Product image of Lenalidomid Medical Valley (Lenalidomide) supplied by GNH India

Lenalidomid Medical Valley

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomid Medical Valley (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomid Medical Valley, is an immunomodulatory imide drug (IMiD) presented as an oral dosage form for oral use. It treats multiple myeloma and myelodysplastic syndromes in adult patients.

GNH India supplies Lenalidomid Medical Valley as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Medical Valley Invest Ab

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Indications & Clinical Uses

Lenalidomide is used in hematologic malignancies and related bone‑marrow disorders, targeting abnormal plasma cells and dysplastic clones.

  • Multiple Myeloma (newly diagnosed): improves progression‑free and overall survival.
  • Multiple Myeloma (relapsed/refractory): provides disease control when other therapies have failed.
  • Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and improves blood counts.

How It Works

  • Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering substrate specificity. This leads to degradation of transcription factors Ikaros and Aiolos, resulting in modulation of cytokine production, inhibition of angiogenesis, and induction of apoptosis in malignant plasma cells and dysplastic hematopoietic clones.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness reported by many patients.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: low platelet levels leading to easy bruising.
  • Diarrhea: loose stools that may require management.
  • Rash: skin eruptions of varying intensity.
  • Constipation: difficulty passing stools.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Secondary primary malignancies: emergence of new cancers.
  • Severe neutropenia: profound immune suppression.
  • Hepatic toxicity: elevated liver enzymes or liver injury.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Tumor lysis syndrome: rapid tumor cell breakdown causing metabolic disturbances.

Precautions & Warnings

Lenalidomid Medical Valley requires careful monitoring and specific safety measures.

  • Pregnancy: contraindicated (Category X); avoid use in pregnant women.
  • Thrombosis risk: assess patient history and consider prophylactic anticoagulation.
  • Renal impairment: adjust dosing and monitor kidney function.
  • Hematologic monitoring: perform regular complete blood counts.
  • Drug interactions: review concomitant medications for potential interactions.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Lenalidomid Medical Valley can interact with several drug classes, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may markedly lower lenalidomide exposure.
  • Anticoagulants (warfarin): increased risk of bleeding.
  • Live vaccines: heightened risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Antiplatelet agents (aspirin, clopidogrel): monitor for bleeding signs.
  • HIV protease inhibitors (ritonavir): may raise lenalidomide plasma levels.
  • Diuretics (furosemide): watch electrolyte balance and renal function.

Frequently Asked Questions

Lenalidomid Medical Valley contains lenalidomide and is indicated for the treatment of adult patients with multiple myeloma, including newly diagnosed and relapsed/refractory disease, as well as for myelodysplastic syndromes that have a deletion of chromosome 5q (del[5q]).

Lenalidomide binds to the cereblon component of the CRL4‑CRBN E3 ubiquitin ligase, altering the degradation of specific transcription factors. This results in immune modulation, inhibition of new blood‑vessel formation, and induction of programmed cell death in malignant plasma cells and dysplastic bone‑marrow clones.

The exact dose and schedule are determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and other individual factors. Healthcare professionals should follow the latest clinical guidelines and product labeling when prescribing.

Lenalidomid Medical Valley 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 (including any cold‑chain requirements), and necessary import documentation.

Lenalidomide is an oral immunomodulatory agent that differs from proteasome inhibitors and monoclonal antibodies. It offers the convenience of oral administration and a distinct mechanism targeting cereblon, often used in combination regimens to enhance efficacy and overcome resistance seen with other drug classes.

Store Lenalidomid Medical Valley below 25 °C in its original packaging, protecting it from moisture and direct sunlight. Do not store in a humid environment such as a bathroom cabinet, and keep the container tightly closed when not in use.

The product is taken orally, usually with or without food, as directed by the prescribing physician. Patients should swallow the tablet whole with a glass of water and follow any specific timing instructions provided by their healthcare provider.

Serious risks include venous thromboembolism, severe neutropenia or thrombocytopenia, secondary primary malignancies, hepatic toxicity, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for signs of these events.

Lenalidomid Medical Valley should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or any excipients, patients with uncontrolled active infections, or those with severe renal impairment without appropriate dose adjustment. Contraindications are detailed in the prescribing information.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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