Medical Device Network on MSN1d
Nearly a third of FDA medical device adverse event reports filed late
A new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year ...
Considerable proportion of medical device adverse events reported late
Although most manufacturer reports of medical device adverse events are reported on time, a considerable proportion are ...
STAT4h
RFK Jr. says the measles vaccine causes deaths ‘every year.’ Scientists disagree
When Robert F. Kennedy Jr. was confirmed as America’s secretary of health and human services, neutral observers might have ...
More than 1.2 million medical device side-effect reports not submitted within legal timeframe, analysis finds
More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...
The Daily Signal1d
Restoring Trust in Public Health: Transparency Urgently Needed in Reporting Adverse Vaccine Effects
COVID-19 showed us that we urgently need more transparency in reporting adverse vaccine effects and that compensation for ...
The BMJ1d
Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study
Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...
Physician's Weekly2d
Late Adverse Events After CAR T-Cell Therapy in Aggressive B-Cell Lymphoma
The following is a summary of “Late Adverse Events After Chimeric Antigen Receptor T-Cell Therapy for Patients With ...
McKnight's Long-Term Care News3d
Adverse drug events more likely in older adults with comorbidities, study shows
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, ...