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No serious systemic adverse events have been documented in peer-reviewed human studies at therapeutic doses
Nor was there any evidence of a difference in the insulin levels between the acute phase and the 3 months follow-up (14.7 vs
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The conflicting safety signal One real-world evidence study found that patients receiving GLP-1 receptor agonists had higher risks of certain autoimmune conditions, including ulcerative colitis, rheumatoid arthritis, autoimmune thyroiditis, ankylosing spondylitis, and psoriasis, compared to those on DPP-4 inhibitors
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