Evaluation of serious adverse drug reactions: A Proactive Pharmacovigilance Program (RADAR) vs safety activities conducted by the Food and Drug Administration and pharmaceutical manufacturers Academic Article uri icon

Overview

MeSH Major

  • Drug Industry
  • Drug-Related Side Effects and Adverse Reactions
  • Product Surveillance, Postmarketing
  • United States Food and Drug Administration

abstract

  • Proactive safety efforts conducted by the RADAR investigators are more comprehensive than those conducted by the FDA and pharmaceutical manufacturers, but dissemination of related safety notifications is less timely.

publication date

  • May 28, 2007

Research

keywords

  • Academic Article

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1001/archinte.167.10.1041

PubMed ID

  • 17533207

Additional Document Info

start page

  • 1041

end page

  • 9

volume

  • 167

number

  • 10