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The active component was sequenced as a nine-residue peptide with no homology to other neuropeptides
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61 The ongoing SURPASS trials evaluating tirzepatide also evidenced a trend towards cardiovascular safety with decreased incidence of MACEs (hazard ratio 0.80
BPC 157, given intragastrically or intraperitoneally in the same dose range, can considerably antagonize the course of succinylcholine and neuromuscular block as a whole [81]
