共 50 条
- [44] How the US Food and Drug Administration defines and detects adverse drug events CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, 2001, 62 (09): : 641 - 649
- [45] SERIOUS ADVERSE EVENTS IN NORPLANT USERS REPORTED TO THE FOOD-AND-DRUG-ADMINISTRATION MEDWATCH SPONTANEOUS REPORTING SYSTEM OBSTETRICS AND GYNECOLOGY, 1995, 86 (02): : 318 - 319
- [46] Monitoring adverse drug events: The Food and Drug Administration MedWatch reporting system REGIONAL ANESTHESIA AND PAIN MEDICINE, 1998, 23 (06): : 190 - 193