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Adverse event
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841	Medical Device Reporting for User Facilities DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Food and Drug Administration Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical sciences MedWatch Medical device Adverse event Center for Devices and Radiological Health Unique Device Identification Good Clinical Data Management Practice Food and Drug Administration Medicine Health
842	142 Guidance for Industry Pharmacovigilance of Veterinary Medicinal Products: Management of Periodic Summary Update Reports (PSUs) VICH GL29 Add to Reading List Source URL: www.fda.gov. Language: English Drug safety Pharmacy Pharmaceutical industry Pharmacovigilance Adverse event Food and Drug Administration Vich Switzerland Advanced Encryption Standard Pharmaceutical sciences Pharmacology Clinical research
843	Microsoft Word - Tables - Jones final report.doc Add to Reading List Source URL: www.unmc.edu Language: English - Date: 2014-07-30 13:30:53 Patient safety Medical ethics Hospice Nursing Medical error Safety culture Pharmacist Council of Australian Humanist Societies Adverse event Medicine Health Medical terms
844	59A[removed]Definitions. For the purpose of this section the word, phrase, or term: (1) “Adverse reaction” means an event where there is potential for the unanticipated transmission of communicable disease or malignanc Add to Reading List Source URL: www.ahca.myflorida.com Language: English - Date: 2013-02-18 17:34:18 Organ donation Organ transplants Organ transplantation Allotransplantation Eye bank Transplantable organs and tissues Tissue National Organization for Organ and Tissues Donation and Transplantation Human Tissue Authority Medicine Transplantation medicine Immunology
845	U.S. Department of Health & Human Services U.S. Food and Drug Administration FDA Facts: MedWatch M Add to Reading List Source URL: www.fda.gov. Language: English Pharmacology Pharmaceutical industry Health Clinical research MedWatch Package insert Serious adverse event Adverse Event Reporting System Adverse event Pharmaceutical sciences Food and Drug Administration Medicine
846	Report of the Section 618 Regulations Subgroup - Summary Add to Reading List Source URL: www.healthit.gov Language: English - Date: 2014-02-28 13:51:01 Pharmaceutical sciences Food and Drug Administration Clinical research Pharmaceuticals policy Medical technology Medical device Patient safety organization Adverse event Good manufacturing practice Medicine Health Pharmaceutical industry
847	Department of Health and Human Services Public Health Service Food and Drug Administration Center for Drug Evaluation and Research Office of Surveillance and Epidemiology Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Otologicals Cyclopropanes Drug safety Ofloxacin Ciprofloxacin Quinolone Pefloxacin Adverse Event Reporting System Piperazines Chemistry Pharmacology
848	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
849	Slide 1 Serious Reportable Events[removed]Madeleine Biondolillo, MD Associate Commissioner Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-08-15 11:07:39 Medical terms Healthcare Hospice Nursing Never events Medical error Bedsore Adverse event ASA physical status classification system Medicine Health Patient safety
850	Date: August 12, 2009 Add to Reading List Source URL: www.fda.gov Language: English Vaccination Pediatrics Gastroenterology Viral diseases Drug safety Rotavirus vaccine Rotavirus Vaccine Adverse Event Reporting System Influenza vaccine Medicine Health Vaccines

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