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... Adverse events should be reported using the Common Terminology Criteria for Adverse Events v3.0 (CTCAE), which is NCI and CTEP ? s standard language for reporting adverse events ...
... X mg/m2, and not as a percent of the previous dose use values for CTCAE grades consistent with the actual definition and, finally, this one is tricky but ...
... : Provide the link for A number of investigators still have pending Special 1. CTCAE v 3.0. Exceptions (SPEX) paperwork with CTEP. Once 2. PMB's ...
... NCI Asymptomatic, transient Recurrent or persistent (> 24 Requiring more than one Life-threatening CTCAE ver 3.0 (< 24 hrs) increase by >20 hrs) or symptomatic ...
... Common Terminology Criteria for Adverse Events v3.0 (CTCAE) Publish Date: August 9, 2006 Quick Reference or diagnosis. A supra-ordinate term is followed by the word ...
... Common Terminology Criteria for Adverse Events (CTCAE) v3.0 March 31, 2003, Publish Date: August 9, 2006 Notice of Modifications The table below details the ...
... be routinely questioned about potential neurotoxicity, and undergo immediate dose reduction for neurotoxicity >CTCAE grade 1. In addition, delivery of IV paclitaxel at a reduced dose ( ...
... Development| Adverse Events/CTCAE Last Updated: 09/21/20 Common Terminology Criteria for Adverse Events (CTCAE) CTEP/NCORP Guidance for Collection of Adverse Events Related to COVID-19 Infection (3/25/2020) ...
... global standard for reporting to regulatory authorities within the U.S. Europe, and Japan. CTCAE Codes Common Terminology Criteria for Adverse Events are based on MedDRA and are used for ...
10. CTEP
... Login CTOIB Last Updated: 02/26/20 Reporting Guidelines Clinical Data Update System (CDUS) CTCAE Adverse Event Information Gender& Minority Accrual Data About the Branch Chief Michael Montello, ...