Literature DB >> 12071780

Signal generation in the New Zealand Intensive Medicines Monitoring Programme: a combined clinical and statistical approach.

David M Coulter1.   

Abstract

The New Zealand Intensive Medicines Monitoring Programme (IMMP) undertakes prospective observational cohort studies on selected new drugs in the early postmarketing period using prescription-event monitoring (PEM) methodology with the purpose of identifying signals of previously unrecognised ADRs and establishing risk profiles for each drug. Events are reviewed by a physician and a relationship is established between each event and the drug. The events are then sorted into reactions and incidents. The latter are used to assist signal detection and control for bias. Rates for reports, reactions and incidents are used to assess the adequacy of reporting, signal detection and identification of confounders. Most signals are identified by clinical evaluation of the reports at a stage when statistical analyses are unlikely to have the power to detect them with confidence. The incident group is used for signal detection and controlling for bias. A low reporting rate indicates that certain types of event are unlikely to be reported. A systematic review of the original case reports at the site of collection provides the best opportunity for early signal detection. More resources need to be invested in the training and support of clinical evaluators. Categorising events into reactions and incidents gives added value to the data. Rates of reporting should be quoted with the results of cohort studies to facilitate assessment of their power to detect new signals.

Mesh:

Year:  2002        PMID: 12071780     DOI: 10.2165/00002018-200225060-00007

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  3 in total

1.  The New Zealand Intensive Medicines Monitoring Programme.

Authors:  D M Coulter
Journal:  Pharmacoepidemiol Drug Saf       Date:  1998-03       Impact factor: 2.890

2.  A comparison of the use, effectiveness and safety of bezafibrate, gemfibrozil and simvastatin in normal clinical practice using the New Zealand Intensive Medicines Monitoring Programme (IMMP).

Authors:  P W Beggs; D W Clark; S M Williams; D M Coulter
Journal:  Br J Clin Pharmacol       Date:  1999-01       Impact factor: 4.335

3.  The New Zealand intensive medicines monitoring programme in pro-active safety surveillance.

Authors:  D M Coulter
Journal:  Pharmacoepidemiol Drug Saf       Date:  2000-07       Impact factor: 2.890

  3 in total
  8 in total

Review 1.  Myopathy including polymyositis: a likely class adverse effect of proton pump inhibitors?

Authors:  David W J Clark; Johanna Strandell
Journal:  Eur J Clin Pharmacol       Date:  2006-04-22       Impact factor: 2.953

2.  Muscular Adverse Drug Reactions Associated with Proton Pump Inhibitors: A Disproportionality Analysis Using the Italian National Network of Pharmacovigilance Database.

Authors:  Alice Capogrosso Sansone; Irma Convertino; Maria Teresa Galiulo; Stefano Salvadori; Stefania Pieroni; Tamara Knezevic; Stefania Mantarro; Alessandra Marino; Manfred Hauben; Corrado Blandizzi; Marco Tuccori
Journal:  Drug Saf       Date:  2017-10       Impact factor: 5.606

Review 3.  Postmarketing safety surveillance : where does signal detection using electronic healthcare records fit into the big picture?

Authors:  Preciosa M Coloma; Gianluca Trifirò; Vaishali Patadia; Miriam Sturkenboom
Journal:  Drug Saf       Date:  2013-03       Impact factor: 5.606

4.  Fluvastatin and hepatic reactions: a signal from spontaneous reporting in Italy.

Authors:  Anita Conforti; Lara Magro; Ugo Moretti; Stefania Scotto; Domenico Motola; Francesco Salvo; Barbara Ros; Roberto Leone
Journal:  Drug Saf       Date:  2006       Impact factor: 5.606

5.  Linking pharmacovigilance with pharmacogenetics.

Authors:  David W J Clark; Emma Donnelly; David M Coulter; Rebecca L Roberts; Martin A Kennedy
Journal:  Drug Saf       Date:  2004       Impact factor: 5.606

Review 6.  Do some inhibitors of COX-2 increase the risk of thromboembolic events?: Linking pharmacology with pharmacoepidemiology.

Authors:  David W J Clark; Deborah Layton; Saad A W Shakir
Journal:  Drug Saf       Date:  2004       Impact factor: 5.606

7.  Implementation and evaluation of adverse drug reaction monitoring system in a tertiary care teaching hospital in Mumbai, India.

Authors:  Dindayal Patidar; Mithun S Rajput; Nilesh P Nirmal; Wenny Savitri
Journal:  Interdiscip Toxicol       Date:  2013-03

8.  Pattern of drug utilization for treatment of uncomplicated malaria in urban Ghana following national treatment policy change to artemisinin-combination therapy.

Authors:  Alexander N O Dodoo; Carole Fogg; Alex Asiimwe; Edmund T Nartey; Augustina Kodua; Ofori Tenkorang; David Ofori-Adjei
Journal:  Malar J       Date:  2009-01-05       Impact factor: 2.979

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.