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

Lenalidomide Stada

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Stada (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Stada, is an immunomodulatory drug (IMiD) presented as an oral tablet for oral use. It is employed in the treatment of certain blood cancers, specifically multiple myeloma and myelodysplastic syndromes, in adult patients.

GNH India supplies Lenalidomide Stada 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‑approved batches for clinical and commercial use. Our distribution network ensures timely delivery across continents.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Lenalidomide is an immunomodulatory agent used in hematologic malignancies.

  • Multiple myeloma: improves progression‑free survival when combined with dexamethasone.
  • Myelodysplastic syndromes with del(5q): reduces transfusion dependence and can induce cytogenetic remission.
  • Relapsed or refractory disease: offers an additional therapeutic option for patients whose disease has progressed after standard treatments.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑E3 ubiquitin ligase complex, altering substrate specificity and promoting ubiquitination of transcription factors Ikaros and Aiolos. This leads to their proteasomal degradation, resulting in modulation of cytokine production, inhibition of angiogenesis, and direct anti‑proliferative and pro‑apoptotic effects on malignant plasma and myeloid cells.

Side Effects

Lenalidomide may cause a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: lowered platelet levels that may cause bleeding.
  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhea: loose stools that may lead to dehydration.
  • Constipation: difficulty passing stools.
  • Rash: mild skin eruptions.

Serious or Rare Side Effects

  • Venous thromboembolism: deep vein thrombosis or pulmonary embolism.
  • Severe neutropenia: markedly low neutrophil counts requiring medical intervention.
  • Serious infections: opportunistic or bacterial infections requiring hospitalization.
  • Secondary primary malignancies: emergence of new cancers unrelated to the original disease.
  • Hepatotoxicity: significant liver enzyme elevations or liver injury.

Precautions & Warnings

When prescribing lenalidomide, clinicians should observe several safety considerations.

  • Blood count monitoring: perform complete blood counts regularly to detect neutropenia or thrombocytopenia.
  • Thrombosis risk assessment: evaluate patient history and consider prophylactic anticoagulation when appropriate.
  • Pregnancy avoidance: the drug is contraindicated in pregnancy; ensure effective contraception.
  • Breastfeeding caution: advise against nursing while on therapy due to unknown excretion.
  • Renal function adjustment: modify dosing in patients with impaired renal clearance.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase lenalidomide exposure.
  • Anticoagulants (e.g., warfarin): heightened risk of bleeding.
  • Live vaccines: reduced vaccine efficacy and potential infection.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): decrease lenalidomide plasma levels.
  • Other myelosuppressive agents: additive risk of severe cytopenias.
  • Diuretics: may affect renal clearance of lenalidomide.

Frequently Asked Questions

Lenalidomide Stada is indicated for the treatment of adult patients with multiple myeloma and for myelodysplastic syndromes that have a deletion of the long arm of chromosome 5 (del[5q]). It is used as part of combination therapy or as a single agent depending on the clinical scenario.

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This triggers degradation of transcription factors Ikaros and Aiolos, leading to modulation of immune responses, inhibition of angiogenesis, and direct anti‑proliferative and pro‑apoptotic effects on malignant cells.

The dosage of Lenalidomide Stada is individualized by the prescribing physician based on the specific indication, disease stage, renal function, and patient tolerance. Only a qualified healthcare professional should determine the appropriate regimen.

Lenalidomide is contraindicated in pregnancy because of the risk of fetal harm. Women of childbearing potential must use effective contraception. Safety during breastfeeding has not been established, and nursing is generally discouraged while on therapy.

To place an order, submit an enquiry on the Lenalidomide Stada product page at gnhindia.com, specifying the required quantity. GNH India supplies 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.

Lenalidomide belongs to the immunomodulatory drug class, offering a distinct mechanism compared with proteasome inhibitors or monoclonal antibodies. It provides oral administration, can be combined with dexamethasone or other agents, and has demonstrated efficacy in both newly diagnosed and relapsed settings, though safety profiles differ among classes.

Store Lenalidomide Stada at temperatures below 25 °C in its original container, protected from moisture and direct light. Do not store in the bathroom or near heat sources. Keep the product out of reach of children.

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

Serious risks include venous thromboembolism, severe neutropenia or thrombocytopenia leading to infection or bleeding, secondary primary malignancies, and significant liver toxicity. Patients should be monitored closely for these events, and any signs of serious adverse reactions require immediate medical attention.

Lenalidomide Stada should not be used by individuals who are pregnant, have uncontrolled infections, have severe renal impairment without dose adjustment, or have known hypersensitivity to lenalidomide or any of the tablet excipients. Contraindications are determined by the treating physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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