Indication
Hereditary angioedema
Hereditary angioedema is a rare genetic disorder characterized by recurrent, self-limiting episodes of nonpitting, nonpruritic subcutaneous and submucosal swelling occurring without urticaria. Read more about Hereditary angioedema
21 drugs 18 manufacturers
Drugs that treat it
Common Hereditary angioedema therapies.
FIRAZYR (icatibant acetate)
BERINERT (C1 esterase inhibitor)
BERINERT (C1 esterase inhibitor)
RUCONEST (C1 esterase inhibitor, recombinant)
RUCONEST (C1 esterase inhibitor, recombinant)
KALBITOR (ecallantide)
RUCONEST (C1 esterase inhibitor, recombinant)
RUCONEST (C1 esterase inhibitor, recombinant)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonHereditary angioedema is a rare genetic disorder characterized by recurrent, self-limiting episodes of nonpitting, nonpruritic subcutaneous and submucosal swelling occurring without urticaria.
The disease predominantly involves the skin of the face and extremities, the gastrointestinal tract—presenting with severe abdominal pain, nausea, and vomiting—and the upper respiratory tract, where laryngeal involvement can cause life-threatening airway obstruction.
Pathophysiologically, the condition is most commonly driven by deficient or dysfunctional C1 esterase inhibitor activity, which leads to unregulated contact-system activation, excessive bradykinin generation, and dramatically increased vascular permeability.
- nih.gov
Hereditary angioedema is a rare genetic disorder characterized by recurrent, self-limiting episodes of nonpitting, nonpruritic subcutaneous and submucosal swelling occurring without urticaria
- dermnetnz.org
Hereditary angioedema is a rare genetic disorder characterized by recurrent, self-limiting episodes of nonpitting, nonpruritic subcutaneous and submucosal swelling occurring without urticaria
- nih.gov
The disease predominantly involves the skin of the face and extremities, the gastrointestinal tract—presenting with severe abdominal pain, nausea, and vomiting—and the upper respiratory tract, where laryngeal involvement can cause life-threatening airway obstruction
- medlineplus.gov
The disease predominantly involves the skin of the face and extremities, the gastrointestinal tract—presenting with severe abdominal pain, nausea, and vomiting—and the upper respiratory tract, where laryngeal involvement can cause life-threatening airway obstruction
- nih.gov
Pathophysiologically, the condition is most commonly driven by deficient or dysfunctional C1 esterase inhibitor activity, which leads to unregulated contact-system activation, excessive bradykinin generation, and dramatically increased vascular permeability
- discoverhae.com
Pathophysiologically, the condition is most commonly driven by deficient or dysfunctional C1 esterase inhibitor activity, which leads to unregulated contact-system activation, excessive bradykinin generation, and dramatically increased vascular permeability
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