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The European Medicines Agency (EMA) and MHRA conduct ongoing pharmacovigilance monitoring of all licensed medicines, including post-marketing surveillance to identify rare adverse events that may not emerge during clinical trials

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It should not be purchased, possessed, or used for anything other than lawful research activities

Patients often report that moderate caffeine use feels 'normal' during GLP-1 therapy once they establish a routine that works with their digestive tolerance

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