Skip To Content

Thought leadership on the clinical impact on workers' compensation and auto no-fault.

Recent blog posts

November 24, 2020 · Clinical Team
The U.S. Food and Drug Administration (FDA) authorized the use of the Lucira™ COVID-19 All-In-One Test Kit under an Emergency Use Authorization (EUA) on November 17, 2020.  This is the first at-home nasal swab test kit to detect SARS-CoV-2  the virus that causes the coronavirus disease 2019 (COVID-19). Read more...
October 30, 2020 · Clinical Team
Evzio auto-injector and naloxone auto-injector have been discontinued and will no longer be available, according to kaléo Inc. (kaléo). According to information Optum has obtained from kaléo, previously dispensed Evzio and its authorized generic are still safe to use until their expiration dates. In addition, pharmacies may dispense current stock, but future refills will not likely be available. Read more...
October 26, 2020 · Clinical Team
Veklury® (remdesivir) is the first medication to be approved for the treatment of coronavirus disease 2019 (COVID-19) by the U.S. Food and Drug Administration (FDA) on October 22, 2020. Read more...
October 14, 2020 · Clinical Team
The U.S. Food and Drug Administration (FDA) reported that the brand-name opioid analgesic, Duragesic (fentanyl transdermal system), manufactured by Janssen Pharmaceuticals, Inc., is being discontinued. According to the FDA’s website, Janssen made a business decision to permanently discontinue all Duragesic transdermal systems and indicated they should be maintained on formularies until the last produced batch expires on July 31, 2021 to maintain continuity of the reimbursement process. No additional information was provided on Janssen’s website related to its business decision. Read more...
September 29, 2020 · Clinical Team
The U.S. Food and Drug Administration (FDA) has issued a labeling change requiring the Boxed Warning and other precautions included in prescribing information to be updated for all benzodiazepines. Read more...
September 23, 2020 · Clinical Team
The U.S. Food and Drug Administration (FDA) announced that Perrigo Pharmaceutical Company issued a voluntary recall for all unexpired albuterol sulfate inhalation aerosol to the retail level. The September 21, 2020 recall announcement was issued due to the potential clogging of the inhaler, which could result in health risks to patients if they do not receive enough or any medication when using the inhaler. Read more...
September 14, 2020 · Clinical Team
The U.S. Food and Drug Administration (FDA) has issued a safety communication regarding the use of hot/cold therapy devices. The September 9, 2020 communication reminds patients and healthcare providers about the importance of following the instructions when providing cold therapy through a water-circulating hot/cold therapy device. Read more...
     Next >>
Page 1 of 5

Subscribe today to receive our latest blogs, articles and more.

Subscribe now button

Download the latest
Pharmacy Resource Guide

Pharmacy Resource Guide