GNH USA

Europe — EMA

Lenalidomida Teva

GNH USA supplies Lenalidomida Teva (Lenalidomide), an immunomodulatory drug for myeloma and del(5q) myelodysplastic syndromes. Request a quote for supply.

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomida Teva, is a Immunomodulatory drug (IMiD) presented as an oral formulation for oral use. It is indicated for the treatment of multiple myeloma and myelodysplastic syndromes with the del(5q) chromosome abnormality.

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

What is Lenalidomide used for?

Lenalidomida Teva is an immunomodulatory agent used in specific hematologic malignancies.

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.

What are the side effects of Lenalidomide?

Lenalidomida Teva may cause a range of adverse reactions.

Common Side Effects: - Neutropenia: reduced neutrophil count increasing infection risk. - Thrombocytopenia: low platelet levels causing bleeding tendencies. - Fatigue: persistent tiredness affecting daily activities. - Diarrhea: loose stools that may lead to dehydration. - Rash: skin irritation or erythema. - Nausea: feeling of sickness often accompanied by vomiting.

Serious or Rare Side Effects: - Venous thromboembolism: deep vein thrombosis or pulmonary embolism. - Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Secondary malignancies: emergence of new cancers. - Hepatotoxicity: elevated liver enzymes or liver injury. - Embryo‑fetal toxicity: severe birth defects if exposure occurs during pregnancy.

What precautions apply to Lenalidomide?

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

Pregnancy contraindication: avoid use in pregnant women; teratogenic risk is category X. Thromboembolic risk: assess need for prophylactic anticoagulation. Renal impairment: adjust monitoring for patients with reduced kidney function. Hematologic monitoring: regular CBC to detect neutropenia or thrombocytopenia. Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

What does Lenalidomide interact with?

Lenalidomida Teva can interact with several concomitant medications.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce drug exposure. - Anticoagulants (e.g., warfarin): increased risk of bleeding. - P-glycoprotein inhibitors: may elevate plasma concentrations.

Moderate Interactions (Monitor Closely): - CYP3A4 inhibitors (e.g., ketoconazole): may increase exposure. - Immunosuppressants (e.g., cyclosporine): potential additive hematologic toxicity. - Vaccines: live attenuated vaccines should be avoided during treatment.

Frequently asked questions

What conditions is Lenalidomida Teva used to treat?+
Lenalidomida Teva is prescribed for patients with multiple myeloma, particularly in relapsed or refractory settings, and for those with myelodysplastic syndromes that carry the del(5q) chromosomal abnormality. In both cases, the drug helps control disease progression and can reduce the need for blood transfusions.
How does lenalidomide work in the body?+
Lenalidomide binds to the cereblon protein within the CRL4CRBN E3 ubiquitin ligase complex, changing its substrate specificity. This triggers the degradation of transcription factors Ikaros and Aiolos, leading to enhanced immune cell activity, inhibition of new blood vessel formation, and direct anti‑tumor effects that suppress malignant plasma cells.
What is the usual dose of Lenalidomida Teva?+
The specific dose and schedule of Lenalidomida Teva are determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Healthcare providers tailor the regimen to achieve optimal therapeutic benefit while minimizing risk.
Is Lenalidomida Teva safe during pregnancy or breastfeeding?+
Lenalidomida Teva is classified as pregnancy category X because it can cause severe fetal harm, including birth defects. It is contraindicated in pregnant women and should not be used by women who are breastfeeding, as the drug may be excreted in breast milk and affect the infant.
How do I order Lenalidomida 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 necessary import documentation.
How does Lenalidomida Teva compare with other treatments for multiple myeloma?+
Lenalidomida Teva belongs to the immunomodulatory drug class, offering a distinct mechanism compared with proteasome inhibitors or monoclonal antibodies. It provides oral administration, which can be more convenient, and has demonstrated efficacy in relapsed or refractory multiple myeloma, often used in combination regimens to enhance response rates.
What are the recommended storage conditions for Lenalidomida Teva?+
Lenalidomida Teva should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.
How is Lenalidomida Teva administered?+
Lenalidomida Teva is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets are swallowed whole with a glass of water, and the dosing schedule (e.g., daily or on specific days of a cycle) is individualized for each patient.
What are the most serious risks associated with Lenalidomida Teva?+
The most serious risks include severe neutropenia and thrombocytopenia, which can lead to infections or bleeding, as well as venous thromboembolism, embryo‑fetal toxicity, and rare but severe skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for these events throughout therapy.
Who should not use Lenalidomida Teva?+
Lenalidomida Teva is contraindicated in pregnant women and in individuals with known hypersensitivity to lenalidomide or any component of the formulation. Caution is also advised for patients with severe renal impairment, uncontrolled infections, or a history of thromboembolic events unless appropriate prophylaxis is in place.
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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