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

Lenalidomide Sandoz

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Sandoz (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Sandoz, is an immunomodulatory drug (IMiD) presented as an oral tablet for systemic use. It is indicated for the treatment of multiple myeloma, myelodysplastic syndromes and mantle cell lymphoma in adult patients.

GNH India supplies Lenalidomide Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑compliant sourcing for global oncology programs.

Manufacturer / TM Owner

Sandoz Pharmaceuticals D.D.

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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 patients with relapsed or refractory disease.
  • Myelodysplastic Syndromes: reduces transfusion dependence and modifies disease course in patients with del(5q) cytogenetic abnormality.
  • Mantle Cell Lymphoma: induces tumor regression and prolongs remission in patients with relapsed or refractory disease.

How It Works

  • Lenalidomide binds to the cereblon subunit of the CRL4‑E3 ubiquitin ligase complex, altering ubiquitination and degradation of transcription factors such as Ikaros and Aiolos. This modulation enhances immune‑mediated tumor cell killing, inhibits angiogenesis, and directly induces apoptosis in malignant plasma cells and other hematologic cancer cells. The resulting shift in cytokine production and T‑cell activation contributes to its antineoplastic activity.

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 accompanied by vomiting.
  • Rash: skin redness or itching.
  • Low blood counts: decreased neutrophils, platelets or red cells.
  • Peripheral neuropathy: tingling or numbness in extremities.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Severe neutropenia: markedly low neutrophil count increasing infection risk.
  • Severe thrombocytopenia: very low platelet count leading to bleeding.
  • Secondary primary malignancies: emergence of new cancers.
  • Hepatotoxicity: liver enzyme elevations or liver injury.

Precautions & Warnings

When prescribing Lenalidomide, clinicians should observe several safety considerations.

  • Pregnancy risk: contraindicated in pregnancy (Category X); ensure effective contraception.
  • Thromboembolic prophylaxis: assess need for anticoagulation in high‑risk patients.
  • Renal impairment: adjust monitoring in patients with reduced kidney function.
  • Infection monitoring: watch for signs of infection due to neutropenia.
  • Hematologic monitoring: regular CBC to detect cytopenias.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers: may reduce lenalidomide exposure.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding when combined with thrombocytopenia.
  • Immunosuppressants: heightened infection risk.

Moderate Interactions (Monitor Closely)

  • P-glycoprotein inhibitors: may increase plasma levels.
  • NSAIDs: additive risk of gastrointestinal bleeding.
  • Vaccines (live attenuated): reduced vaccine efficacy; avoid during therapy.

Frequently Asked Questions

Lenalidomide Sandoz is prescribed for adult patients with certain blood cancers, specifically multiple myeloma, myelodysplastic syndromes that have a del(5q) chromosome abnormality, and mantle cell lymphoma that has relapsed or is refractory to prior therapy.

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, changing the degradation of transcription factors such as Ikaros and Aiolos. This leads to enhanced immune‑mediated tumor cell killing, inhibition of new blood‑vessel formation, and direct induction of cancer cell apoptosis.

The dose of Lenalidomide Sandoz is individualized by the treating physician based on the specific indication, disease stage, renal function and other patient‑specific factors. Only a qualified prescriber can determine the appropriate regimen.

Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated during pregnancy because it can cause fetal harm. Women of child‑bearing potential must use effective contraception, and breastfeeding is not recommended while taking the drug.

To request Lenalidomide Sandoz, 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 the necessary import documentation.

The primary alternative within the same class is thalidomide, while pomalidomide is a newer IMiD. Compared with thalidomide, lenalidomide generally offers a more favorable safety profile, especially lower rates of peripheral neuropathy, and stronger anti‑angiogenic activity. Pomalidomide may be used after lenalidomide failure, but it can have higher rates of cytopenias.

Lenalidomide Sandoz tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and light, and ensure the blister pack remains sealed until use.

The medication is taken orally as a whole tablet, usually once daily. It may be taken with or without food, but patients should follow the specific instructions provided by their healthcare professional and swallow the tablet whole with water.

Key serious risks include deep vein thrombosis or pulmonary embolism, severe neutropenia or thrombocytopenia that can lead to infection or bleeding, secondary primary cancers, and significant liver injury. Patients should be monitored closely for signs of these events.

Lenalidomide Sandoz should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or any component of the formulation, and patients with uncontrolled severe renal impairment unless dose adjustments and close monitoring are implemented.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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