Living with Factor X Deficiency

Factor X deficiency is a rare bleeding disorder. It is caused by having too little of a protein called factor X in the blood.1,2

  • Factor X plays an important role in blood clotting (coagulation)
  • People with factor X deficiency have a higher risk of excess bleeding

Factor X Deficiency Can Be Hereditary

Factor X deficiency can be caused by a genetic defect that is passed down from parents to their children.1,2

  • To have hereditary factor X deficiency, a person must receive a defective factor X gene from both parents
  • Hereditary factor X deficiency affects approximately 1 in every 1,000,000 people

Symptoms of Factor X Deficiency

The symptoms of factor X deficiency can range from mild to severe. Women may experience additional symptoms as compared with men.1,2

Symptoms of severe factor X deficiency may include:

  • Bleeding of umbilical cord
  • Joint bleeds and bruising
  • Intramuscular bleeds
  • Spontaneous bleeding in the head, spinal cord, or gastrointestinal tract (for example: stomach or intestines)

Symptoms of mild factor X deficiency may include:

  • Easy bruising
  • Nosebleeds
  • Mouth bleeds
  • Bleeding longer than normal after injury or surgery

Women with factor X deficiency may experience:

  • Heavy or prolonged bleeding during menstruation (periods)
  • Complications during pregnancy or childbirth

Diagnosing Factor X Deficiency

A healthcare provider may suspect a bleeding disorder like factor X deficiency based on:

  • A personal history of bleeding symptoms
  • A family history of a bleeding disorder

When factor X deficiency is suspected, the diagnosis is made through blood tests that measure the time it takes for blood to clot. An additional test that measures the activity of factor X in the blood can be used to confirm the diagnosis.1,3

Learn more about COAGADEX — the first and only treatment specifically for hereditary factor X deficiency

Get help and support for your COAGADEX prescription

Indications and Usage for COAGADEX

COAGADEX, a plasma-derived blood coagulation factor X concentrate, is indicated in adults and children with hereditary factor X deficiency for:

  • Routine prophylaxis to reduce the frequency of bleeding episodes
  • On-demand treatment and control of bleeding episodes
  • Perioperative management of bleeding in patients with mild and moderate hereditary factor X deficiency

Limitation of Use

Perioperative management of bleeding in major surgery in patients with severe hereditary factor X deficiency has not been studied.

Contraindication for COAGADEX

COAGADEX is contraindicated in patients with known hypersensitivity to any of the components of the product.

Important Safety Information for COAGADEX

Allergic type hypersensitivity reactions, including anaphylaxis, are possible with COAGADEX. If symptoms occur, patients should discontinue use of the product immediately, contact their physician, and administer appropriate treatment.

The formation of neutralizing antibodies (inhibitors) to factor X is a possible complication in the management of individuals with factor X deficiency. Carefully monitor patients taking COAGADEX for the development of inhibitors by appropriate clinical observations and laboratory tests.

COAGADEX is made from human plasma and may contain infectious agents, e.g. viruses, the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent. No cases of transmission of viral diseases, vCJD or CJD, have been associated with the use of COAGADEX.

In clinical studies, the most common adverse reactions (frequency ≥5% of subjects) with COAGADEX were infusion site erythema, infusion site pain, fatigue and back pain.

Please see complete Prescribing Information for COAGADEX.

References: 1. National Hemophilia Foundation. Factor X. Bleeding-Disorders/Other-Factor-Deficiencies/Factor-X. Accessed April 11, 2019. 2. MedlinePlus Medical Encyclopedia. Factor X deficiency. Accessed April 11, 2019. 3. MedlinePlus Medical Encyclopedia. Factor X assay. Accessed April 11, 2019.

Adrian, Carly, Maritza, and Pam are living with factor X deficiency.
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