior therapies.
  • Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and cytopenias.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering substrate specificity and leading to degradation of transcription factors Ikaros and Aiolos. This results in modulation of the immune response, inhibition of angiogenesis, and induction of apoptosis in malignant plasma cells and dysplastic progenitors.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhoea: loose stools that may require fluid replacement.
  • Constipation: reduced bowel movements causing discomfort.
  • Rash: mild skin eruptions that resolve with or without treatment.
  • Nausea: feeling of sickness that may be transient.
  • Peripheral neuropathy: tingling or numbness in extremities.

Serious or Rare Side Effects

  • Neutropenia: dangerously low neutrophil counts increasing infection risk.
  • Thrombocytopenia: low platelet levels leading to bleeding tendencies.
  • Venous thromboembolism: formation of blood clots in deep veins or lungs.
  • Secondary primary malignancies: emergence of new cancers unrelated to the original disease.
  • Severe allergic reactions: anaphylaxis or Stevens‑Johnson syndrome.
  • Hepatotoxicity: elevated liver enzymes indicating liver injury.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for toxicity.

  • Monitor blood counts: perform regular CBCs to detect neutropenia or thrombocytopenia.
  • Assess thromboembolic risk: consider prophylactic anticoagulation in high‑risk patients.
  • Contraindicated in pregnancy: enforce strict contraception and avoid use in pregnant women.
  • Adjust for renal impairment: dose may need modification based on creatinine clearance.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lenalidomide can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce lenalidomide exposure.
  • Live vaccines: increased risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (warfarin, DOACs): may heighten bleeding risk when combined with thrombocytopenia.
  • NSAIDs: can exacerbate platelet suppression.
  • Other immunomodulatory agents (e.g., pomalidomide): additive myelosuppression.
  • P‑glycoprotein inhibitors (e.g., verapamil): may increase plasma concentrations.

Frequently Asked Questions

Lenalidomide Eugia (Uk) is indicated for the treatment of adult patients with multiple myeloma, including relapsed or refractory disease, and for myelodysplastic syndromes that carry the del(5q) chromosomal abnormality. In these settings, the drug helps control disease progression and can reduce the need for blood transfusions.

Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering its substrate specificity. This triggers degradation of transcription factors such as Ikaros and Aiolos, leading to enhanced immune activation, inhibition of new blood‑vessel formation, and programmed cell death of malignant plasma cells and dysplastic progenitors.

The specific dose and schedule of Lenalidomide Eugia (Uk) are determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and prior therapies. Clinicians tailor the regimen to achieve optimal efficacy while minimizing toxicity.

Lenalidomide is contraindicated in pregnancy because it can cause fetal harm. Women of childbearing potential must use effective contraception before, during, and after treatment. Safety during breastfeeding has not been established, and nursing is generally discouraged while on therapy.

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 necessary import documentation.

Lenalidomide belongs to the immunomodulatory imide drug class, offering a distinct mechanism from proteasome inhibitors or monoclonal antibodies. It is often combined with dexamethasone and can be used after failure of other agents, providing an oral option that targets both the tumor micro‑environment and malignant cells.

Store Lenalidomide Eugia (Uk) at room temperature, below 25 °C, in the original blister or bottle. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Lenalidomide Eugia (Uk) is taken orally, usually once daily on a schedule prescribed by the treating physician. The tablets should be swallowed whole with water and taken at the same time each day, unless otherwise directed.

The most serious risks include severe neutropenia and thrombocytopenia, which can lead to life‑threatening infections or bleeding, and venous thromboembolism. Patients should be monitored regularly for blood‑cell counts and signs of clot formation, and appropriate prophylactic measures should be considered.

Lenalidomide should not be used by individuals who are pregnant, have uncontrolled infections, or have a known hypersensitivity to lenalidomide or any of its excipients. Caution is also advised in patients with severe renal impairment unless dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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