Article: Adverse events with placebo: representative of real life?

Article: An adverse event for food companies? (Regulatory ...
Food Processing;  October 1, 2002 ;     700+ words ... ... and analyze adverse events associated with ... acknowledged that adverse event reporting involving ... qualifies as an adverse event?" Presumably ... physicians report adverse events associated with ... reportable) adverse event is one that ...

Article: Preventing compelled disclosure of adverse event ...
Defense Counsel Journal;  January 1, 1996 ;     700+ words ... ... production or in the reported adverse events themselves. Pursuant to ... Identities of Reporters of Adverse Events and Patients; Preemption ... and others involved with adverse events, the FDA in January 1994 ... person associated with an adverse event involving a human ...

Article: Adverse events after inactivated influenza ...
Pediatrics;  February 1, 2005 ;     700+ words ...ABBREVIATIONS. VAERS, Vaccine Adverse Event Reporting System; TIV, trivalent ... proportional reporting ratio; AE, adverse event; DC, disease category. Influenza ... this age, this review compares the adverse event (AE) experience before the guidelines ...

Article: Adverse events--can we trust the data?
Bandolier;  March 1, 2001 ;     700+ words ... ... Reporting adverse events Adverse event reporting ... because of adverse events were reported ... specific type of adverse event leading to ... reason for adverse event discontinuations ... of clinical adverse events was found ...

Article: Purdue improves e-record tracking of Oxycontin adverse ...
Validation Times;  January 1, 2003 ;     700+ words ... ... to handle the increased adverse event information being received ... OTC and non-NDA product adverse events that could come in from the ... establishing SOPs for handling adverse events, compiling adverse event reports and filing adverse ...

Article: Purdue improves e-record tracking of Oxycontin adverse ...
Inspection Monitor;  December 1, 2002 ;     700+ words ... ... to handle the increased adverse event information being received ... OTC and non-NDA product adverse events that could come in from the ... establishing SOPs for handling adverse events, compiling adverse event reports and filing adverse ...

Article: Getting on the right path: when it comes to research, development ...
Nutraceuticals World;  September 1, 2006 ;     700+ words ... ... research and dietary supplements, presenting an opportunity to discuss the meanings of research studies, adverse events, adverse event reporting and product development. These exact areas are of particular importance and hopefully are of interest ...