angioedema


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Related to angioedema: Hereditary angioedema
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.angioedema - recurrent large circumscribed areas of subcutaneous edema; onset is sudden and it disappears within 24 hours; seen mainly in young women, often as an allergic reaction to food or drugs
atrophedema, giant hives, periodic edema, Quincke's edema
dropsy, edema, hydrops, oedema - swelling from excessive accumulation of watery fluid in cells, tissues, or serous cavities
Translations

angioedema

n angioedema m
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Summary: This report on the global Hereditary Angioedema Market analyzes the current and future prospects of the market.
Hereditary Angioedema Market Size, Share, Trends and Future Growth Predictions till 2025
[UKPRwire, Tue Jul 02 2019] This report on the global Hereditary Angioedema Market analyzes the current and future prospects of the market.
Hereditary Angioedema Market Size, Share, Trends and Future Growth Predictions till 2025
M2 PRESSWIRE-June 19, 2019-: Hereditary Angioedema (HAE) Market Spotlight 2019: With Takhzyro Approval, Shire Could Reclaim HAE Prophylaxis Market from CSL Behring
Hereditary Angioedema (HAE) Market Spotlight 2019: With Takhzyro Approval, Shire Could Reclaim HAE Prophylaxis Market from CSL Behring
M2 PHARMA-May 29, 2019-KalVista Pharmaceuticals Presents KVD900 Data at C1-Inhibitor Deficiency and Angioedema Workshop
KalVista Pharmaceuticals Presents KVD900 Data at C1-Inhibitor Deficiency and Angioedema Workshop
Hereditary angioedema (HAE) due to C1 inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease with deficiency (type I C1-INH-HAE) or dysfunction (type II C1-INH-HAE) of C1 inhibitor (C1-INH) due to mutations in the SERPING1 gene (1-3).
HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA --FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES
Angioedema is defined as increased permeability and dilatation of the capillaries in the deep dermis or subcutaneous or submucosal tissues leading to localized swelling, often affecting the upper respiratory and gastrointestinal tracts.
Angioedema and Urticaria Associated with Fluoxetine in a Preadolescent Boy/Preadolesan Bir Erkek Cocukta Fluoksetinle Iliskili Anjiyoodem ve Urtiker
In 1882, Quincke first described isolated uvular angioedema. It is a relatively rare presentation of angioedema of the upper airway (1).
Life-Threatening Upper Airway Compression: Quincke's Disease
Hereditary angioedema (HAE) is a rare disease with an autosomal dominant inheritance and an estimated prevalence of 1:50,000 (1).
Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)
BioCryst presented data showing that an oral formulation of BCX7353 was rapidly absorbed and exhibited a long half-life, two important characteristics of desired new acute treatments for hereditary angioedema, or HAE, attacks at the American College of Allergy, Asthma & Immunology, or ACAAI, meeting.
BioCryst presents BCX7353 data at ACAAI meeting
An experimental agent reduced swelling episodes markedly in patients with hereditary angioedema, according to results from a phase 2 randomized, dose-ranging, placebo-controlled trial.
Oral drug seen preventing angioedema attacks
The United States Food and Drug Administration (FDA) has approved Ireland-based Shire's Takhzyro (lanadelumab-flyo) injection as a preventative treatment for hereditary angioedema in patients 12 years of age and older, it was reported yesterday.
US Food and Drug Administration approves Shire's Takhzyro injection
THURSDAY, July 26, 2018 (HealthDay News) -- A small-molecule inhibitor of plasma kallikrein, BCX7353, results in a significantly lower rate of hereditary angioedema attacks compared with placebo, according to a study published in the July 26 issue of the New England Journal of Medicine.
Daily BCX7353 Cuts Rate of Hereditary Angioedema Attacks; Oral administration of BCX7353 at dose of ≥125 mg results in lower rate of attacks versus placebo

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