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Adverse event
Results: 2359

#	Item
641	National Action Plan for Adverse Drug Event Prevention Add to Reading List Source URL: health.gov Language: English - Date: 2014-09-18 06:35:00 Health informatics Patient safety Pharmacology Hospice Electronic health record Health information technology Food and Drug Administration Pay for performance Adverse Event Reporting System Medicine Health Medical terms
642	Guidance for Industry: Addendum to E2C Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Drug safety Pharmaceutical industry Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Food and Drug Administration Adverse event Addendum Pharmacovigilance Pharmaceutical sciences Clinical research Research
643	FDA Patient Safety News: Show #68, October 2007 Add to Reading List Source URL: www.fda.gov Language: English Pyridines Food and Drug Administration Pharmaceutical industry Sulfoxides MedWatch Adverse event Esomeprazole Omeprazole Ventricular assist device Medicine Pharmacology Proton pump inhibitors
644	National Action Plan for Adverse Drug Event Prevention Add to Reading List Source URL: health.gov Language: Czech - Date: 2014-09-18 06:35:00
645	Summary of 2009 Monovalent H1N1 Influenza Vaccine Data--Vaccine Adverse Event Reporting System--Data through January 8, 2010 Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2010-01-14 10:31:35 Health Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Influenza vaccine Flu pandemic vaccine FluMist Flu pandemic Medicine Vaccines Vaccination
646	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:39:39 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
647	Summary of[removed]Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through Jan. 25, 2011 Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2011-03-07 13:19:30 Prevention Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Anthrax vaccines Vaccine injury Vaccines Vaccination Medicine
648	Post-Approval Study Status Report 18-Month Report A Study to Evaluate the Effectiveness of Essure Post-NovaSure Radiofrequency Endometrial Ablation Procedure Following a Successful Essure Confirmation Test Essure-NovaSur Add to Reading List Source URL: www.fda.gov Language: English Science Technology Design of experiments Pharmacology Medical statistics Essure Clinical trial Birth control Adverse event Clinical research Pharmaceutical industry Research
649	FDA Patient Safety News: Show #37, March 2005 Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmaceutical industry Clinical research Adverse Event Reporting System MedWatch Adverse event Package insert Levofloxacin Infliximab Pharmacology Medicine Pharmaceutical sciences
650	Summary of 2009 Monovalent H1N1 Influenza Vaccine Data - November 24, 2009 Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2009-12-04 09:53:08 Health Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Influenza vaccine Flu pandemic vaccine FluMist Flu pandemic Medicine Vaccines Vaccination

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