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 imide drug (IMiD) presented as an oral tablet for oral use. It treats multiple myeloma, myelodysplastic syndromes, and mantle cell lymphoma in adult patients.

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

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

Lenalidomide is an immunomodulatory agent used in hematologic malignancies.

  • Multiple Myeloma: improves progression‑free survival and overall response rates in adult patients.
  • Myelodysplastic Syndromes: reduces transfusion dependence and delays transformation to acute leukemia.
  • Mantle Cell Lymphoma: enhances response when combined with standard chemotherapy in relapsed or refractory disease.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑E3 ubiquitin ligase complex, promoting ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos. This leads to anti‑proliferative, pro‑apoptotic, and anti‑angiogenic effects, while also modulating cytokine production and immune‑cell activity to target malignant plasma cells and other hematologic cancers.

Side Effects

Lenalidomide may cause a range of adverse reactions.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: lowered platelet count leading to easy bruising.
  • Anemia: decreased red blood cells causing weakness.
  • Constipation: infrequent bowel movements.
  • 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.
  • Secondary primary malignancies: emergence of new cancers.
  • Hepatotoxicity: liver enzyme elevations or liver injury.
  • Stevens‑Johnson syndrome: severe skin reaction with blistering.
  • Tumor lysis syndrome: rapid tumor cell breakdown causing metabolic disturbances.

Precautions & Warnings

Before initiating therapy, several safety considerations are essential.

  • Pregnancy: contraindicated (Category X); avoid use in pregnant women.
  • Thrombosis risk: assess for prior clotting events and consider prophylactic anticoagulation.
  • Hematologic monitoring: perform regular CBCs to detect neutropenia, thrombocytopenia, or anemia.
  • Renal/hepatic function: adjust therapy in patients with impaired kidney or liver function.
  • Drug interactions: review concomitant medications for potential additive toxicity.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lenalidomide interacts with several drug classes that may alter its safety or efficacy.

Major Interactions (Avoid)

  • Thalidomide: combined use increases teratogenic and neurotoxic risk.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): raise lenalidomide plasma levels.
  • Live vaccines: may cause uncontrolled infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): reduce lenalidomide exposure.
  • Anticoagulants (e.g., warfarin): heightened risk of thromboembolic events.
  • NSAIDs: may exacerbate hematologic toxicity, especially neutropenia.

Frequently Asked Questions

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

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos. This triggers anti‑proliferative, pro‑apoptotic, and anti‑angiogenic actions while also modulating cytokine release and immune‑cell activity against malignant cells.

The specific dose and schedule of Lenalidomide Sun are determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. No fixed dosing regimen is provided here.

Lenalidomide Sun 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 because it may be excreted in breast milk.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity of Lenalidomide Sun. 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 belongs to the immunomodulatory imide drug (IMiD) class, offering a distinct mechanism of action compared with proteasome inhibitors or monoclonal antibodies. It is often used in combination regimens and provides benefits in progression‑free survival, though safety profiles differ, especially regarding hematologic toxicity and thrombotic risk.

Store Lenalidomide Sun at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture, heat, and direct sunlight to maintain potency.

Lenalidomide Sun is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

The most serious risks include venous thromboembolism, severe neutropenia or other profound blood‑cell deficiencies, secondary primary malignancies, and rare but severe skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for these events.

Lenalidomide Sun should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or its excipients, and patients with uncontrolled active infections or severe organ dysfunction unless a specialist determines that benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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