FDA launches new AI-powered system to track drug and vaccine side effects in real time, replacing outdated databases and saving $120 million annually.

The US Food and Drug Administration (FDA) launched a new unified platform for analyzing adverse event reports. This platform — called the FDA Adverse Event Monitoring System (AEMS) — represents a ...

"It's probably one of the most egregious demonstrations of government overreach imaginable." | Opinion ...

FDA launches single adverse event platform to consolidate drug, vaccine, and device reports, improving transparency and saving $120 million annually.

In another development, 25 states have petitioned to join a lawsuit and defend the EPA’s decision to rescind the climate endangerment finding ...

Yesterday, the Food and Drug Administration (FDA) announced the launch of the Adverse Event Monitoring System ( AEMS ), a new platform for assessing adverse event reports made to the FDA for drugs, ...

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Malware is evolving to evade sandboxes by pretending to be a real human behind the keyboard. The Picus Red Report 2026 shows 80% of top attacker techniques now focus on evasion and persistence, ...

AI is creating more realistic content that is harder to debunk. Tal Hagin, an open-source intelligence analyst based in Israel, compiles misinformation and shares his findings on X daily. He said he’s ...

Bengaluru: The U.S. Food and Drug Administration said on Wednesday it has introduced a unified platform designed to ...

Stuck on Protect/Destroy 3 in Marathon? Here’s where to install the UV Protocol and tag the marked locations on Dire Marsh.

The tool can quickly review submitted questionnaires that document medical evidence to determine a disability rating and ...