We collaborate with the world's leading lawyers to deliver news tailored for you. Sign Up for any (or all) of our 25+ Newsletters. Some states have laws and ethical rules regarding solicitation ...

The FDA, the U.S. Food and Drug Administration ... a violative product will cause serious adverse health consequences or death.” Many other products from Cal Yee Farm that were a part of ...

database to identify common and repeated patterns of preventable adverse drug events (ADEs) was analyzed. ADR reports collected from 1994 through 2000 were extracted from a teaching hospital's ADR ...

The Food and Drug Administration on Thursday approved a new type of nonopioid painkiller from ... very good or excellent at treating their pain. About 37% experienced some kind of adverse event, but ...

the FDA updated its guidance, classifying it under a Class 1 recall — its highest risk classification — which means exposure or consumption of the chips could cause "serious adverse health ...

The Food and Drug Administration (FDA) recently issued a final rule updating the definition of the term “healthy” for use on food labels. This change aims to align with modern nutrition ...

But now, the U.S. Food and Drug Administration is raising alarms about Librela, warning veterinarians of potential adverse effects, including death, in some dogs receiving the treatment.

While clinical trials have highlighted the safety and efficacy of amiodarone, there is limited real-world data on adverse events (AEs) associated with different administration routes. This study aims ...