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The answer depends on which side effect you are experiencing and whether you are still in the dose escalation phase or have reached maintenance dosing

The process for a biosimilar GLP-1 has several distinct stages: Development and clinical testing The manufacturer conducts analytical studies, pharmacokinetic trials, and (in some cases) clinical immunogenicity studies to demonstrate biosimilarity to the reference product BLA submission A Biologics License Application is filed with the FDA, including all comparability data FDA review Typically 12 months from filing

It resolves on its own

while toxic, in small enough doses, it shouldnt be too harmful

The bottle is designed to keep moisture away from the pills, ensuring they stay effective