Literature DB >> 28548608

A descriptive review of additional risk minimisation measures applied to EU centrally authorised medicines 2006-2015.

Annalisa Rubino1, Esther Artime2.   

Abstract

BACKGROUND: Guidance on therapeutic risk management, first released in EU in 2005, was updated in 2012-2013 with increased requirements on additional risk minimisation measures (aRMM). This study describes aRMM imposed at initial EU central marketing authorisation of medicines in 2006-2015.
METHODS: Non-generic medicines authorised between 01/01/2006 and 31/12/2015 were identified in the European Public Assessment Report (EPAR) database. Data on aRMM, including effectiveness measures were extracted, tabulated and analysed with Excel 2016 for chi-square p value estimates and linear regression modelling as appropriate.
RESULTS: The EPAR database encompassed 717 medicines, including 550 non-generic products authorised in 2006-2015. Those authorised with aRMM accounted for 26% (144/550). Yearly frequency ranged from 12% (6/49) in 2008 to 41% (13/32) in 2010, though no time-trend was detected. Antineoplastic/immunomodulating products were the most prevalent (26%, 38/144). All aRMM consisted of educational interventions, mostly targeting physicians/nurses (96%, 139/144). Patients were targeted in 50% of instances (72/144). Effectiveness evaluation was limited to 31% (44/144) of medicines, though an accelerated increase by year was detected.
CONCLUSIONS: Through 2006-2015, aRMM were imposed to approximately a quarter of EU centrally authorised medicines. No time-trends were observed. Updated regulatory guidance did not appear to impact frequency of aRMM, type of interventions, or target population, however, further investigation is required. Effectiveness measurements, though increasing in time, remained limited to a minority of instances.

Entities:  

Keywords:  Risk minimisation measures; educational interventions; effectiveness evaluation; pharmacovigilance; risk management

Mesh:

Year:  2017        PMID: 28548608     DOI: 10.1080/14740338.2017.1335303

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  7 in total

1.  Measuring the impact of pharmacovigilance activities, challenging but important.

Authors:  Florence van Hunsel; Helga Gardarsdottir; Anthonius de Boer; Agnes Kant
Journal:  Br J Clin Pharmacol       Date:  2019-07-31       Impact factor: 4.335

2.  Evaluation of the Effectiveness of Additional Risk Minimization Measures for Voriconazole in the EU: Findings and Lessons Learned from a Healthcare Professional Survey.

Authors:  Joanna Lem; Muhammad Younus; Jalal A Aram; Shahrzad Moosavi; Klaus Freivogel; Anne Lewis; Rachel E Sobel
Journal:  Pharmaceut Med       Date:  2019-04

Review 3.  EU postmarket surveillance plans for medical devices.

Authors:  Josep Pane; Reynold D C Francisca; Katia M C Verhamme; Marcia Orozco; Hilde Viroux; Irene Rebollo; Miriam C J M Sturkenboom
Journal:  Pharmacoepidemiol Drug Saf       Date:  2019-07-18       Impact factor: 2.890

4.  Description of the Risk Management of Medication Errors for Centrally Authorised Products in the European Union.

Authors:  Christina E Hoeve; Reynold D C Francisca; Inge Zomerdijk; Miriam C J M Sturkenboom; Sabine M J M Straus
Journal:  Drug Saf       Date:  2020-01       Impact factor: 5.606

5.  Pharmacists' perception of educational material to improve patient safety: A cross-sectional study on practices and awareness in Germany.

Authors:  André Said; Leonard Freudewald; Natalie Parrau; Matthias Ganso; Martin Schulz
Journal:  Medicine (Baltimore)       Date:  2021-03-19       Impact factor: 1.817

6.  Proposals for Engaging Patients and Healthcare Professionals in Risk Minimisation from an Analysis of Stakeholder Input to the EU Valproate Assessment Using the Novel Analysing Stakeholder Safety Engagement Tool (ASSET).

Authors:  Priya Bahri; Daniel R Morales; Adrien Inoubli; Jean-Michel Dogné; Sabine M J M Straus
Journal:  Drug Saf       Date:  2020-10-30       Impact factor: 5.606

7.  Patient Preferences for Rituximab Additional Risk Minimization Measures: Results From an International Online Survey.

Authors:  Kristyna Schneiderova; Nathalie Bere; Doris Irene Stenver; Sabine M J M Straus
Journal:  J Patient Saf       Date:  2021-10-05       Impact factor: 2.243

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.