GNH USA

Europe — EMA

Lenalidomid Fresenius Kabi

GNH USA supplies Lenalidomid Fresenius Kabi (Lenalidomide), an immunomodulatory imide drug for multiple myeloma, myelodysplastic syndromes and mantle cell

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomid Fresenius Kabi, is an immunomodulatory imide drug (IMiD) presented as an oral tablet for oral use. It treats multiple myeloma, myelodysplastic syndromes and mantle cell lymphoma in adult patients.

GNH USA supplies Lenalidomid Fresenius Kabi as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Lenalidomide used for?

Lenalidomide is employed in hematologic malignancies that involve abnormal plasma or lymphoid cells.

- Multiple Myeloma: improves progression‑free survival and overall response rates in adult patients. - Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and can induce cytogenetic remission. - Mantle Cell Lymphoma: provides disease control in relapsed or refractory cases.

What are the side effects of Lenalidomide?

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

Common Side Effects: - Fatigue: mild to moderate tiredness. - Diarrhea: loose stools, often transient. - Rash: skin erythema or pruritus. - Nausea: occasional upset stomach. - Constipation: reduced bowel movements. - Peripheral edema: mild swelling of extremities.

Serious or Rare Side Effects: - Thromboembolic events: deep‑vein thrombosis or pulmonary embolism. - Severe neutropenia or leukopenia: markedly reduced white blood cell counts. - Secondary primary malignancies: rare occurrence of new cancers. - Hepatotoxicity: elevated liver enzymes or liver injury. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

What precautions apply to Lenalidomide?

Before initiating therapy, clinicians should assess patient‑specific risk factors and monitor for known adverse events.

- Pregnancy: contraindicated (Category X); teratogenic risk requires effective contraception. - Renal impairment: dose adjustment may be needed based on creatinine clearance. - Thrombotic risk: consider prophylactic anticoagulation in high‑risk patients. - Hematologic monitoring: regular CBCs to detect neutropenia or anemia. - Drug interactions: review concomitant medications for CYP3A4 inducers or inhibitors. - Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

What does Lenalidomide interact with?

Lenalidomide can interact with several drug classes, affecting its efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may markedly reduce lenalidomide exposure. - Anticoagulants (e.g., warfarin, DOACs): increased risk of bleeding. - Live vaccines: reduced efficacy and potential infection risk.

Moderate Interactions (Monitor Closely): - P‑glycoprotein inhibitors (e.g., cyclosporine): may raise plasma concentrations. - Immunosuppressants (e.g., corticosteroids): additive immunomodulatory effects. - NSAIDs: may exacerbate renal toxicity when combined with lenalidomide.

Frequently asked questions

What conditions is Lenalidomid Fresenius Kabi used to treat?+
Lenalidomid Fresenius Kabi, containing lenalidomide, is indicated for adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) cytogenetic abnormality, and mantle cell lymphoma, particularly in relapsed or refractory settings.
How does lenalidomide work in the body?+
Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos. This action modifies the immune response, inhibits new blood‑vessel formation, and directly suppresses malignant plasma and lymphoid cells.
What is the usual dose of Lenalidomid Fresenius Kabi?+
The dose of lenalidomide is individualized by the prescribing physician based on the specific indication, disease stage, renal function, and patient tolerance. The prescriber determines the appropriate strength, frequency and duration of therapy.
Is lenalidomide safe during pregnancy or breastfeeding?+
Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because of a high risk of fetal malformations and embryotoxicity. It is also not recommended while breastfeeding, as it may be excreted in milk and harm the infant.
How do I order Lenalidomid Fresenius Kabi 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 worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including any cold‑chain requirements) and import documentation.
How does lenalidomide compare with thalidomide?+
Both lenalidomide and thalidomide belong to the immunomodulatory imide drug class, but lenalidomide is more potent, has a more favorable safety profile, and exhibits stronger anti‑angiogenic and immune‑activating effects. Thalidomide is associated with higher rates of peripheral neuropathy, whereas lenalidomide carries greater risk of hematologic toxicity and thromboembolic events.
What are the recommended storage conditions for Lenalidomid Fresenius Kabi?+
Store below 25 °C in a dry place. Keep the tablets in the original blister pack or container, protect them from moisture, heat and direct sunlight, and ensure the packaging remains tightly closed until use.
How is Lenalidomid Fresenius Kabi administered?+
The medication is taken orally, usually as a tablet swallowed whole with a glass of water. It may be taken with or without food, according to the prescriber’s instructions, and the dosing schedule is set by the treating physician.
What are the most serious risks associated with lenalidomide?+
Serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe neutropenia or leukopenia that can predispose to infection, and rare secondary primary malignancies. Patients should be monitored closely for signs of clotting, infection and blood‑count changes.
Who should not use lenalidomide?+
Lenalidomide should not be used by pregnant women, individuals with known hypersensitivity to the drug or its excipients, patients with uncontrolled severe renal impairment without dose adjustment, and anyone for whom the risk–benefit assessment is unfavorable, such as those with active 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
Fresenius Kabi Austria Gmbh
Origin
EU

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