Health IT Pulse:

adverse event reporting


June 23, 2015  3:12 PM

FDA makes a deal with online patient group to study patient-reported drug safety data

Alex Delvecchio Alex Delvecchio Profile: Alex Delvecchio
adverse event reporting, drug safety, FDA, patient engagement, social media

The U.S. Food and Drug Administration (FDA) is teaming up with the largest online patient network to collect and study patient-reported drug safety data. 0 Comments     RSS Feed     Email a friend

November 30, 2011  1:56 PM

Vendors need to better support legal EHR

Don Fluckinger Profile: Don Fluckinger
adverse event reporting, AHIMA, HIPAA audits, Legal EHR, RSNA

CHICAGO -- Here at the Radiological Society of North America's RSNA 2011 annual meeting, I had a flashback. A presenter was going over how his large radiology group handles fuzzy or errant scans. It involved a multi-step rigmarole that...


November 9, 2011  1:02 PM

10 things you need to know from the IOM HIT safety report

Don Fluckinger Profile: Don Fluckinger
adverse event reporting, EHR security, FDA, IOM, ONC

Research is inconclusive about how safe health IT is for patients overall -- and poorly designed software can cause errors in an already complex national system of health care delivery -- making government oversight of HIT safety and serious adverse events (death serious injury and unsafe...


October 20, 2011  11:11 AM

AAMI glossary helps standardize terms for adverse event reporting

AnneSteciw Profile: AnneSteciw
adverse event reporting, device safety, medical devices, patient safety organizations

When it comes to the use of medical devices, adverse event reporting is a key factor in maintaining patient safety. Data collected from adverse event reports can be...


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