Product image of Lenalidomid Pharmevid (Lenalidomide) supplied by GNH India

Lenalidomid Pharmevid

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomid Pharmevid (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomid Pharmevid, is an immunomodulatory drug presented as an oral tablet for oral use. It is employed in the treatment of certain blood cancers, including multiple myeloma, myelodysplastic syndromes, and mantle cell lymphoma, in adult patients.

GNH India supplies Lenalidomid Pharmevid 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 global distribution. Customers benefit from reliable supply chains and responsive technical support.

Manufacturer / TM Owner

Pharmevid S.R.O.

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Indications & Clinical Uses

  • Lenalidomide is used in hematologic malignancies that involve abnormal plasma or lymphoid cells.
  • Multiple Myeloma: improves progression‑free survival and overall response rates in adult 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: contributes to disease control when combined with other agents in relapsed or refractory adult cases.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4 E3 ubiquitin ligase complex, promoting ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos. This leads to modulation of cytokine production, inhibition of angiogenesis, and induction of apoptosis in malignant plasma and lymphoid cells, while enhancing immune‑mediated tumor surveillance.

Side Effects

Adverse reactions may occur with lenalidomide therapy.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Diarrhea: loose stools that may require supportive care.
  • Rash: mild skin eruptions that are usually self‑limiting.
  • Constipation: difficulty passing stools.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Severe neutropenia or thrombocytopenia: markedly low blood cell counts.
  • Secondary primary malignancies: emergence of new cancers.
  • Hepatotoxicity: significant liver enzyme elevations.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: severe skin reactions.

Precautions & Warnings

  • Safety considerations are essential when prescribing lenalidomide.
  • Monitor blood counts: perform regular CBC to detect cytopenias.
  • Assess thrombotic risk: evaluate history of clotting and consider prophylaxis.
  • Avoid in pregnancy: teratogenic; contraindicated for women of childbearing potential.
  • Use effective contraception: both male and female patients must employ reliable methods.
  • Adjust for renal impairment: dose modifications may be required in reduced kidney function.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lenalidomide may interact with several concomitant medications.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lenalidomide exposure.
  • Anticoagulants (e.g., warfarin): heightened risk of bleeding.
  • Other teratogenic agents: additive risk of fetal harm.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): may reduce drug levels.
  • P‑glycoprotein inhibitors (e.g., verapamil): modest increase in exposure.
  • Live vaccines: potential for reduced vaccine efficacy.
  • NSAIDs: may increase risk of thrombosis when combined with lenalidomide.

Frequently Asked Questions

Lenalidomid Pharmevid contains lenalidomide and is indicated for the treatment of adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) cytogenetic abnormality, and mantle cell lymphoma, typically in relapsed or refractory settings.

Lenalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, leading to degradation of transcription factors Ikaros and Aiolos. This results in immunomodulation, anti‑angiogenic activity, and induction of apoptosis in malignant plasma and lymphoid cells.

The specific dose and schedule of Lenalidomid Pharmevid are determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. The prescriber will tailor the regimen to each individual case.

Lenalidomid Pharmevid is classified as Pregnancy Category X because it is teratogenic and can cause fetal harm. It should not be used by pregnant women, and effective contraception is required for both male and female patients of childbearing potential. 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 (including any cold‑chain requirements), and necessary import documentation.

Lenalidomid Pharmevid (lenalidomide) belongs to the immunomodulatory drug class, offering a distinct mechanism of action compared with proteasome inhibitors or monoclonal antibodies. It is often used in combination regimens and provides benefits in progression‑free survival, especially in relapsed or refractory disease, while having a different safety profile.

Lenalidomid Pharmevid should be stored at temperatures below 25 °C in its original packaging. Protect the tablets from moisture, heat, and direct sunlight to maintain stability throughout its shelf life.

Lenalidomid Pharmevid is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. The tablets should be swallowed whole with water and not crushed or chewed unless otherwise instructed.

The most serious risks include venous thromboembolism, severe neutropenia or thrombocytopenia, secondary primary malignancies, and serious skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for signs of infection, clotting, or unusual skin changes.

Lenalidomid Pharmevid is contraindicated in pregnant women, patients with known hypersensitivity to lenalidomide or its excipients, and individuals with severe renal impairment unless dose adjustments are made. It should also be avoided in patients with uncontrolled thrombotic risk without appropriate prophylaxis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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