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Medical Device Network on MSNNearly a third of FDA medical device adverse event reports filed lateA new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year ...
Although most manufacturer reports of medical device adverse events are reported on time, a considerable proportion are ...
Gastrointestinal adverse events partially mediated the weight loss effects among patients with obesity who received tirzepatide vs placebo.
More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...
COVID-19 showed us that we urgently need more transparency in reporting adverse vaccine effects and that compensation for ...
The COVID-19 vaccine has prompted more than 10 times as many reports of adverse symptoms than the measles vaccine.
Most medical devices in the United States come to market with limited clinical data, and device surveillance is viewed as a ...
The following is a summary of “Late Adverse Events After Chimeric Antigen Receptor T-Cell Therapy for Patients With ...
Adverse drug events are more common in older people with comorbidities, a new study finds. Factors that are independently linked with adverse drug events are being female, taking more drugs daily, ...
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