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Faxed prescriptions will only be accepted from a prescribing practitioner. Patients must bring an original prescription to the pharmacy, and cannot fax these referral forms to Sender. Hemophilia Enrollment
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01
Wash your hands thoroughly with soap and water before handling the Factor I Recombinant.
02
Ensure that the Factor I Recombinant has been stored properly and has not expired.
03
Check the dosage instructions provided by your healthcare provider.
04
Draw up the correct amount of Factor I Recombinant into a sterile syringe.
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Choose an injection site, usually in the belly or thigh, and clean it with an alcohol swab.
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Pinch the skin and fat at the injection site to create a small fold.
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Insert the needle into the fold at a 90-degree angle and push the plunger to inject the Factor I Recombinant.
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Carefully remove the needle and dispose of it in a sharps container.
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Apply gentle pressure to the injection site with a sterile cotton ball or gauze pad if needed.
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Wash your hands again after administering the Factor I Recombinant.

Who needs factor i recombinant?

01
Factor I Recombinant is needed by individuals with a deficiency or dysfunction of Factor I, a protein involved in the blood clotting process.
02
It is typically prescribed to people with congenital afibrinogenemia or hypofibrinogenemia, as well as those with certain bleeding disorders.
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Factor I recombinant is a genetically engineered form of the human complement Factor I protein, which plays a crucial role in regulating the immune system and preventing excessive inflammation.
Typically, entities involved in the production, distribution, or use of Factor I recombinant in a clinical or research setting are required to file the necessary documentation regarding its use.
To fill out Factor I recombinant documentation, you need to provide specific details regarding the product's use, dosage, patient information, and adherence to regulatory guidelines.
The purpose of Factor I recombinant is to treat complement deficiencies and related conditions, helping to prevent infections and complications caused by immune system dysfunction.
Information that must be reported includes the manufacturing details, usage data, adverse effects, patient demographics, and compliance with safety regulations.
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