Tirzepatide
Dual GIP/GLP-1 receptor agonist for superior weight loss
Aperçu
Tirzepatide is a first-in-class dual GIP and GLP-1 receptor agonist. It produces greater weight loss than semaglutide by targeting two incretin pathways simultaneously.
Key Information
Mechanism
Dual agonism of GIP and GLP-1 receptors, providing enhanced appetite suppression and improved insulin sensitivity compared to GLP-1-only agonists.
Benefits
- Up to 22.5% weight loss
- Dual GIP/GLP-1 mechanism
- Superior to semaglutide
- Weekly dosing
Side Effects
- Nausea
- Diarrhea
- Vomiting
- Decreased appetite
Contraindications
- Medullary thyroid carcinoma
- MEN2 syndrome
- Pregnancy
Evidence Summary
SURMOUNT trials showed up to 22.5% weight loss at 72 weeks.
Research
SURMOUNT trials showed up to 22.5% weight loss at 72 weeks, significantly outperforming semaglutide in head-to-head comparisons.
View ResearchSafety
Similar GLP-1 class side effects: nausea, diarrhea, vomiting. Boxed warning for thyroid C-cell tumors.
Legal Status
FDA-approved as Zepbound (weight) and Mounjaro (diabetes).
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Rating Breakdown
Avis
Tirzepatide is a beast. Lost 22 lbs in 4 months. Better than semaglutide in my experience - less nausea, more energy. The dual GIP/GLP-1 mechanism really makes a difference.
Switched from semaglutide after stalling. Tirz broke through my plateau - another 12 lbs in 2 months. Side effects are similar but milder. Worth the extra cost.
After trying everything, tirzepatide finally worked. 28 lbs in 5 months. The appetite suppression is unmatched. Weekly dosing makes it easy to stick with.