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Adverse event
Results: 2359

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31	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: 2016-08-04 23:26:37 RTT Allergology Clinical pharmacology Neuropeptides Neurotransmitters Oxytocin Anaphylaxis Adverse effect
32	Expanded Access to Investigational Drugs and Biologics _______________________________When All Else Fails__________________________ Add to Reading List Source URL: www.reaganudall.org Language: English - Date: 2016-05-24 12:16:34 Clinical pharmacology Food and Drug Administration Medical research Clinical research Pharmaceutical industry Expanded access Investigational New Drug Adverse event Clinical trial Adverse effect Treatment IND Managed access program
33	∙ Tips for Talking With and Helping Children and Youth Cope After a Disaster or Traumatic Event: A GUIDE FOR PARENTS, CAREGIVERS, AND TEACHERS Adult support and reassurance is the key to helping children through a tra Add to Reading List Source URL: www.nhstudentwellness.org Language: English - Date: 2016-07-08 14:01:00 Stress Caregiving Posttraumatic stress disorder Anxiety disorders Mental health Caregiver Psychological trauma Grief Major trauma Substance Abuse and Mental Health Services Administration Child abuse Adverse Childhood Experiences Study
34	PHARMACOVIGILANCE GUIDE FOR ADVERSE DRUG REACTION MONITORING AND CAUSALITY ASSESSMENT, 2015 Post marketing Control Division, Add to Reading List Source URL: dra.gov.bt Language: English - Date: 2016-07-27 06:22:23 Pharmaceuticals policy Clinical research Clinical pharmacology Drug safety World Health Organization Pharmacovigilance Uppsala Monitoring Centre VigiBase Adverse effect Adverse drug reaction Serious adverse event Adverse event
35	REVIEW ARTICLE A New, Evidence-based Estimate of Patient Harms Associated with Hospital Care John T. James, PhD Add to Reading List Source URL: s3.amazonaws.com Language: English - Date: 2013-09-17 22:16:55 Medical terminology Patient safety Healthcare quality Clinical pharmacology Medical ethics Medical error Electronic health record Adverse effect Adverse event Never events Antimicrobial stewardship Adverse drug reaction
36	QuarterWatch Monitoring FDA MedWatch Reports Why Reports of Serious Adverse Drug Events Continue to Grow October 3, 2012 Data from 2012 Quarter 1 Add to Reading List Source URL: www.ismp.org Language: English - Date: 2012-10-03 12:53:27 Food and Drug Administration Clinical research Thiophenes Healthcare quality Medical terminology Adverse Event Reporting System Duloxetine Pharmacovigilance Rivaroxaban Adverse effect Adverse event MedWatch
37	Improving Patient Care Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement John P.A. Ioannidis, MD; Stephen J.W. Evans, MSc; Peter C. Gøtzsche, MD, DrMedSci; Robert T. O’Neill, PhD; D Add to Reading List Source URL: www.consort-statement.org Language: English - Date: 2013-08-14 20:08:36 Clinical research Randomized controlled trial Consolidated Standards of Reporting Trials Adverse effect Pharmacovigilance Serious adverse event Evidence-based medicine Clinical trial Cochrane Adverse event Systematic review Reporting bias
38	Pharmacovigilance: Monitoring the Safety & Efficacy of Animal Medicines Summary This document Add to Reading List Source URL: www.noah.co.uk Language: English - Date: 2016-05-20 12:52:44 Pharmaceuticals policy Clinical research Drug safety Clinical pharmacology Healthcare quality Veterinary Medicines Directorate Pharmacovigilance European Medicines Agency Suspected Adverse Reaction Surveillance Scheme Adverse effect Adverse event National Office of Animal Health
39	FAHSS Research Ethics Committee (FREC) Form: End of project report April 2014 Add to Reading List Source URL: ahss.tcd.ie Language: English - Date: 2014-07-17 07:53:01 Adverse event Clinical research Pharmaceutical industry Ethics Research ethics Adverse effect
40	IMDRF Presentation: Adverse Event Terminology and Coding Working Group Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2016-03-29 00:18:15 Standards organizations Technical specifications International Organization for Standardization

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