Product image of Lenalidomide Olainfarm (Lenalidomide) supplied by GNH India

Lenalidomide Olainfarm

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Olainfarm (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Olainfarm, is an immunomodulatory drug presented as an oral formulation for oral use. It is indicated for the treatment of multiple myeloma, mantle cell lymphoma, and myelodysplastic syndromes with deletion 5q, typically in adult patients who have received prior therapy.

GNH India supplies Lenalidomide Olainfarm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory documentation for import.

Manufacturer / TM Owner

Jsc Olainfarm

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Indications & Clinical Uses

Lenalidomide Olainfarm is employed in hematologic malignancies and related disorders where immunomodulation and anti‑angiogenic activity are therapeutic goals.

  • Multiple Myeloma: improves progression‑free survival and overall response rates in patients with relapsed or refractory disease.
  • Mantle Cell Lymphoma: contributes to disease control when combined with other agents in relapsed settings.
  • Myelodysplastic Syndromes with del(5q): induces transfusion independence and cytogenetic remission in eligible patients.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4 E3 ubiquitin ligase complex, redirecting it to ubiquitinate the transcription factors Ikaros and Aiolos. Their degradation alters downstream signaling, leading to enhanced T‑cell and NK‑cell activation, inhibition of angiogenesis, and direct anti‑tumor effects through apoptosis and cell‑cycle arrest in malignant plasma cells and lymphocytes.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: lowered platelet levels leading to bruising.
  • Anemia: decreased red blood cells causing weakness.
  • Diarrhea: loose stools that may require supportive care.
  • Rash: mild skin eruptions.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Severe neutropenia or thrombocytopenia: profound marrow suppression.
  • Secondary primary malignancies: emergence of new cancers.
  • Severe liver injury: marked elevation of hepatic enzymes.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: life‑threatening skin reactions.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for known risks.

  • Monitor blood counts: perform regular CBCs to detect cytopenias.
  • Assess thromboembolic risk: consider prophylactic anticoagulation in high‑risk patients.
  • Contraindicated in pregnancy: enforce strict contraception for both sexes.
  • Adjust for renal impairment: dose modifications may be required based on creatinine clearance.
  • Avoid live vaccines: immunosuppression can reduce vaccine efficacy.
  • Store at below 25°C: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Lenalidomide can interact with several drug classes, necessitating careful review of concomitant medications.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Antiplatelet agents (e.g., aspirin, clopidogrel): may heighten bleeding tendency.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): potential additive renal toxicity.
  • Other immunomodulatory agents (e.g., pomalidomide, thalidomide): can cause additive myelosuppression.

Frequently Asked Questions

Lenalidomide Olainfarm is prescribed for adult patients with multiple myeloma, mantle cell lymphoma, and myelodysplastic syndromes that carry a deletion of chromosome 5q. In each indication, the drug aims to control disease progression, improve response rates, and, in the case of del(5q) syndromes, achieve transfusion independence.

Lenalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, causing the targeted degradation of the transcription factors Ikaros and Aiolos. This leads to enhanced immune cell activity, inhibition of new blood‑vessel formation, and direct anti‑tumor effects such as apoptosis and cell‑cycle arrest in malignant cells.

The prescribed dose is individualized by the treating physician based on the specific indication, prior therapies, and the patient’s renal function, hematologic parameters, and overall health status. No universal dosing schedule is provided; clinicians adjust the regimen to balance efficacy with safety.

Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because of a high risk of fetal harm. Women of child‑bearing potential must use effective contraception, and breastfeeding is not recommended while taking 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 necessary import documentation.

Lenalidomide shares the same class (immunomodulatory drug) as thalidomide and pomalidomide but generally offers a more favorable safety profile, especially regarding peripheral neuropathy. It is more potent than thalidomide in anti‑angiogenic activity and is often preferred for the approved indications, while pomalidomide is typically reserved for later‑line therapy in multiple myeloma.

Store the product at temperatures below 25 °C in its original container, protecting it from moisture and direct sunlight. Do not refrigerate or freeze the tablets, and keep them out of reach of children.

Lenalidomide Olainfarm is taken orally, usually once daily, with or without food, as directed by the prescriber. Tablets should be swallowed whole with a full glass of water and not crushed or chewed to maintain proper absorption.

The most critical risks include severe neutropenia or thrombocytopenia, which can lead to infections or bleeding, and venous thromboembolism such as deep‑vein thrombosis or pulmonary embolism. Patients should also be monitored for secondary primary malignancies and rare but severe skin reactions like Stevens‑Johnson syndrome.

Lenalidomide should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or its excipients, and patients with severe renal impairment unless dose‑adjusted by a specialist. It is also contraindicated in patients receiving live vaccines due to the risk of infection.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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