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When you work with compounded semaglutide or tirzepatide from a vial, you handle the syringe selection yourself

They must ensure their products are safe and that label claims are not misleading, but the burden of proving a product is unsafe falls on the FDA, not the manufacturer

Reconstitution example: 5 mg vial You have a 5 mg vial of lyophilized semaglutide and you want a 2.5 mg/mL concentration

Novo Nordisk and Eli Lilly will attack the reliability of plaintiff experts, challenge causation opinions, and argue that gastroparesis and other GI injuries are too complicated or too multifactorial to blame on the drugs