Initial trial results have shown that a wearable patch, which delivers small amounts of peanut protein, can protect children and young adults with peanut allergies from the effects of accidental ingestion or exposure.
Kaléo announced today that they will reintroduce AUVI-Q (epinephrine injection, USP) to the U.S. market in the first half of 2017.
About 80% of patients with a penicillin allergy lose their sensitivity by 10 years following their reaction.
Taking antibiotics at a very young age could increase the risk of certain allergic conditions later in life, according to research presented at the annual European Respiratory Society International Congress, held from in London.
Mylan announced it is taking steps to expand patient access to EpiPen (epinephrine injection) and EpiPen Jr. Auto-Injectors by enhancing existing programs to assist patients who face higher costs.
A retrospective study found that the nausea and vomiting preventative treatment, ondansetron, was more effective than traditional therapy in inducing remission of vomiting in patients with acute food protein induced enterocolitis syndrome (FPIES).
A study reported that close to 80% of peanut-allergic preschool children successfully integrated peanut-containing foods into their diets after treatment with peanut oral immunotherapy (OIT).
For patients with allergic rhinitis (AR), house dust mite (HDM) sublingual immunotherapy is effective and seems safe, according to a study published online July 29 in Allergy.
The OTC treatment is for symptoms associated with seasonal and perennial allergies in patients aged ≥2 years.
Adamis Pharmaceuticals announced that the Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) to the New Drug Application (NDA) for Epinephrine Injection USP 1:1000 0.3mg Pre-filled Single Dose Syringe (PFS) for the emergency treatment of acute anaphylaxis.
For the management of angiotensin-converting enzyme inhibitor (ACEI)-induced angioedema, use of fresh frozen plasma and complement 1 esterase (C1) inhibitor appear to be safe and effective whereas ecallantide should be avoided, a study published in the American Journal of Health-System Pharmacy concluded.
The labeling for several epinephrine injection products has been updated to include information regarding injection-related injury and serious infections at the injection site.
Xlear have announced that their line of xylitol-based products for adults with upper respiratory problems will be available at 1,300 Target stores nationwide.
Older patients taking anticholinergic (AC) medication scored significantly lower on three separate brain atrophy and dysfunction tests compared to matched controls who took no AC medication.
The Food and Drug Administration (FDA) issued a safety communication recommending against the use of OxySure Portable Emergency Oxygen System, Model 615.
NOW Health Group announced a voluntary recall of 6 dietary supplements that were mislabeled due to a printing error by the label supplier.
The FDA has proposed a ban on most powdered gloves in the United States.
Early changes in immune T-cell populations may aid researchers in determining which patients with peanut allergies will respond well to oral immunotherapy. They can also pinpoint which immune mechanisms are involved in the response, according to a study conducted by Stanford University researchers.
Less than 40% of parents recall their pediatricians explaining when they are to use epinephrine in the event of their child having an allergic reaction.
Delaying immunization with diphtheria-tetanus-acellular pertussis (DTaP) vaccine was not associated with reduced risk of food allergy but children with delayed DTaP were found to have less eczema and used less eczema drugs, according to a study published in Allergy.
Children with certain allergies are at double the risk of developing high blood pressure and cholesterol, a study conducted by researchers at Northwestern Medicine reported.
Sanofi announced the voluntary recall of all Auvi-Q (epinephrine injection) due to a potentially inaccurate dosage delivery.
Merck has issued a letter to healthcare professionals letting them know that Nasonex (mometasone furoate monohydrate) Nasal Spray 50mcg is currently out of stock due to a manufacturing issue.
Infants who developed intolerance to cow's milk showed significant differences in gut bacteria after being treated with probiotics, a new study conducted by researchers from the University of Chicago has found.
The American Academy of Pediatrics (AAP) has issued interim guidance, in conjunction with 10 other medical organizations, supporting early rather than delayed peanut introduction during the period of complementary food introduction in infants.
In a new article published in the Annals of of Allergy, Asthma and Immunology, experts recommend the use of epinephrine for all severe allergic reactions, even for patients at risk of an anaphylactic reaction.
