GNH USA

Europe — EMA

Lenalidomide Stada

GNH USA supplies Lenalidomide Stada (Lenalidomide), an antineoplastic agent for multiple myeloma and del(5q) MDS. Request a quote for international supply.

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomide Stada, is an immunomodulatory drug (IMiD) presented as an oral formulation for oral use. It is employed in the treatment of certain blood cancers, specifically multiple myeloma and myelodysplastic syndromes with deletion 5q, and is prescribed for adult patients under specialist supervision.

GNH USA supplies Lenalidomide Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to hospitals, pharmacies and clinical trial sites.

What is Lenalidomide used for?

Lenalidomide is an immunomodulatory agent used in hematologic malignancies and related disorders. - Multiple Myeloma: improves disease control and prolongs survival in patients with relapsed or refractory disease. - Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and can lead to cytogenetic remission. - Mantle Cell Lymphoma: used in relapsed or refractory cases to achieve tumor reduction.

What are the side effects of Lenalidomide?

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

Common Side Effects: - Neutropenia: decreased neutrophil count. - Thrombocytopenia: reduced platelet levels. - Fatigue: persistent tiredness. - Diarrhea: loose stools. - Rash: skin irritation. - Constipation: difficulty passing stool.

Serious or Rare Side Effects: - Venous thromboembolism: blood clots in veins. - Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Secondary primary malignancies: emergence of new cancers. - Hepatic failure: serious liver injury. - Tumor lysis syndrome: rapid tumor cell breakdown. - Anaphylaxis: life‑threatening allergic reaction.

What precautions apply to Lenalidomide?

When prescribing Lenalidomide, clinicians should observe several safety measures to minimize risk. - Pregnancy: contraindicated; teratogenic, use effective contraception. - Thromboembolism risk: assess and consider prophylactic anticoagulation. - Hematologic monitoring: regular CBC to detect neutropenia or thrombocytopenia. - Infection risk: monitor for signs of infection and manage promptly. - Renal impairment: adjust dose in patients with reduced kidney function. - Store at ambient temperature: keep below 25 °C, in original container, protect from moisture.

What does Lenalidomide interact with?

Lenalidomide interacts with several drug classes; awareness of these interactions helps avoid adverse outcomes.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lenalidomide exposure. - Strong CYP3A4 inducers (e.g., rifampin): may reduce efficacy. - Anticoagulants (e.g., warfarin): heightened bleeding risk.

Moderate Interactions (Monitor Closely): - NSAIDs: additive risk of gastrointestinal bleeding. - Antiplatelet agents (e.g., aspirin): monitor for bleeding. - Hormonal contraceptives: reduced effectiveness, consider alternative methods. - Live vaccines: increased infection risk, avoid during therapy.

Frequently asked questions

What conditions is Lenalidomide Stada used to treat?+
Lenalidomide Stada is indicated for the treatment of multiple myeloma, myelodysplastic syndromes that carry a deletion of chromosome 5q, and mantle cell lymphoma that has relapsed or is refractory to prior therapy. These are hematologic malignancies where the drug’s immunomodulatory and anti‑angiogenic actions provide clinical benefit.
How does Lenalidomide work in the body?+
Lenalidomide binds to the cereblon subunit of the CRL4‑E3 ubiquitin ligase complex, changing its target profile. This leads to the ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos, which suppresses malignant plasma‑cell growth, inhibits new blood‑vessel formation, and enhances immune‑mediated tumor killing.
What is the usual dose of Lenalidomide Stada?+
The specific dose of Lenalidomide Stada is determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Dosing regimens may differ between multiple myeloma, MDS with del(5q), and mantle‑cell lymphoma, and should follow the latest approved labeling and clinical guidelines.
Is Lenalidomide safe to use during pregnancy or breastfeeding?+
Lenalidomide is classified as Pregnancy Category X because it is known to cause fetal harm. It is contraindicated in pregnancy, and effective contraception must be used by both male and female patients of reproductive potential. The drug is also not recommended while breastfeeding, as it may be excreted in milk and affect the infant.
How do I order Lenalidomide Stada from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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 the necessary import documentation.
How does Lenalidomide compare with other treatments for multiple myeloma?+
Lenalidomide belongs to the immunomodulatory drug class, offering a distinct mechanism from proteasome inhibitors or monoclonal antibodies. It is often used in combination regimens and provides benefits such as oral administration and anti‑angiogenic effects. Compared with older agents like thalidomide, Lenalidomide generally has a more favorable side‑effect profile, especially regarding neuropathy.
What are the recommended storage conditions for Lenalidomide Stada?+
Lenalidomide Stada should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and avoid storing it in bathrooms or other humid environments.
How is Lenalidomide Stada administered?+
Lenalidomide Stada is taken orally, usually once daily, with or without food, as directed by the treating physician. The tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.
What are the most serious risks associated with Lenalidomide therapy?+
The most serious risks include severe neutropenia or thrombocytopenia that can lead to infection or bleeding, venous thromboembolism, life‑threatening skin reactions such as Stevens‑Johnson syndrome, secondary primary malignancies, and hepatic failure. Patients should be monitored closely for these events throughout treatment.
Who should not take Lenalidomide Stada?+
Lenalidomide Stada is contraindicated in pregnant women, patients with known hypersensitivity to lenalidomide or any component of the formulation, and individuals who cannot comply with required contraception measures. Caution is also advised for patients with severe renal impairment, uncontrolled infections, or a history of thromboembolic events.
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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