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The dual-hormone option
Tirzepatide is the newer of the two molecules used for weight management and the one people increasingly ask for by name. It acts on two gut hormones rather than one, and in direct comparison it produced greater average weight loss than semaglutide.
Two hormones
Semaglutide mimics GLP-1. Tirzepatide mimics GLP-1 and also GIP, a second gut hormone thought to affect how the body handles sugar and fat alongside its effect on appetite.
In practice patients describe the appetite effect as similar in kind and stronger in degree. The trial data supports that: in head-to-head comparison tirzepatide produced a greater average reduction in body weight.
It is not automatically the better choice. Tolerance varies between people more than between molecules, and cost, coverage and availability all bear on which one you can actually stay on. See Semaglutide vs tirzepatide, How GLP-1 medications work and Weight loss timeline for the rest of it.
Dosing
As with any GLP-1, the opening dose is about tolerance. It is not expected to do much beyond letting your body adjust.
Steps at set intervals, usually every four weeks, conditional on the current dose being tolerated.
The appetite effect tends to be pronounced. Smaller, more frequent, protein-forward meals are what most people settle into.
The aim is the lowest dose that holds the effect, not the maximum on the label.
Who it suits
The thresholds are the same as for semaglutide: BMI 30 and above, or 27 and above with a documented weight-related condition. The exclusions are also broadly the same, including thyroid cancer history and pregnancy.
It is often considered where semaglutide has plateaued or was not tolerated, and switching between the two is a normal clinical move rather than starting again from nothing. Related reading: Who should not take it, Common side effects and Medication cost.
Related
The brands tirzepatide is sold under, and the molecule it is compared with.
Common questions
How it differs, whether it is stronger, and whether you can switch to it.
Plateaued on the other one around month five. The switch was suggested at a review and things moved again within six weeks.
The appetite effect was stronger than I was ready for. Smaller meals more often was the fix and it was advice given upfront.
My plan would not fund it so I stayed on the other. They were clear that staying on something affordable beats stopping the better one.
Four weeks per step, no rushing. Two of my friends on this from elsewhere went faster and had a far worse time.
From the blog
Next step
Whether it is the right molecule depends on your history, what you tolerate and what you can obtain and afford. That is decided at the consultation.
Licensed clinicians · Eligibility reviewed before any prescription · Virtual appointments