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Adverse Event Reporting System
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#	Item
121	CDER Data Standards Strategy Action Plan Add to Reading List Source URL: www.fda.gov Language: English Clinical research Medical informatics Pharmacology Food and Drug Administration Clinical Data Management Clinical Data Interchange Standards Consortium Center for Biologics Evaluation and Research Electronic Common Technical Document Adverse Event Reporting System Pharmaceutical sciences Research Medicine
122	Summary of 2009 Monovalent H1N1 Influenza Vaccine Data--Vaccine Adverse Event Reporting System--Data Through December 23, 2009 Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2009-12-30 14:42:51 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
123	Summary of 2009 Monovalent H1N1 Influenza Vaccine Data – Vaccine Adverse Event Reporting System Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2010-03-04 14:38:08 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
124	Summary of 2009 Monovalent H1N1 Influenza Vaccine Data--Vaccine Adverse Event Reporting System Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2009-12-10 12:13:44 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
125	Brenda J. Rose, Pharm. D. Office of Special Health Issues Food and Drug Administration October 20, 2011 Add to Reading List Source URL: www.fda.gov Language: English MedWatch Clinical research Medicinal chemistry Adverse Event Reporting System Serious adverse event Pharmacology Food and Drug Administration Pharmaceutical sciences
126	FDA Patient Safety News: Show #48, February 2006 Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmaceutical industry Pharmacology MedWatch Adverse Event Reporting System Medical device Package insert Adverse event Center for Devices and Radiological Health Medicine Food and Drug Administration Health
127	Web Summary AE VAERS Updated[removed] Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2010-06-03 16:19:38 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
128	Guidance for Industry: MedWatch Form FDA 3500A: Mandatory Reporting of Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps) Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Center for Biologics Evaluation and Research Adverse effect Adverse Event Reporting System MedWatch Allotransplantation Adverse event Medical device Medicine Food and Drug Administration Health
129	FDA Patient Safety News: Show #73, March 2008 Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Clinical research Pharmaceutical industry Adverse Event Reporting System MedWatch Adverse event Phenylketonuria Alendronic acid Carbamazepine Medicine Food and Drug Administration Health
130	National Action Plan for Adverse Drug Event Prevention Add to Reading List Source URL: www.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