The Food and Drug Administration on Friday authorized the first at-home syphilis test amid surging cases of the bacterial ...
(The Hill) – The Food and Drug Administration (FDA) granted market authorization to the first at-home syphilis test amid a decades-long rise of cases in the U.S. The test, which detects syphilis ...
On October 7, 2024, FDA granted marketing authorization for the over‑the‑counter combination flu and COVID-19 combination test, Healgen Rapid ...
The test kits are part of the COVID ... is longer than was known when the test was first authorized. To see if the expiration ...
meaning it correctly identified 93.4% of positive specimens when compared to three FDA cleared laboratory tests. Results from the First to Know ® Syphilis Test alone are not sufficient to ...
“We hope this is the first step towards seeing a resolution to this shortage, and that HHS and FDA will continue to take steps to ensure that communities never experience a syphilis treatment ...
The Food and Drug Administration said on Monday it has authorized the first over-the-counter flu and COVID-19 combination test for the public to have access to outside of emergency use.
Nowdiagnostics Inc. established an exclusive agreement with Laboratory Holdings Inc. for distribution of its First To Know syphilis test in the U.S. The test provides results in 15 minutes with as ...
The community can now test ... home. The Food and Drug Administration (FDA) just granted the authorization of a COVID-19 and flu test that can be used without a prescription. This is the first ...
Last year, cases of the most infectious stages of syphilis fell 10% from the year before — the first substantial decline in ...
A new proven protocol in which doxycycline is used to prevent sexually transmitted infections, called doxyPEP, has been an ...
Although sexually transmitted infections are still at an epidemic level in the US, scientists at the US Centers for Disease ...