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Human Plasma Coagulation Factor Viii
Human Plasma Coagulation Factor Viii

Human Plasma Coagulation Factor Viii

Price 110.0 USD ($)/ Pack

MOQ : 1000 Packs

Human Plasma Coagulation Factor Viii Specification

  • Origin of Medicine
  • India
  • Salt Composition
  • Nefopam Hydrochloride Injection 20mg
  • Drug Type
  • Specific Drug
  • Ingredients
  • HUMAN PLASMA COAGULATION FACTOR VIII
  • Physical Form
  • Liquid
  • Function
  • Other
  • Dosage
  • AS PER INSTRUCTION
  • Dosage Guidelines
  • AS PER INSTRUCTION
  • Quantity
  • 10000 Pieces
  • Storage Instructions
  • AS PER INSTRUCTIONS
 

Human Plasma Coagulation Factor Viii Trade Information

  • Minimum Order Quantity
  • 1000 Packs
  • FOB Port
  • Mundra & Nhava Sheva
  • Payment Terms
  • Letter of Credit (L/C), Telegraphic Transfer (T/T)
  • Supply Ability
  • 1000 Packs Per Month
  • Delivery Time
  • 2 Week
  • Sample Available
  • No
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Packaging Details
  • SINGLE PACK
  • Main Export Market(s)
  • North America, Asia, Australia, Central America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Certifications
  • AS PER AVAILABILITY
 

About Human Plasma Coagulation Factor Viii

PRODUCT NAME:HUMAN PLASMA COAGULATION FACTOR VIII

GENERIC NAME: HUMAN PLASMA COAGULATION FACTOR VIII

MANUFACTURER: OCEAN

PACKING: SINGLE PACK

USES: used in: haemorrhages treatment and prophylaxis of patients with congenital deficit of factor VIII (haemophilia A); treatment of acquired deficit of factor VIII; treatment of haemophilic patients with developed antibody against factor VIII (inhibitors).




Key Role in Hemostasis

Human Plasma Coagulation Factor VIII plays a crucial part in the blood clotting process, helping individuals with certain clotting disorders to prevent and control bleeding. It is specifically formulated to replace missing or deficient factor VIII, allowing for more reliable management of hereditary coagulation deficiencies like hemophilia A.


Strict Dosage and Storage Guidelines

This medication is available in liquid form and should be dosed strictly according to medical instructions. Appropriate storage conditions, as outlined by the manufacturer, maintain the products stability and effectiveness. Following correct guidelines ensures the medicine retains its therapeutic potential, making it safe for use.

FAQs of HUMAN PLASMA COAGULATION FACTOR VIII:


Q: How is Human Plasma Coagulation Factor VIII administered?

A: This medication is typically administered by intravenous infusion under the supervision of a healthcare professional. It is important that both preparation and injection follow the specific instructions provided to ensure safety and effectiveness.

Q: What conditions does Factor VIII treat?

A: Human Plasma Coagulation Factor VIII is primarily used to manage and prevent bleeding episodes in individuals with hemophilia A or other congenital deficiencies of factor VIII. It is not effective for treating von Willebrand disease or factor IX deficiencies.

Q: When should Factor VIII be used?

A: Factor VIII should be administered when prescribed by a physician, often in response to bleeding episodes, during surgeries, or as preventive therapy. Follow the recommended schedule and dosage determined by your healthcare provider.

Q: Where should I store the Factor VIII formulation?

A: Store the liquid formulation exactly as indicated in the manufacturers instructions, typically in a controlled environment that protects from temperature extremes. Always check the packaging for specific storage conditions.

Q: What is the process for using Human Plasma Coagulation Factor VIII safely?

A: To use this medication safely, ensure that preparation and administration are handled by a trained healthcare professional. Adhere strictly to all dosing, handling, and storage instructions provided by your medical team and the manufacturer.

Q: What are the main benefits of using Factor VIII therapy?

A: The primary benefit of Factor VIII therapy is to restore normal clotting activity in individuals with factor VIII deficiency, significantly reducing the risk of spontaneous and severe bleeding episodes, and improving quality of life.

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