Ausgabe 11/2009
Inhalt (9 Artikel)
Do Biological Medicinal Products Pose a Risk to the Environment?
Thomas C. Kühler, Mikael Andersson, Gunnar Carlin, Ann Johnsson, Lennart Åkerblom
A Benefit-Risk Assessment of Imatinib in Chronic Myeloid Leukaemia and Gastrointestinal Stromal Tumours
Dominik Wolf, Holger Rumpold
Predicting the Clinical Relevance of Drug Interactions From Pre-Approval Studies
Silvio Caccia, Silvio Garattini, Luca Pasina, Alessandro Nobili
Differences in Adverse Effect Reporting in Placebo Groups in SSRI and Tricyclic Antidepressant Trials
Winfried Rief, Yvonne Nestoriuc, Anna von Lilienfeld-Toal, Imis Dogan, Franziska Schreiber, Stefan G. Hofmann, Arthur J. Barsky, Jerry Avorn
Risk Management Policy and Black-Box Warnings
Daniel M. Cook, Rama K. Gurugubelli, Lisa A. Bero
Consumer Reporting of Adverse Drug Reactions
Lise Aagaard, Lars Hougaard Nielsen, Ebba Holme Hansen
Effectiveness of Safety Warnings in Atypical Antipsychotic Drugs
Gabriel Sanfélix-Gimeno, Pedro Cervera-Casino, Salvador Peiró, Beatriz González López-Valcarcel, Amparo Blázquez, Teresa Barbera
Mortality Associated with Attention-Deficit Hyperactivity Disorder (ADHD) Drug Treatment
Suzanne McCarthy, Noel Cranswick, Laura Potts, Eric Taylor, Ian C. K. Wong
Attention-Deficit Hyperactivity Disorder (ADHD) Treatment and Sudden Death
Frank M.C. Besag