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Adverse Event Reporting System
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581	MINUTES OF THE PEDIATRIC ADVISORY COMMITTEE Bethesda Marriott Hotel 5151 Pooks Hill Road, Bethesda, Maryland[removed]Monday, March 22, 2010 The meeting was convened at approximately 8:00 a.m. Add to Reading List Source URL: www.fda.gov Language: English Immunosuppressants Macrolides Safety Drug safety Vaccination Center for Biologics Evaluation and Research Vaccine Adverse Event Reporting System Tacrolimus Pimecrolimus Medicine Health Food and Drug Administration
582	Microsoft Word - FINAL Agenda Day 1 Monday, May 7th.doc Add to Reading List Source URL: www.fda.gov Language: English Clinical pharmacology Pharmacology Therapeutics United States Public Health Service Chemistry Adverse Event Reporting System Oseltamivir Center for Drug Evaluation and Research Food and Drug Administration Pharmaceutical sciences Clinical research
583	What Types of Events Should I Report? You should report any adverse event that happens after getting a vaccine, even if you are not sure that the vaccine caused the adverse event. It is especially important to report any Add to Reading List Source URL: www.fda.gov Language: English Health Vaccine Adverse Event Reporting System Vaccine injury Adverse effect Vaccine Vaccination schedule Vaccination National Childhood Vaccine Injury Act Anthrax vaccines Drug safety Safety Medicine
584	U.S. Department of Health and Human Services Food and Drug Administration Center for Food Safety and Applied Nutrition CFSAN Adverse Event Reporting System Voluntary Reports on Red Bull Energy Drink January 1, 2004, thro Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Pharmaceutical industry Drug safety Red Bull Adverse event Adverse Event Reporting System MedWatch Energy drink Pharmaceutical sciences Pharmacology Food and Drug Administration
585	A MEDWATCH CONTINUING EDUCATION ARTICLE Provided as a service by the National Institutes of Health/Foundation for Advanced Education in the Sciences (NIH/FAES), Bethesda, MD, and the U.S. Food and Drug Administration (F Add to Reading List Source URL: www.fda.gov Language: English Vaccines Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Vaccine injury National Childhood Vaccine Injury Act Varicella vaccine Adverse effect Medicine Health Vaccination
586	Immunization Safety Office - Scientific Agenda Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2011-03-16 17:13:51 Health Drug safety Centers for Disease Control and Prevention Public safety Food and Drug Administration Vaccine Adverse Event Reporting System Vaccine injury National Childhood Vaccine Injury Act Varicella vaccine Vaccination Medicine Vaccines
587	Consumer Health Information www.fda.gov/consumer WANTED: Consumers to Report Problems A Add to Reading List Source URL: www.fda.gov Language: English Clinical research MedWatch Medicine FDA Consumer Consumer Reports Adverse Event Reporting System Package insert Food and Drug Administration Pharmacology Pharmaceutical sciences
588	Table of Contents EXECUTIVE SUMMARY ................................................................................................ 1 I. SENTINEL SYSTEM VISION......................................................... Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceutical sciences MedWatch Electronic health record Adverse Event Reporting System Harvard Pilgrim Health Care Medical device Clinical trial Patient safety organization Food and Drug Administration Medicine Health
589	FDA Notifying Health Care Providers about the Risks of Purchasing Unapproved Injectable Cancer Medications from Unlicensed Sources Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Office of Criminal Investigations Center for Drug Evaluation and Research Federal Food Drug and Cosmetic Act Online pharmacy Adverse Event Reporting System Food and Drug Administration Health Medicine
590	This graph depicts what happens to an adverse event report that is submitted to FDA. First, FDA may receive one of two types of reports: mandatory or voluntary. A mandatory report is sent to FDA by a manufacturer, import Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical research Pharmaceutical industry Therapeutics Adverse event Adverse Event Reporting System Unique Device Identification Pharmaceutical sciences Pharmacology Research

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