National Pharma announced the launch of Naramin (diphenhydramine), an oral solution in prefilled single-dose whistles.
DBV Technologies announced that based its meeting with the Food and Drug Administration (FDA), it plans to initiate a global Phase 3 study of its investigational Viaskin Peanut epicutaneous immunotherapy (EPIT) patch for the treatment of peanut allergies.
The Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to AR101, an oral immunotherapy for children and adolescents 4 to 17 years of age who are allergic to peanuts.
Aimmune Therapeutics announced that the Phase 2 study of a novel investigational oral immunotherapy (AR101) for the treatment of peanut allergy met its primary endpoint of tolerating a cumulative amount of peanut protein of at least 443mg.
The American College of Allergy, Asthma, and Immunology has developed an infographic titled "Scope and Impact of the Asthma Epidemic" that addresses vital statistics for asthma sufferers as well as the benefits of consulting an allergist for their care.
An over-the-counter (OTC) medication indicated to treat allergy symptoms could potentially be used to treat hepatitis C virus (HCV) infection after a new study showed that it limited HCV virus activity in infected mice. The research was funded by the National Institutes of Health (NIH).
A new blood test may be able to predict who will have severe allergic reactions to foods, researchers from Mount Sinai have reported.
The Food and Drug Administration (FDA) has strengthened an existing warning regarding serious and potentially fatal allergic reactions that can occur with Feraheme (ferumoxytol; AMAG Pharmaceuticals).
Despite the widely accepted assumption that the rise in allergic disorders may be due to improved hygiene, a new study has found no connection between development of allergies and asthma and personal hygiene or home cleanliness.
A new study has found that maternally reported gastrointestinal (GI) symptoms in children are more common in children with autism spectrum disorder (ASD) in the first three years of life compared to children with typical development or developmental delay (DD).
The Food and Drug Administration (FDA) is recommending that manufacturers stop using the labels "latex-free" or "does not contain latex" due to the scientific inaccuracy of these claims.
Allergic disease associated with Cannabis sativa and use has been reported with increasing frequency, although it is still relatively uncommon. A new article published in the Annals of Allergy, Asthma and Immunology presents data on how Cannabis sativa can act as an allergen.
Introducing peanut products into the diets of infants at high risk of developing peanut allergy was safe and led to an 81% reduction in the subsequent allergy development, reports a new study.
Meda announced that the Food and Drug Administration (FDA) has approved Dymista (azelastine HCl and fluticasone propionate) for the relief of symptoms of seasonal allergic rhinitis (SAR) in patients ages 6-11 who require treatment with both components.
Data from a Phase 2b trial showed that patients with peanut allergy using Viaskin Peanut (DBV Technologies) showed significant improvement using this epicutaneous immunotherapy (EPIT) after one year.
Loratadine, an antihistamine found in over-the-counter allergy medicines, may be able to help kill the bacteria associated with Lyme disease (Borrelia burgdorferi).
A new oral therapy that combines a probiotic and peanut protein appears to be a successful immunotherapy for peanut allergy, based on a study conducted by researchers at Murdoch Childrens Research Institute at the Royal Children's Hospital in Australia.
The Food and Drug Administration (FDA) is warning about a slightly increased risk of cardiovascular and cerebrovascular events among patients being treated with Xolair (omalizumab; Genentech and Novartis) for asthma compared to those not treated with Xolair.
Vicks announced the launch of QlearQuil, a line of over-the-counter (OTC) products for the treatment of sinus and allergy symptoms.
The Food and Drug Administration (FDA) has issued an alert regarding an ingredient commonly found in gluten-free products that may cause anaphylaxis in patients with a legume allergy.
GlaxoSmithKline announced that the FDA has approved Flonase Allergy Relief (fluticasone propionate 50mcg spray) as a once-daily over-the-counter (OTC) treatment indicated for symptoms of seasonal and perennial allergic and nonallergic rhinitis in patients ≥4 years of age
Greer laboratories announced the launch of Oralair (Sweet Vernal, Orchard, Perennial Rye, Timothy and Kentucky Blue Grass Mixed Pollens Allergen Extract) sublingual allergy immunotherapy tablet.
