GNH USA

Europe — EMA

Lenalidomidum Stada Arzneimittel Ag

GNH USA supplies Lenalidomidum Stada Arzneimittel Ag (Lenalidomide), a immunomodulatory drug for multiple myeloma, myelodysplastic syndromes, and mantle cell

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomidum Stada Arzneimittel Ag, is an immunomodulatory drug presented as a tablet for oral use. It treats certain blood cancers such as multiple myeloma, myelodysplastic syndromes, and mantle cell lymphoma in adult patients.

GNH USA supplies Lenalidomidum Stada Arzneimittel Ag as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres, and pharmacies worldwide.

What is Lenalidomide used for?

Lenalidomide is used in the treatment of hematologic malignancies and related disorders.

- Multiple Myeloma: improves progression‑free survival and overall response rates in patients with relapsed or refractory disease. - Myelodysplastic Syndromes: reduces transfusion dependence and improves blood counts in patients with del(5q) cytogenetic abnormality. - Mantle Cell Lymphoma: contributes to disease control in patients with relapsed or refractory mantle cell lymphoma.

What are the side effects of Lenalidomide?

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. - Nausea: feeling of sickness often accompanied by loss of appetite. - Rash: mild skin eruptions or itching.

Serious or Rare Side Effects: - Thromboembolic events: deep vein thrombosis or pulmonary embolism requiring immediate medical attention. - Severe neutropenia: markedly reduced neutrophil count increasing infection risk. - Secondary primary malignancies: emergence of new cancers distinct from the original disease.

What precautions apply to Lenalidomide?

When prescribing lenalidomide, clinicians should consider several safety precautions.

- Pregnancy risk: contraindicated in pregnancy due to teratogenicity; ensure effective contraception. - Thrombosis prophylaxis: assess need for anticoagulation in patients with additional risk factors. - Hematologic monitoring: perform regular complete blood counts to detect neutropenia or anemia. - Renal function: adjust use in patients with impaired kidney function and monitor creatinine. - Drug interactions: review concomitant medications for potential CYP or immunosuppressive interactions. - Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

What does Lenalidomide interact with?

Lenalidomide can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inducers: agents such as rifampicin may markedly reduce lenalidomide exposure. - Anticoagulants: concurrent use with warfarin can increase bleeding risk; close monitoring required.

Moderate Interactions (Monitor Closely): - Immunosuppressants: drugs like cyclosporine may enhance immunomodulatory effects, requiring dose adjustment. - Live vaccines: administration may be less effective and increase infection risk; avoid during therapy. - NSAIDs: may increase risk of renal impairment when combined with lenalidomide in susceptible patients.

Frequently asked questions

What is Lenalidomidum Stada Arzneimittel Ag used for?+
Lenalidomidum Stada Arzneimittel Ag contains lenalidomide, which is indicated for the treatment of adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) chromosomal abnormality, and mantle cell lymphoma, particularly in relapsed or refractory disease settings.
How does lenalidomide work in the body?+
Lenalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, leading to the ubiquitination and degradation of transcription factors Ikaros and Aiolos. This action modifies cytokine production, inhibits angiogenesis, and enhances immune‑mediated anti‑tumor activity, thereby reducing proliferation of malignant plasma cells.
What is the usual dose of lenalidomide?+
The specific dose of lenalidomide is individualized by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and prior therapies. Dosing regimens are detailed in the product’s prescribing information and should be followed exactly as directed by a qualified healthcare professional.
Is lenalidomide safe during pregnancy or breastfeeding?+
Lenalidomide is classified as pregnancy category X because it is teratogenic and can cause fetal harm. It is contraindicated in pregnancy, and effective contraception is required for both male and female patients of reproductive potential. Use during breastfeeding is not recommended due to potential secretion in milk.
How do I order Lenalidomidum Stada Arzneimittel Ag from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies, and procurement teams across international markets. After submission, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details (including any cold‑chain requirements), and required import documentation.
How does lenalidomide compare with the main alternative drug or class?+
Lenalidomide belongs to the immunomodulatory drug (IMiD) class and is structurally related to thalidomide. Compared with thalidomide, lenalidomide generally shows greater potency, a more favorable side‑effect profile, and reduced neurotoxicity, while retaining anti‑angiogenic and immunomodulatory properties. Both agents are used in similar hematologic malignancies, but choice depends on efficacy, tolerability, and regulatory approval.
How should Lenalidomidum Stada Arzneimittel Ag be stored and handled?+
Store the tablets at ambient temperature, preferably below 25 °C, in the original blister pack or container. Protect from moisture, excessive heat, and direct sunlight. Keep out of reach of children and do not use if the packaging is damaged or the tablets appear discolored.
How is lenalidomide administered to patients?+
Lenalidomide is administered orally, usually once daily on a schedule defined by the prescriber (e.g., 21 days on followed by 7 days off). Tablets should be swallowed whole with water and taken at the same time each day, preferably with or without food as directed in the prescribing information.
What are the most serious risks to watch for while on lenalidomide?+
Serious risks include thromboembolic events such as 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 regularly for signs of clotting, infection, and new cancer diagnoses.
Who should not use lenalidomide?+
Lenalidomide should not be used by individuals who are pregnant, planning to become pregnant, or not using effective contraception. It is also contraindicated in patients with known hypersensitivity to lenalidomide or any component of the formulation, and caution is advised in those with severe renal impairment or uncontrolled infections.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Lenalidomide
Route
Oral Use
Manufacturer
Stada Arzneimittel Ag
Origin
EU

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