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Dose-limiting toxicity: Severe sympathomimetic symptoms and rhabdomyolysis reported at 6 mg dose [4]
More clinical trials of other peptides are likely, potentially bringing FDA approval and mainstream acceptance to compounds currently limited to research use
The European Medicines Agency refused marketing authorisation for phentermine topiramate due to concerns about cardiovascular safety, psychiatric and cognitive adverse effects, and significant teratogenic risks including orofacial clefts
Most users experience zero side effects
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