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Pegreligrast Inj 6mg Pegfilgrastim

Pegreligrast Inj 6mg Pegfilgrastim
Pegreligrast Inj 6mg Pegfilgrastim

Pegreligrast Inj 6mg Pegfilgrastim Specification

  • Measurement Range
  • 6 mg/0.6 ml
  • Shelf Life
  • 24 Months
  • Instruments Type
  • Pharmaceutical Injection
  • Features
  • Filgrastim pegylated for longer half-life, single use
  • Accuracy
  • Standardized medical dosage
  • Storage Instructions
  • Store at 2C - 8C, Do not freeze
  • Frequency
  • Single dose per chemotherapy cycle
  • Usage Type
  • Single Use
  • Function
  • Stimulates white blood cell production
  • Equipment Type
  • Injection
  • Material
  • Sterile aqueous solution
  • Condition
  • New
  • Technology
  • Recombinant DNA technology
  • Portable
  • Yes
  • Wall Mounted
  • No
  • Operating Type
  • Parenteral
  • Use
  • Medical, Oncology, Chemotherapy Induced Neutropenia
  • Dimension (L*W*H)
  • Prefilled syringe (1 ml)
  • Weight
  • Approx. 1g per syringe
  • Color
  • Clear colorless solution
  • Brand Name
  • Pegreligrast
  • Packaging Type
  • Prefilled syringe
  • Indication
  • Reduction of neutropenia duration in chemotherapy patients
  • Prescription/Non Prescription
  • Prescription Only
  • Therapeutic Class
  • Hematopoietic Agent
  • Route of Administration
  • Subcutaneous injection
  • Marketed By
  • Zydus Cadila
  • Strength
  • 6 mg
  • Generic Name
  • Pegfilgrastim
 

Pegreligrast Inj 6mg Pegfilgrastim Trade Information

  • Minimum Order Quantity
  • 100 Packs
  • FOB Port
  • AHMEDABAD
  • Payment Terms
  • Paypal, Cash Advance (CA), Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Delivery Time
  • 3 Days
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • Box
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
 

About Pegreligrast Inj 6mg Pegfilgrastim

Pegreligrast 6mg Injection contains Pegfilgrastim, a long-acting form of granulocyte colony-stimulating factor (G-CSF). It is primarily used to stimulate the production of neutrophils, a type of white blood cell that plays a key role in fighting infections. Pegfilgrastim is especially beneficial for patients who experience neutropenia (low white blood cell count) due to chemotherapy.

Key Uses:

  1. Chemotherapy-Induced Neutropenia: Pegfilgrastim is used to prevent neutropenia in cancer patients undergoing chemotherapy. Chemotherapy often leads to a decrease in white blood cells, making the body more vulnerable to infections. Pegreligrast 6mg helps increase neutrophil counts, reducing the risk of infections.
  2. Bone Marrow Disorders: It can be used in patients with certain conditions that cause low white blood cell counts or following bone marrow transplantation.

Mechanism of Action:

Pegfilgrastim is a modified version of the natural granulocyte colony-stimulating factor (G-CSF). It works by binding to receptors on bone marrow cells, stimulating the production of neutrophils and enhancing the immune system's ability to fight infections.

Common Side Effects:

  • Bone pain: This is the most frequent side effect, as the bodys bone marrow increases its production of white blood cells.
  • Fatigue or general weakness.
  • Headache.
  • Injection site reactions: Pain, redness, or swelling at the injection site.

Serious Side Effects:

  • Splenic rupture: A rare but serious side effect where the spleen may become enlarged and rupture, causing left abdominal or shoulder pain.
  • Acute respiratory distress syndrome (ARDS): Rare, but severe lung complications.
  • Severe allergic reactions: Symptoms can include rash, swelling, difficulty breathing, and dizziness.

Dosage:

The usual dose of Pegreligrast 6mg is 6 mg, given once per chemotherapy cycle. The injection is typically administered subcutaneously (under the skin) at least 24 hours after chemotherapy. The injection is usually given in the thigh or abdomen.

Precautions:

  • Bone pain: Pain relief may be required to manage bone pain associated with the increased production of white blood cells.
  • Pregnancy and breastfeeding: The use of Pegfilgrastim during pregnancy or breastfeeding should be avoided unless absolutely necessary, and only under the supervision of a healthcare provider.
  • Monitoring: Regular monitoring of blood counts is necessary to track the effectiveness of treatment and ensure safety.

Summary:

Pegreligrast 6mg Injection is a key treatment for preventing neutropenia in cancer patients undergoing chemotherapy, helping reduce the risk of infections. The injection works by stimulating the production of neutrophils in the bone marrow. While it is generally well-tolerated, it may cause side effects like bone pain and injection site reactions. Serious risks include splenic rupture and allergic reactions, requiring careful monitoring throughout the treatment.



Efficient Neutropenia Management

Pegreligrast provides targeted support for chemotherapy patients, significantly reducing episodes and duration of neutropenia. This helps lower infection risk, safeguarding the patient's overall health during intensive cancer treatment. Its pegylated design guarantees extended action with just one dose per chemotherapy cycle.


User-Friendly Administration

Delivered as a prefilled, portable syringe, Pegreligrast offers single-use convenience and standardized doses with each injection. Healthcare professionals can administer this subcutaneous injection with ease, optimizing workflow in oncology clinics while maintaining patient comfort.


Innovative Technology and Quality Assurance

Pegreligrast is produced via advanced recombinant DNA technology, ensuring high purity and efficacy. Stringent manufacturing processes and rigorous quality controls uphold its standardized dose and sterile composition, giving healthcare providers and patients peace of mind.

FAQ's of Pegreligrast Inj 6mg Pegfilgrastim:


Q: How is Pegreligrast Inj 6mg Pegfilgrastim administered?

A: Pegreligrast is administered as a single subcutaneous injection using a prefilled syringe. A qualified healthcare professional will inject the medication, typically once per chemotherapy cycle, as directed by your oncologist.

Q: What is the main benefit of using Pegreligrast for chemotherapy patients?

A: The primary benefit of Pegreligrast is its ability to stimulate white blood cell production, thereby reducing the duration and severity of neutropenia. This helps to decrease the risk of infection during chemotherapy treatment.

Q: When should Pegreligrast be given during the chemotherapy cycle?

A: Pegreligrast is usually administered at least 24 hours after chemotherapy as a single dose per treatment cycle. Your doctor will determine the precise timing based on your specific chemotherapy schedule.

Q: Where should Pegreligrast be stored before use?

A: Pegreligrast should be stored in a refrigerator at 2C to 8C. It must not be frozen. Keep the prefilled syringe in its original packaging until ready for use to maintain sterility and efficacy.

Q: What process is used to manufacture Pegreligrast?

A: Pegreligrast is produced using recombinant DNA technology, which enables precise pegylation of filgrastim, resulting in a longer half-life and sustained effect compared to standard filgrastim formulations.

Q: Is Pegreligrast suitable for home use by patients?

A: Pegreligrast is typically administered by healthcare professionals in a medical setting. If patients are to receive it at home, they should first be trained by a professional on the correct subcutaneous injection technique and safe handling of the single-use syringe.

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