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Hemophilia Premium

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Program Status

Open - We are accepting applications for new and renewal patients. If your application for assistance is approved you can begin receiving funding immediately.


Assistance Amount

$4,500 per year. Patients may apply for a second grant during their eligibility period subject to availability of funding.


Premium Assistance Information

Eligibility Criteria

  1. The patient must be getting treatment for hemophilia.
  2. The patient must have health insurance that covers his or her qualifying medication or product. 
  3. The patient’s medication or product must be listed on PAN’s list of covered medications.
  4. The patient’s income must fall at or below 400% of the Federal Poverty Level.
  5. The patient must reside and receive treatment in the United States or U.S. territories. (U.S. citizenship is not a requirement.)
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See the list of medications covered in this program
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  • Advate (antihemophilic factor (fviii) recombinant,full length)
  • Adynovate (antihemophilic factor (fviii) recombinant, full length, peg)
  • Afstyla (antihemophilic factor viii recomb,single-chn,b-dom truncated)
  • Alphanate (antihemophilic factor, human/von willebrand factor,human)
  • Alphanine Sd (factor ix)
  • Alprolix (factor ix recombinant, fc fusion protein)
  • Amicar (aminocaproic acid)
  • Aminocaproic Acid (aminocaproic acid)
  • Bebulin (factor ix complex, prothrombin cplx conc(pcc) no.6, 3-factor)
  • Benefix (factor ix human recombinant)
  • Cyklokapron (tranexamic acid)
  • Ddavp (desmopressin acetate (non-refrigerated))
  • Desmopressin Acetate (desmopressin acetate)
  • Eloctate (antihemophilic factor (fviii) recombinant, fc fusion protein)
  • Esperoct (antihemophilic factor (fviii) rec, b-dom truncated peg-exei)
  • Feiba Nf (anti-inhibitor coagulant complex)
  • Helixate Fs (antihemophilic factor (fviii) recombinant,full length)
  • Hemlibra (emicizumab-kxwh)
  • Hemofil M (antihemophilic factor, human)
  • Humate-p (antihemophilic factor, human/von willebrand factor,human)
  • Idelvion (factor ix recombinant,albumin fusion protein)
  • Ixinity (factor ix human recombinant, threonine 148)
  • Jivi (antihemophilic factor (fviii) rec, b-domain deleted peg-aucl)
  • Koate (antihemophilic factor, human)
  • Kogenate Fs (antihemophilic factor (fviii) recombinant,full length)
  • Kovaltry (antihemophilic factor (fviii) recombinant,full length)
  • Lysteda (tranexamic acid)
  • Monoclate-p (antihemophilic factor, human)
  • Mononine (factor ix)
  • Novoeight (antihemophilic factor viii recombinant, b-domain truncated)
  • Novoseven Rt (coagulation factor viia (recombinant))
  • Nuwiq (antihemophilic factor viii rec hek cell, b-domain deleted)
  • Obizur (antihemophilic factor viii, recombinant porcine sequence)
  • Profilnine (factor ix complex, prothrombin cplx conc(pcc) no.4, 3-factor)
  • Rebinyn (factor ix (human) recombinant, pegylated)
  • Recombinate (antihemophilic factor viii, human recombinant)
  • Rixubis (factor ix human recombinant)
  • Stimate (desmopressin acetate)
  • Tranexamic Acid (tranexamic acid)
  • Tranexamic Acid-nacl (tranexamic acid in sodium chloride,iso-osmotic)
  • Wilate (antihemophilic factor, human/von willebrand factor,human)
  • Xyntha (antihemophilic factor (factor viii) recomb,b-domain deleted)
  • Xyntha Solofuse (antihemophilic factor (factor viii) recomb,b-domain deleted)

Diagnosis Codes:

ICD-10: D66, D67, D68.1, D68.311, D68.4


About the Disease:

Hemophilia is a disorder in which the blood doesn't clot normally. It is a rare disease that affects the circulatory system. Subtypes include hemophilia A, hemophilia B and hemophilia C.


Source: National Institutes of Health


Related Organizations: