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G. Caleb Alexander is past Chair of the US FDA’s Peripheral and Central Nervous System Advisory Committee and a co-founding Principal and equity holder in Stage Analytics. Sebastian Schneeweiss (ORCID ID: 0000-0003-2575-467X) is participating in investigator-initiated grants to the Brigham and Women’s Hospital from Boehringer Ingelheim, Takeda, and UCB, unrelated to the topic of this study. He is a consultant to Aetion Inc., a software manufacturer of which he owns equity, and is also an advisor to Temedica GmbH, a patient-oriented data generation company. His interests were declared, reviewed, and approved by the Brigham and Women’s Hospital in accordance with their institutional compliance policies. Daniel Budnitz, Carmel Hughes, Renke Maas, Alpana Mair, Emily G. McDonald, Andreas D. Meid, Rupert Payne, Hanna M. Seidling, Saad Shakir, Samy Suissa, Cara Tannenbaum, and Tobias Dreischulte have no potential conflicts of interest relevant to the contents of this study.
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Appendices
Appendix: Speaker Biographies
Tobias Dreischulte, MPharm, MSc, PhD, is Professor of Clinical Health Services Research at the Department of General Practice and Family Medicine at University Hospital of the Ludwig Maximilian University of Munich. In addition to using large electronic databases to characterize the risks of ambulatory therapeutics, including novel approaches to identify adverse drug events, his work focuses on the design, conduct and evaluation of complex interventions to improve prescribing safety in primary care.
G. Caleb Alexander, MD, MS, is a Visiting Professor at Ludwig Maximilian University of Munich and a Professor of Epidemiology and Medicine at Johns Hopkins Bloomberg School of Public Health, where he serves as a founding co-Director of the Center for Drug Safety and Effectiveness and Principal Investigator of the Johns Hopkins Center of Excellence in Regulatory Science and Innovation (CERSI). He is a practicing general internist and pharmacoepidemiologist and is internationally recognized for his research examining prescription drug utilization, safety, and effectiveness.
Daniel Budnitz, MD, MPH, is currently a Global Medical Safety Officer with Kenvue, where he is responsible for the safety of cough and cold products. Previously, he served in the US Public Health Service, including as the founding Director of the Medication Safety Program at the US Centers for Disease Control and Prevention (CDC), where he designed and implemented a national adverse drug event surveillance system.
Carmel Hughes, PhD, is Professor of Primary Care at the School of Pharmacy, Queen’s University Belfast. She was the first pharmacist to have been appointed to a Harkness Fellowship in Healthcare Policy, the only pharmacist to receive a Primary Care Career Scientist Award and a former Cochrane Fellow. Her research interests center on prescribing in older people, intervention development, and evidence-based healthcare.
Renke Maas, MD, is a physician and board-certified specialist in Clinical Pharmacology and a Professor of Clinical Pharmacology and Drug Therapy Safety at the Friedrich-Alexander-University Erlangen-Nürnberg. His work focuses on the identification and characterization of risk markers and the detection and prevention of adverse drug reactions and medication errors.
Alpana Mair, PhD, is responsible for coordinating delivery of the Government’s work program, and advising Ministers on quality, prescribing, safety and effective use of medicines. She is the principle investigator and coordinator of the EU-funded projects iSIMPATHY and SIMPATHY, and is responsible for the development of Scottish National Polypharmacy guidance, as well as quality prescribing guidelines, patient app and shared decision-making tools.
Emily G. McDonald, MD, MSc, FRCPC, is an Associate Professor of Medicine and subspecialist in General Internal Medicine at McGill University. She is the Associate Chair of Quality and Safety for the Department of Medicine and the Scientific Director of the Canadian Medication Appropriateness and Deprescribing Network.
Andreas D. Meid, PhD, is head of the Pharmacoepidemiology Section in the Department of Clinical Pharmacology and Pharmacoepidemiology at Heidelberg University Hospital. His research interests include examining pharmacoepidemiologic databases to determine individualized treatment recommendations.
