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

Lenalidomide Mylan

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Mylan (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Mylan, is an immunomodulatory agent presented as a tablet for oral use. It treats multiple myeloma, myelodysplastic syndromes with del(5q), and mantle cell lymphoma in adult patients.

GNH India supplies Lenalidomide Mylan as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mylan Pharmaceuticals Limited

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Indications & Clinical Uses

Lenalidomide is used in hematologic malignancies and related disorders, targeting abnormal plasma cells and myeloid clones.

  • Multiple Myeloma: improves progression‑free survival and overall response rates in patients who have received prior therapy.
  • Myelodysplastic Syndromes (del(5q)): reduces transfusion dependence and can lead to cytogenetic remission in eligible adults.
  • Mantle Cell Lymphoma: used in combination regimens to achieve disease control in relapsed or refractory cases.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4 E3 ubiquitin ligase complex, altering substrate specificity. This leads to degradation of transcription factors Ikaros and Aiolos, resulting in anti‑angiogenic, immunomodulatory, and direct anti‑tumor effects that inhibit proliferation of malignant plasma cells and myeloid clones.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhea: loose stools that may require fluid replacement.
  • Nausea: upset stomach often occurring after dosing.
  • Rash: mild skin eruptions or itching.
  • Constipation: difficulty passing stool.
  • Peripheral edema: swelling of extremities.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Severe neutropenia: marked reduction in neutrophil count increasing infection risk.
  • Severe thrombocytopenia: low platelet counts leading to bleeding.
  • Secondary primary malignancies: emergence of new cancers.
  • Hepatotoxicity: elevated liver enzymes or liver injury.

Precautions & Warnings

Before initiating Lenalidomide, several safety considerations should be reviewed.

  • Pregnancy risk: contraindicated in pregnancy (Category X); ensure effective contraception.
  • Thromboembolic prophylaxis: assess need for anticoagulation in high‑risk patients.
  • Renal function: adjust monitoring in patients with impaired kidney function.
  • Hematologic monitoring: perform regular CBC to detect neutropenia or thrombocytopenia.
  • Infection risk: monitor for signs of infection and manage promptly.
  • Store at ambient temperature: keep tablets below 25°C in the original container, protect from moisture and light.

Avoid Interactions

Lenalidomide can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may reduce plasma concentrations of lenalidomide.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding when combined with lenalidomide.

Moderate Interactions (Monitor Closely)

  • P-glycoprotein inhibitors (e.g., verapamil): may increase lenalidomide exposure.
  • Immunosuppressants (e.g., cyclosporine): may enhance immunomodulatory effects.
  • Vaccines (live attenuated): reduced efficacy; avoid concurrent administration.

Frequently Asked Questions

Lenalidomide Mylan is indicated for the treatment of adult patients with multiple myeloma, myelodysplastic syndromes that have a deletion of chromosome 5q (del(5q)), and mantle cell lymphoma, typically in relapsed or refractory disease settings.

Lenalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, modifying its activity. This triggers degradation of specific transcription factors, leading to anti‑angiogenic, immunomodulatory, and direct anti‑tumor actions that suppress malignant cell growth.

The appropriate dose of Lenalidomide is individualized by the prescribing clinician based on the specific indication, disease stage, renal function, and patient tolerance. Patients should follow the exact regimen provided by their healthcare professional.

Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal harm. It is also not recommended for breastfeeding mothers, as it may be excreted in breast milk and affect the infant.

To order Lenalidomide Mylan, 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 and any necessary import documentation.

Lenalidomide shares a similar mechanism with thalidomide and pomalidomide but generally offers greater potency and a more favorable safety profile, especially regarding peripheral neuropathy. Compared with thalidomide, it often requires less dose reduction for hematologic toxicities, while pomalidomide is typically reserved for later‑line therapy.

Lenalidomide tablets should be stored at ambient temperature, below 25 °C, in the original blister or container. Keep them away from moisture, direct sunlight, and excessive heat to maintain product stability.

Lenalidomide 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 a glass of water and not crushed or chewed unless specifically instructed.

The most serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe neutropenia or thrombocytopenia that can lead to infections or bleeding, and the potential development of secondary primary malignancies. Patients should be monitored closely for these complications.

Lenalidomide should not be used by individuals who are pregnant, planning to become pregnant, or not using effective contraception. It is also contraindicated in patients with known hypersensitivity to lenalidomide or any component of the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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