Watch list
The list shows a new FDA count for a watched page, and a new count is not a finding.
Your pages
FDA says:
Many factors can influence whether or not an event will be reported, such as the time a product has been marketed and publicity about an event.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
The information in these reports cannot be used to estimate the incidence (occurrence rates) of the events reported.
Source: FDA, FDA Adverse Event Monitoring System (AEMS) Public Dashboard. Content current as of . The site read the page on .
FDA says:
MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices.
Source: openFDA, Manufacturer and User Facility Device Experience. The site read the page on .
The watch list is empty. To add a page, open a drug page or a device page and select "Watch this page".
The watch list is not available, because this browser blocks site storage.
How the list works
- The list stays in this browser. The site does not send it to a server.
- If you clear the site data of the browser, the browser deletes the list.
- The list follows the reports that FDA received in the latest closed quarter, with two counts and the quarter of each count.
- The feed of updates (RSS) and the list of updates show the changes for all pages.
- A report does not show that a drug or a device caused the event. A new count is not a statement about a product.