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To date, GLP-1R has been identified presynaptically on GABAergic nerve terminals ( ex vivo dopaminergic neurotransmission in the amygdala and striatum ( Another aspect that should be explored is the treatment effect in female rodents

After needle withdrawal, there may be minimal residual tenderness at the injection site, though this typically resolves within minutes

This article was previously distributed in the August 22, 2023, educational email of the Patient Safety Authority, available at About the Author Patient Safety Authority (patientsafety.pa.gov) is an independent state agency that oversees the Pennsylvania Patient Safety Reporting System (PA-PSRS), the largest database of its kind in the United States.

In February 2026, the FDA announced it was restricting GLP-1 active pharmaceutical ingredients from being used in unapproved compounded drugs