Psychiatric adverse events associated with GLP-1 receptor agonists: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database
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That's why the standard titration protocol uses 4-week intervals between dose increases
We know that in the world of peptide research, even minor impurities can compromise your data
This is due to the fact that the drug can accumulate in the body leading to increased side effects including dehydration, electrolyte imbalance, or worsening renal function
For example, liraglutide, a GLP-1 analog, is resistant to the action of dipeptidyl peptidase IV (DPP IV)