Anaphylaxis News and Research

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Anaphylaxis is an acute multi-system severe type I hypersensitivity reaction. Due in part to the variety of definitions, between 1% and 15% of the population of the United States can be considered "at risk" for having an anaphylactic reaction if they are exposed to one or more allergens. Of those people who actually experience anaphylaxis, up to 1% may die as a result.
Baxter to commence second GAMMAGARD LIQUID Phase III trial in Alzheimer's

Baxter to commence second GAMMAGARD LIQUID Phase III trial in Alzheimer's

FDA approves product label change for Biogen Idec's TYSABRI to treat MS

FDA approves product label change for Biogen Idec's TYSABRI to treat MS

Baxter submits GAMMAGARD LIQUID sBLA to FDA for treatment of MMN

Baxter submits GAMMAGARD LIQUID sBLA to FDA for treatment of MMN

ACAAI allergist available to discuss importance of immediate access to epinephrine

ACAAI allergist available to discuss importance of immediate access to epinephrine

CMS assigns permanent J-code for Savient's KRYSTEXXA to treat RCG

CMS assigns permanent J-code for Savient's KRYSTEXXA to treat RCG

Baxter commences BAX 855 Phase I trial in hemophilia A

Baxter commences BAX 855 Phase I trial in hemophilia A

FDA approves CSL Behring's Berinert for treatment of HAE attacks

FDA approves CSL Behring's Berinert for treatment of HAE attacks

FDA approves Pfizer's Prevnar 13 pneumococcal conjugate vaccine as a single dose for adults

FDA approves Pfizer's Prevnar 13 pneumococcal conjugate vaccine as a single dose for adults

Researchers warn food allergy blood tests should never be used as standalone diagnostics

Researchers warn food allergy blood tests should never be used as standalone diagnostics

Baxter receives FDA approval for ADVATE to prevent hemophilia A

Baxter receives FDA approval for ADVATE to prevent hemophilia A

Health Alliance, Bayer sign outcomes-based contract to support MS patients

Health Alliance, Bayer sign outcomes-based contract to support MS patients

FDA approves EUSA's orphan drug ERWINAZE for acute lymphoblastic leukemia

FDA approves EUSA's orphan drug ERWINAZE for acute lymphoblastic leukemia

EUSA Pharma receives FDA approval for Erwinaze to treat ALL

EUSA Pharma receives FDA approval for Erwinaze to treat ALL

Feraheme as safe and effective as iron sucrose in patients with anemia, CKD

Feraheme as safe and effective as iron sucrose in patients with anemia, CKD

Positive results from Alkermes VIVITROL addiction study

Positive results from Alkermes VIVITROL addiction study

Experts share latest buzz on allergies to alcohol and tobacco

Experts share latest buzz on allergies to alcohol and tobacco

New data from Savient's KRYSTEXXA Phase III trial on refractory chronic gout

New data from Savient's KRYSTEXXA Phase III trial on refractory chronic gout

Human Genome Sciences to present abstracts regarding BENLYSTA, SLE at ACR/ARHP meeting

Human Genome Sciences to present abstracts regarding BENLYSTA, SLE at ACR/ARHP meeting

Single-parent status, household income linked to increased rate of hospital readmissions of asthmatic children

Single-parent status, household income linked to increased rate of hospital readmissions of asthmatic children

States lack policies to curb classroom burden of asthma and severe allergies

States lack policies to curb classroom burden of asthma and severe allergies

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