Ranbaxy has announced a voluntary recall of 29,790 blister packs of an over-the-counter (OTC) allergy medication in the U.S. after an unacceptable number of blister defects were identified.
The FDA announced the approval of Ragwitek (Ambrosia artemisiifolia; Merck), the first sublingual allergen extract to treat short ragweed pollen induced allergic rhinitis, with or without conjunctivitis.
Merck announced that the FDA has approved Grastek (Timothy grass pollen allergen extract) Tablet for Sublingual Use as immunotherapy for the treatment of grass pollen-induced allergic rhinitis with or without conjunctivitis.
Greer Laboratories announced that the FDA has approved Oralair sublingual allergy immunotherapy tablet for the treatment of grass pollen-induced allergic rhinitis with or without conjunctivitis.
Genentech announced that the FDA has approved Xolair (omalizumab) injection for the treatment of chronic idiopathic urticaria (CIU).
Allergy prevalence is uniform across varying regions in the U.S, except in children ≤5 years old, according to an NIH study.
Adjuvant high-dose vitamin D3 is beneficial for patients with chronic urticaria.
"Talking" medical devices and apps, among other techy health-focused inventions, can help people manage everyday wellness routines, such as taking pills and checking blood sugar levels, as well as dire medical circumstances.
Sanofi and its consumer healthcare division Chattem announced that Nasacort (triamcinolone acetonide) Allergy 24hr Nasal Spray is now available over-the-counter (OTC).
Peanut oral immunotherapy (OIT) is efficacious for desensitization of children with peanut allergy.
Early allergen exposure may increase tolerance and lowers risk of childhood food allergy.
The delay of solid foods until ≥17 weeks of age and continued breastfeeding when cow's milk protein is introduced to infants' diets correlate with a reduced likelihood of food allergies.
President Obama signed a new law meant to increase the availability of life-saving epinephrine in U.S. schools on Wednesday.
Merck announced data for its investigational Timothy grass sublingual allergy immunotherapy tablet (MK-7243) to treat the underlying cause of allergic rhinitis.
Non-celiac wheat sensitivity (NCWS) may be a non-immunoglobulin E-mediated food allergy.
Mothers' receipt of immunotherapy during pregnancy may reduce the risk of any type of allergy in offspring.
Multiple chronic conditions are associated with worse health in terms of activities of daily living and health-related quality of life in older adults.
Patients with egg allergy face no increased danger from receiving injectable inactivated influenza vaccine as a single dose.
Childhood food allergies result in significant direct medical costs for the U.S. health care system and even larger total costs for families of food-allergic children.
Probiotic exposure in early life may reduce total immunoglobulin E level (IgE) and protect against atopic sensitization, but does not seem to protect against asthma/wheezing.
AidaPak is initiating a voluntary recall for strip packs at the hospital/user level after learning of possible incorrect labeling.
Children treated successfully for milk allergies with oral immunotherapy lose tolerance after several years.
About a fifth of patients who have received a spinal injection of fungus-contaminated methylprednisolone but have not sought medical care are likely to be infected.
Amedra announced the relaunch of Adrenaclick (epinephrine) auto-injector for the emergency treatment of anaphylaxis.
Atriphen has been recalled due to the possibility of causing a severe allergic reaction from two undeclared allergens.
The FDA has accepted for review the Biologics License Application for ragweed pollen sublingual allergy immunotherapy tablet.
Parental sucking of their infant's pacifier is associated with a reduced risk of allergy development.
For U.S. children aged younger than 18 years, the prevalence of allergies increased from 1997-2011, with age, race/ethnicity, and income all affecting the prevalence.
Saratoga Therapeutics recalled 900 bottles of ebA Multivitamin Supplement because they may contain undeclared milk components such as milk protein(s) and lactose.
