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These issues highlighted the vulnerabilities of a market that had rapidly expanded around temporary shortage exemptions rather than long-term regulatory frameworks

The analytical data were integrated using RapidFire Integrator software (version 4.0

Food and Drug Administration (FDA) approval for Rybelsus in the treatment of type 2 diabetes patients who are at risk of the major adverse cardiovascular events (MACE), such as heart attack, stroke, or cardiovascular death

Adverse events were described as mild to moderate and were mostly gastrointestinal (GI) in patients treated with exenatide

Moreover, a serious limitation with these datasets is the lack of sufficient patient level data to assess key variables, including other PDAC risk factors (particularly diabetes and obesity) as well as dosing and duration of drug exposure