Finished product reference
Plasma, Fresh Frozen
Injection · Parenteral
- List code
- 51566
- Pharmacologic class
- Blood component (human plasma)
What it is and how it works
Fresh frozen plasma is plasma separated from donated whole blood or collected by apheresis and frozen rapidly to preserve labile coagulation factors. It replaces all plasma clotting factors and natural anticoagulants (protein C, protein S, antithrombin).
Indications
Correction of multiple coagulation factor deficiencies with bleeding or before invasive procedures (e.g. massive transfusion, liver disease, disseminated intravascular coagulation); plasma exchange in thrombotic thrombocytopenic purpura; replacement of single factors when no specific concentrate is available.
Dosage and administration (summary)
Dosing is individualised by the treating specialist according to clinical response and coagulation tests (typically around 12–15 mL/kg), given by intravenous infusion through a blood administration set after thawing; must be ABO-compatible.
Contraindications
Not to be used as a volume expander or nutritional source; contraindicated in known IgA deficiency with anti-IgA antibodies unless IgA-deficient plasma is used.
Warnings and precautions
Risks include transfusion-associated circulatory overload, transfusion-related acute lung injury (TRALI), allergic and anaphylactic reactions, and transmission of infection. Administer within the time limits set by the blood service after thawing and monitor the patient closely.
Pregnancy
May be used in pregnancy when clinically indicated, for example in obstetric haemorrhage.
Storage and supply
Store frozen at or below −25 °C; once thawed, use promptly according to blood-service guidance and do not refreeze.
Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
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