Pfizer didn't say hantavirus is side effect of its COVID-19 vaccine, contrary to online claims

Those eager to discredit Pfizer's mRNA vaccine, which is safe and effective, exploited the cruise ship outbreak.
STAT

FDA says it will publish reports of adverse events tied to drugs on daily basis

Lizzy Lawrence leads STAT’s coverage of the Food and Drug Administration. She was previously a medical devices reporter. You can reach Lizzy on Signal at lizzylaw.53. WASHINGTON — The Food and Drug ...

2-Day Medical Device Studies Training Course: Regulatory Requirements and Adverse Event Reporting (Online: Sept 17th-18th, 2026)

The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting (Sept 17th - Sept 18th, 2026)" training course has been added to ResearchAndMarkets.com's offering. Delve into the ...
TCTMD

Watchman Adverse Events: Analysis Digs Into What’s Been Reported to the FDA

SAN FRANCISCO, CA—In the 3-and-a-half years after the Watchman device (Boston Scientific) was approved for left atrial appendage (LAA) occlusion in high-risk patients with atrial fibrillation, ...