TRACKING DIRECT REPORTED ADVERSE EVENTS
First Claim
1. A method in a medical information computing environment for tracking one or more adverse event reports, the method comprising:
- communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties;
receiving one or more received receipts from the one or more end-user receiving parties for each of the one or more communicated electronic forms;
recording indicia corresponding to the one or more received receipts in one or more records associated with the one or more communicated electronic forms;
querying the status of one or more adverse event reports communicated to the one or more end-user receiving parties as an electronic form; and
providing a user interface on a display to allow a user to at least one of view, query, audit, and create reports for one or more data corresponding to the one or more adverse event reports.
1 Assignment
0 Petitions
Accused Products
Abstract
Systems, methods, and computer readable media are described for communicating an adverse event report directly to an end-user receiving party and tracking one or more adverse event reports. An adverse event may be detected manually or automatically by a system and an electronic adverse event reporting form presented to a user with one or more data fields pre-populated with data from a patient'"'"'s electronic health record (EHR). The user may enter and edit data in the electronic form and may submit the data in the electronic form directly to an end-user receiving party such as the U.S. Food and Drug Administration. One or more receipts may be received from the receiving party and indicia from the receipts recorded to one or more records. The submitted adverse event reports may be tracked, accessed, and interacted with through a user interface and additional information may be provided to a user therein.
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Citations
20 Claims
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1. A method in a medical information computing environment for tracking one or more adverse event reports, the method comprising:
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communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties; receiving one or more received receipts from the one or more end-user receiving parties for each of the one or more communicated electronic forms; recording indicia corresponding to the one or more received receipts in one or more records associated with the one or more communicated electronic forms; querying the status of one or more adverse event reports communicated to the one or more end-user receiving parties as an electronic form; and providing a user interface on a display to allow a user to at least one of view, query, audit, and create reports for one or more data corresponding to the one or more adverse event reports. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12)
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13. A system in a medical information computing environment for facilitating the tracking of one or more adverse event reports, the system comprising:
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a communication component for communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties; a receiving component for receiving at least one of a receipt and a unique identifier; a recording component for recording the at least one of receipts and identifiers in one or more records associated with each of the one or more adverse event reports; and a displaying component for presenting on a display one or more data corresponding to the one or more adverse event reports. - View Dependent Claims (14, 15, 16, 17, 18, 19)
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20. A method in a medical information computing environment for tracking one or more adverse event reports, the method comprising:
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communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties as an electronic mail message; receiving one of a successful transmission receipt and a transmission failure receipt for each of the one or more communicated electronic forms; receiving a unique identifier for each of the one or more electronic forms from one or more of the one or more end-user receiving parties; receiving an acknowledgment receipt for each of the one or more communicated electronic forms; recording indicia corresponding to one or more of the acknowledgment receipt, the one of successful transmission receipt and transmission failure receipt, and the unique identifier in one or more records associated with the one or more communicated electronic forms; querying the status of one or more adverse event reports communicated to the one or more end-user receiving parties as an electronic form; providing a user interface on a display to allow a user to at least one of view, query, audit, and create reports for one or more data corresponding to the one or more adverse event reports; and providing a user interface on a display to present to a user one or more of statistics, related reports, safety warnings, notices and related data based on at least one of the groups of all, and a subset of all, adverse event reports communicated to the one or more end-user receiving parties by one or more users.
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Specification