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  • Everolimus
  • Everolimus
  • Everolimus
  • Everolimus

Everolimus(LuciEver)

Another NameAfinitor、飞尼妥、依维莫司

IndicationsIndicated for the treatment of advanced hormone receptor-positive, HER2-negative breast cancer; neuroendocrine tumors of pancreatic, gastrointestinal, and pulmonary origin; advanced renal cell carcino

Specs

  • 5mg*30Tablets
  • Reg No.02 L 1303/25
  • Inspection NO.425-25
  • Dosage FormTablet
  • Indate24 months
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    Telegram name: Vira

  • Name: LUCIUS

    No.:0085253923643

Warm tips:Please purchase and use the medication under pharmacist guidance as the outer packaging is for reference only and the information is intended for professionals.
Introduction of Everolimus

Everolimus produced by Lucius Pharmaceuticals is a multi-targeted kinase inhibitor with well-established clinical efficacy and favorable tolerability, demonstrating significant therapeutic value in the treatment of various solid tumors and rare disease-related lesions.

Medicine-related columns

Instructions of Everolimus

Overview of Key Information for Everolimus.

Active Ingredient

The main active ingredient is everolimus.

Indications

Indicated for adult and pediatric patients with various cancers and tuberous sclerosis complex (TSC)-associated lesions.

Dosage and Administration

The recommended general dosage is 10 mg orally once daily. The specific dosage should be adjusted based on the indication, body surface area, and blood concentration.

Use in Specific Populations

Dosage adjustment is required for patients with hepatic impairment.

Men and women of reproductive potential should use effective contraceptive measures during treatment.

Overdosage

In case of overdosage, seek medical attention immediately and initiate symptomatic and supportive treatment.

Storage Conditions

Store the drug in its original packaging at 20–25°C, protected from moisture and light.

Pharmacokinetics

Everolimus is metabolized by CYP3A4. Its blood concentration is affected by food and concurrent medications, requiring blood concentration monitoring.

FDA,2022.02