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 oral tablets for oral use. It is employed in the treatment of certain hematologic malignancies, including multiple myeloma, myelodysplastic syndromes, and mantle cell lymphoma, in adult patients.

GNH India supplies Lenalidomide Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, with strict quality assurance and regulatory compliance. The company ensures batch consistency, proper labeling, and adherence to EU pharmacopeial standards.

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 and overall response rates in adult patients.
  • Myelodysplastic syndromes with del(5q): reduces transfusion dependence and induces cytogenetic remission.
  • Mantle cell lymphoma: contributes to disease control when combined with other therapies 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 induces ubiquitination and proteasomal degradation of transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), leading to modulation of cytokine production, inhibition of angiogenesis, and direct anti‑proliferative effects on malignant plasma cells and other hematologic tumor cells.

Side Effects

Lenalidomide may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Fatigue: persistent tiredness reported by many patients.
  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools, often self‑limiting.
  • Rash: skin irritation or erythema.
  • Neutropenia: reduced neutrophil count requiring monitoring.
  • Thrombocytopenia: lowered platelet levels.

Serious or Rare Side Effects

  • Venous thromboembolism: risk of deep‑vein thrombosis or pulmonary embolism.
  • Severe neutropenia: markedly low neutrophils increasing infection risk.
  • Secondary primary malignancies: emergence of new cancers.
  • Tumor lysis syndrome: rapid tumor cell breakdown causing metabolic disturbances.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess patient‑specific risk factors and monitor laboratory parameters.
  • Pregnancy: contraindicated (Category X); avoid exposure.
  • Thromboembolic risk: assess and consider prophylaxis.
  • Renal impairment: dose adjustment may be required.
  • Hematologic monitoring: regular CBC to detect cytopenias.
  • Drug interactions: avoid concomitant use with strong CYP inducers without monitoring.
  • Store at ambient temperature below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Lenalidomide can interact with several medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may reduce efficacy.
  • Anticoagulants (warfarin): increased bleeding risk.
  • Live vaccines: risk of infection.

Moderate Interactions (Monitor Closely)

  • Antiplatelet agents (aspirin): additive bleeding risk.
  • Other immunomodulatory drugs (e.g., thalidomide): enhanced toxicity.
  • P‑glycoprotein inhibitors (e.g., verapamil): may increase plasma levels.

Frequently Asked Questions

Lenalidomide Stada contains the active ingredient lenalidomide, an immunomodulatory drug indicated for the treatment of multiple myeloma, myelodysplastic syndromes (especially those with del(5q)), and mantle cell lymphoma in adult patients.

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos. This results in altered cytokine production, inhibition of angiogenesis, and direct anti‑proliferative activity against malignant cells.

The prescribed dose of lenalidomide is determined by the treating physician based on the specific indication, patient characteristics, and renal function. Dosing regimens are individualized and should follow the prescriber’s instructions.

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

To place an order, 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 required import documentation.

Lenalidomide is an oral immunomodulatory agent that offers a different mechanism of action compared with proteasome inhibitors or monoclonal antibodies. It is often used in combination regimens and provides benefits in progression‑free survival, but choice of therapy depends on disease stage, prior treatments and patient tolerance.

Store Lenalidomide Stada tablets at ambient temperature below 25 °C. Keep the product in its original container, protect it from moisture and light, and avoid storing in humid or excessively hot environments.

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

Serious risks include venous thromboembolism, severe neutrop

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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