Europe — EMA
Human Albumin Kedrion
Human Albumin Kedrion is a prescription intravenous albumin solution used to expand plasma volume in hypovolemia, shock, burns, and hypoalbuminemia.
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What is Human Albumin Solution?
Human Albumin Kedrion is a sterile human albumin solution for injection supplied as an intravenous colloid plasma volume expander. The product contains purified human albumin protein in a sterile aqueous solution, marketed in the European Union and available by prescription only. It is used to increase plasma oncotic pressure and restore intravascular volume in clinical situations such as hypovolemia, shock, burns, and hypoalbuminemia or related conditions.
What is Human Albumin Solution used for?
Human Albumin Kedrion is indicated for clinical situations that require rapid plasma volume expansion and correction of low serum albumin levels.
- Treatment of hypovolemia due to blood loss, dehydration, or sepsis. - Management of circulatory shock when fluid resuscitation is needed. - Support of patients with extensive burns to maintain intravascular volume. - Correction of hypoalbuminemia associated with liver disease, nephrotic syndrome, or malnutrition. - Adjunctive therapy during major surgery or trauma to reduce edema.
What are the side effects of Human Albumin Solution?
Adverse reactions to Human Albumin Kedrion are generally related to the infusion process or the protein nature of the product.
Common: - Fever or chills - Headache - Nausea or vomiting
Serious: - Anaphylactic or severe allergic reaction - Volume overload leading to pulmonary edema - Thromboembolic events
What precautions apply to Human Albumin Solution?
Before administering Human Albumin Kedrion, clinicians should evaluate patient-specific factors that may increase the risk of complications.
- Known hypersensitivity to human albumin or any component of the solution. - Pre‑existing cardiac failure or severe pulmonary edema. - Renal impairment or oliguria. - Active bleeding or uncontrolled coagulopathy. - Pregnancy and lactation status, as safety data are limited. - Ongoing fluid overload or hypervolemia. - Need for regular monitoring of serum albumin and fluid balance.
What does Human Albumin Solution interact with?
Potential drug interactions should be considered when prescribing Human Albumin Kedrion.
Avoid: - Concurrent administration of other colloid plasma expanders (e.g., hydroxyethyl starch). - High‑dose diuretics that may exacerbate volume depletion.
Use with caution: - Anticoagulants (warfarin, heparin) due to potential bleeding risk. - ACE inhibitors or ARBs because of additive hypotensive effect. - Vasopressors, as volume status may alter response.
Frequently asked questions
What is the primary clinical purpose of Human Albumin Kedrion?+
How is Human Albumin Kedrion administered?+
Can Human Albumin Kedrion be used in pregnant women?+
What monitoring is recommended during infusion of Human Albumin Kedrion?+
What are common adverse reactions to Human Albumin Kedrion?+
What serious side effects require immediate medical attention?+
Is Human Albumin Kedrion contraindicated in patients with heart failure?+
Can Human Albumin Kedrion be given together with other plasma expanders?+
What drug classes should be used cautiously with Human Albumin Kedrion?+
How does Human Albumin Kedrion differ from crystalloid solutions?+
Is there a need for special storage conditions for Human Albumin Kedrion?+
What regulatory status does Human Albumin Kedrion have in the EU?+
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