GNH USA

Europe — EMA

Lenalidomida Stada

GNH USA supplies Lenalidomida Stada (Lenalidomide), an immunomodulatory agent indicated for multiple myeloma, del(5q) myelodysplastic syndromes and mantle

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Lenalidomida Stada, is an immunomodulatory agent (IMiD) presented as an oral tablet for systemic use. It is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with del(5q), and mantle cell lymphoma in adult patients.

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

What is Lenalidomide used for?

Lenalidomide is used in hematologic malignancies and related disorders, targeting abnormal plasma cells and dysplastic clones. - Multiple Myeloma: improves progression‑free survival and overall response rates in adult patients. - Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and induces 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, which are categorized by frequency and severity.

Common Side Effects: - Fatigue: persistent tiredness affecting daily activities. - Diarrhea: loose stools that may require fluid replacement. - Rash: skin redness or itching. - Nausea: feeling of sickness that may lead to vomiting.

Serious or Rare Side Effects: - Thromboembolic events: blood clots such as deep vein thrombosis or pulmonary embolism. - Severe neutropenia: markedly reduced neutrophil count increasing infection risk. - Secondary primary malignancies: emergence of new cancers unrelated to the original disease.

What precautions apply to Lenalidomide?

When prescribing Lenalidomida Stada, clinicians should consider several safety and handling precautions. - Pregnancy risk: avoid use in pregnant women; a risk management program is required. - Thrombosis prophylaxis: assess need for anticoagulation in patients with additional risk factors. - Renal impairment: adjust monitoring in patients with reduced kidney function. - Hepatic impairment: monitor liver function tests regularly. - Drug interactions: review concomitant medications for potential interactions. - Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and light.

What does Lenalidomide interact with?

Lenalidomide can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inducers: may lower lenalidomide exposure (e.g., rifampin, carbamazepine). - Anticoagulants: increased risk of bleeding when combined with warfarin or direct oral anticoagulants. - Immunosuppressants: may enhance immunosuppression, raising infection risk.

Moderate Interactions (Monitor Closely): - P-glycoprotein inhibitors: may increase plasma levels (e.g., verapamil, quinidine). - NSAIDs: can exacerbate renal toxicity. - Vaccines: live attenuated vaccines may be less effective; avoid during therapy.

Frequently asked questions

What is Lenalidomida Stada used for?+
Lenalidomida Stada contains lenalidomide, an immunomodulatory drug approved for adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) chromosomal abnormality, and mantle cell lymphoma, particularly in relapsed or refractory settings.
How does lenalidomide work?+
Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, triggering degradation of transcription factors Ikaros and Aiolos. This leads to anti‑angiogenic, anti‑inflammatory, and immunomodulatory effects that suppress malignant cell growth and enhance immune‑mediated tumor clearance.
What is the usual dose of Lenalidomida Stada?+
The specific dose of Lenalidomida Stada is determined by the treating physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Prescribers follow approved dosing guidelines and adjust as needed.
Is Lenalidomida Stada safe in pregnancy or breastfeeding?+
Lenalidomida Stada is contraindicated in pregnancy because it can cause fetal harm. Women of childbearing potential must use effective contraception. Safety during breastfeeding has not been established, so nursing is generally discouraged while on therapy.
How do I order Lenalidomida Stada from GNH USA?+
To order Lenalidomida Stada, 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 lenalidomide compare with thalidomide?+
Both lenalidomide and thalidomide belong to the same immunomodulatory class, but lenalidomide is more potent, has a better safety profile, and is approved for a broader range of hematologic cancers. Thalidomide is associated with higher rates of peripheral neuropathy and sedation, whereas lenalidomide shows fewer neurotoxic effects.
What are the storage and handling requirements for Lenalidomida Stada?+
Lenalidomida Stada should be stored at ambient temperature, preferably below 25 °C, in the original blister or bottle. Keep the product away from moisture, direct sunlight, and excessive heat. Do not refrigerate or freeze the tablets.
How is Lenalidomida Stada administered?+
Lenalidomida Stada is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets are swallowed whole with a glass of water. Patients should follow the dosing schedule provided by their healthcare professional.
What are the most serious risks to watch for while taking Lenalidomida Stada?+
Serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe neutropenia that can predispose to infections, and the possible development of secondary primary malignancies. Patients should be monitored regularly for signs of clotting, infection, and new cancer diagnoses.
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 active infections. Caution is also advised in those with severe renal or hepatic impairment, where dose adjustments may be required.
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 Lda.
Origin
EU

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