Literature DB >> 28007050

An adverse drug event manager facilitates spontaneous reporting of adverse drug reactions.

Siri Vinther1, Pia Klarskov, Hanne Borgeskov, Perle Darsø, Anette Kvindebjerg Christophersen, Bille Borck, Catrine Christensen, Melissa Voigt Hansen, Natalie Monica Løvland Halladin, Mikkel Bring Christensen, Kirstine Moll Harboe, Marie Lund, Espen Jimenez-Solem.   

Abstract

INTRODUCTION: Spontaneous reporting of adverse drug reactions (ADRs) is used for continuous risk-benefit evaluation of marketed pharmaceutical products and for signal detection. The Adverse Drug Event Manager (ADEM) is a service offered to clinicians employed at hospitals in the Capital Region of Denmark. The ADEM assists healthcare professionals in reporting suspected ADRs to the Danish Health Authority. The aim of this retrospective observational study was to quantify and describe ADRs reported via the ADEM in 2014.
METHODS: All ADR reports handled by the ADEM in 2014 were recorded anonymously and analysed descriptively.
RESULTS: A total of 484 ADRs were reported through the ADEM in 2014 (the median number of reports per month was 37; range: 17-78). The majority of the reports came from departments of internal medicine (61%), psychiatry (14%) and dermatology, ophthalmology or otorhinolaryngology (11%). The drugs most frequently reported were lisdexamphetamine (n = 40), rivaroxaban (n = 16) and warfarin (n = 15) (vaccines excluded). In 13 out of 484 reports, the ADR was associated with a fatal outcome.
CONCLUSION: The findings of this study indicate that an ADEM promotes and facilitates spontaneous ADR reporting and helps raise awareness about ADRs, including how and why they should be reported. Hopefully, this will assist national and European spontaneous reporting systems in their work to increase patient safety nationally and abroad. FUNDING: none. TRIAL REGISTRATION: not relevant. .

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Year:  2017        PMID: 28007050

Source DB:  PubMed          Journal:  Dan Med J        ISSN: 2245-1919            Impact factor:   1.240


  4 in total

1.  Intracranial Hemorrhage Following Anticoagulant Treatment in Denmark: Spontaneous Adverse Drug Reaction Reports Versus Real-World Data.

Authors:  Benedikte Irene von Osmanski; Astrid Blicher Schelde; Espen Jimenez-Solem; Martin Erik Nyeland; Henrik Horwitz
Journal:  Drug Saf       Date:  2022-03-19       Impact factor: 5.228

2.  Medical students as adverse drug event managers, learning about side effects while improving their reporting in clinical practice.

Authors:  M Reumerman; J Tichelaar; M C Richir; M A van Agtmael
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2021-03-05       Impact factor: 3.000

3.  ACE-Inhibitor Related Angioedema Is Not Sufficiently Reported to the Danish Adverse Drug Reactions Database.

Authors:  Johan Emil Lundbek Cornwall; Anette Bygum; Eva Rye Rasmussen
Journal:  Drug Healthc Patient Saf       Date:  2019-12-16

4.  The potential of training specialist oncology nurses in real-life reporting of adverse drug reactions.

Authors:  M Reumerman; J Tichelaar; R van Eekeren; E P van Puijenbroek; M C Richir; M A van Agtmael
Journal:  Eur J Clin Pharmacol       Date:  2021-05-12       Impact factor: 2.953

  4 in total

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