Europe — EMA
Human Albumin Takeda
Human Albumin Takeda is a prescription intravenous albumin solution used for plasma volume expansion in hypovolemia, shock, burns, and major surgery.
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What is Human Serum Albumin?
Human Albumin Takeda is a sterile intravenous solution containing human serum albumin as the active ingredient. It is supplied as a colloid plasma expander for use in clinical settings within the European Union. The product is prescription‑only and is administered intravenously to support plasma volume and oncotic pressure in patients with fluid loss or hypovolemia.
What is Human Serum Albumin used for?
Human Albumin Takeda is indicated for conditions where plasma volume expansion is required. It is commonly employed in the following clinical situations:
- Management of hypovolemia due to trauma, hemorrhage, or dehydration - Treatment of shock, including septic or hypovolemic shock - Support during major surgery or extensive burns - Adjunct therapy for plasma volume expansion in patients with liver disease or hypoalbuminemia - Resuscitation in patients undergoing massive transfusion protocols
What are the side effects of Human Serum Albumin?
Human Albumin Takeda may be associated with adverse reactions ranging from mild to severe. Monitoring for these events is recommended during and after administration.
Common: - Mild fever or chills - Transient hypotension or hypertension - Headache or dizziness - Nausea or vomiting - Local irritation at the infusion site
Serious: - Anaphylactic or severe allergic reactions - Volume overload leading to pulmonary edema - Hemolysis or renal impairment - Coagulopathy or thrombosis - Transmission of infectious agents (rare)
What precautions apply to Human Serum Albumin?
Human Albumin Takeda should be used with careful clinical assessment and monitoring. Important precautions include:
- Assess fluid status and cardiac function before infusion to avoid volume overload - Use caution in patients with renal or hepatic impairment, as albumin metabolism may be altered - Monitor for signs of allergic reaction, especially in individuals with a history of serum protein sensitivity - Adjust dosage in patients with severe hypoproteinemia or malnutrition - Avoid rapid infusion rates that may precipitate hypotension or cardiovascular stress - Ensure proper storage and handling to maintain sterility and potency
What does Human Serum Albumin interact with?
Human Albumin Takeda may interact with other therapies, influencing efficacy or safety. Consider the following:
Avoid: - Concurrent use of high‑dose diuretics that may exacerbate hypovolemia - Simultaneous administration of other volume expanders without adjusting total fluid balance
Use with caution: - Vasopressors, as changes in intravascular volume can affect hemodynamic response - Anticoagulants, because volume expansion may alter coagulation parameters - Nephrotoxic drugs, given the potential for renal stress in volume‑overloaded states - Blood products, to prevent additive volume overload
Frequently asked questions
What is the primary indication for Human Albumin Takeda?+
How is Human Albumin Takeda administered?+
Can Human Albumin Takeda be used in patients with kidney disease?+
What monitoring is required during infusion of Human Albumin Takeda?+
Is Human Albumin Takeda safe for pregnant women?+
What are common side effects of Human Albumin Takeda?+
What serious adverse reactions can occur with Human Albumin Takeda?+
Should diuretics be stopped before giving Human Albumin Takeda?+
Can Human Albumin Takeda be combined with blood transfusions?+
What is the mechanism by which Human Albumin Takeda expands plasma volume?+
Is Human Albumin Takeda available over the counter?+
How is the quality and safety of Human Albumin Takeda ensured?+
Product details
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