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Adverse event
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#	Item
771	MERP Program & Medication Safety Loriann De Martini, Pharm.D. Chief Pharmaceutical Consultant Center for Healthcare Quality Add to Reading List Source URL: cdph.ca.gov Language: English - Date: 2014-11-25 18:00:36 Adverse event Medical error Health Patient safety Medicine Middle-earth Role Playing
772	VFC Provider Manual Resources Add to Reading List Source URL: www.health.ny.gov Language: English - Date: 2012-08-17 08:56:22 Drug safety Vaccines Vaccination Centers for Disease Control and Prevention Public safety Vaccination schedule National Childhood Vaccine Injury Act Vaccine Adverse Event Reporting System Vaccine Health Medicine Prevention
773	I. Current Illinois Law on Caregiver Information  Illinois Adverse Health Care Event Reporting Law of[removed]R]eports, findings, and plans shall not be available to the public and shall not be discoverable or admissibl Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2007-10-15 09:38:08 Journalism sourcing Secrecy Healthcare in the United States Medicine Health informatics Health Ethics Confidentiality
774	Adverse Events Policy and Reporting Guidelines The Queen’s University and Affiliated Teaching Hospitals Health Sciences Research Ethics Board (REB) has developed a policy with reporting requirements for Serious Adverse Add to Reading List Source URL: www.queensu.ca Language: English - Date: 2014-11-04 15:10:37 Adverse event Clinical research Pharmaceutical industry Serious adverse event
775	ADVERSE EVENT REPORTING GUIDELINES CCF Clinical Research Unit-CRU The RSA must be informed of adverse events to assess if the risk: benefit status of the study has changed. In general, an Adverse Event (AE) is any unto Add to Reading List Source URL: www.lerner.ccf.org Language: English - Date: 2014-10-31 14:07:24 Pharmaceutical sciences Pharmaceutics Adverse event Serious adverse event Clinical trial Randomized controlled trial Risk Clinical research coordinator Adverse effect Clinical research Pharmaceutical industry Research
776	CTRG WEBSITE GLOSSARY AE Adverse event AR Add to Reading List Source URL: www.admin.ox.ac.uk Language: English - Date: 2013-11-21 07:29:44 Science Clinical Trials Directive Clinical trial Serious adverse event Ethics Committee Good Clinical Practice Data monitoring committees Adverse event EudraCT Clinical research Research Scientific method
777	SRTR Consensus Conference on Transplant Program Quality and Surveillance February 13-15, 2012 INTERMACS The Interagency Registry for Add to Reading List Source URL: srtr.org Language: English - Date: 2012-03-15 15:36:05 Pharmacology Clinical research Pharmaceutical industry Prosthetics Interventional cardiology Destination therapy Adverse event Clinical trial Food and Drug Administration Medicine Health Science
778	01-05 STATEMENT OF POLICY VACCINE SAFETY Policy Confidence in the safety of the vaccines used to protect the residents of our nation is critical to assuring that the vaccines are used as widely, effectively and appropria Add to Reading List Source URL: www.naccho.org Language: English - Date: 2013-07-23 11:31:15 Prevention Centers for Disease Control and Prevention Vaccination Public safety Pediatrics Vaccine Safety Datalink Vaccine Adverse Event Reporting System Pertussis Vaccine Medicine Health Drug safety
779	RASCAL Study Description Help Text Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-01-08 12:20:51 Science Pharmaceutical sciences Design of experiments Pharmacology Food and Drug Administration Clinical trial Informed consent Internet privacy Adverse event Clinical research Pharmaceutical industry Research
780	Microsoft Word - FINAL IMM DDL#2 Letterhead[removed]doc Add to Reading List Source URL: us.merial.com Language: English - Date: 2011-09-30 12:09:30 Pharmaceutical industry Merial Medical informatics Dirofilaria immitis Food and Drug Administration Package insert Adverse event Medicine Veterinary medicine Health

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