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Adverse event
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#	Item
871	GUIDELINE FOR GOOD CLINICAL PRACTICE Add to Reading List Source URL: www.fda.gov. Language: English Medicine Clinical research Pharmaceutical industry Pharmaceuticals policy Drug safety Pharmacovigilance Serious adverse event Adverse event Adverse effect Pharmaceutical sciences Pharmacology Health
872	CONTENTS EXECUTIVE SUMMARY ............................................................................................................. 2 1 BACKGROUND ................................................................... Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Abatacept Rheumatoid arthritis Adverse Event Reporting System Adalimumab Uveitis Juvenile idiopathic arthritis Rituximab Co-stimulation Medicine Immunosuppressants Health
873	Understanding the Vaccine Adverse Event Reporting System (VAERS) Add to Reading List Source URL: www.fda.gov. Language: English Vaccines Prevention Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Vaccine injury Anthrax vaccines Medicine Safety Drug safety
874	Serious Reportable Events[removed]Madeleine Biondolillo, MD Associate Commissioner Public Health Council August 2014 Add to Reading List Source URL: www.hcfama.org Language: English - Date: 2014-08-14 15:44:41 Patient safety Hospice Nursing Never events Adverse event Patient safety organization Medicine Health Medical terms
875	Guidance for Industry: How to Complete the Vaccine Adverse Events Reporting System Form (VAERS-1) Add to Reading List Source URL: www.fda.gov. Language: English Drug safety Food and Drug Administration Pharmacology Vaccines Vaccination Vaccine Adverse Event Reporting System Vaccine injury Adverse effect National Childhood Vaccine Injury Act Medicine Health Safety
876	Improving the basis for FDA CBER identification of adverse effects of blood products and vaccines Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Safety Drug safety Centers for Disease Control and Prevention Public safety Center for Biologics Evaluation and Research Adverse Event Reporting System Biologic Postmarketing surveillance Medicine Health Pharmacology
877	Serious Reportable Events[removed]Madeleine Biondolillo, MD Associate Commissioner Public Health Council August 2014 Add to Reading List Source URL: www.hcfama.org Language: English - Date: 2014-08-14 15:44:41 Patient safety Hospice Nursing Never events Adverse event Patient safety organization Medicine Health Medical terms
878	Pharmaceuticals and Medical Devices Agency This English version is intended to be a reference material to provide convenience for users. In the event of inconsistency between the Japanese original and this English transl Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2014-08-06 20:44:52 Drug eruptions Piperazines Toxic epidermal necrolysis Package insert Carvedilol Adverse effect Stevens–Johnson syndrome Medicine Health Chemistry
879	Department of Health and Human Services Public Health Service Food and Drug Administration Center for Drug Evaluation and Research Office of Surveillance and Epidemiology Date: Add to Reading List Source URL: www.fda.gov Language: English Drug safety Adverse Event Reporting System Food and Drug Administration Pharmacovigilance ISTA Pharmaceuticals Pharmaceutical sciences Pharmacology Clinical research
880	QUALITY MONITORING USING CASE MIX AND ADVERSE EVENT OUTCOME REPORTS Implementing Outcome-Based Quality Improvement at a Home Health Agency 2001 Department ofHealth andHumanServices Health Care FinancingAdministration Add to Reading List Source URL: www.cms.gov Language: English - Date: 2013-08-07 15:29:24 Healthcare reform in the United States Presidency of Lyndon B. Johnson Geriatrics Healthcare Medicare Medicaid Nursing home Home care Patient safety Medicine Health Federal assistance in the United States

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