BioMedWire Stocks

FDA Issues Warning about Reliability of Food Allergy Skin Tests

An estimated 32 million Americans, including around 5.6 million children and 26 million adults, suffer from food allergies. The severity of these food allergies ranges from hives and swelling of the face to difficulty breathing, abdominal pain and diarrhea. Currently one of the most common ways of testing for food allergies is a skin prick test that involves placing a small amount of a certain food on a patient’s skin to see if it will cause an adverse reaction.

This method is the most accessible food allergy test, and it usually provides immediate results, allowing patients to discuss means of dealing with the allergy with their allergist during a single hospital visit. However, a recent announcement from the U.S. Food and Drug Administration has revealed that skin tests for food allergies aren’t always effective. The FDA has revealed that commonly used skin tests can produce false negative results and give patients with potentially deadly allergies a false sense of security.

The March 3, 2023, announcement stated that these ineffective food allergy tests have been associated with anaphylaxis after patients were exposed to an allergen they had been led to believe wouldn’t affect them. According to the announcement, the FDA became aware of the presence of food-allergen skin tests that provided false results after analyzing data from the FDA Adverse Event Reporting System. The analysis found that there has been an increase in reports of false-negative tests after patients used certain skin tests to check for potential allergies.

Some of the reports seen by the FDA revealed that patients with peanut allergies faced the risk of life-threatening anaphylaxis after being exposed to peanuts due to false negative results.

The announcement came a few months after the FDA notified the public that food allergen skin test manufacturer ALK-Abelló Inc. had voluntarily withdrawn four lots of tests due to increased reports of false-negative tests.

Before the announcement of product recalls, the FDA had listed certain product lots that were increasingly associated with false-negative skin test results.

The FDA concluded that all allergenic extracts used to check for food allergies had a risk of providing negative skin-test results. It now requires all manufacturers of these allergenic extracts to include language explaining the risk of false results and anaphylaxis in the Warnings and Precautions section of their products’ Prescribing Information.

With better approaches to managing allergies being developed by enterprises such as Aditxt Inc. (NASDAQ: ADTX), the need for skin tests that have proven to be minimally reliable will decrease as novel approaches to allergy detection and management take root.

NOTE TO INVESTORS: The latest news and updates relating to Aditxt Inc. (NASDAQ: ADTX) are available in the company’s newsroom at https://ibn.fm/ADTX

About BioMedWire

BioMedWire (BMW) is a bio-med news and content distribution company that provides (1) access to a network of wire services via InvestorWire to reach all target markets, industries and demographics in the most effective manner possible, (2) article and editorial syndication to 5,000+ news outlets (3), enhanced press release services to ensure maximum impact, (4) social media distribution via the Investor Brand Network (IBN) to millions of social media followers, (5) a full array of corporate communications solutions, and (6) a total news coverage solution with BMW Prime. As a multifaceted organization with an extensive team of contributing journalists and writers, BMW is uniquely positioned to best serve private and public companies that desire to reach a wide audience of investors, consumers, journalists and the general public. By cutting through the overload of information in today’s market, BMW brings its clients unparalleled visibility, recognition and brand awareness. BMW is where news, content and information converge.

To receive SMS text alerts from BioMedWire, text “Biotech” to 888-902-4192 (U.S. Mobile Phones Only)

For more information, please visit https://www.biomedwire.com

Please see full terms of use and disclaimers on the BioMedWire website applicable to all content provided by BMW, wherever published or re-published: http://BMW.fm/Disclaimer

BioMedWire (BMW)
San Francisco, California
www.biomedwire.com
415.949.5050 Office
Editor@BioMedWire.com

BioMedWire is part of the InvestorBrandNetwork.

Chris@BMW

Share
Published by
Chris@BMW

Recent Posts

Soligenix Inc. (NASDAQ: SNGX) Strengthens Advisory Leadership in Cutaneous T-Cell Lymphoma

Soligenix revealed updates to its U.S. Medical Advisory Board for CTCL designed to support the…

12 hours ago

Sapu Nano Reveals the Initial In-Human Clinical Trial of Sapu-003, Intravenous Everolimus (Afinitor(R)) at Australian Translational Breast Cancer Symposium

The company revealed the trial at the Australia Translational Breast Cancer Research Symposium (“ATBCR”) Sapu-003…

12 hours ago

How Rural Health Care is Being Impacted by the Federal Funding Landscape

Approximately 20% of people in the U.S. live in a rural area, and they face…

4 days ago

$37.5M Grant Announced to Boost Management of Infectious Diseases in the US

On October 15, NETEC (National Emerging Special Pathogens Training & Education Center) announced a grant…

5 days ago

What Patients Need to Know About the Remission Rate of Glioblastomas

Patients are overwhelmed when they are diagnosed with glioblastoma, the most deadly primary brain cancer.…

7 days ago

Soligenix Inc. (NASDAQ: SNGX) Research Highlights Breakthrough in High-Temperature Vaccine Stability

Thermostable vaccine technology is considered a significant unmet need in epidemic preparedness. Soligenix has been…

7 days ago