GNH USA

Europe — EMA

Kleder Stada

GNH USA supplies Kleder Stada (Lenalidomide), an antineoplastic agent for multiple myeloma and del(5q) myelodysplastic syndromes. Request a quote for supply.

Lenalidomide

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What is Lenalidomide?

Lenalidomide, the active ingredient in Kleder Stada, is a immunomodulatory drug presented as an oral tablet for oral use. It is indicated for the treatment of multiple myeloma and myelodysplastic syndromes with del(5q) in adult patients. GNH USA supplies Kleder 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 rely on abnormal plasma‑cell proliferation and ineffective hematopoiesis. - Multiple myeloma: improves progression‑free and overall survival when combined with dexamethasone in relapsed or refractory disease. - Myelodysplastic syndromes (del(5q)): reduces transfusion dependence and prolongs survival in patients with the 5q deletion.

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: persistent tiredness affecting daily activities. - Diarrhea: loose stools occurring intermittently. - Nausea: mild to moderate upset stomach. - Rash: skin redness or itching. - Constipation: difficulty passing stool. - Peripheral edema: swelling of the lower extremities.

Serious or Rare Side Effects: - Thromboembolic events: deep‑vein thrombosis or pulmonary embolism. - Severe neutropenia: markedly reduced neutrophil count increasing infection risk. - Hepatotoxicity: elevated liver enzymes or liver injury. - Secondary malignancies: emergence of new cancers. - Severe cutaneous 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 laboratory parameters regularly. - Pregnancy testing: confirm negative result before starting; discontinue if pregnancy occurs. - Thrombosis prophylaxis: consider anticoagulation in patients with additional risk factors. - Renal function: adjust monitoring in patients with impaired clearance. - Hepatic function: evaluate liver enzymes prior to and during treatment. - Contraception: use effective methods during treatment and for at least four weeks after the last dose. - Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

What does Lenalidomide interact with?

Lenalidomide may interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inducers: may reduce lenalidomide exposure. - Anticoagulants (e.g., warfarin): increased risk of bleeding.

Moderate Interactions (Monitor Closely): - P-glycoprotein inhibitors: may raise plasma concentrations. - NSAIDs: additive risk of renal impairment. - Vaccines: live vaccines should be avoided during therapy.

Frequently asked questions

What conditions is Kleder Stada used to treat?+
Kleder Stada, which contains lenalidomide, is approved for adult patients with multiple myeloma and for myelodysplastic syndromes that have a deletion of the chromosome 5q region. It is used as part of combination regimens to control disease progression and reduce transfusion needs.
How does lenalidomide work in the body?+
Lenalidomide binds to cereblon, a component of an E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos. This action modifies the immune environment, inhibits new blood‑vessel formation, and directly induces death of malignant plasma cells and dysplastic progenitors.
What is the usual dose of Kleder Stada?+
The dosage of Kleder Stada is individualized by the prescribing physician based on the specific indication, disease stage, renal function, and patient tolerance. Only a qualified healthcare professional should determine the appropriate dose and schedule.
Is Kleder Stada 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 harm. Women of child‑bearing potential must use effective contraception, and breastfeeding is not recommended while taking the medication.
How do I order Kleder Stada from GNH USA?+
To request Kleder 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 Kleder Stada compare with other treatments for multiple myeloma?+
Compared with older immunomodulatory agents such as thalidomide, lenalidomide offers a more favorable safety profile, especially regarding neuropathy, while maintaining strong anti‑myeloma activity. It is often used in combination with dexamethasone or proteasome inhibitors, providing synergistic efficacy.
What are the recommended storage conditions for Kleder Stada?+
Kleder Stada tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect the product from moisture, excessive heat and direct sunlight to maintain potency throughout its shelf life.
How is Kleder Stada administered?+
Kleder Stada is taken orally, usually once daily, with or without food, as directed by the treating physician. The tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.
What are the most serious risks associated with Kleder Stada?+
The most serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe neutropenia that can predispose to infections, and rare but life‑threatening skin reactions like Stevens‑Johnson syndrome. Patients should be monitored closely for these complications.
Who should not use Kleder Stada?+
Kleder Stada should not be used by pregnant women, individuals with known hypersensitivity to lenalidomide or its excipients, and patients with uncontrolled severe infections. Caution is also advised for those with significant renal or hepatic impairment, and the drug should be avoided in patients receiving live vaccines.
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 Arzneimittel Ag
Origin
EU

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