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Adverse event
Results: 2359

#	Item
811	YouScript Risk Assessment ® To find out if you are at risk for an adverse drug event, complete the following YouScript Risk Assessment and Add to Reading List Source URL: genelex.com Language: English - Date: 2014-03-14 05:35:33 Pharmacy Organochlorides Nicotinic antagonists Selective serotonin reuptake inhibitors Clopidogrel Bupropion Pharmacogenetics Pharmacist Medical prescription Chemistry Pharmacology Medicine
812	Herbert Irving Comprehensive Cancer Center Columbia University Medical Center DATA AND SAFETY MONITORING PLAN S t e p h e n G . E m e r s o n , M D , P h D , Director Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2014-01-14 14:49:56 Medicine Health Clinical trial Investigational Device Exemption Institutional review board Investigational New Drug Safety monitoring Eastern Cooperative Oncology Group Adverse event Clinical research Research Pharmaceutical industry
813	D2[removed]University of Kentucky Policy on Prompt Reporting For Unanticipated Problems, Serious or Life-Threatening Events, and Anticipated or Unanticipated Related Deaths to the Institutional Review Board (IRB) and Insti Add to Reading List Source URL: www.research.uky.edu Language: English - Date: 2012-09-14 14:44:36 Drug safety Scientific method Pharmacology Science Medical ethics Adverse event Serious adverse event Institutional review board Clinical research coordinator Clinical research Pharmaceutical industry Research
814	Adverse events can be broadly divided into three categories: 1. Implantation Reactions: These usually occur relatively soon after implantation and are commonly linked to the implantation procedure e.g. haematomas (bleed Add to Reading List Source URL: www.vmd.defra.gov.uk Language: English Pharmaceutical sciences Radio-frequency identification Animal identification Microchip implant Veterinary Medicines Directorate Pharmacovigilance Ferret Adverse effect Adverse event Medicine Pharmacology Health
815	F10.0000 UK External Prompt Reporting Form F10.0000 UK External Prompt Reporting Form For Unanticipated Problems, Serious or Life-Threatening Events, and Related Anticipated and Unanticipated Deaths Add to Reading List Source URL: www.research.uky.edu Language: English - Date: 2014-03-10 14:39:02 Science Pharmacology Ethics Design of experiments Drug safety Adverse event Serious adverse event Institutional review board Clinical trial Clinical research Pharmaceutical industry Research
816	Microsoft PowerPoint - Tues_11h40_RonBone [Read-Only] Add to Reading List Source URL: www.gs1.org Language: English - Date: 2013-10-07 04:20:09 Pharmacology Health Barcode National Drug Code Center for Devices and Radiological Health Adverse event Identifier Food and Drug Administration Pharmaceutical sciences Unique Device Identification
817	Guideline for Industry The Extent of Population Exposure to Assess Clinical Safety: For Drugs Intended for Longterm Treatment of Non-LifeThreatening Conditions Add to Reading List Source URL: www.fda.gov Language: English Health Clinical trial Pharmacovigilance Adverse drug reaction Adverse event Food and Drug Administration Pharmaceutical drug Phases of clinical research Adverse effect Pharmacology Pharmaceutical sciences Medicine
818	Follow-up Discussion of Serious Adverse Event OBA Protocol Number 705 Add to Reading List Source URL: osp.od.nih.gov Language: English - Date: 2014-01-14 14:54:11 Monoclonal antibodies Molecular biology Biotechnology Immunosuppressants Tumor necrosis factor-alpha TNF inhibitor Rheumatoid arthritis Adalimumab Vector Biology Medicine Gene delivery
819	University of South Alabama Add to Reading List Source URL: www.southalabama.edu Language: English - Date: 2011-12-09 13:48:38 Scientific method Science Design of experiments Pharmacology Drug safety Institutional review board Good Clinical Practice Adverse event Clinical research coordinator Clinical research Research Pharmaceutical industry
820	FDA INSPECTIONS OF CLINICAL INVESTIGATORS Add to Reading List Source URL: www.research.uky.edu Language: English - Date: 2013-04-05 15:07:07 Health Pharmacology Food and Drug Administration Pharmaceutical industry Design of experiments Institutional review board Clinical trial Investigational New Drug Adverse event Clinical research Research Medicine

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