[DOI] [PMC free article] [PubMed] [Google Scholar] 36.Broedbaek K, Ribel-Madsen R, Henriksen T, Weimann A, Petersen M, Andersen JT, Afzal S, Hjelvang B, Roberts LJ, 2nd, Vaag A, Poulsen P, Poulsen HE
Research peptides may have limited stability data available, making appropriate storage and handling more challenging
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1,4 Adverse events 5% in SUSTAIN 4 9 AEs occurring in 5% of participants treated with Ozempic injection in SUSTAIN 4 SUSTAIN 4 was not designed to evaluate relative safety between Ozempic injection and Lantus In placebo-controlled trials, the most common adverse reactions reported in 5% of patients treated with Ozempic injection are nausea, vomiting, diarrhea, abdominal pain, and constipation 1 Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trials of another drug and may not reflect the rates observed in practice 1 Comparator AE rates are not an adequate basis for comparison of safety between products 1 Incidence of severe hypoglycemia was 1.5% across all placebo-controlled trials 1 Incidence of severe hypoglycemia or blood glucose-confirmed hypoglycemia (% of patients) was 4% with Ozempic injection 0.5 mg, 6% with Ozempic injection 1 mg, and 11% with Lantus 9,a Adverse events 5% in SUSTAIN FORTE 4 AEs occurring in 5% of patients receiving Ozempic injection 1 mg and 2 mg in SUSTAIN FORTE In placebo-controlled trials, the most common adverse reactions reported in 5% of patients treated with Ozempic injection are nausea, vomiting, diarrhea, abdominal pain, and constipation 1 No new safety signals were identified
