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

Lenalidomide Zentiva

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Zentiva (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Zentiva, is a Immunomodulatory agent presented as a tablet for oral use. It is used to treat certain blood cancers, primarily in adult patients.
GNH India supplies Lenalidomide Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Zentiva Pharma Uk Limited

1
Pack/s
This product is added to your enquiry list

Request a Quote

Please fill out the form below and our team will get back to you shortly with pricing and further information.

A minimum order value applies. Our team will confirm the exact amount or quantity after reviewing your requirements.

Indications & Clinical Uses

Lenalidomide is an immunomodulatory antineoplastic that targets malignant plasma cells and dysplastic bone‑marrow clones.

  • Multiple myeloma: helps control disease progression and improve survival in patients who have received prior therapy.
  • Myelodysplastic syndromes: reduces transfusion dependence and may modify disease course in patients with del(5q) cytogenetic abnormality.

How It Works

  • Lenalidomide exerts its antitumor activity by binding to cereblon, a component of the E3 ubiquitin ligase complex, leading to degradation of transcription factors Ikaros and Aiolos. This results in inhibition of angiogenesis, modulation of cytokine production, and enhancement of natural killer and T‑cell mediated immune responses against malignant cells.

Side Effects

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

Common Side Effects

  • Neutropenia: reduced white blood cell count increasing infection risk.
  • Thrombocytopenia: lowered platelet count causing bleeding tendency.
  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhea: loose stools that may lead to dehydration.
  • Constipation: difficulty passing stools.
  • Rash: mild skin irritation or redness.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Severe neutropenia: profound immune suppression requiring medical intervention.
  • Hepatotoxicity: liver enzyme elevations indicating possible liver injury.
  • Secondary malignancies: emergence of new cancers during treatment.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmias: irregular heart rhythms in susceptible patients.

Precautions & Warnings

Patients receiving Lenalidomide should be monitored closely for safety concerns.

  • Blood monitoring: regular complete blood counts to detect cytopenias.
  • Thrombotic risk assessment: evaluate need for prophylactic anticoagulation.
  • Pregnancy avoidance: enforce strict contraception due to teratogenic potential.
  • Renal function: adjust therapy in patients with impaired kidney function.
  • Drug interaction review: assess concomitant medications for potential interactions.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase lenalidomide exposure.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): heightened risk of thromboembolic events.
  • Live vaccines: risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce drug effectiveness.
  • NSAIDs: potential additive effect on platelet inhibition.
  • Antihypertensives: monitor blood pressure as lenalidomide can cause fluid shifts.

Frequently Asked Questions

Lenalidomide Zentiva is indicated for the treatment of multiple myeloma and myelodysplastic syndromes, particularly those with a del(5q) chromosomal abnormality. It is used in adult patients who have received prior therapies and require disease control or reduction in transfusion dependence.

Lenalidomide binds to the cereblon component of the E3 ubiquitin ligase complex, leading to selective degradation of transcription factors Ikaros and Aiolos. This action suppresses angiogenesis, alters cytokine production, and boosts immune‑mediated anti‑tumor activity, thereby inhibiting the growth of malignant cells.

The specific dose of Lenalidomide Zentiva is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and prior treatment history. Healthcare professionals tailor the regimen to achieve optimal therapeutic benefit while minimizing risk.

Lenalidomide is classified as teratogenic and is contraindicated in pregnancy. Women of child‑bearing 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 needs), and necessary import documentation.

Lenalidomide is a second‑generation immunomodulatory agent, often compared with thalidomide. Compared with thalidomide, lenalidomide generally offers greater potency, a more favorable peripheral neuropathy profile, and a broader spectrum of activity in multiple myeloma and certain myelodysplastic syndromes.

Lenalidomide Zentiva tablets should be stored at room temperature, below 25 °C. Keep them in the original blister pack or container, protect from moisture and direct sunlight, and ensure they are out of reach of children.

Lenalidomide Zentiva is taken orally, usually once daily in the evening with or without food, as directed by the prescribing physician. The tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.

The most serious risks include severe neutropenia, thrombocytopenia, venous thromboembolism, hepatotoxicity, and the potential for secondary malignancies. Patients should be monitored regularly for blood count changes, liver function, and signs of clot formation.

Lenalidomide is contraindicated in patients with known hypersensitivity to the drug, in pregnant women, and in individuals who cannot adhere to strict contraceptive measures. Caution is also advised for patients with severe renal impairment or uncontrolled infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

Disclaimer

At GNH India, we aim to provide information that is expert-reviewed, accurate, and reliable. However, all content on this platform is intended for general informational purposes only and does not constitute professional medical advice, diagnosis, or treatment. While efforts are made to maintain accuracy and currency, the information may contain errors, omissions, or may not reflect the latest developments. Always consult a qualified healthcare professional regarding any medical concerns.

All product names, brand names, trademarks and registered trademarks displayed on this website are the property of their respective owners. This website and its operator are not affiliated with, endorsed by, or authorized by any such trade mark owners unless expressly stated. Any reference to product names or trademarks is made solely for descriptive and informational purposes. No commercial relationship, sponsorship, approval, or association with any trademark owner should be inferred. Information provided herein does not constitute promotion, advertising, or an offer for sale of any medicinal product and is intended solely for general informational purposes.

All trademarks and brand names displayed on this website are used strictly in accordance with the provisions of the Trade Marks Act, 1999, specifically Sections 30 and 30(1) governing fair use. Trademark ownership has been accurately attributed under the "Manufacturer/ TM Owner" section in compliance with statutory requirements.

Ordering Process

Simple, Secure, and Seamless

Learn how our streamlined ordering process guarantees fast, compliant, and reliable access to essential medicines worldwide.

Quote request form

01

Submit Quote Request Form

Tell us what medications you need by filling out our simple form and uploading a valid document.

Price estimate review

02

We Review & Send Estimate

Our licensed pharmacists will verify your details and provide you with a detailed cost estimate.

Secure payment

03

Confirm & Make Payment

Discuss any queries, approve the estimate, and complete your payment.

Worldwide delivery

04

Get Delivered

Your medicines, safely packed and delivered to your door or nearest airport — hassle-free.

Quality You Can Trust

Our internationally recognized certifications underscore our commitment to safety, quality, and excellence.