A cross-sectional survey to evaluate prescribers' knowledge and understanding of safety messages following Dengvaxia® product information update
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Author(s): Mariana F Almas 1, Massoud Toussi 2, Elisa Valero 3, Annick Moureau 4, Lydie Marcelon |
Affiliations(s): 1IQVIA Real World Solutions, Porto Salvo, Portugal.
2IQVIA Real World &Analytics Solutions, La Défense, France.
3Global Pharmacovigilance, Sanofi Pasteur, Lyon, France.
4Global Biostatistical Sciences, Sanofi Pasteur, Marcy l'Etoile, France.
5Epidemiology and Benefit Risk, Global Pharmacovigilance, Sanofi Pasteur, Lyon, France. |
Publication(s): Pharmacoepidemiol Drug Saf
. 2022 Jul;31(7):758-768. doi: 10.1002/pds.5447. Epub 2022 May 13
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Document Type(s): Article, |
Countries: Brazil, Thailand, |
Click here for the abstract |
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Immunology and Vaccination, Risk Management & REMS, 2022 |
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English Clinical setting: Primary care, Epidemiological study, Survey research, |
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Insights from a review of publicly available information on Post Authorisation Safety Studies (PASS)
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Author(s): Almas MF, Hoogendoorn WE, Sayeed S, Blackburn S, Bosco J, Parmenter L
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Affiliations(s): IQVIA
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Document Type(s): Poster, |
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Drug safety, Risk Management & REMS, 2022 |
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English Review, |
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A review of the sampling methodology used in studies evaluating the effectiveness of risk minimisation measures in Europe. |
Author(s): Jouaville LS, Paul T, Almas MF |
Affiliations(s): IQVIA |
Publication(s): Pharmacoepidemiol Drug Saf. 2021 Sep;30(9):1143-1152. doi: 10.1002/pds.5301.
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Document Type(s): Article, |
Countries: Europe, |
Click here for the abstract |
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Guidelines, Methodology, Risk Management & REMS, 2021 |
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English Literature Review, |
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A review of the sampling methodology used in studies evaluating the effectiveness of risk minimisation measures in Europe
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Author(s): Laurence Sophie Jouaville 1, Tulika Paul 2, Mariana Ferreira Almas |
Affiliations(s): QVIA Real World Solutions, La Defense, France.
2IQVIA Real World Solutions, Gurugram, Haryana, India.
3IQVIA Real World Solutions, Porto Salvo, Portugal. |
Publication(s): Pharmacoepidemiol Drug Saf
. 2021 Sep;30(9):1143-1152. doi: 10.1002/pds.5301. Epub 2021 Jun 24.
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Document Type(s): Article, |
Countries: |
Click here for the abstract |
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Methodology, Risk Management & REMS, 2021 |
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English Database Study, |
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Evaluation of the Effectiveness of Risk Minimisation Measures Targeting Physicians on Prescribing Practices of Thiocolchicoside Containing Medicinal Products for Systemic Use |
Author(s): Jouaville LS, Ehrhardt C, Kürzinger ML, de Voogd H, Toussi M |
Affiliations(s): IQVIA |
Publication(s): Epidemiology (Sunnyvale) 9: 372. DOI: 10.4172/2161-1165.1000372
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Document Type(s): Article, |
Countries: France, Greece, Italy, Portugal, |
Click here for the abstract |
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Musculoskeletal disease, Rheumatology, Risk Management & REMS, 2019 |
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English Survey research, |
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. Lessons learned on the design and the conduct of Post-Auhorization Safety Studies: Review of 3 years of Pharmacovigilance Risk Assessment Committee (PRAC) oversight. |
Author(s): Engel P, Almas MF, De Bruin ML, Starzyk K, Blackburn, Dreyer NA. |
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Publication(s): British Journal of Clinical Pharmacology
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Document Type(s): Article, |
Countries: |
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Risk Management & REMS, 2017 |
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English
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Evaluation of the effectiveness of risk minimisation measures: a survey among health care professionals to assess their knowledge and attitudes on prescribing conditions of Instanyl® in France and the Netherlands. |
Author(s): Toussi M1, Garofano A1, Jouaville L1, Bardoulat I1, Mitrofan L1 |
Affiliations(s): 1 QuintilesIMS, La Défense, France |
Publication(s): 33rd International Conference on Pharmacoepidemiology & Therapeutic Risk Management, 2017, August 26-30, Montreal, Canada
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Document Type(s): Poster, |
Countries: France, Netherlands, |
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Drug safety, Pain, Risk Management & REMS, 2017 |
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L: A: |
English Clinical setting: hospital, Clinical setting: Primary care, clinical setting: Secondary care, Public Health, Survey research, |
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Between Risk Management and Pharmacoepidemiology: Where Do Post-Authorisation Safety Studies Stand Today?
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Author(s): Mariana F. Almas1, Pierre Engel2, Marieke L. De Bruin3, Kathryn Starzyk4, Blackburn Stella1 and Dreyer A. Nancy5 |
Affiliations(s): 1Real-World & Late Phase Research, Reading, Berkshirek, United Kingdom; 2Real-World & Late Phase Research, France; 3Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht, Netherlands; 4Real-World & Late Phase Research, Cambridge, United States; 5University of North Carolina, Chapel Hill, United States |
Publication(s): |
Document Type(s): Abstract, |
Countries: |
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Drug safety, Regulatory, Risk Management & REMS, 2016 |
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English Review, |
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Risk Management in Pharmacoepidemiology |
Author(s): Blackburn SCF. |
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Publication(s): Risk Management in Pharmacoepidemiology, 5th edition. Edited Strom, Kimmel & Hennessy 2012 Wiley Blackwell
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Document Type(s): Book chapter, |
Countries: |
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Risk Management & REMS, 2012 |
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L: A: |
English RWLPR (Real-World Late Phase Research-quintiles, |
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Risk minimisation activities of centrally authorised products in the european union: A descriptive study |
Author(s): Zomerdijk IM, Sayed-Tabatabaei FA, Trifirò G, Blackburn SCF, Sturkenboom MCJM, Straus SMJM |
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Publication(s): Pharmacoepidemiology and Drug Saf. 2011; 20:S228-S9
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Document Type(s): Abstract, |
Countries: |
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Risk Management & REMS, 2011 |
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L: A: |
English RWLPR (Real-World Late Phase Research-quintiles, |
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