Rupert Payne, PhD, FRCPE, MRCGP, FBPhS, is Professor of Primary Care and Clinical Pharmacology at the University of Exeter, UK. He is based in the Exeter Collaboration for Academic Primary Care and leads a program of research around medication optimization, with a particular focus on polypharmacy, and has particular expertise in the use of routine electronic health records.
Sebastian Schneeweiss, MD, ScD, is a Professor of Medicine at Harvard Medical School and Chief of the Division of Pharmacoepidemiology in the Department of Medicine, Brigham and Women’s Hospital, Boston. His research focuses on assessing the effectiveness and safety of biopharmaceuticals in clinical practice.
Hanna M. Seidling, PhD, is head of the Cooperation Unit Clinical Pharmacy at the University Hospital Heidelberg. As a pharmacist specialized in drug information, her research interests include the development, implementation and evaluation of strategies to improve medication safety.
Saad Shakir, MB, ChB, LRCP&S, FRCP, FFPM, MRCGP, is Director of the Drug Safety Research Unit (DSRU) in Southampton, an academic Unit associated with the University of Portsmouth. Here he leads a research team with an active program for monitoring and studying the safety of medicines
Samy Suissa, PhD, FRSC, FCAHS, is a Distinguished James McGill Professor of Epidemiology and Biostatistics and Medicine at McGill University, and the Director of the Centre for Clinical Epidemiology, Lady Davis Institute of the Jewish General Hospital, Montreal, Canada. He established the McGill Pharmacoepidemiology Research Unit and was the founding Director of the Quebec Research Network on Medication Use, funded by the FRSQ.
Cara Tannenbaum, MD, MSc, is the co-founder and inaugural scientific director of the Canadian Deprescribing Network. She is a Professor of Medicine and practicing geriatrician at the Université de Montréal, where she held the Michel Saucier Endowed Chair in Geriatric Pharmacology, Health and Aging from 2008 to 2022.
Participants
Tobias Dreischulte – Organizer
Professor of Clinical Health Services and Research
Ludwig Maximilian University of Munich, Munich, Germany
G. Caleb Alexander – Organizer
Professor of Epidemiology and Medicine
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
Sebastian Schneeweiss – Keynote
Professor of Medicine
Harvard, Cambridge, MA, USA
Darren Ashcroft
Professor of Pharmacoepidemiology
University of Manchester, Manchester, UK
Vita Brisnik
Pharmacist Doctoral Student
Ludwig Maximilian University of Munich, Munich, Germany
Daniel Budnitz – Speaker
Global Medical Safety Officer
Kenvue, Fort Washington, PA, USA
Marieke De Bruin
Professor of Drug Policy and Regulation
Utrecht University, Utrecht, The Netherlands
Petra Denig
Professor of Drug Utilization Quality
University of Groningen, Groningen, The Netherlands
Stefan Endres
Director of Clinical Pharmacology
Ludwig Maximilian University of Munich, Munich, Germany
Daniela Fialová
Associate Professor at the Department of Social and Clinical Pharmacy
Charles University, Prague, Czech Republic
Ronja Flemming
Chair of Health Economics
Technical University of Munich, Munich, Germany
Martin Fromm
Chair of Clinical Pharmacology and Clinical Toxicology
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany
Helga Gardarsdottir
Associate Professor at Division of Pharmacoepidemiology and Clinical Pharmacology
Utrecht University, Utrecht, The Netherlands
Jochen Gensichen
Director, Professor of General Medicine
Ludwig Maximilian University of Munich, Munich, Germany
Tobias Gerhard
Director, Center for Pharmacoepidemiology and Treatment Science
Rutgers University, New Brunswick, NJ, USA
Eva Grill
Professor of Epidemiology
