The company announced on Wednesday that Ralphs became the first retailer in the United States to provide rapid antibody testing at 77 pharmacies in Southern California and the Central Coast.
According to a statement by Ralphs, the results of a finger prick test are usually available within 15 minutes, which will help patients determine if they have the virus that causes COVID-19.
The FDA-authorized rapid antibody test provided by Whitmire Medical is available to Ralph customers who think they may have been infected with COVID-19 before and are currently asymptomatic. The price is $25.
In September, the American Society for Microbiology reported that 73% of the test laboratories surveyed encountered a shortage of commercial test kits for SARS-CoV-2, a capability challenge that may hinder the accessibility of tests for many Americans.
According to investigations in many states, as COVID-1
“Rapid antibody testing at Ralphs Pharmacy not only provides an affordable and convenient testing solution for patients who want to know whether they have previously been infected with the virus that causes COVID-19, but it also helps clinicians understand the long-term effects of dealing with this. COVID-19 and potential public health strategies.”
Ralphs’ rapid antibody test is performed by licensed health professionals using fingertip blood samples and Assure COVID-19 IgG/IgM rapid test equipment, which is a rapid lateral flow chromatography immunoassay-similar to the blood glucose test method-for Detection is for SARS-CoV-2.
The test received an emergency use authorization from the FDA in July and a broader immediate medical service authorization in September. The company stated that Kroger, the parent company of Ralfs, was the first retailer to provide customers with test solutions.
Research is ongoing to determine how long the antibodies are present after infection and whether the presence of antibodies provides protective immunity. Regardless of the test results, all patients should continue to follow the safety guidelines recommended by the FDA, including keeping their distance from society and wearing masks. The Assure COVID-19 IgG / IgM rapid test should not be used to diagnose active infections because the test only detects antibodies against the virus, not the virus itself.