{"id":16007,"date":"2020-05-15T08:55:12","date_gmt":"2020-05-15T12:55:12","guid":{"rendered":"https:\/\/medicarereport.org\/?p=16007"},"modified":"2020-05-15T08:55:12","modified_gmt":"2020-05-15T12:55:12","slug":"fda-says-abbotts-5-minute-covid-19-test-may-miss-infected-patients","status":"publish","type":"post","link":"https:\/\/medicarereport.org\/?p=16007","title":{"rendered":"FDA says Abbott\u2019s 5-minute Covid-19 test may miss infected patients"},"content":{"rendered":"<p>(By Matthew Herper for ST<em>A<\/em>T)<\/p>\n<p>The Food and Drug Administration said late Thursday that the Abbott ID Now rapid test for Covid-19 \u2014 touted by the White House and widely used nationally \u2014 may return false negative results, meaning it can incorrectly indicate that patients who are infected with the novel coronavirus are not. Continue reading article <a href=\"https:\/\/www.statnews.com\/2020\/05\/15\/fda-says-abbotts-5-minute-covid-19-test-may-miss-infected-patients\/\">here&#8230;<\/a><\/p>\n<p><a href=\"https:\/\/medicarereport.org\/wp-content\/uploads\/2016\/09\/STAT-Logo.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-4372\" src=\"https:\/\/medicarereport.org\/wp-content\/uploads\/2016\/09\/STAT-Logo-300x32.png\" alt=\"\" width=\"300\" height=\"32\" srcset=\"https:\/\/medicarereport.org\/wp-content\/uploads\/2016\/09\/STAT-Logo-300x32.png 300w, https:\/\/medicarereport.org\/wp-content\/uploads\/2016\/09\/STAT-Logo.png 453w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<pre><strong>Notice:<\/strong> The link provided above connects readers to the full content of the posted article. The URL (internet address) for this link is valid on the posted date; medicarereport.org cannot guarantee the duration of the link\u2019s validity. Also, the opinions expressed in these postings are the viewpoints of the original source and are not explicitly endorsed by AMAC, Inc.; the AMAC Foundation, Inc.; or medicarereport.org.<\/pre>\n","protected":false},"excerpt":{"rendered":"<p>(By Matthew Herper for STAT) The Food and Drug Administration said late Thursday that the Abbott ID Now rapid test<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[17,31,14],"tags":[],"class_list":["post-16007","post","type-post","status-publish","format-standard","hentry","category-emerging-health-issues","category-fda","category-medical-technology"],"_links":{"self":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/16007","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=16007"}],"version-history":[{"count":1,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/16007\/revisions"}],"predecessor-version":[{"id":16008,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/16007\/revisions\/16008"}],"wp:attachment":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=16007"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=16007"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=16007"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}