Product image of Lenalidomid +pharma (Lenalidomide) supplied by GNH India

Lenalidomid +pharma

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomid +pharma (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomid +pharma, is an Immunomodulatory imide drug (IMiD) presented as an oral dosage form for oral use. It is employed in the treatment of certain blood cancers and related disorders in adult patients.
GNH India supplies Lenalidomid +pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

+pharma Arzneimittel Gmbh

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Indications & Clinical Uses

Lenalidomide is used in hematologic malignancies and related syndromes, targeting abnormal cell growth and immune dysregulation.

  • Multiple myeloma: improves progression‑free survival and overall response rates in patients with relapsed or refractory disease.
  • Myelodysplastic syndromes with del(5q): reduces transfusion dependence and induces cytogenetic remission.
  • Mantle cell lymphoma: contributes to disease control when combined with other agents in relapsed settings.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering ubiquitination of transcription factors such as Ikaros and Aiolos. This leads to reduced cytokine production, inhibition of angiogenesis, and induction of apoptosis in malignant plasma cells and other hematologic tumor cells, while modulating the immune microenvironment.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Diarrhea: loose stools that may require hydration.
  • Rash: mild skin eruptions or itching.
  • Nausea: occasional upset stomach.
  • Low blood counts: reduced neutrophils, platelets, or red cells.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Secondary malignancies: emergence of new cancers.
  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Severe infections: opportunistic or bacterial infections requiring prompt treatment.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient risk factors and monitor laboratory parameters regularly.

  • Pregnancy risk: contraindicated in pregnancy; use effective contraception.
  • Thrombosis risk: evaluate need for prophylactic anticoagulation.
  • Renal function: adjust monitoring for patients with impaired kidney function.
  • Hepatic function: monitor liver enzymes in patients with liver disease.
  • Drug interactions: review concomitant medications for potential interactions.
  • Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and direct light.

Avoid Interactions

Lenalidomide can interact with several drug classes, affecting efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce plasma concentrations.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants (e.g., cyclosporine): may enhance immunomodulatory effects.
  • CYP3A4 inhibitors (e.g., ketoconazole): may modestly increase exposure.
  • Vaccines: live attenuated vaccines should be avoided during treatment.
  • NSAIDs: may increase risk of thrombosis when combined with lenalidomide.

Frequently Asked Questions

Lenalidomid +pharma, containing the active ingredient lenalidomide, is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with del(5q) chromosomal abnormality, and mantle cell lymphoma. These are hematologic malignancies where the drug helps control disease progression and improve patient outcomes.

Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering the degradation of specific transcription factors. This results in reduced cytokine production, inhibition of new blood‑vessel formation, and promotion of apoptosis in malignant cells, while also modulating immune cell activity.

The dosage of Lenalidomid +pharma is individualized by the prescribing physician based on the specific indication, disease stage, renal function, and patient tolerance. Only a qualified healthcare professional can determine the appropriate dose and schedule.

Lenalidomid +pharma is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal harm. Women of child‑bearing 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, and any necessary import documentation.

Both lenalidomide and thalidomide belong to the immunomodulatory imide drug class, but lenalidomide has a more favorable safety profile, especially regarding peripheral neuropathy, and exhibits stronger anti‑angiogenic and anti‑myeloma activity. Clinical guidelines often prefer lenalidomide for newer treatment regimens.

Store Lenalidomid +pharma at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, excessive heat, and direct sunlight to maintain stability and potency.

Lenalidomid +pharma is taken orally, usually as a tablet, with or without food as directed by the prescriber. The exact timing and frequency depend on the treatment protocol established by the healthcare provider.

The most serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe skin reactions like Stevens‑Johnson syndrome, secondary malignancies, and significant reductions in blood cell counts that can lead to infection or bleeding.

Lenalidomid +pharma should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or its excipients, and patients with uncontrolled infections or severe renal impairment unless closely monitored. The prescribing physician will assess suitability on a case‑by‑case basis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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