The AAFP has partnered with PDR Alerts to help you receive FDA-mandated and product-related patient safety alerts as soon as they are issued.
Features of PDR Drug Alerts include:
Drug Alerts and Adverse Event Reporting
PDR Drug Alerts
- Ability to appoint a family medicine team member to manage practice alerts
- Free for U.S.-based prescribers
- Traditional "dear doctor letter" (DDL) sent when online alert has not been reviewed within 72 hours (weekends not included)
- Email addresses kept secure and confidential
- Access to 12-month alert history master file
- No advertisements
- Information paid for by manufacturers required by the FDA to deliver safety alerts
- Exclusive specialty-specific service fulfilling FDA guidance for electronic delivery of drug warnings
Register to receive urgent FDA-mandated and product-related patient-safety alerts via email from the AAFP's partner, PDR Drug Alerts.
Adverse Drug Events
Using RxEvent, U.S. physicians and other health care providers can easily and effectively report adverse drug events. This service is a collaboration of medical professional insurance carriers and governmental experts.
Features of RxEvent include:
Features of RxEvent include:
- Easy-to-use, standardized report form with pre-populated information
- Minimal required questions
- Prompt acknowledgment sent upon submission of a report
RxEvent has been established for initial use by U.S. health care professionals only, for reporting adverse events on U.S.-distributed drugs.
Report adverse drug events.
Report adverse drug events.
