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While these results provide a robust basis for investigating GLP-1 agonist use in SUDs, there are some potential drawbacks that should be weighed

It is not approved by the Medicines and Healthcare products Regulatory Agency (MHRA) as confirmed by the MHRA's Product Information search and the Electronic Medicines Compendium (emc) nor by the European Medicines Agency (EMA) , and no European Public Assessment Report (EPAR) exists for this medicine

Now, that may be easier said than done

Packer M, Zile MR, Kramer CM, et al Tirzepatide for Heart Failure with Preserved Ejection Fraction and Obesity

A significant shift in color that was not present initially suggests degradation or contamination

There are many reasons why someone might want to try GLP-1 microdosing