Dutch Group Alleges GSK Failed to Communicate Serious Risks
A formal claim will be made against GlaxoSmithKline by more than 20 people in the Netherlands who used Seroxat (paroxetine) in their youth. (GSK sells paroxetine as Paxil in America.) The group states GSK failed to inform them about the serious psychological side effects of the drug, including aggressive behavior and an increased risk of suicide. These adverse drug effects were apparently not listed on GSK’s Seroxat label at the time these teens were given the drug.
See: https://www.dutchnews.nl/news/2019/02/dutch-seroxat-teen-users-to-sue-drug-maker-for-side-effects/
Drug Approval Process Raises Consumer’s Questions
MISSD Board member, Kim Witzack, discusses the recent FDA approval of esketamine, a nasal spray to be marketed as an antidepressant. Witzack serves as a consumer representative on the FDA Advisory Committee. The FDA reviewed only one positive clinical trial before approving the drug.
See: https://www.madinamerica.com/2019/02/nasal-spray-for-depression/
Excellent Podcast Spotlighting Adverse Drug Effects
The Human Givens Institute provides an informative podcast with psychotherapist Marion Brown who sheds light on adverse drug effects. MISSD sincerely appreciates Brown’s reference to our work. Listen at: https://www.hgi.org.uk/resources/podcasts/why-antidepressants-need-be-understood