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Adverse event
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#	Item
851	Consumer Health Information www.fda.gov/consumer www.fda.gov/consumer/updates/reporting_guide061008.html Your Guide to Reporting Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical sciences MedWatch Adverse Event Reporting System FDA Consumer Medical device Drug recall Office of Regulatory Affairs Food and Drug Administration Medicine Health
852	Microsoft Word - PDUFA IV Annual IT Assessment _FY2010_.doc Add to Reading List Source URL: www.fda.gov Language: English Health Clinical research Pharmaceuticals policy Prescription Drug User Fee Act Medical informatics Drug safety Regulated Product Submissions Center for Biologics Evaluation and Research Adverse Event Reporting System Food and Drug Administration Medicine Research
853	Pharmaceuticals and Medical Devices Agency This English version is intended to be a reference material to provide convenience for users. In the event of inconsistency between the Japanese original and this English transl Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2014-08-06 20:44:51 Adverse effect Patient safety Package insert Carboplatin Chemistry Medicine Pharmacology
854	Reporter Quick Reference Guide Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2014-06-16 17:13:03 Medical terms Safety Pharmaceutical industry Hospice Near miss Medical error Adverse event Medical record Patient safety organization Medicine Health Patient safety
855	Pharmaceuticals and Medical Devices Agency This English version is intended to be a reference material to provide convenience for users. In the event of inconsistency between the Japanese original and this English transl Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2014-10-14 01:32:29 Immunosuppressants Monoclonal antibodies Schering-Plough Bodybuilding supplements Infliximab Biologic Adverse effect Creatine Rhabdomyolysis Medicine Health Pharmacology
856	Version Date[removed]Faculty Senate Approved INSTITUTIONAL REVIEW BOARD FWA: [removed] \| IRB: [removed] Add to Reading List Source URL: www.pacificu.edu Language: English - Date: 2014-11-26 19:43:48 Applied ethics Institutional review board Investigational New Drug Investigational Device Exemption Public Responsibility in Medicine and Research Declaration of Helsinki Belmont Report Adverse event Clinical research coordinator Clinical research Research Medicine
857	Safety Data Issues for Discussion Email, April 4, [removed]Laviv Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Food and Drug Administration Clinical trial Design of experiments MedDRA Adverse event Pharmacology Pharmaceutical sciences Research
858	Pediatric Medical Devices: Neurotherapeutics Add to Reading List Source URL: www.fda.gov Language: English Neurotechnology Surgery Vagus nerve stimulation Medical terms Epilepsy Adverse event Deep brain stimulation Vagus nerve Neurologist Medicine Electrotherapy Neuroprosthetics
859	Pharmaceuticals and Medical Devices Agency This English version is intended to be a reference material to provide convenience for users. In the event of inconsistency between the Japanese original and this English transl Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2014-10-14 01:32:32 Morpholines Organofluorides Pfizer Metabolic acidosis Acidosis Lactic acidosis Adverse effect Glycogen storage disease type I Medicine Health Linezolid
860	PLAN OF ACTION FOR IMPLEMENTATION OF 510(K) AND SCIENCE RECOMMENDATIONS In August 2010, the Food and Drug Administration’s Center for Devices and Radiological Health (CDRH or the Center) Add to Reading List Source URL: www.fda.gov Language: English Clinical research Health Pharmaceutical industry Pharmacology Therapeutics Center for Devices and Radiological Health Medical device Adverse event Clinical trial Medicine Food and Drug Administration Pharmaceutical sciences

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