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Serious adverse event
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171	Blood Collection Guidelines Add to Reading List Source URL: www.compliance.iastate.edu Language: English - Date: 2010-02-10 15:30:15 Medicine Science Institutional review board Clinical trial Serious adverse event Adverse event Investigational New Drug Investigational Device Exemption Medical error Clinical research Research Pharmaceutical industry
172	DCP SAE Form Instructions for Completion Version 1.2 DCP SAE Form Instructions for Completion Version 1.2 SAE Report Form: Instructions for Completion Version 1.2 Add to Reading List Source URL: prevention.cancer.gov Language: English - Date: 2013-06-27 17:24:28 Serious adverse event Adverse event Clinical research Pharmaceutical industry Research
173	DOC Document Add to Reading List Source URL: www.compliance.iastate.edu Language: English - Date: 2011-08-04 11:07:13 Research Medical ethics Scientific method Design of experiments Pharmacology Institutional review board Serious adverse event Informed consent Adverse event Clinical research Ethics Pharmaceutical industry
174	PROTECTED WHEN COMPLETED Health Canada’s Special Access Programme (SAP) Instructions for Filling out a Follow-up Form FORM C Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-06-24 11:34:22 Health Patient safety Medical terms Pharmacy Adverse effect Medical prescription Adverse drug reaction Pefloxacin Serious adverse event Pharmacology Medicine Pharmaceutical sciences
175	Microsoft Word - sapf3_pasf3_e.doc Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-07-08 16:46:01 Health Patient safety Medical terms Pharmacy Adverse effect Medical prescription Adverse drug reaction Serious adverse event Pharmacology Medicine Pharmaceutical sciences
176	Bannatyne Campus Research Ethics Boards P126-770 Bannatyne Avenue Winnipeg, Mb R3E 0W3 Phone: (204) Phone: ([removed] Add to Reading List Source URL: umanitoba.ca Language: English - Date: 2014-08-28 08:15:14 Adverse event Serious adverse event Safety monitoring Pharmaceutical industry Clinical research Research
177	OCTOBER 24, 2008 ADVISORY RE CLINICAL DRUG TRIAL REPORTING To manufacturers and labelers of prescription drugs: Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-29 09:00:49 Pharmaceutics Pharmaceutical sciences Pharmacology Food and Drug Administration Adverse event ClinicalTrials.gov Clinical trial Serious adverse event Pharmaceutical industry Clinical research Research
178	Serious Adverse Events: Proposyphene and Darvocet (memo, December 15, 2008) Add to Reading List Source URL: www.fda.gov Language: English Eli Lilly and Company Combination drugs Amines Antitussives Dextropropoxyphene Propionates Adverse Event Reporting System Carbamazepine Paracetamol Pharmacology Chemistry Medicine
179	Adverse Event Form STUDY NAME Site Number: Pt_ID: ______________________ Add to Reading List Source URL: www.nia.nih.gov Language: English - Date: 2011-09-21 08:32:40 Research Pharmaceutical sciences Medicine Serious adverse event Adverse event Dose Adverse effect Clinical research Pharmaceutical industry Pharmacology
180	Gammagard Liquid, subcutaneous route of administration, PediatrSafety and Utilization Review for the Pediatric Advisory Committ(PAC) Meeting Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Clinical research Pharmaceutical industry Drug safety Medical terms Pharmacovigilance Adverse effect Idiopathic thrombocytopenic purpura Serious adverse event Health Medicine Pharmacology

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