Product image of Lenalidomidă Teva (Lenalidomide) supplied by GNH India

Lenalidomidă Teva

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomidă Teva (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomidă Teva, is an immunomodulatory agent (IMiD) presented as an oral dosage form for oral use. It is employed in the treatment of multiple myeloma and certain myelodysplastic syndromes in adult patients, and is authorized for use within the European Union.

GNH India supplies Lenalidomidă Teva as a licensed, GDP‑compliant international pharmaceutical supplier, serving hospitals, oncology centres, pharmacies and clinics worldwide through regulated supply chains and adhering to global quality standards, ensuring product integrity and compliance with import regulations.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Lenalidomide is an immunomodulatory agent used in hematologic malignancies and related disorders.
  • Multiple myeloma: improves progression‑free survival and overall response rates in adult patients.
  • Multiple myeloma (maintenance therapy): prolongs remission after initial treatment or stem‑cell transplantation.
  • Myelodysplastic syndromes with del(5q): reduces transfusion dependence and improves peripheral blood counts.

How It Works

  • Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering substrate specificity and leading to degradation of transcription factors such as Ikaros and Aiolos. This results in modulation of cytokine production, inhibition of angiogenesis, and direct anti‑tumor activity by reducing proliferation of malignant plasma cells and myelodysplastic clones.

Side Effects

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

Common Side Effects

  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: low platelet levels leading to bleeding tendency.
  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhea or constipation: gastrointestinal disturbances.
  • Rash or pruritus: mild skin irritation.
  • Nausea: upset stomach, sometimes with vomiting.

Serious or Rare Side Effects

  • Venous thromboembolism: deep vein thrombosis or pulmonary embolism.
  • Secondary primary malignancies: emergence of new cancers.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatotoxicity: significant elevation of liver enzymes.
  • Severe infections: opportunistic or bacterial infections requiring hospitalization.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient suitability and monitor for potential complications.

  • Monitor blood counts: perform regular complete blood count tests to detect cytopenias.
  • Assess thrombotic risk: evaluate history of clotting disorders and consider prophylactic anticoagulation.
  • Evaluate renal and hepatic function: adjust therapy if impairment is present.
  • Contraindicated in pregnancy: enforce effective contraception and avoid use in pregnant women.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lenalidomide may interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Immunosuppressants (e.g., cyclosporine): heightened toxicity and infection risk.
  • Live vaccines: reduced efficacy and potential for infection.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): may raise lenalidomide exposure.
  • CYP3A4 inducers (e.g., rifampin): may lower drug levels.
  • NSAIDs: combined use can increase renal adverse effects.
  • Hormonal contraceptives: may reduce contraceptive effectiveness.
  • Antiplatelet agents (e.g., aspirin): additive risk of bleeding.

Frequently Asked Questions

Lenalidomidă Teva contains the active ingredient lenalidomide and is prescribed for adult patients with multiple myeloma and for those with myelodysplastic syndromes that have a del(5q) chromosomal abnormality. It is used to control disease progression, reduce transfusion needs, and improve blood cell counts.

Lenalidomide binds to the cereblon component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering the degradation of specific transcription factors. This leads to reduced production of pro‑inflammatory cytokines, inhibition of new blood‑vessel formation, and direct anti‑tumor effects on malignant plasma cells and dysplastic bone‑marrow clones.

The dose of Lenalidomidă Teva is individualized by the prescribing physician based on the specific indication, disease stage, renal function, and patient tolerance. Only a qualified health‑care professional can determine the appropriate dosing schedule and any necessary adjustments.

Lenalidomidă Teva is contraindicated during pregnancy because it can cause fetal harm. Effective contraception is required for both male and female patients of reproductive potential. Limited data are available for breastfeeding, and the drug is generally not recommended while nursing.

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 (including any cold‑chain requirements) and the necessary import documentation.

The primary alternative to lenalidomide is thalidomide, another immunomodulatory agent, and pomalidomide, a newer IMiD. Compared with thalidomide, lenalidomide generally has a more favorable neuropathy profile but a higher risk of cytopenias. Pomalidomide may be used after lenalidomide failure and can have a different safety spectrum.

Store Lenalidomidă Teva at room temperature, below 25 °C, in the original container to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiration date printed on the label.

Lenalidomidă Teva is taken orally, usually 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 the development of venous thromboembolism, severe infections, secondary primary malignancies, and significant liver enzyme elevations. Patients should report any signs of clotting, unexplained fever, persistent abdominal pain, or yellowing of the skin or eyes to their health‑care provider promptly.

Lenalidomidă Teva should not be used by individuals with known hypersensitivity to lenalidomide or any of its excipients, pregnant women, or patients who cannot use effective contraception. Caution is also advised for patients with severe renal or hepatic impairment, uncontrolled infections, or a history of thromboembolic events.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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