Skip to main content
Log in

Erfassung und Bewertung von Arzneimittelrisiken durch Spontanmeldungen

Detection of drug risks by spontaneous reporting

  • Risikoerfassung Bei Antibakteriell Wirksamen Chemotherapeutika
  • Published:
Infection Aims and scope Submit manuscript

Zusammenfassung

Die Risiko-Nutzen-Abwägung der Arzneimittelbehandlung setzt die Erfassung und Dokumentation von Arzneimittelnebenwirkungen, im Rahmen Klinischer Prüfungen, ein Spontanerfassungssystem zur Erfassung seltener Arzneimittelnebenwirkungen voraus. Im Rahmen dieses Spontanerfassungssystems muß durch eine eingehende Fallanalyse eine Kausalitätsbewertung erreicht werden. Die Erfassung der Inzidenz von Nebenwirkungen muß das Spontanmeldesystem ergänzen, um über die qualitative Beschreibung von unerwünschten Arzneimittelreaktionen hinaus die Häufigkeit von Arzneimittelrisiken festzulegen.

Summary

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Literatur

  • Rawlins M. D.: National adverse drug reaction reporting — a silver jubilee. Adverse Drug Reaction Bulletin, October 1989, No. 138, 516–519.

  • Faich, G. A. Special report: Adverse-drug-reaction monitoring, The New England Journal of Medicine, 314, 24 (1986) 1589–1592.

    Google Scholar 

  • Scott, H. D. Adverse drug reaction reporting, physician reporting of adverse drug reactions — Results of the Rhode Island Adverse Drug Reaction Reporting Project. JAMA, 263 (1990) 1785–1788.

    Google Scholar 

  • Janknegt, R. Fluoroquinolones, adverse reactions during clinical trials and postmarketing surveillance. Pharmaceutisch Weekblad Scientific edition, 11 (1989) 124–127.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Weidmann, E., Jüngst, G. Erfassung und Bewertung von Arzneimittelrisiken durch Spontanmeldungen. Infection 19 (Suppl 1), S16–S18 (1991). https://doi.org/10.1007/BF01644729

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01644729

Navigation