Literature DB >> 2007509

[Comprehension and evaluation of drug risks through spontaneous notification].

E Weidmann1, G Jüngst.   

Abstract

Risk/benefit analysis of drugs requires not only the reporting and documentation of adverse drug reactions in clinical trials but also a spontaneous reporting system for the detection of rare adverse reactions to drugs. A central aspect of any spontaneous reporting system is assessment of causality on the basis of detailed case histories. However, besides the qualitative description of adverse drug reactions, information about the incidence of such reactions has to be obtained as well so that their frequency, and thus the risk involved, can be established.

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Year:  1991        PMID: 2007509     DOI: 10.1007/bf01644729

Source DB:  PubMed          Journal:  Infection        ISSN: 0300-8126            Impact factor:   3.553


  3 in total

1.  Physician reporting of adverse drug reactions. Results of the Rhode Island Adverse Drug Reaction Reporting Project.

Authors:  H D Scott; A Thacher-Renshaw; S E Rosenbaum; W J Waters; M Green; L G Andrews; G A Faich
Journal:  JAMA       Date:  1990-04-04       Impact factor: 56.272

2.  Adverse-drug-reaction monitoring.

Authors:  G A Faich
Journal:  N Engl J Med       Date:  1986-06-12       Impact factor: 91.245

Review 3.  Fluoroquinolones. Adverse reactions during clinical trials and postmarketing surveillance.

Authors:  R Janknegt
Journal:  Pharm Weekbl Sci       Date:  1989-08-25
  3 in total

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