Product image of Lenalidomide Accord (Lenalidomide) supplied by GNH India

Lenalidomide Accord

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Accord (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Accord, is a Immunomodulatory imide drug (IMiD) presented as a tablet for oral use. It is employed in the treatment of certain blood‑related cancers, primarily multiple myeloma and myelodysplastic syndromes, in adult patients.
GNH India supplies Lenalidomide Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Lenalidomide is an immunomodulatory agent used in hematologic malignancies and related disorders.

  • Multiple myeloma: improves progression‑free and overall survival when combined with dexamethasone or other agents.
  • Myelodysplastic syndromes with del(5q): reduces transfusion dependence and improves blood counts.
  • Mantle cell lymphoma (relapsed/refractory): provides clinical benefit as part of combination therapy.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering substrate specificity and promoting ubiquitination of transcription factors such as Ikaros and Aiolos. This leads to reduced proliferation of malignant plasma cells, enhanced immune‑mediated tumor cell clearance, and inhibition of angiogenesis, collectively contributing to its antineoplastic activity.

Side Effects

Lenalidomide may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Neutropenia: lowered neutrophil count increasing infection risk.
  • Thrombocytopenia: reduced platelet count, may cause easy bruising.
  • Diarrhea: loose stools, sometimes leading to dehydration.
  • Constipation: difficulty passing stool.
  • Rash: mild skin irritation or redness.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Severe neutropenia: markedly low neutrophils requiring medical intervention.
  • Severe thrombocytopenia: dangerously low platelets with bleeding risk.
  • Secondary primary malignancies: emergence of new cancers.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: severe skin reactions.

Precautions & Warnings

Lenalidomide requires careful monitoring and specific safety measures.

  • Pregnancy contraindication: teratogenic; ensure effective contraception for both patient and partner.
  • Thrombosis risk: assess need for prophylactic anticoagulation, especially with additional risk factors.
  • Hematologic monitoring: regular CBCs to detect neutropenia or thrombocytopenia.
  • Renal impairment: dose adjustment may be needed in patients with reduced kidney function.
  • Drug interaction vigilance: avoid concurrent use with strong CYP3A4 inhibitors without supervision.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

Avoid Interactions

Lenalidomide can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma levels.
  • Thalidomide: additive teratogenic and hematologic toxicity.
  • Anticoagulants (e.g., warfarin): heightened risk of thromboembolic events.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce effectiveness.
  • Live vaccines: immunosuppression can diminish vaccine response.
  • NSAIDs: may increase risk of renal impairment when combined with lenalidomide.

Frequently Asked Questions

Lenalidomide Accord is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with a del(5q) chromosomal abnormality, and relapsed or refractory mantle cell lymphoma. It is used as part of combination regimens to improve disease control and patient outcomes.

Lenalidomide binds to the cereblon component of an E3 ubiquitin ligase complex, redirecting the complex to degrade specific transcription factors. This action reduces malignant cell proliferation, enhances immune‑mediated tumor cell killing, and inhibits new blood‑vessel formation, collectively contributing to its antineoplastic effects.

The specific dose and schedule of Lenalidomide Accord are determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Lenalidomide is classified as Pregnancy Category X because it is known to cause severe birth defects. It should not be used by pregnant women, and effective contraception is required for both patients and male partners. Use during breastfeeding is also contraindicated.

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.

Both lenalidomide and thalidomide belong to the immunomodulatory imide drug class, but lenalidomide generally offers a more favorable safety profile, especially regarding peripheral neuropathy. Lenalidomide also has stronger anti‑angiogenic activity and is approved for a broader range of hematologic indications.

Lenalidomide Accord should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack or container, protect them from moisture, heat, and direct sunlight to maintain product stability.

Lenalidomide Accord is taken orally, usually once daily, 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.

The most serious risks include severe neutropenia, severe thrombocytopenia, venous thromboembolism, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored regularly for blood counts and signs of clotting or severe skin changes.

Lenalidomide should not be used by pregnant women, individuals who cannot practice effective contraception, patients with uncontrolled infections, or those with severe renal impairment without dose adjustment. It is also contraindicated in patients with known hypersensitivity to lenalidomide or any component of the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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