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Patients should review contraindications and urgent warning signs with the prescriber and seek medical care for severe symptoms

The FDA also required changes to the labels to achieve a more uniform presentation of side effects and risk information for all of the drugs in the GLP-1 category, including adding or changing subsections for Acute Pancreatitis and Severe Gastrointestinal Adverse Reactions and revising the Patient Counseling section and Medication Guide. Some of the labels were also updated with post-marketing reports of hair loss (alopecia) and the neurological symptom of altered sense of touch, or dysethesia

The difference is the timeline and side effect profile, not the final result

doi: 10.1016/j.peptides.2018.10.013 249 ScottRMinnionJTanTBloomSR