Ludwig Maximilian University of Munich, Munich, Germany
Larus Steinþór Guðmundsson
Associate Professor of Pharmaceutical Science
University of Iceland, Reykjavik, Iceland
Christine Hallgreen
Associate Professor at Copenhagen Centre for Regulatory Science
University of Copenhagen, Copenhagen, Denmark
Annette Härdtlein
Pharmacist
Ludwig Maximilian University of Munich, Munich, Germany
Carmel Hughes – Speaker
Professor of Primary Care Pharmacy
Queens University, Belfast, Northern Ireland
Ulrich Jaehde
Professor of Clinical Pharmacy
University of Bonn, Bonn, Germany
Kristina Johnell
Professor in Geriatric Pharmacoepidemiology
Karolinska Institute, Solna, Sweden
Thomas Kühlein
Chair of General Medicine
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany
Renke Maas – Speaker
Professor of Drug Therapy Safety and Clinical Pharmacology
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany
Alpana Mair – Speaker
Head of Effective Prescribing and Therapeutics
The Scottish Government, Edinburgh, UK
Emily McDonald – Speaker
Associate Professor of Medicine
McGill University, Montreal, QC, Canada
Andreas Meid – Speaker
Post-Doctoral Researcher in Clinical Pharmacology and Pharmacoepidemiology
University of Heidelberg, Heidelberg, Germany
Eva-Lisa Meldau
Data Scientist
Uppsala Monitoring Centre, Uppsala, Sweden
Achim Mortsiefer
Chair of General and Family Medicine
Universität Witten Herdecke, Witten, Germany
Christiane Muth
Head of General and Family Medicine
University of Bielefeld, Bielefeld, Germany
Rupert Payne – Speaker
Professor of Primary Care and Clinical Pharmacology
University of Exeter, Exeter, UK
Cristin Ryan
Professor in Pharmacy Practice
Trinity College Dublin, Dublin, Ireland
Andre Said
Head of the Office of the Drug Commission of German Pharmacists
ABDA – Federal Union of German Associations of Pharmacists, Berlin, Germany
Miriam Schechner
Pharmacist
Ludwig Maximilian University of Munich, Munich, Germany
Sven Schmiedl
Professor of Clinical Studies and Regulatory Aspects
University of Witten/Herdecke, Witten, Germany
Oliver Schwalbe
Managing Director
The Scientific Institute of the Westphalia-Lippe Chamber of Pharmacists for Health Research in Pharmacies, Münster, Germany
Hanna Seidling – Speaker
Head of Cooperation Unit Clinical Pharmacy
University of Heidelberg, Heidelberg, Germany
Faiza Shahid
Pharmacist
Ludwig Maximilian University of Munich, Munich, Germany
Saad Shakir – Speaker
Director of the Drug Safety Research Unit
Drug Safety Research Unit, University of Portsmouth, Southampton, UK
Tim Steimle
Head of Medicines
Techniker Krankenkasse, Hamburg, Germany
Derek Stewart
Professor of Clinical Pharmacy and Practice
University of Qatar, Doha, Qatar
Dorothea Strobach
Head of Clinical Pharmacy Services
Ludwig Maximilian University of Munich, Munich, Germany
Samy Suissa – Speaker
Distinguished James McGill Professor of Epidemiology, Biostatistics and Medicine
McGill University, Montreal, QC, Canada
Cara Tannenbaum – Speaker
Scientific Director of the Canadian Institutes of Health Research
Canadian Institutes of Health Research, Ottawa, ON, Canada
Bart van den Bemt
Professor of Personalized Pharmaceutical Care
Radboud University, Nijmegen, The Netherlands
Anita Elaine Weidmann
Professor of Clinical Pharmacy
University of Innsbruck, Innsbruck, Austria
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Alexander, G.C., Budnitz, D., Hughes, C. et al. Proceedings of the International Ambulatory Drug Safety Symposium: Munich, Germany, June 2023. Drug Saf 47, 103–111 (2024). https://doi.org/10.1007/s40264-023-01362-9
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DOI: https://doi.org/10.1007/s40264-023-01362-9