CINRYZE (C1 esterase inhibitor [human]) for Hereditary Angioedema
CINRYZE is an injectable prescription medicine indicated for use in children (6 years old and above), teenagers and adults with HAE. Do not use if you have had hypersensitivity reactions to CINRYZE. See important safety information and patient labeling.
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Learn all about identifying and treating hereditary angioedema (HAE), a rare disease that causes swelling anywhere in the body. Attacks can be painful and, in some cases, lifethreatening. Symptoms often include hand or foot swelling, stomach pain, or swelling in the throat.
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Alpha1-Proteinase Inhibitor (Human), ZEMAIRA® is indicated to raise the plasma level of alpha1-proteinase inhibitor (A1-PI) in patients with A1-PI deficiency and related emphysema.
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Common Variable Immunodeficiency CVID, Hypogammaglobulinaemia, Agammaglobulinaemia, Severe Combined Immunodeficiency SCID and X-linked SCID, Neutropenia, Hereditary Angioedema HAE, X-linked agammaglobulinaemia Brutons Disease XLA, Wiskott-Aldrich Syndrome, IgG sub-classes, IgA deficiency, Hyper IgM, Selective IgA deficiency, Selective IgG sub-class deficiences, X-linked Lymphoproliferative Syndrome Duncans Syndrome, C1 esterase inhibitor deficiency, Hyper IgE Syndrome Jobs Syndrome
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We are a global non-profit network of patient associations and we are dedicated to raising awareness of C1-inhibitor deficiencies around the world.
Learn about BERINERT C1-INH replacement therapy. BERINERT helps you be prepared for on-demand treatment of an HAE attack.
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