GNH USA

Europe — EMA

Lenalidomid Teva

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

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomid Teva, is an immunomodulatory imide drug (IMiD) presented as an oral formulation for oral use. It is employed in the treatment of certain blood cancers, including multiple myeloma, myelodysplastic syndromes with del(5q), and mantle‑cell lymphoma, typically in adult patients under specialist supervision.

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

What is Lenalidomide used for?

Lenalidomid Teva is an immunomodulatory agent used in hematologic malignancies and related disorders. - Multiple myeloma: helps control disease progression and improve survival when used in combination regimens. - Myelodysplastic syndromes with del(5q): reduces transfusion dependence and may achieve cytogenetic remission. - Mantle cell lymphoma: contributes to disease control as part of approved therapeutic protocols.

What are the side effects of Lenalidomide?

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

Common Side Effects: - Neutropenia: reduced neutrophil count increasing infection risk. - Thrombocytopenia: lowered platelet levels leading to bleeding tendencies. - Fatigue: persistent tiredness affecting daily activities. - Nausea: upset stomach often occurring after dosing. - Constipation: difficulty passing stools. - Rash: mild skin irritation or erythema.

Serious or Rare Side Effects: - Venous thromboembolism: blood clots in deep veins or lungs. - Secondary primary malignancies: emergence of new cancers. - Tumor lysis syndrome: rapid tumor cell breakdown causing metabolic disturbances. - Severe allergic reactions: anaphylaxis or angioedema. - Hepatotoxicity: liver enzyme elevations indicating potential liver injury.

What precautions apply to Lenalidomide?

Before initiating therapy with Lenalidomid Teva, several safety considerations should be observed. - Monitor blood counts: perform regular CBC to detect cytopenias. - Assess renal function: adjust use in patients with impaired kidney clearance. - Avoid pregnancy: teratogenic risk requires strict contraception for both sexes. - Counsel on contraception: use effective methods throughout treatment and for a defined period after cessation. - Watch for thrombotic events: evaluate risk factors and consider prophylaxis when indicated. - Store at room temperature: keep in original packaging, protect from moisture and light.

What does Lenalidomide interact with?

Lenalidomid Teva can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase lenalidomide exposure. - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic levels. - Live vaccines: risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - Anticoagulants (warfarin, DOACs): heightened bleeding risk. - NSAIDs: may exacerbate renal toxicity. - Other myelosuppressive agents: additive bone‑marrow suppression. - ACE inhibitors or ARBs: monitor renal function and electrolytes.

Frequently asked questions

What conditions is Lenalidomid Teva used to treat?+
Lenalidomid Teva contains lenalidomide and is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with a deletion of chromosome 5q, and mantle‑cell lymphoma. In each case the drug is used as part of a prescribed therapeutic regimen aimed at controlling disease activity and improving patient outcomes.
How does lenalidomide work in the body?+
Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex. This binding changes the complex’s substrate specificity, leading to the ubiquitination and degradation of transcription factors Ikaros and Aiolos. The resulting actions include anti‑angiogenic effects, modulation of the immune response, and direct inhibition of malignant cell proliferation.
What is the usual dose of Lenalidomid Teva?+
The specific dose of Lenalidomid Teva is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and other individual factors. Healthcare professionals follow approved labeling and clinical guidelines to select the appropriate dosage and schedule for each patient.
Is Lenalidomid Teva safe to use during pregnancy or breastfeeding?+
Lenalidomid Teva is classified as teratogenic and is contraindicated in pregnancy. Women of childbearing potential must use effective contraception before, during, and after treatment. Safety during breastfeeding has not been established, and breastfeeding is generally not recommended while taking lenalidomide.
How do I order Lenalidomid Teva 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 Lenalidomid Teva compare with other treatments for the same diseases?+
Lenalidomid Teva belongs to the immunomodulatory imide drug class, offering a distinct mechanism compared with proteasome inhibitors or monoclonal antibodies used in similar indications. Its oral administration and ability to target cereblon‑mediated pathways provide an alternative or complementary option, often selected based on patient tolerance, prior therapy, and specific disease characteristics.
What are the recommended storage conditions for Lenalidomid Teva?+
Lenalidomid Teva should be stored at room temperature, below 25 °C, in its original packaging. The container protects the product from moisture and light, helping maintain stability throughout its shelf life.
How is Lenalidomid Teva administered?+
Lenalidomid Teva is taken orally, usually with or without food, as directed by the prescribing physician. The tablets are swallowed whole with a glass of water and the dosing schedule is individualized for each patient.
What are the most serious risks associated with Lenalidomid Teva?+
The most serious risks include severe neutropenia or thrombocytopenia, which can lead to infections or bleeding, venous thromboembolism, secondary primary malignancies, and rare but life‑threatening reactions such as tumor lysis syndrome or severe hypersensitivity. Patients should be monitored closely for these events.
Who should not use Lenalidomid Teva?+
Lenalidomid Teva is contraindicated in patients with known hypersensitivity to lenalidomide or any component of the formulation, in pregnant women, and in individuals who cannot adhere to strict contraceptive measures. Caution is also advised for patients 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
Teva B.V
Origin
EU

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