Product image of Lenalidomida Tecnigen (Lenalidomide) supplied by GNH India

Lenalidomida Tecnigen

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomida Tecnigen (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomida Tecnigen, is an immunomodulatory drug (IMiD) presented as an oral tablet for systemic use. It is employed in the treatment of certain blood cancers, including multiple myeloma, myelodysplastic syndromes with del(5q) and mantle cell lymphoma, targeting malignant cell growth and immune modulation.

GNH India supplies Lenalidomida Tecnigen 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 documentation for import and distribution.

Manufacturer / TM Owner

Tecnimede España Ind. Fca., S.A.

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Indications & Clinical Uses

Lenalidomide is used in hematologic malignancies that involve abnormal plasma or lymphoid cells.

  • Multiple myeloma: reduces disease progression and improves survival in patients with relapsed or refractory disease.
  • Myelodysplastic syndromes with del(5q): induces transfusion independence and cytogenetic remission.
  • Mantle cell lymphoma: contributes to disease control in patients who have received prior therapies.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4^CRBN E3 ubiquitin ligase complex, altering its substrate specificity. This leads to ubiquitination and proteasomal degradation of transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), resulting in modulation of cytokine production, inhibition of angiogenesis, and induction of apoptosis in malignant plasma and lymphoid cells. The downstream effects also include enhanced natural killer cell activity and reduced tumor‑supporting microenvironment.

Side Effects

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

Common Side Effects

  • Fatigue
  • Neutropenia
  • Thrombocytopenia
  • Diarrhea
  • Rash
  • Constipation

Serious or Rare Side Effects

  • Venous thromboembolism
  • Secondary primary malignancies
  • Severe neutropenia
  • Severe infections
  • Hepatotoxicity
  • Tumor lysis syndrome

Precautions & Warnings

When prescribing Lenalidomida Tecnigen, clinicians should observe several safety measures to minimize risk.

  • Pregnancy contraindication: drug is teratogenic (Category X) and must not be used during pregnancy.
  • Thrombosis risk: assess patient history and consider prophylactic anticoagulation.
  • Hematologic monitoring: perform regular complete blood counts to detect neutropenia or thrombocytopenia.
  • Renal/hepatic function: adjust dose in patients with impaired clearance.
  • Drug interaction vigilance: avoid concomitant use with strong CYP3A4 inducers.
  • Store at ambient temperature: keep below 25 °C, in original container, protected from moisture and light.

Avoid Interactions

Lenalidomide interacts with several medicines that can alter its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce plasma concentrations and therapeutic effect.
  • Live vaccines: concurrent use can increase risk of severe infection.
  • Anticoagulants (warfarin): may increase bleeding risk when combined with lenalidomide‑induced thrombocytopenia.

Moderate Interactions (Monitor Closely)

  • Antiplatelet agents (aspirin, clopidogrel): monitor platelet counts and bleeding signs.
  • P‑glycoprotein inhibitors (e.g., verapamil): may increase lenalidomide exposure.
  • Non‑live vaccines: timing should be coordinated with treatment cycles.

Frequently Asked Questions

Lenalidomida Tecnigen, containing lenalidomide, is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with the del(5q) cytogenetic abnormality, and mantle cell lymphoma. These are hematologic cancers where the drug helps control disease progression and improve patient outcomes.

Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, changing its substrate specificity. This triggers degradation of transcription factors Ikaros and Aiolos, leading to altered cytokine production, reduced angiogenesis, enhanced immune cell activity, and programmed cell death of malignant plasma and lymphoid cells.

The specific dose of Lenalidomida Tecnigen is determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal and hepatic function, and prior therapies. Dosage regimens are individualized and should follow the prescriber’s instructions and local regulatory guidelines.

Lenalidomida Tecnigen is classified as Pregnancy Category X, indicating it is contraindicated in pregnancy because of a high risk of fetal harm. Women of childbearing potential must use effective contraception, and the drug should not be used while breastfeeding.

To order Lenalidomida Tecnigen, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and any required import documentation.

Both lenalidomide and thalidomide belong to the immunomodulatory drug (IMiD) class, but lenalidomide has a more favorable safety profile, especially regarding peripheral neuropathy. Lenalidomide also shows stronger anti‑angiogenic and anti‑myeloma activity, making it the preferred option for many approved indications.

Lenalidomida Tecnigen should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture, light and excessive heat to maintain product stability throughout its shelf life.

Lenalidomida Tecnigen is taken orally, usually once daily, with or without food, as directed by the prescriber. Swallow the tablet whole with water and follow the dosing schedule provided in the prescription to ensure optimal therapeutic effect.

Serious risks include venous thromboembolism, severe neutropenia, severe infections, secondary primary malignancies, and hepatotoxicity. Patients should be monitored regularly for signs of blood clots, low blood counts, liver enzyme changes, and any new cancer development.

Lenalidomida Tecnigen should not

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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