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B., Drmic, D., Grgic, T., Strbe, S., Zukanovic, G., Crvenkovic, D., Madzarac, G., Rukavina, I., Sucic, M., Baric, M., Starcevic, N., Krstonijevic, Z., Bencic, M

a)(semaglutide)0.1-10 mg/ml(semaglutide)0.5-10 mg/ml(semaglutide)b)0.1%(w/w)c)5.0-7.0 mg/ml5.46.7 mg/mld)e)60%f)In some embodiments, the pharmaceutical formulation comprises a) semaglutide, such as 0.1-10 mg/ml semaglutide or 0.5-10 mg/ml semaglutide, optionally b ) Not more than 0.1% (w/w) phenol, c) 5.0-7.0 mg/ml, such as 5.4 or 6.7 mg/ml sodium chloride, d) buffer, e) at least 60% water, and f) histamine acid

Molecular weight340.38 g/mol CHCuNO

The tolerability gap may be less significant in practice than the raw nausea percentages suggest