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Adverse Event Reporting System
Results: 638

#	Item
501	FDAAA Accomplishments – One Year After Enactment Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Prescription Drug User Fee Act Boxed warning Priority review voucher Adverse Event Reporting System ClinicalTrials.gov Ofloxacin Center for Devices and Radiological Health Pharmaceutical industry Food and Drug Administration Medicine Health
502	September[removed]AAP IMMUNIZATION INITIATIVES NEWSLETTER Inside this issue: Add to Reading List Source URL: www2.aap.org Language: English - Date: 2009-12-08 10:39:50 Vaccines Drug safety Centers for Disease Control and Prevention Immunology National Center for Immunization and Respiratory Diseases National Childhood Vaccine Injury Act Influenza vaccine Vaccination schedule Vaccine Adverse Event Reporting System Medicine Health Vaccination
503	ORIGINAL ARTICLE Evaluation and Overview of the National Electronic Injury Surveillance System-Cooperative Adverse Drug Event Surveillance Project (NEISS-CADES) Michael A. Jhung, MD, MPH,* Daniel S. Budnitz, MD, MPH,* A Add to Reading List Source URL: www.effectivehealthcare.ahrq.gov Language: English - Date: 2009-10-30 06:58:00 Pharmaceutical sciences Clinical surveillance Adverse Event Reporting System U.S. Consumer Product Safety Commission Pharmacovigilance Adverse effect Food and Drug Administration Patient safety Adverse drug reaction Medicine Health Pharmacology
504	Patient Safety Surveillance and Improvement System - Final Rule Add to Reading List Source URL: www.healthvermont.gov Language: English - Date: 2011-07-21 16:25:41 Medical terms Safety Pharmacology Hospice Adverse Event Reporting System Adverse effect Root cause analysis Adverse event Near miss Medicine Health Patient safety
505	FDA’s Adverse Event Surveillance Systems and MedWatch Add to Reading List Source URL: www.fda.gov Language: English Health Medicine Clinical research Pharmaceutical industry MedWatch Pharmacovigilance Clinical trial Adverse Event Reporting System Serious adverse event Pharmacology Pharmaceutical sciences Food and Drug Administration
506	Adverse Event Reporting Via NYPORTS System Add to Reading List Source URL: www.health.ny.gov Language: English - Date: 2013-05-30 11:45:58 Nursing Clinical research Pharmaceutical industry Patient safety Adverse event Patient Methadone Patient safety organization Adverse effect Medicine Health Medical terms
507	SOPP 8002 Appendix 2 - Draft Guidance.doc Add to Reading List Source URL: www.fda.gov Language: English Medicine Health Vaccine Adverse Event Reporting System Adverse Event Reporting System Center for Biologics Evaluation and Research Validation Electronic Common Technical Document Postmarketing surveillance Food and Drug Administration Clinical research Research
508	Guidance for Industry Postmarketing Safety Reporting for Human Drug and Biological Products Including Vaccines DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Research Adverse Event Reporting System Center for Biologics Evaluation and Research Validation Regulatory requirement New Drug Application Biologic Center for Drug Evaluation and Research Postmarketing surveillance Food and Drug Administration Medicine Pharmaceutical sciences
509	New York Patient Occurrence Reporting and Tracking System - NYPORTS[removed] Add to Reading List Source URL: www.health.ny.gov Language: English - Date: 2012-05-16 13:36:16 Medical terms Healthcare Safety Patient safety organization Medical error Adverse Event Reporting System Adverse event Never events Near miss Medicine Health Patient safety
510	Microsoft Word[removed]Draft NYPORTS report[removed]doc Add to Reading List Source URL: www.health.ny.gov Language: English - Date: 2012-05-16 13:36:18 Medical terms Healthcare Hospice Nursing Medical error Agency for Healthcare Research and Quality Adverse Event Reporting System Adverse effect Patient safety organization Medicine Health Patient safety

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