Literature DB >> 8134741

Alert systems for post-marketing surveillance of adverse drug reactions.

M Praus1, F Schindel, R Fescharek, S Schwarz.   

Abstract

When monitoring spontaneous reports of adverse reactions to registered drugs, it is important to detect any change in the number of reported adverse reactions in the course of time. Sales adjusted adverse drug reaction rates are usually compared in order to be able to take drug exposure into account. Here we review the so-called arithmetic and some statistical procedures which could form the basis for an alert system. The advantages and disadvantages of each of these methods are discussed. The importance of data requirements and the problems which arise when using an alert system are pointed out and then clarified with the help of the example of diphtheria/tetanus vaccine.

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Year:  1993        PMID: 8134741     DOI: 10.1002/sim.4780122414

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  4 in total

1.  Is reporting rate a good predictor of risks associated with drugs?

Authors:  C Pierfitte; B Bégaud; R Lagnaoui; N D Moore
Journal:  Br J Clin Pharmacol       Date:  1999-03       Impact factor: 4.335

Review 2.  Quantitative methods in pharmacovigilance: focus on signal detection.

Authors:  Manfred Hauben; Xiaofeng Zhou
Journal:  Drug Saf       Date:  2003       Impact factor: 5.606

3.  Defining 'surveillance' in drug safety.

Authors:  Jeffrey K Aronson; Manfred Hauben; Andrew Bate
Journal:  Drug Saf       Date:  2012-05-01       Impact factor: 5.606

4.  A Qualitative Evaluation of Adverse Drug Reaction Reporting System in Pakistan: Findings from the Nurses' Perspective.

Authors:  Rabia Hussain; Mohamed Azmi Hassali; Anees Ur Rehman; Jaya Muneswarao; Muhammad Atif; Zaheer-Ud-Din Babar
Journal:  Int J Environ Res Public Health       Date:  2020-04-27       Impact factor: 3.390

  4 in total

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