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The FDA Adverse Event Reporting System includes post-marketing reports of insomnia, anxiety, and sleep disturbance in patients taking tirzepatide

The different receptor profiles mean your side effect experience may change substantially

Now, the tirzepatide shortage is over and deadlines for producing new copies of tirzepatide have passed, Eli Lilly is cracking down

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It is included on the 2026 WADA Monitoring Program alongside semaglutide, allowing WADA to gather data on GLP-1 receptor agonist use patterns ahead of a possible Prohibited List decision by late 2026 or 2027