MyAllergyTest, a lab-based quantitative IgE and allergy diagnostic, is the first FDA-approved at-home test that allows allergy patients to test themselves against 10 key allergens.
Immunoglobulin E antibody specific for galactose-α1,3-galactose, which is associated with delayed anaphylaxis and urticaria that occurs several hours after eating beef, pork, or lamb, has been identified in children reporting idiopathic anaphylaxis or urticaria.
The FDA has approved the New Drug Application for Tris Pharma's Karbinal Extended-Release Oral Suspension. Karbinal is used to treat seasonal and perennial allergic rhinitis in children 2 years of age and older.
After visible particulates were found in product vials, Pallimed Solutions is voluntarily recalling all sterile compounds dispensed since January 1, 2013. Particulate matter can potentially damage or obstruct blood vessels.
Merck's Biologics License Application was accepted for its investigational Timothy grass pollen allergy immunotherapy tablet (AIT). In March, the company submitted a BLA for its investigational ragweed pollen AIT.
Complications linked to tattoos and tattoo inks include allergic reactions, serious infections, and reactions that can be mistaken for skin cancer.
Genentech and Novartis announced the results from a Phase 3 study, ASTERIA II, which showed that omalizumab, met its primary endpoint in patients with moderate to severe chronic idiopathic urticaria (CIU), who remained symptomatic despite treatment with approved H1 antihistamine doses.
Acupuncture produces statistically significant improvements in disease-specific quality of life and reduces antihistamine use in patients with seasonal allergic rhinitis (SAR), although further study is required to determine whether these results are clinically significant.
Sanofi announced that Auvi-Q (epinephrine injection) is now available.
For children with food allergy, bullying is common, and correlates with decreased quality of life and increased distress for children and their parents.
Just over half of children with hen egg allergies can tolerate baked eggs in an oral food challenge (OFC); and more than a quarter of children over the age of 10 with food allergies develop tolerance.
People with both hay fever and asthma have a modestly reduced risk of dying from colorectal cancer.
Local allergic rhinitis (LAR) is prevalent among patients with rhinitis, affecting about one in four, and is often associated with childhood onset and persistent, severe conjunctivitis and/or asthma.
Perceived stress correlates with an increased risk of adult-onset asthma, allergic rhinitis, and atopic dermatitis as well as asthma medication use.
Nearly one-third of parent-reported food allergies are not formally diagnosed by a physician
When a drug switches from prescription-only to over-the-counter (OTC) there is a shift in the direct-to-consumer advertising (DTCA), with less presentation of potential harms and frequent omission of identification by generic names.
Patients with unpredictable and recurring attacks of acute hereditary angioedema (HAE) may be effectively treated with ecallantide, with relapse occurring in a small proportion of patients and little evidence of rebound.
Mylan Specialty announced the EpiPen4Schools program, which offers four free EpiPen (epinephrine 0.3mg; DEY Pharma) or EpiPen Jr (epinephrine 0.15mg; DEY Pharma) Auto-Injectors upon qualification.
Sanofi announced that the FDA has approved Auvi-Q (epinephrine injection) for the emergency treatment of life-threatening allergic reactions in people who are at risk for or have a history of anaphylaxis.
There appears to be an inverse relationship between elevated allergy biomarker levels (immunoglobulin E [IgE]) and the risk of developing glioma, which is detectable many years before tumor diagnosis.
Individuals who have been bitten by the lone star tick may develop immunoglobulin E (IgE) to the carbohydrate galactose-α-1,3-galactose (alpha-gal), which puts them at risk for delayed anaphylaxis after consumption of meat containing alpha-gal on glycoproteins or glycolipids.
Sunovion announced the nationwide availability of Zetonna (ciclesonide) Nasal Aerosol, 74mcg once-daily, for the treatment of allergic rhinitis (AR), also known as hay fever or nasal allergies.
Concentrations of several fragrance allergens applied to test chambers well in advance of patient testing may be reduced by >20% within hours when stored at room temperature.