GNH USA

Europe — EMA

Lenalidomida Stada

GNH USA supplies Lenalidomida Stada (Lenalidomide), a immunomodulatory imide drug for multiple myeloma, myelodysplastic syndromes with del(5q) and mantle

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomida Stada, is an immunomodulatory imide drug (IMiD) presented as an oral formulation for oral use. It treats multiple myeloma, myelodysplastic syndromes with del(5q), and mantle cell lymphoma in appropriate patients.

GNH USA supplies Lenalidomida Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

What is Lenalidomide used for?

Lenalidomide is used in hematologic malignancies that respond to immunomodulatory therapy.

Multiple Myeloma: improves progression‑free survival and overall response rates when combined with dexamethasone or proteasome inhibitors. Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and cytopenias. Mantle Cell Lymphoma: enhances response when added to standard chemo‑immunotherapy regimens.

What are the side effects of Lenalidomide?

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

Common Side Effects: - Neutropenia: reduced neutrophil count, increasing infection risk. - Thrombocytopenia: low platelet levels, may cause bleeding. - Fatigue: persistent tiredness. - Nausea: upset stomach and vomiting. - Diarrhea: loose stools. - Rash: mild skin irritation.

Serious or Rare Side Effects: - Venous thromboembolism: blood clots in deep veins or lungs. - Severe neutropenia: profound immune suppression. - Secondary primary malignancies: emergence of new cancers. - Tumor lysis syndrome: rapid tumor cell breakdown. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Hepatic failure: liver dysfunction with jaundice.

What precautions apply to Lenalidomide?

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor laboratory parameters.

Pregnancy: contraindicated; ensure effective contraception. Renal impairment: assess renal function and adjust dose if needed. Thromboembolic risk: consider prophylactic anticoagulation in high‑risk patients. Hematologic monitoring: perform regular CBC to detect cytopenias. Drug interactions: review concomitant medications for potential CYP3A4 effects. Store at ambient temperature: keep below 25 °C, in original packaging, protected from moisture and light.

What does Lenalidomide interact with?

Lenalidomide can interact with several agents, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin): may markedly reduce lenalidomide exposure. - Anticoagulants (e.g., warfarin): increased risk of bleeding. - Live vaccines: heightened infection risk due to immunosuppression. - Teratogenic agents: combined exposure contraindicated in pregnancy.

Moderate Interactions (Monitor Closely): - CYP3A4 inhibitors (e.g., ketoconazole): may increase drug levels. - NSAIDs: potential additive renal toxicity. - Antihistamines: may enhance sedation or dizziness.

Frequently asked questions

What conditions is Lenalidomida Stada used for?+
Lenalidomida Stada contains lenalidomide and is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with deletion 5q, and mantle cell lymphoma, typically as part of combination therapy prescribed by a qualified oncologist.
How does lenalidomide work in the body?+
Lenalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, altering its activity. This triggers degradation of specific transcription factors, leading to anti‑angiogenic, immunomodulatory, and direct anti‑tumor effects that help control malignant cell growth.
What is the usual dose of Lenalidomida Stada?+
The prescribed dose of Lenalidomida Stada is determined individually by the treating physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Patients should follow the exact dosing instructions provided by their healthcare professional.
Is Lenalidomida Stada safe during pregnancy or breastfeeding?+
Lenalidomida Stada is contraindicated in pregnancy because lenalidomide is teratogenic. Women of child‑bearing potential must use effective contraception. Safety during breastfeeding has not been established, and breastfeeding is generally not recommended while receiving the drug.
How do I order Lenalidomida 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, and any necessary import documentation.
How does Lenalidomida Stada compare with other treatments for multiple myeloma?+
Lenalidomida Stada (lenalidomide) belongs to the immunomodulatory imide drug class, offering a distinct mechanism compared with proteasome inhibitors or monoclonal antibodies. It is often combined with dexamethasone or other agents to improve response rates, whereas alternative classes target proteasome activity or surface antigens.
What are the recommended storage conditions for Lenalidomida Stada?+
Store Lenalidomida Stada at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat, and direct sunlight to maintain stability and potency.
How is Lenalidomida Stada administered?+
Lenalidomida Stada is taken orally, usually as a tablet or capsule, with or without food as directed by the prescriber. The exact administration schedule, including any dose interruptions, is determined by the treating physician based on therapeutic response and tolerability.
What are the most serious risks associated with Lenalidomida Stada?+
Serious risks include venous thromboembolism, severe neutropenia or thrombocytopenia, secondary primary malignancies, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for signs of infection, clotting, or unusual skin changes.
Who should not use Lenalidomida Stada?+
Lenalidomida Stada should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or its excipients, and patients with uncontrolled severe infections or certain uncontrolled cardiac conditions unless specifically advised by a specialist.
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
Laboratorio Stada, S.L.
Origin
EU

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