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

Lenalidomide Krka

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Krka (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Krka, is an immunomodulatory agent presented as a tablet for oral use. It is indicated for the treatment of multiple myeloma and myelodysplastic syndromes in adult patients.

GNH India supplies Lenalidomide Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory support for global distribution.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

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

  • Multiple myeloma: reduces disease progression and improves survival in patients with relapsed or refractory disease.
  • Myelodysplastic syndromes: decreases transfusion dependence and modifies disease course in patients with lower‑risk MDS.

How It Works

  • Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, altering substrate specificity and promoting degradation of transcription factors such as Ikaros and Aiolos. This leads to modulation of cytokine production, inhibition of angiogenesis, and enhanced immune‑mediated tumor cell killing, while also exerting anti‑inflammatory effects.

Side Effects

Lenalidomide may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhea: loose stools that may require fluid replacement.
  • Rash: mild to moderate skin eruptions.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Nausea: upset stomach often alleviated with food.
  • Constipation: reduced bowel movements.

Serious or Rare Side Effects

  • Deep vein thrombosis or pulmonary embolism: blood clots requiring immediate medical attention.
  • Severe neutropenia: markedly low white blood cell count increasing infection risk.
  • Secondary primary malignancies: emergence of new cancers unrelated to the original disease.

Precautions & Warnings

When prescribing Lenalidomide, clinicians should consider several safety and handling measures.

  • Monitor blood counts: perform regular complete blood count assessments to detect cytopenias.
  • Assess renal function: adjust use in patients with impaired kidney function.
  • Evaluate thromboembolic risk: consider prophylactic anticoagulation in high‑risk individuals.
  • Counsel on teratogenic potential: enforce strict contraception for patients of child‑bearing potential.
  • Store at ambient temperature: keep tablets in original container, protect from moisture and light.

Avoid Interactions

Lenalidomide interacts with several drug classes, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may lower plasma concentrations of lenalidomide.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding when combined.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants (e.g., cyclosporine): may enhance hematologic toxicity.
  • Vaccines (live attenuated): reduced vaccine efficacy; avoid during treatment.
  • NSAIDs (e.g., ibuprofen): may increase risk of renal impairment.

Frequently Asked Questions

Lenalidomide Krka is prescribed for adult patients with multiple myeloma, especially in relapsed or refractory settings, and for certain lower‑risk myelodysplastic syndromes where it helps reduce transfusion needs and modify disease progression.

Lenalidomide binds to the cereblon protein within the CRL4‑E3 ubiquitin ligase complex, altering the degradation of specific transcription factors. This results in immune modulation, inhibition of new blood‑vessel formation, and direct anti‑tumor activity against malignant plasma cells and dysplastic marrow clones.

The exact dose of Lenalidomide Krka is determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and prior therapies. Dosage regimens are individualized and should follow the latest clinical guidelines.

Lenalidomide is classified as having unknown pregnancy and lactation categories, and it is considered potentially teratogenic. Women of child‑bearing potential must use effective contraception, and breastfeeding is generally discouraged 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 and any necessary import documentation.

Both lenalidomide and thalidomide belong to the immunomodulatory drug class, but lenalidomide has a more favorable safety profile, stronger anti‑angiogenic activity, and greater efficacy in multiple myeloma and certain myelodysplastic syndromes, while thalidomide is associated with higher rates of neuropathy.

Lenalidomide Krka tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, direct sunlight, and excessive heat to maintain potency.

The medication is taken orally, usually once daily on a scheduled cycle (e.g., 21 days on, 7 days off), as directed by the treating physician. It should be swallowed with water and can be taken with or without food, depending on the prescriber’s advice.

Serious risks include deep vein thrombosis or pulmonary embolism, severe neutropenia or other cytopenias that increase infection risk, and the potential development of secondary primary malignancies. Patients should be monitored closely for signs of clotting, infection, or unusual bleeding.

Lenalidomide is contraindicated in patients with known hypersensitivity to the drug or its excipients, in individuals with uncontrolled active infections, and in pregnant women or those who cannot adhere to strict contraceptive measures. Caution is also advised for patients with severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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