Safety Communication Tools and Healthcare Professionals’ Awareness of Specific Drug Safety Issues in Europe: A Survey Study

Author:

de Vries Sieta T.ORCID, ,van der Sar Maartje J. M.,Coleman Anna Marie,Escudero Yvette,Rodríguez Pascual Alfonso,Maciá Martínez Miguel-Ángel,Cupelli Amelia,Baldelli Ilaria,Šipić Ivana,Andrić Adriana,Michan Line,Denig Petra,Mol Peter G. M.

Funder

The work was conducted in the context of a European Commission sponsored joint action, Strengthening Collaboration for Operating Pharmacovigilance in Europe (SCOPE).

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Toxicology

Reference15 articles.

1. European Medicines Agency. European Medicines Agency recommends suspension of Avandia, Avandamet and Avaglim. [Internet]. http://www.ema.europa.eu/docs/en_GB/document_library/Press_release/2010/09/WC500096996.pdf . Accessed 23 Jan 2018.

2. European Medicines Agency. European Medicines Agency recommends suspension of marketing authorisations for sibutramine. [Internet]. http://www.ema.europa.eu/docs/en_GB/document_library/Press_release/2010/01/WC500069995.pdf . Accessed 23 Jan 2018.

3. Dusetzina SB, Higashi AS, Dorsey ER, Conti R, Huskamp HA, Zhu S, et al. Impact of FDA drug risk communications on health care utilization and health behaviors: a systematic review. Med Care. 2012;50(6):466–78.

4. Piening S, Haaijer-Ruskamp FM, de Vries JT, van der Elst ME, de Graeff PA, Straus SM, et al. Impact of safety-related regulatory action on clinical practice: a systematic review. Drug Saf. 2012;35(5):373–85.

5. Piening S, Reber KC, Wieringa JE, Straus SM, de Graeff PA, Haaijer-Ruskamp FM, et al. Impact of safety-related regulatory action on drug use in ambulatory care in the Netherlands. Clin Pharmacol Ther. 2012;91(5):838–45.

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