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Serious adverse event
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#	Item
141	Adverse Event Review and Reporting as Mandated by Best Pharmaceuticals for Children Act: Summary of Committee Feedback and Options for Improvement Pediatric Advisory Committee Meeting Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-08-08 12:21:00 Pharmacology Pharmaceutics Piperazines Drug safety Boxed warning Adverse event Pharmacovigilance Serious adverse event Pharmaceutical industry Pharmaceutical sciences Clinical research
142	CENTRAL DEPARTMENT OF ENERGY INSTITUTIONAL REVIEW BOARD Report of Unanticipated Problems Involving Risks to Subject or Others (UP) Including Unanticipated Serious Adverse Events (USAE) The protocol must be submitted in t Add to Reading List Source URL: humansubjects.energy.gov Language: English - Date: 2012-08-29 10:08:10 Scientific method Science Design of experiments Pharmacology Drug safety Institutional review board Adverse event Serious adverse event Clinical research coordinator Clinical research Pharmaceutical industry Research
143	Serious Reportable Events in Massachusetts Hospitals: January 1, 2008 – December 31, 2008 Add to Reading List Source URL: www.mass.gov Language: English - Date: 2013-08-30 23:26:54 Patient safety Never events Medical error Adverse event Patient safety organization Medicine Health Medical terms
144	Serious Reportable Events in Massachusetts Acute Care Hospitals: January 1, 2009 – December 31, 2009 A report by the Add to Reading List Source URL: www.mass.gov Language: English - Date: 2013-08-30 23:26:19 Patient safety Healthcare Nursing Medical error Never events Adverse event Acute care Patient safety organization Medicine Health Medical terms
145	Division of Microbiology and Infectious Diseases SAE Reporting Guidelines For questions on SAE reporting or SAE form completion, contact DMID-CROMS Pharmacovigilance: Email: [removed] SAE Hotline: [removed] Add to Reading List Source URL: www.dmidcroms.com Language: English - Date: 2013-06-17 14:47:07 Serious adverse event Horsepower Measurement Clinical research Pharmaceutical industry
146	QuarterWatch: 2008 Quarter 2 January 15, 2009 Executive Summary Reports of serious injury, disability, and death associated with drug therapy exceeded 20,000 cases for a second consecutive quarter in[removed]For the first Add to Reading List Source URL: www.ismp.org Language: English - Date: 2009-05-06 13:43:21 Pharmacology Food and Drug Administration Pharmaceutical industry Piperazines Patient safety Varenicline Boxed warning Adverse effect Adverse Event Reporting System Medicine Health Pharmaceutical sciences
147	Federation of the European Academies of Medicine Palais des Académies Rue Ducale 1 B-1000 Brussels Tel: +[removed] Fax: +[removed]65 [removed] www.feam.eu.com FEAM Response to Consultation on Func Add to Reading List Source URL: www.feam-site.eu Language: English - Date: 2012-06-07 04:11:38 Scientific method Ethics Committee Clinical trial Clinical Trials Directive Institutional review board EudraCT Serious adverse event Evidence-based medicine Declaration of Helsinki Clinical research Research Science
148	Microsoft Word - Glossary of terms.doc Add to Reading List Source URL: www.who-umc.org Language: English - Date: 2011-08-25 10:12:54 Medicine Clinical research Drug safety Pharmacy Pharmaceutical industry Pharmacovigilance EudraVigilance Adverse effect Serious adverse event Pharmacology Pharmaceutical sciences Health
149	Reviewer Guidance Conducting a Clinical Safety Review of a New Product Application and Preparing a Report on the Review U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-04-14 09:11:03 Health Clinical research Pharmaceutical industry Food and Drug Administration Drug safety Adverse effect Serious adverse event Clinical trial Adverse event Pharmacology Pharmaceutical sciences Medicine
150	Appendix II Determining whicfh Adverse Events are Unanticipated Problems: DAIDS Responsibilities Add to Reading List Source URL: www.niaid.nih.gov Language: English - Date: 2012-11-13 15:35:04 Serious adverse event Medicine Norfloxacin Health Technology Clinical research Pharmaceutical industry Adverse event

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