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The European Medicines Agencys 2025 synthetic peptide quality guideline treats peptide-related impurities as first-class critical quality attributes: deletion and truncated sequences, dimers, oligomers, and degradation products each need characterization, with European Pharmacopoeia practice pointing to reporting thresholds at 0.1% and identification thresholds above 0.5% for peptide-related impurities in pharmaceutical use

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People who experience persistent vomiting or who have kidney disease may be at higher risk for electrolyte disturbances.Keep in mind that electrolytes often work in concert with each other

In some cases, the drugs contain impurities