Human Serum Albumin-I.P Grifols 100 ml

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Human Serum Albumin-I.P Grifols 100 ml Specification

Indication
Hypovolemia, burns, hypoalbuminemia, shock, plasma exchange, volume replacement

Salt Composition
Human Serum Albumin (20% Solution)

Dosage Form
Injection / Infusion

Enzyme Types
Not an enzyme; plasma-derived protein

Feature
Sterile, pyrogen-free, high protein content, ready-to-use, approved for clinical use

Ingredients
Human Albumin, Stabilizers (e.g. sodium caprylate, sodium chloride)

Application
Medical, intravenous administration

Ph Level
6.7 - 7.3

Physical Color/Texture
Clear, slightly viscous liquid

Fermentation Smell
Odorless

Enzymatic Activity
None (not an enzyme)

Storage Instructions
Store below 25C. Do not freeze. Protect from light.

Shelf Life
3 years from date of manufacture

Volume
100 ml

Contraindication
Severe anemia, cardiac failure with normal or increased intravascular volume

Concentration
20% (20 g/100 ml)

Route of Administration
Intravenous

Manufactured By
Grifols Therapeutics

Country of Approval
Canada, EU, UK, USA, Australia as displayed

Compatibility
Compatible with common IV solutions

Packaging Type
Glass Bottle / Vial

Adverse Effects
Allergic reactions, increased blood volume (hypervolemia), mild pyrexia

Prescription Status
Prescription only

Human Serum Albumin-I.P Grifols 100 ml About

Human Serum Albumin-I.P Grifols 100 ml is an incomparable solution used to treat hypovolemia, burns, hypoalbuminemia, shock, and for plasma exchange and volume replacement. This first-string, plasma-derived protein is manufactured by Grifols Therapeutics and features a highlighted concentration of 20% in a reduced, 100 ml glass bottle/vial for intravenous infusion. Clinically approved across Canada, the EU, UK, USA, and Australia, it is sterile, pyrogen-free, and compatible with common IV solutions. Buy online as a prescription-only product, with secure storage, unmatched sterility, and long shelf life guaranteed.

Essential Application Details

Human Serum Albumin-I.P Grifols 100 ml is widely used as an infusion for managing hypovolemia, shock, burns, and hypoalbuminemia. The direction of use mandates administration through intravenous infusion by a healthcare professional under prescription. Material features include a high-protein, ready-to-use, sterile and pyrogen-free solution, presented in a clear, slightly viscous liquid. Its stable pH and absence of enzymatic activity ensure optimal clinical safety and efficacy for diverse medical scenarios.

Payment, Packaging & Delivery Specifics

Payment terms are flexible and tailored to buyer needs. Secure shipping methods ensure integrity through the entire packing & dispatch process. Each 100 ml vial is encased in durable glass packaging and protected against light, maintaining safety standards during transit. Standard delivery timelines apply, with expedited options available upon request. Meticulous packaging and careful logistics ensure the product arrives promptly and in optimal condition, ready for immediate clinical application.

FAQ's of Human Serum Albumin-I.P Grifols 100 ml:

Q: How should Human Serum Albumin-I.P Grifols 100 ml be administered?

A: This product must be administered intravenously under the guidance of a qualified healthcare professional. Dosage and infusion rates are tailored to individual patient needs and clinical indications.

Q: What are the main medical uses of Human Serum Albumin-I.P Grifols 100 ml?

A: It is employed for the treatment of hypovolemia, burns, hypoalbuminemia, shock, plasma exchange, and for volume replacement in various clinical settings.

Q: When is Human Serum Albumin-I.P Grifols contraindicated?

A: The product is contraindicated in cases of severe anemia and cardiac failure with normal or increased intravascular volume. It should not be used if allergic reactions to albumin are known.

Q: Where has Human Serum Albumin-I.P Grifols 100 ml been approved for clinical use?

A: It is approved for use in Canada, the EU, UK, USA, and Australia, ensuring trust in its quality and efficacy across major global markets.

Q: What are the product's key features and composition?

A: It consists of human serum albumin (20%), stabilized with sodium caprylate and sodium chloride, ensuring a sterile, pyrogen-free, and ready-to-use clear solution suitable for intravenous infusion.

Q: How is the product shipped and packaged to ensure quality?

A: Each vial is securely packaged in light-resistant glass bottles, shipped under conditions below 25C, and dispatched using secure shipping methods to avoid breakage or compromise.

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