[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
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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
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