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Package leaflet: Information for the user Berliner 1500 1500 IU Powder and solvent for solution for injection. Human C1esterase inhibitor Read all of this leaflet carefully before you start using
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How to fill out berinert 1500 iu powder

01
Wash your hands thoroughly before handling the berinert 1500 iu powder.
02
Use a syringe and needle to draw up the appropriate amount of sterile water for injection.
03
Slowly inject the sterile water into the vial containing the berinert 1500 iu powder.
04
Gently swirl the vial until the powder is completely dissolved.
05
Inspect the solution for any particles or discoloration. Do not use if it appears to be contaminated.
06
Attach a new sterile syringe and needle to the vial.
07
Draw up the desired dose of the reconstituted berinert solution into the syringe.
08
Administer the berinert 1500 iu powder as directed by your healthcare provider, following proper injection techniques and guidelines.

Who needs berinert 1500 iu powder?

01
Berinert 1500 iu powder is typically used by individuals with hereditary angioedema (HAE), a genetic disorder that causes swelling in various parts of the body. It may be prescribed for those who experience frequent or severe HAE attacks. It should only be used under the guidance and prescription of a healthcare professional.
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Berinert 1500 IU powder is a medication used to treat hereditary angioedema (HAE) by replacing the C1 inhibitor protein that is deficient or dysfunctional in patients with this condition.
Healthcare professionals and institutions that administer berinert 1500 IU powder may be required to file reports or documentation regarding its use and inventory, depending on regulatory requirements.
To fill out berinert 1500 IU powder, follow the manufacturer's instructions for reconstitution and dosage calculation, ensuring proper storage and handling practices are adhered to.
The purpose of berinert 1500 IU powder is to prevent or treat acute attacks of hereditary angioedema by providing the necessary C1 inhibitor protein.
Information that must be reported may include patient details, dosage administered, date of administration, and any adverse reactions experienced.
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