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Yes - Google "Recombinant Factor 8" (FVIII) or "Human Factor 8". Bayer, Baxter, CSL Behring, Grifols, Pfizer, and Octapharma sell Factor 8 products.

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Q: How can you buy the factor 8 for hemophilia?
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What is the difference between Hemophilia A and Hemophilia B?

There are two types of hemophilia: hemophilia A (sometimes called classical hemophilia) and hemophilia B (sometimes called Christmas disease). Both are caused by a low level or absence of one of the proteins in the blood (called factors) that control bleeding. Hemophilia A is caused by a deficiency of factor VIII, and hemophilia B is caused by a deficiency of factor IX. There is no difference between the two types of hemophilia, except that hemophilia B is about five times less common than hemophilia A.


Hemophilia is caused by an?

Hemophilia is caused by missing or low levels of factor VIII


Excessive bleeding caused by congenital lack of factor VII or IX?

A lack of factor VIII is hemophilia A, and a lack in factor IX is hemophilia B. They can cause excessive bleeding because the person is unable to clot.


Which clotting factor is deficient in Hemophilia A?

Hemophilia A is an X-linked, hereditary bleeding disorder caused by the absence or defect of a blood clotting protein, Factor VIII. As a result, when a person with hemophilia A has a bleeding episode, the bleeding may be prolonged due to the body's inability to form blood clots. Patients who are affected with hemophilia A experience frequent spontaneous bleeding, most commonly into their joints and soft tissues, with bleeding into vital organs that may ... be life-threatening. Bleeding episodes may be painful, and over time, recurrent joint bleeding may result in debilitating destruction of the joints. Currently, patients with hemophilia A are dependent on injections of Factor VIII produced by genetic engineering or purified from human plasma, to help control a bleeding episode. It is estimated that approximately 50,000 individuals worldwide are affected with hemophilia A. Hemophilia A - Clotting Factor VIII Hemophilia B - Clotting Factor IX Hemophilia C - Clotting Factor XI


What is factor VIII deficiency?

Hemophilia


Hemophilia is caused by a defiency of what clotting factor?

factor VIII


Cures for hemophilia?

There no cure for hemophilia. It can be controlled. Typically there is a deficiency of a clotting factor, therefore the individual must have regular infusions of this deficient factor.


Royal hemophilia is the result of what inheritance?

Hemophilia is broken into three subcategories; Hemophilia A, Hemophilia B, and Hemophilia C. These subcategories designate a person as having a deficiency of one of three specific clotting proteins. Hemophilia A is the deficiency of the protein called Clotting Factor VIII. Hemophilia B is the deficiency of Clotting Factor IX. Hemophilia C is the deficiency of Clotting Factor XI. "Royal" hemophilia is simply a reference to Hemophilia B and is therefore a result of a deficiency in the Clotting Factor IX protein. It is sometimes called the royal disease because it has been known to have been passed through some royal families throughout history.


How do you treat heamophilia?

Standards of care for Hemophilia vary greatly around the world and from one doctor to another there are variations of care. Most doctors agree treatment of Hemophilia is administration of anti-hemophiliac factor. The main treatment for hemophilia is called replacement therapy. Concentrates of clotting factor VIII (for hemophilia A) or clotting factor IX (for hemophilia B) are slowly dripped in or injected into a vein. These infusions help replace the clotting factor that's missing or low.


What is the protein that hemophiliacs lack?

In the most common type, Hemophilia A, the person lacks clotting factor VIII. In Hemophilia B, clotting factor IX is lacking.


What is an inherited abnormality that causes a deficiency of a specific clotting factor resulting in a reduced ablitity to clot blood?

Hemophilia is a bleeding disorder that slows down the blood clotting process. People who have hemophilia often have longer bleeding after an injury or surgery. People who have severe hemophilia have spontaneous bleeding into the joints and muscles. Hemophilia occurs more commonly in males than in females.The two most common types of hemophilia are hemophilia A (also known as classic hemophilia) and hemophilia B (also known as Christmas disease). People who have hemophilia A have low levels of a blood clotting factor called factor eight (FVIII). People who have hemophilia B have low levels of factor nine (FIX).The two types of hemophilia are caused by permanent gene changes (mutations) in different genes.


The absence of Factor VIII is indicative of which condition?

Hemophilia