FDA authorizes 1st over-the-counter combo flu and COVID test outside of emergency use
The FDA has authorized the first over-the-counter combination COVID-19 and flu test outside of emergency use, which delivers ...
Medpage Today on MSN15h
Tirzepatide Shortage Resolved; Compounder Sues FDA; Menopause Mistaken as Dementia
All doses of the diabetes and weight management injectable tirzepatide (Mounjaro, Zepbound) were taken off the FDA's shortage ...
The FDA is warning of serious health effects, possibly death, from a Wisconsin farm's eggs
A recall of eggs from a Wisconsin farm has been upgraded to "Class 1 status," meaning consumers may be at risk of serious ...
Zealand, Boehringer win FDA breakthrough status to treat fatty liver
Denmark's Zealand Pharma and German partner Boehringer Ingelheim have won the U.S. Food and Drug Administration's ...
Merck immune from antitrust claim that it misled FDA about mumps vaccine, court rules
Merck is immune from an antitrust lawsuit accusing it of misleading regulators about the effectiveness of its mumps vaccine ...
Were FDA's 'Black Box' Warnings on Antidepressants a Mistake? Youth Suicides Rose Afterwards
The FDA required that a Black Box warning be placed on antidepressants in 2005, notifying doctors of this possible effect in ...
Compounding Group Sues FDA for Removing Lilly's Weight Loss Drug From Shortage List
In a lawsuit in Fort Worth, Texas federal court, the Outsourcing Facilities Association claims the FDA removed tirzepatide ...
FDA antidepressant warnings of suicide risk among kids may have the opposite effect, study finds
FDA black box warnings that antidepressants may be linked with suicidality among youth may have unintended, yet harmful, ...
Medscape23h
FDA Antidepressant Warnings Tied to Increase in Suicidality
New data suggest that black box warnings of suicidality risk are associated with a decline in mental health care and an ...
FDA's promised guidelines on pulse oximeters unlikely to end decades of racial bias
For decades, widely used pulse oximeters have underestimated the oxygen needs of darker-skinned patients. Will the FDA's new ...
Vegetable Recall Update: Warning for State As FDA Sets Highest Risk Level
The vegetable products were recalled due to a possible contamination with the bacteria Listeria monocytogenes.
FDA upgrades recall of eggs linked to salmonella to 'serious' health risks. Any KY cases?
The original recall notification stated 65 people in nine states were infected with salmonella linked to eggs supplied by ...