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Adverse Event Reporting System
Results: 638

#	Item
391	National Vaccine Advisory Committee (NVAC) February 6, 2009 Meeting on the draft strategic National Vaccine Plan: Goal 2 – Enhance the safety of vaccines and vaccination practices Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2014-09-01 00:35:37 Medicine Vaccination Centers for Disease Control and Prevention Vaccines Public safety Vaccine Adverse Event Reporting System Vaccine Vaccination schedule Prevention Safety Drug safety
392	Quarterly Review of Literature April—September 2010 Acquired Long QT Syndrome Antimicrobials and the risk of torsades de pointes: the contribution from data mining of the US FDA Adverse Event Reporting System. Add to Reading List Source URL: www.sads.org Language: English - Date: 2011-04-29 19:50:40 Implants Neuroprosthetics Barry A. Love Medicine Cardiac electrophysiology Implantable cardioverter-defibrillator
393	FDA - Adverse Event Reporting System (AERS) ISR Information Report for ISR #[removed]ISR Information: Manufacturer Information: Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-04-09 13:27:49 Necrotizing enterocolitis Adverse Event Reporting System Octreotide Coarctation of the aorta Pneumatosis intestinalis Surgery Medicine Pediatrics Health
394	Immune Globulins and Thromboembolic Events – Characterizing Risks and Improving Safety Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Adverse Event Reporting System Adverse effect Pharmacovigilance Food and Drug Administration Vaccine Gamma globulin Pharmacology Medicine Health
395	K:G FILESRLISTATear post-pediatric postmarketing exclusivity review[removed]Swann D030559.doc Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-04-09 09:20:39 Adverse Event Reporting System Food and Drug Administration Drug safety Orlistat Pharmacovigilance Phenytoin Medicine Pharmaceutical sciences Pharmacology
396	Microsoft Word - CDER Pharmacovigilance Review Background.doc Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical research Pharmaceutical industry Drug safety Pharmacovigilance Center for Drug Evaluation and Research Adverse event Clinical trial Adverse Event Reporting System Pharmacology Pharmaceutical sciences Research
397	FDA Science Board Subcommitte Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Research Clinical research Pharmaceutical industry Drug safety Pharmacovigilance Postmarketing surveillance Adverse Event Reporting System Adverse event Pharmacology Pharmaceutical sciences Health
398	3 - Francis - CDER Slider Add to Reading List Source URL: www.fda.gov Language: English Adverse Event Reporting System Food and Drug Administration Drug safety Pharmacovigilance MedDRA Adverse effects of fluoroquinolones COSTART Pharmacology Pharmaceutical sciences Clinical research
399	PDUFA IV Postmarket Safety Subgroup Tradename Discussion Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Food and Drug Administration Clinical research Medical terms Drug safety Adverse Event Reporting System Pharmacovigilance Postmarketing surveillance Adverse effect Medicine Health Pharmacology
400	PHARMACY BOARD[removed]Adopted and Filed Emergency After Notice Pursuant to the authority of Iowa Code section[removed]and 2013 Iowa Acts, Senate File 353, the Board of Pharmacy hereby amends Chapter 8, “Universal Practic Add to Reading List Source URL: www.state.ia.us Language: English - Date: 2014-01-03 10:04:35 Vaccines Drug safety Centers for Disease Control and Prevention Influenza vaccine Virology Medical prescription Pharmacist Vaccine Adverse Event Reporting System Immunization registry Medicine Health Vaccination

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