{"id":8851,"date":"2017-12-06T10:05:50","date_gmt":"2017-12-06T15:05:50","guid":{"rendered":"https:\/\/medicarereport.org\/?p=8851"},"modified":"2017-12-06T10:05:50","modified_gmt":"2017-12-06T15:05:50","slug":"fda-urges-maker-to-recall-limbrel-after-liver-and-lung-injury-reports","status":"publish","type":"post","link":"https:\/\/medicarereport.org\/?p=8851","title":{"rendered":"FDA urges maker to recall Limbrel after liver and lung injury reports"},"content":{"rendered":"<p>(By Andrew Joseph for ST<em>A<\/em>T)<\/p>\n<p>The Food and Drug Administration has asked Primus Pharmaceuticals to recall a product touted to address \u201cthe metabolic processes associated with osteoarthritis\u201d but that the agency says comes with a risk of liver injury and a lung condition. <a href=\"https:\/\/www.statnews.com\/2017\/12\/05\/fda-urges-maker-to-recall-limbrel-after-liver-and-lung-injury-reports\/?_hsenc=p2ANqtz-8_hSz6728XGFOvZjJ8AI0WnUA7Mm3qxeo2JOtykRDy-RlYmzSdzN5vDa0vRdPPj_j16QymLkIqHr8MLgSsQntRSAECfA&amp;_hsmi=59129301\">Continue reading article 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>Notice: 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<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>(By Andrew Joseph for STAT) The Food and Drug Administration has asked Primus Pharmaceuticals to recall a product touted to<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[31,15],"tags":[],"class_list":["post-8851","post","type-post","status-publish","format-standard","hentry","category-fda","category-part-dprescription-drugs"],"_links":{"self":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/8851","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=8851"}],"version-history":[{"count":1,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/8851\/revisions"}],"predecessor-version":[{"id":8852,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/8851\/revisions\/8852"}],"wp:attachment":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=8851"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=8851"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=8851"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}