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 a immunomodulatory imide drug (IMiD) presented as an oral formulation for oral use. It is indicated for the treatment of certain blood cancers 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 employed in hematologic malignancies that rely on abnormal plasma or lymphoid cells.

  • Multiple myeloma: helps control disease progression and improve survival in patients with relapsed or refractory disease.
  • Myelodysplastic syndromes: reduces transfusion dependence and delays transformation to acute leukemia.
  • 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 substrate specificity and 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 cells, while enhancing immune‑mediated tumor cell clearance.

Side Effects

Lenalidomid Medical Valley may cause a range of adverse reactions.

Common Side Effects

  • Fatigue: persistent tiredness reported by many patients.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: lowered platelet levels that may cause easy bruising.
  • Diarrhea: loose stools occurring during treatment.
  • Rash: skin irritation or erythema.
  • Constipation: difficulty passing stool.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Secondary primary malignancies: emergence of new cancers unrelated to the original disease.
  • Severe neutropenia: profound drop in neutrophils requiring medical intervention.
  • Hepatic failure: significant liver dysfunction.
  • Tumor lysis syndrome: rapid tumor cell breakdown causing metabolic disturbances.
  • Interstitial lung disease: inflammation of lung tissue leading to breathing difficulties.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor laboratory parameters.

  • Pregnancy: contraindicated (Category X); avoid use in pregnant women.
  • Thrombosis risk: assess history of clotting disorders and consider prophylaxis.
  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hematologic monitoring: perform regular complete blood counts to detect cytopenias.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lenalidomid Medical Valley can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers: may markedly lower lenalidomide exposure and reduce efficacy.
  • Anticoagulants: concurrent use can increase bleeding risk.
  • Live vaccines: heightened risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Macrolide antibiotics (e.g., erythromycin): may raise lenalidomide plasma levels.
  • Azole antifungals (e.g., ketoconazole): potential increase in drug concentration.
  • Other immunosuppressants: may amplify overall immunosuppressive effect.

Frequently Asked Questions

Lenalidomid Medical Valley contains lenalidomide and is prescribed for adult patients with certain hematologic cancers, specifically multiple myeloma, myelodysplastic syndromes, and mantle cell lymphoma, to help control disease progression and improve survival outcomes.

Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering its substrate specificity. This triggers degradation of transcription factors Ikaros and Aiolos, leading to reduced angiogenesis, enhanced immune‑mediated tumor cell killing, and induction of apoptosis in malignant cells.

The specific dose and schedule are individualized by the treating physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Only a qualified prescriber can determine the appropriate regimen.

Lenalidomid Medical Valley is classified as Pregnancy Category X, meaning it is contraindicated in pregnant women because it can cause fetal harm. It is also not recommended for breastfeeding mothers, as it may be excreted in breast milk and affect the infant.

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 often compared with thalidomide and pomalidomide, other immunomodulatory imide drugs. Compared with thalidomide, lenalidomide generally shows greater potency, a more favorable side‑effect profile regarding neuropathy, and stronger anti‑angiogenic activity. Pomalidomide is a newer agent with activity in lenalidomide‑refractory disease but may have a different safety spectrum.

Store the product at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and avoid exposure to excessive heat or humidity to maintain product stability.

The medication is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious risks include severe neutropenia, which can predispose to infections; venous thromboembolism, leading to potentially life‑threatening clots; secondary primary malignancies; and rare events such as hepatic failure or interstitial lung disease. Prompt medical attention is required if symptoms of these conditions appear.

Patients who are pregnant, have a known hypersensitivity to lenalidomide or any excipients, or have uncontrolled severe infections should avoid this medication. Additionally, individuals with severe renal impairment without appropriate dose adjustment may be unsuitable candidates.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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