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32 When the adverse event reports start rolling inand they have, with over 1,000 reports filed by July 2025the regulators will not look at your batch records

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Four studies (50%) were Phase 4 trials, which typically emphasize safety surveillance post-market approval, indicating a focus on long-term safety and efficacy in real-world settings

In a review conducted by scientists from the United Kingdom and Canada, researchers examined numerous studies to determine how these drugs affect cognitive abilities and mental health