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PEGYLATED (rHu G-CSF)

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Product Details:

Salt Composition Pegfilgrastim
Dosage Form Injection
Indication Neutropenia, particularly chemotherapy-induced neutropenia
Pacakaging (Quantity Per Box) 1 vial per box
Life Span 24 months from manufacturing date
Packaging Type Vial
Origin of Medicine Biotechnology, Recombinant DNA Technology
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PEGYLATED (rHu G-CSF) Price And Quantity

Minimum Order Quantity 100 Kit

PEGYLATED (rHu G-CSF) Product Specifications

Suitable For Adults
Pacakaging (Quantity Per Box) 1 vial per box
Function Stimulates production of neutrophils, reduces risk of infection
Physical Form Lyophilized Powder
Dosage As directed by physician, typically 6mg as single subcutaneous injection per cycle
Storage Instructions Store at 2C to 8C, Do not freeze
Recommended For Cancer Patients Undergoing Chemotherapy
Salt Composition Pegfilgrastim
Dosage Form Injection
Indication Neutropenia, particularly chemotherapy-induced neutropenia
Ingredients Pegylated Recombinant Human Granulocyte Colony Stimulating Factor (rHu G-CSF)
Dosage Guidelines Follow strictly as per healthcare provider
Quantity 6 mg
Packaging Type Vial
Origin of Medicine Biotechnology, Recombinant DNA Technology
Drug Type Biological Product
Life Span 24 months from manufacturing date

Side Effects May cause bone pain, headache, or injection site reactions
Reconstitution Reconstitute with provided sterile water for injection
Route of Administration Subcutaneous
Contraindications Hypersensitivity to Pegfilgrastim or Filgrastim
Prescription Status Prescription only
Molecular Weight Approximately 39 kDa (pegylated)
Color White to off-white powder
Stability Stable for up to 24 months at recommended conditions

Product Description

Pegylated G-CSF Inhibits Blood Cell Depletion, Increases Platelets, Blocks Splenomegaly, and Improves Survival after Whole-Body Ionizing Irradiation but Not after Irradiation Combined with Burn - PMC Skip to main content. An official website of the United States government.

How Leupag Works

Leupag stimulates the bone marrow to enhance the production of neutrophils, a type of white blood cell essential for fighting infections. This mechanism is particularly valuable for cancer patients who are at increased risk of neutropenia, especially during chemotherapy. By elevating neutrophil counts, Leupag helps to minimize the likelihood of infection, supporting more effective and uninterrupted cancer treatment regimens.

Usage and Administration Guidelines

Leupag should only be used as directed by a qualified healthcare professional. The recommended dosage is a single 6 mg subcutaneous injection per chemotherapy cycle. Before administration, the lyophilized powder must be reconstituted with the provided sterile water for injection. Strictly follow your physician's instructions, including correct reconstitution and injection practices, to ensure safety and effectiveness.

Storage, Stability, and Handling

This biological product remains stable for up to 24 months when stored at 2C to 8C. Leupag must not be frozen and should be kept away from light until use. Each box contains one vial, ensuring precise dosing and minimizing contamination. Always check the manufacturing date and do not use past the stated shelf life for optimal results.

FAQ's of PEGYLATED (rHu G-CSF):

Q: How does Leupag (PEGYLATED rHu G-CSF) benefit cancer patients undergoing chemotherapy?

A: Leupag stimulates the bone marrow to increase neutrophil production, significantly reducing the risk of neutropenia and subsequent infections in patients undergoing chemotherapy. This enables patients to follow their prescribed treatment schedule more safely.

Q: What is the recommended process for reconstituting and administering Leupag?

A: Leupag should be reconstituted using the sterile water provided in the packaging. After complete dissolution, it is administered as a single subcutaneous injection, typically at a dose of 6 mg per chemotherapy cycle, strictly as per your healthcare provider's directions.

Q: When should Leupag be administered during chemotherapy?

A: Leupag is usually given once per chemotherapy cycle, following your physician's advice. The timing of the injection in relation to chemotherapy is critical, so always adhere to your healthcare provider's instructions for scheduling.

Q: Where should Leupag be stored and how should it be handled?

A: Store Leupag at temperatures between 2C to 8C and keep the vial protected from light. Do not freeze the product. Handle the vial with care during reconstitution and administration to maintain sterility.

Q: What precautions and contraindications should be observed with Leupag?

A: Leupag is contraindicated in individuals with known hypersensitivity to Pegfilgrastim or Filgrastim. Inform your healthcare provider about allergies and follow their guidance. Common side effects may include bone pain, headaches, or reactions at the injection site.

Q: Who is Leupag intended for and is it suitable for all adults?

A: Leupag is intended for adult patients undergoing chemotherapy who are at risk of developing neutropenia. It should be used only under medical supervision and is not recommended for individuals with hypersensitivity to its ingredients.

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