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

Lenalidomide Sun

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Sun (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Sun, is an immunomodulatory drug presented as a tablet for oral use. It is employed in the treatment of certain blood cancers, including multiple myeloma, myelodysplastic syndromes, and mantle‑cell lymphoma, in adult patients. The medication modulates the immune system and inhibits angiogenesis, contributing to disease control.

GNH India supplies Lenalidomide Sun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. Our distribution network ensures reliable delivery and regulatory compliance across multiple regions.

Manufacturer / TM Owner

Sun Pharma France

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Indications & Clinical Uses

  • Lenalidomide is used in hematologic malignancies and related disorders, targeting abnormal plasma cells and dysplastic bone‑marrow clones.
  • Multiple Myeloma: Reduces disease progression and improves survival in adult patients.
  • Myelodysplastic Syndromes: Decreases transfusion dependence and modifies disease course in patients with del(5q) cytogenetic abnormality.
  • Mantle Cell Lymphoma: Provides therapeutic benefit in relapsed or refractory disease.

How It Works

  • Lenalidomide binds to the cereblon subunit of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This triggers ubiquitination and proteasomal degradation of transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), leading to reduced proliferation of malignant plasma cells, enhanced immune‑mediated tumor cell killing, and inhibition of angiogenic factors. The combined immunomodulatory, anti‑angiogenic, and direct anti‑myeloma actions underlie its therapeutic effect.

Side Effects

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

Common Side Effects

  • Fatigue: Persistent tiredness affecting daily activities.
  • Nausea: Stomach upset often occurring after dosing.
  • Diarrhea: Loose stools that may be mild to moderate.
  • Rash: Skin redness or itching.

Serious or Rare Side Effects

  • Neutropenia: Significant reduction in neutrophil count increasing infection risk.
  • Thromboembolic events: Deep vein thrombosis or pulmonary embolism.
  • Teratogenicity: Potential to cause fetal malformations; contraindicated in pregnancy.

Precautions & Warnings

  • When prescribing Lenalidomide, clinicians should observe several safety considerations.
  • Pregnancy: Contraindicated; use effective contraception for both patient and partner.
  • Thrombosis risk: Assess and manage pre‑existing clotting disorders; consider anticoagulation.
  • Renal impairment: Adjust dosing and monitor renal function closely.
  • Hematologic monitoring: Perform regular complete blood counts to detect cytopenias.
  • Infection vigilance: Monitor for signs of infection and treat promptly.
  • Store at ambient temperature: Keep below 25 °C in the original container, protected from moisture and light.

Avoid Interactions

Lenalidomide interacts with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): May reduce lenalidomide exposure, compromising efficacy.
  • Anticoagulants (e.g., warfarin): Increased risk of bleeding; concurrent use should be avoided.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants (e.g., cyclosporine): May enhance immunosuppression, monitor infection signs.
  • Vaccines: Live attenuated vaccines may be less effective; avoid during therapy.
  • Contraceptives: Hormonal methods may have reduced effectiveness; advise additional barrier methods.

Frequently Asked Questions

Lenalidomide Sun is an immunomodulatory antineoplastic medication indicated for the treatment of adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) cytogenetic abnormality, and mantle‑cell lymphoma, particularly in relapsed or refractory settings.

The drug binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, changing its substrate profile. This leads to the degradation of transcription factors Ikaros and Aiolos, which suppresses malignant plasma‑cell growth, enhances immune‑mediated tumor killing, and reduces angiogenesis.

The prescribed dose of Lenalidomide Sun is individualized by the treating physician based on the specific indication, disease stage, renal function, and patient tolerance. No universal dosing regimen is provided here; the prescriber sets the appropriate schedule.

Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal malformations. Women of child‑bearing potential must use effective contraception, and breastfeeding is not recommended while on therapy.

To place an order, submit an enquiry on the Lenalidomide Sun 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 the same cereblon‑binding mechanism as thalidomide and pomalidomide but generally offers greater potency with a more favorable safety profile, especially regarding peripheral neuropathy. Pomalidomide is often reserved for patients who have progressed after lenalidomide therapy, while thalidomide is used less frequently due to its higher toxicity.

Store Lenalidomide Sun at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture and direct light, and ensure the container is tightly closed to maintain stability.

Lenalidomide Sun is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole; do not crush or split unless specifically instructed.

The most serious adverse events include severe neutropenia or other cytopenias, thromboembolic complications such as deep‑vein thrombosis or pulmonary embolism, and teratogenic effects that can cause birth defects. Prompt monitoring and risk‑mitigation strategies are essential.

Lenalidomide Sun should not be used by pregnant women, individuals who cannot use effective contraception, patients with uncontrolled severe infections, or those with severe renal impairment without dose adjustment. Clinicians should also exercise caution in patients with a history of thromboembolic disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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