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Exhibit I itself acknowledges that direct incidence comparisons to approved peptide drugs are limited because the nominated substances data rely disproportionately on passive reporting, while the approved-drug comparators come from trials, registries, and meta-analyses with active adverse-event capture

The relevance of these findings to humans is not established, and this is not classified as a formal contraindication in UK or EU labelling (unlike in the United States)

PAMPs, pathogen-associated molecular patterns

For best handling, slowly add the bacteriostatic water down the inside wall of the vial rather than directly onto the powder