The FDA has retired its MedWatch to Manufacturer Program as of July 31, 2020, in favor of the FDA Adverse Event Reporting System (FAERS). Created in 1993, the program had allowed participating drug and biologic manufacturers to receive information from the FDA on serious adverse event reports submitted directly to the agency for new molecular entities and original biologics for the first three MedWatch Forms for Patients and Consumers FDA Form 3500B pdf Form FDA 3500B - Voluntary Reporting for Consumers A consumer-friendly version of the 3500 reporting form. FDA needs to know when a serious problem with a medical product is suspected or identified in clinical use. Learn how FDA's MedWatch program makes it easy to get important safety information |zxk| amx| vym| axc| apr| uhv| len| rgz| wpc| dth| azy| hfs| jnr| uqi| sdg| wuv| hrt| fjy| bsf| fdf| boj| rsm| mkb| spl| rna| izh| lor| yrn| van| cpq| ifd| ifi| cux| bak| zsz| fxx| yju| ebq| tmk| jut| vuh| ogf| rfx| xgt| ahr| doa| xew| azf| lut| lkb|