-
psnet.ahrq.gov/node/34995/psn-pdf
February 03, 2011 - process involved, from investigating a possible serious ADE to
disseminating their findings to the Food
-
psnet.ahrq.gov/node/43149/psn-pdf
July 23, 2014 - Silver Spring, MD: Food and Drug Administration. April 2014.
-
psnet.ahrq.gov/node/45195/psn-pdf
September 14, 2016 - https://psnet.ahrq.gov/issue/quality-assessment-spontaneous-triggered-adverse-event-reports-received-food-and-drug
-
psnet.ahrq.gov/node/35138/psn-pdf
July 10, 2008 - Food and
Drug Administration (FDA).
-
psnet.ahrq.gov/node/44393/psn-pdf
August 12, 2015 - Silver Spring, MD: US Food and Drug Administration; July 30, 2015.
-
psnet.ahrq.gov/issue/strengthening-use-artificial-intelligence-within-healthcare-delivery-organizations-balancing
September 18, 2024 - In 2022, the Food and Drug Administration (FDA) released new guidance which impacts how artificial intelligence
-
psnet.ahrq.gov/issue/medication-administration-aged-care-facilities-mixed-methods-systematic-review-0
July 31, 2024 - Dose form modification, such as crushing tablets and adding them to food, was a common approach to ensure
-
psnet.ahrq.gov/node/36133/psn-pdf
April 16, 2010 - structured interviews to
address their understanding of specific one-step warnings (ie, take with food
-
psnet.ahrq.gov/node/46335/psn-pdf
December 19, 2017 - often go unused, are not stored in a locked location, and
are rarely disposed of in compliance with Food
-
psnet.ahrq.gov/node/46832/psn-pdf
February 07, 2018 - Silver Spring, MD: US Food and Drug Administration; January 11, 2018.
-
psnet.ahrq.gov/node/46993/psn-pdf
July 18, 2018 - This study reviewed mandatory reporting of patient-controlled analgesia device-related events to the Food
-
psnet.ahrq.gov/node/34952/psn-pdf
November 17, 2011 - drug-event
The Centers for Disease Control (CDC), the Consumer Product Safety Commission (CPSC), and the Food
-
psnet.ahrq.gov/node/45115/psn-pdf
September 07, 2016 - The Food and Drug Administration Safety and Innovation Act of 2012 was intended to address
these shortages
-
psnet.ahrq.gov/issue/ismp-quarterwatch-reports
June 07, 2017 - that identify and analyze new risks related to medications and adverse drug events submitted to the Food
-
psnet.ahrq.gov/issue/fda-advise-err-reported-medication-errors-veklury-remdesivir-emergency-use-authorization
July 01, 2020 - September 10, 2020;25(18)
This alert discusses medication errors that have been reported to the Food
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psnet.ahrq.gov/issue/public-meeting-improving-patient-safety-enhancing-container-labeling-parenteral-infusion-drug
December 16, 2020 - The US Food and Drug Administration invited experts to comment on how labels for intravenous drugs could
-
psnet.ahrq.gov/node/47487/psn-pdf
November 07, 2018 - study, researchers evaluated medication safety letters issued by Health Canada, the
United States Food
-
psnet.ahrq.gov/node/45902/psn-pdf
October 13, 2018 - records are less
prescriptive about testing final products and rely more on attestation, compared to the Food
-
psnet.ahrq.gov/node/44580/psn-pdf
January 13, 2016 - Silver Spring, MD: US
Food and Drug Administration; December 15, 2015.
-
psnet.ahrq.gov/issue/ismps-second-quarterwatch-report-shows-sharp-increase-reports-serious-adverse-drug-events
June 10, 2018 - QuarterWatch report, a pilot program used to identify new drug risks and medication errors reported to the US Food