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The program allows 340B hospitals to stretch limited federal resources to reduce the price of outpatient pharmaceuticals for patients and expand health services to the patients and communities they serve.
Who is eligible for HRSA grants?
Who can apply: These types of domestic* organizations may apply: Public institutions of higher education Private institutions of higher education Non-profits with or without a 501(c)(3) IRS status For-profit organizations, including small businesses State, county, city, township, and special district governments,
What is the 340B program for hemophilia?
Congress created the 340B program to allow safety-net health care providers, like hemophilia treatment centers (HTCs) who serve vulnerable populations, to purchase discounted outpatient drugs, provide them to their patients, and use the income generated to stretch their scarce federal funding and resources that support
What to do if my child has hemophilia?
Managing hemophilia may include: Taking part in activities and exercise, but not ones that may cause injury. Getting special care before surgery including dental work. Preventing dental and gum problems with good dental hygiene. Getting vaccines under the skin instead of in the muscle to prevent bleeding in the muscle.
What kind of medical assistance is needed for hemophilia B?
Healthcare providers typically treat hemophilia B with factor replacement therapy. In factor replacement therapy, providers inject concentrated factor 9 into peoples bloodstreams. The concentrated factor 9 takes the place of the missing factor and helps prevent excessive bleeding or control bleeding when it happens.
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HRSA Hemophilia Treatment CentersHemophilia Treatment centers near meList of Hemophilia Treatment CentersCDC HemophiliaHemophilia centers of excellenceHRSA eligibilitySprans hemophiliaHemophilia government programs
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The new medication, marketed as Hympavzi by Pfizer, is a monoclonal antibody that reduces the amount of the anticoagulation protein known as tissue factor pathway inhibitor.
What is the national program for hemophilia?
National Hemophilia Program Coordinating Center (NHPCC): Tracking national, regional, and patient-level data to assess patient outcomes. Providing an ongoing forum for education, communication, and collaboration. This helps RHN and HTC practitioners improve care to patients and implement best practices.
Related links
Mid-Atlantic Region III Core Center: Regional Grants
Mid-Atlantic Region III is awarded federal grants that support programs and activities for the Core Center and regional hemophilia treatment centers.
Provides accessible, family-centered, continuous, comprehensive, coordinated, and culturally effective care for individuals with hemophilia and other bleeding
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