In 1983 Congress enacted the Orphan Drug Act, which was designed to offer incentives to drug companies to promote development of new treatments for people with rare diseases.
Americans who need FDA-approved orphan drugs are sometimes temporarily or permanently denied access to them because their health insurance companies tend to exclude certain medications from their drug "formularies" due to low demand and/or the high cost of orphan products.
Access to orphan drugs can be substantially delayed when patients must obtain pre-authorization for a drug not included on their insurers' drug formulary. When insurers refuse to pay for an orphan drug, patients who cannot afford to pay are denied treatment.
Reimbursement policy for drug expenses is set by the insurance company and is outlined in your insurance policy.
Many drug companies offer special programs to patients who need their drugs but cannot afford them. Check with your drug's manufacturer or contact HAE Association's Patient Services for additional information.
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