Special Offer! - Free Pharmacy Design - Limited Time Offer, Hurry Up & Register Now

My Cart
In stock

Fasturtec 1.5 mg Powder and solvent for solution for infusion 1ml Vial 3pcs

In stock
Only 1 left
SKU
10331014325

Fasturtec 1.5 mg Powder and Solvent for Infusion is a prescription medicine containing rasburicase, used for the rapid reduction of plasma uric acid levels in cancer patients. It effectively prevents and treats hyperuricemia, a common complication of chemotherapy, especially in cases of Tumor Lysis Syndrome. This essential treatment helps avert acute renal failure and is administered intravenously under medical supervision.

For comprehensive product information and availability, please refer to leading e-commerce platforms like Nahdi Online, , or .


Product Overview


Fasturtec 1.5 mg Powder and Solvent for Solution for Infusion is a vital medication designed for the effective management and prevention of hyperuricemia in patients with cancer.
This condition, characterized by excessively high levels of uric acid in the blood, often arises as a complication of chemotherapy, particularly in cases involving rapid cell lysis known as Tumor Lysis Syndrome (TLS).
Fasturtec, containing the active ingredient rasburicase, works by rapidly converting uric acid into a more soluble compound called allantoin, which is easily excreted by the kidneys, thereby preventing potentially life-threatening complications such as acute renal failure.
Developed by Sanofi-Aventis, Fasturtec is a prescription-only medicine administered under strict medical supervision in a clinical setting.

Benefits of Use


  • Rapid Uric Acid Reduction: Fasturtec provides a swift and highly effective means to lower plasma uric acid levels, crucial during acute phases of hyperuricemia.
  • Prevention of Acute Renal Failure: By facilitating the removal of uric acid, it significantly reduces the risk of uric acid crystallizing in the kidneys, thereby preventing acute renal injury and failure.
  • Management of Tumor Lysis Syndrome (TLS): It is a cornerstone therapy in managing and preventing the severe metabolic abnormalities associated with TLS in patients undergoing chemotherapy for hematologic malignancies.
  • Improved Patient Outcomes: Early intervention with Fasturtec can help improve overall patient prognosis and reduce the need for more invasive treatments like dialysis.

How to Use


Fasturtec is intended for intravenous administration exclusively by healthcare professionals in a hospital or clinic setting.
The following outlines the general process; specific instructions will be provided by your treating physician:

  1. Reconstitution: The powder in the vial is reconstituted with the provided solvent to form a clear solution.
  2. Dilution: The reconstituted solution is then further diluted in an appropriate intravenous fluid (e.g., 0.9% sodium chloride).
  3. Administration: The diluted solution is administered as an intravenous infusion over a specified period, typically 30 minutes.
  4. Dosage: Dosage and duration of treatment are determined by the physician based on the patient's body weight, baseline uric acid levels, and clinical response.
  5. Monitoring: During and after administration, patients will be closely monitored for uric acid levels, kidney function, and potential adverse reactions.

Caution & Warnings


  • Hypersensitivity Reactions: Severe hypersensitivity reactions, including anaphylaxis, can occur. Patients should be closely monitored during and after infusion.
  • G6PD Deficiency: Fasturtec is contraindicated in patients with Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency due to the risk of hemolytic anemia and methemoglobinemia. Screening for G6PD deficiency is recommended prior to treatment.
  • Hemolysis and Methemoglobinemia: These serious adverse events can occur, particularly in patients with G6PD deficiency.
  • Pregnancy and Lactation: Not recommended during pregnancy unless clearly necessary and the potential benefits outweigh the risks. Women of childbearing potential should use effective contraception during and for a period after treatment. Consult your doctor regarding use during lactation.
  • Drug Interactions: Discuss all medications, including over-the-counter drugs and supplements, with your physician to avoid potential interactions.
  • Storage: Store unopened vials in a refrigerator (2°C - 8°C) and protect from light. Do not freeze. Reconstituted and diluted solutions have specific stability guidelines and should be used promptly.

Ingredients


  • Active Ingredient: Rasburicase 1.5 mg
  • Inactive Ingredients: Mannitol, Disodium Phosphate Dodecahydrate, Disodium Phosphate Dihydrate, Tromethamine.

Product Details


Strength: 1.5 mg Rasburicase per vial
Form: Powder and solvent for solution for infusion
Package Size: 3 Vials (each with 1.5 mg powder and 1 ml solvent)
Manufacturer: Sanofi-Aventis
More Information
Gtin 1301221587
Recommended Sale Price 979.75
Is Wasfaty Product No
Brand Not Defined
Ingredient Name RASBURICASE
SFDA Reg. No 1301221587
IBC 1301221587
Drug Type Prescription
Scientific Name Rasburicase
Strength 1.5 mg
Strength Unit mg
Form Powder and solvent for solution for infusion
Admin Route Intravenous
Size 1.5
Size Unit mg
Package Types Vial
Package Size 3 Vials
shelfLife 36 months
Storage conditions Store unopened vials in a refrigerator (2°C - 8°C) and protect from light. Do not freeze. Reconstituted and diluted solutions have specific stability guidelines and should be used promptly.
Refrigerator Storage Yes