Literature DB >> 18523760

Pharmacovigilance: methods, recent developments and future perspectives.

L Härmark1, A C van Grootheest.   

Abstract

BACKGROUND: Pharmacovigilance, defined by the World Health Organisation as 'the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem' plays a key role in ensuring that patients receive safe drugs. Our knowledge of a drug's adverse reactions can be increased by various means, including spontaneous reporting, intensive monitoring and database studies. New processes, both at a regulatory and a scientific level, are being developed with the aim of strengthening pharmacovigilance. On a regulatory level, these include conditional approval and risk management plans; on a scientific level, transparency and increased patient involvement are two important elements.
OBJECTIVE: To review and discuss various aspects of pharmacovigilance, including new methodological developments.

Entities:  

Mesh:

Year:  2008        PMID: 18523760     DOI: 10.1007/s00228-008-0475-9

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  52 in total

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Journal:  Pharmacoepidemiol Drug Saf       Date:  1998-03       Impact factor: 2.890

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Authors:  Deborah A Zarin; Julia L Young; Joyce C West
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2005-01       Impact factor: 4.328

3.  Report criticizes lack of FDA oversight.

Authors:  Mike Mitka
Journal:  JAMA       Date:  2006-08-23       Impact factor: 56.272

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Authors:  Rebecca Coombes
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6.  Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial.

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Journal:  N Engl J Med       Date:  2005-02-15       Impact factor: 91.245

7.  MI risks linked to rosiglitazone.

Authors:  Tracy Hampton
Journal:  JAMA       Date:  2007-09-12       Impact factor: 56.272

Review 8.  Prescription-event monitoring--recent progress and future horizons.

Authors:  R D Mann
Journal:  Br J Clin Pharmacol       Date:  1998-09       Impact factor: 4.335

9.  [Direct reporting of side effects by the patient: favourable experience in the first year].

Authors:  A C van Grootheest; J L M Passier; E P van Puijenbroek
Journal:  Ned Tijdschr Geneeskd       Date:  2005-03-05

Review 10.  Patients' role in reporting adverse drug reactions.

Authors:  Kees van Grootheest; Lolkje de Jong-van den Berg
Journal:  Expert Opin Drug Saf       Date:  2004-07       Impact factor: 4.250

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  67 in total

1.  Adverse drug reactions: analysis of spontaneous reporting system in Europe in 2007-2009.

Authors:  Jindrich Srba; Veronika Descikova; Jiri Vlcek
Journal:  Eur J Clin Pharmacol       Date:  2012-02-01       Impact factor: 2.953

2.  Completeness of published case reports on suspected adverse drug reactions: evaluation of 100 reports from a company safety database.

Authors:  Piero Impicciatore; Massimiliano Mucci
Journal:  Drug Saf       Date:  2010-09-01       Impact factor: 5.606

3.  The out-of-focus bias in drug surveillance.

Authors:  Markus Gnädinger; Hans-Ulrich Mellinghoff
Journal:  Eur J Clin Pharmacol       Date:  2012-08-16       Impact factor: 2.953

4.  EUROmediCAT signal detection: a systematic method for identifying potential teratogenic medication.

Authors:  Johannes M Luteijn; Joan K Morris; Ester Garne; Joanne Given; Lolkje de Jong-van den Berg; Marie-Claude Addor; Marian Bakker; Ingeborg Barisic; Miriam Gatt; Kari Klungsoyr; Anna Latos-Bielenska; Nathalie Lelong; Vera Nelen; Amanda Neville; Mary O'Mahony; Anna Pierini; David Tucker; Hermien de Walle; Awi Wiesel; Maria Loane; Helen Dolk
Journal:  Br J Clin Pharmacol       Date:  2016-08-04       Impact factor: 4.335

5.  Safety-related regulatory actions for orphan drugs in the US and EU: a cohort study.

Authors:  Harald E Heemstra; Thijs J Giezen; Aukje K Mantel-Teeuwisse; Remco L A de Vrueh; Hubert G M Leufkens
Journal:  Drug Saf       Date:  2010-02-01       Impact factor: 5.606

Review 6.  Postmarketing surveillance for "modified-risk" tobacco products.

Authors:  Richard J O'Connor
Journal:  Nicotine Tob Res       Date:  2011-01-20       Impact factor: 4.244

7.  An educational intervention's effect on healthcare professionals' attitudes towards pharmacovigilance.

Authors:  Nisha Jha; Devendra Singh Rathore; P Ravi Shankar; Sudesh Gyawali; Mohamed Alshakka; Shital Bhandary
Journal:  Australas Med J       Date:  2014-12-31

8.  Lack of essential information in spontaneous reports of adverse drug reactions in Catalonia-a restraint to the potentiality for signal detection.

Authors:  Lorraine Plessis; Ainhoa Gómez; Núria García; Gloria Cereza; Albert Figueras
Journal:  Eur J Clin Pharmacol       Date:  2017-03-01       Impact factor: 2.953

9.  Development of a Controlled Vocabulary-Based Adverse Drug Reaction Signal Dictionary for Multicenter Electronic Health Record-Based Pharmacovigilance.

Authors:  Suehyun Lee; Jongsoo Han; Rae Woong Park; Grace Juyun Kim; John Hoon Rim; Jooyoung Cho; Kye Hwa Lee; Jisan Lee; Sujeong Kim; Ju Han Kim
Journal:  Drug Saf       Date:  2019-05       Impact factor: 5.606

10.  Effect of Educational Interventions on Adverse Drug Reaction Reporting in a Cancer Institute in Japan: A Questionnaire Study.

Authors:  Masami Tsuchiya; Akihisa Esashi; Taku Obara; Kyoko Inooka; Nariyasu Mano; Chizuko Takamura
Journal:  Hosp Pharm       Date:  2018-04-13
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