GLP-1 Medications Compared: What Each One Means for Eating
Every drug people ask about, with its status stated plainly and its practical eating implications.
Why a nutrition page cares which drug it is
For the most part it does not. Every drug on this page works through the same two levers, appetite and stomach emptying, so the eating advice is the same: protein first, small and often, fat down, fibre and fluid on purpose.
Three things do differ, and each changes something practical:
- How it is taken. A weekly injection concentrates side effects into the days after the dose. A daily drug spreads them. Oral semaglutide, uniquely, dictates your first half-hour of the day.
- How much weight comes off. Bigger losses mean more lean tissue in play, which raises the stakes on protein and resistance training rather than changing the principles.
- Whether it is a licensed medicine at all. Two of the entries below are not approved anywhere, and one of those is being bought and used anyway. One more has been discontinued in the UK entirely, which matters mainly because everyone on it has been switched to something considerably stronger.
A note on status, since it moves fast
The status column reflects the position at the review date at the foot of this page. This field changes every few months: new approvals, new strengths, new routes. Check with your prescriber or the current MHRA and NHS guidance rather than trusting any web page, including this one, to be current on the day you read it.
The one that is different in kind
Semaglutide, tirzepatide, liraglutide and dulaglutide are licensed medicines with published trial programmes and a clinician between you and the vial. Retatrutide is not. It is a genuinely impressive drug in trials, still in phase 3, approved by nobody, and sold widely as a "research peptide" to people who inject it without supervision. An unlicensed vial has no guarantee of purity, dose accuracy or sterility, which is a different category of risk from a side effect, and no nutrition plan compensates for it. The same reasoning applies across our peptides reference.
Each one, and what it means for eating
The table below is the at-a-glance version; the sections beneath it give the detail for each drug, including what the trials found, how appetite and digestion typically behave, and the practical eating implications.
| Medicine | What it acts on | How it is taken | Status |
|---|---|---|---|
| SemaglutideWegovy, Ozempic, Rybelsus | GLP-1 receptor agonist | Weekly injection, or a daily tablet | Licensed in the UK |
| TirzepatideMounjaro, Zepbound | Dual GIP and GLP-1 receptor agonist | Weekly injection | Licensed in the UK |
| LiraglutideSaxenda, Victoza | GLP-1 receptor agonist | Daily injection | Licensed in the UK |
| DulaglutideTrulicity | GLP-1 receptor agonist | Weekly injection | Licensed in the UK |
| ExenatideByetta, Bydureon | GLP-1 receptor agonist (the original one) | Twice-daily or weekly injection | Discontinued in the UK |
| OrforglipronFoundayo | Non-peptide GLP-1 receptor agonist (a small molecule, not an injectable peptide) | Daily tablet | Licensed elsewhere, not yet routine in the UK |
| Cagrilintide with semaglutide (CagriSema) | Amylin analogue combined with a GLP-1 receptor agonist | Weekly injection | Not approved anywhere |
| Retatrutide | Triple GIP, GLP-1 and glucagon receptor agonist | Weekly injection | Not approved anywhere |
Semaglutide
Wegovy, Ozempic, Rybelsus
Licensed in the UK
- What it acts on
- GLP-1 receptor agonist
- How it is taken
- Weekly injection, or a daily tablet
- Where it stands
- Licensed in the UK for weight management (Wegovy) and type 2 diabetes (Ozempic, Rybelsus). A higher-strength injection and an oral 25 mg weight-management tablet were both cleared by the MHRA during 2026.
- What the trials found
- About 15% average body-weight reduction at 68 weeks on the 2.4 mg injection in STEP 1, against 2.4% on placebo.
- Appetite and digestion
- The reference profile everything else gets compared with: strong appetite suppression, marked early fullness, and gastrointestinal effects in roughly three-quarters of people, overwhelmingly mild to moderate and concentrated around dose increases.
What it means for how you eat
- Because the injection is weekly, side effects often follow a rhythm: the day or two after the dose is when small, low-fat meals matter most.
- The oral form is the exception to almost every rule here. It has to be swallowed on an empty stomach with a small sip of water, with nothing else to eat or drink for at least 30 minutes, or you absorb far less of it. That makes the first half-hour of the day a fixed appointment.
- Protein first at every meal, because a full week of appetite suppression is a full week of under-eating protein if you leave it to chance.
- Wilding JPH, et al. Once-weekly semaglutide in adults with overweight or obesity (STEP 1). NEJM 2021
- Wharton S, et al. Gastrointestinal tolerability of once-weekly semaglutide 2.4 mg in adults with overweight or obesity. Diabetes Obes Metab 2022
- NHS. Semaglutide: a medicine to manage type 2 diabetes or treat obesity
Tirzepatide
Mounjaro, Zepbound
Licensed in the UK
- What it acts on
- Dual GIP and GLP-1 receptor agonist
- How it is taken
- Weekly injection
- Where it stands
- Licensed in the UK for weight management and type 2 diabetes, and the most-prescribed option here as NHS access widened through 2026.
- What the trials found
- Up to about 21% average body-weight reduction at 72 weeks on the 15 mg dose in SURMOUNT-1.
- Appetite and digestion
- Similar in kind to semaglutide but generally stronger in effect on weight; the added GIP action is thought to temper nausea somewhat, though gastrointestinal symptoms are still the most common complaint and still cluster around dose increases.
What it means for how you eat
- Larger and faster weight loss raises the stakes on protein and resistance training, not lowers them.
- Appetite suppression can be profound enough that people forget to eat entirely. A scheduled protein-led breakfast is the cheapest insurance there is.
- In the SURMOUNT-1 body-composition substudy about 74% of the weight lost was fat and 26% lean, essentially the same split as placebo, so the muscle question is about the size of the loss rather than the drug being unusually unkind to muscle.
Liraglutide
Saxenda, Victoza
Licensed in the UK
- What it acts on
- GLP-1 receptor agonist
- How it is taken
- Daily injection
- Where it stands
- Licensed in the UK for weight management (Saxenda) and type 2 diabetes (Victoza); the older, shorter-acting option, now also available as a generic.
- What the trials found
- Typically around 5 to 10% average body-weight reduction, less than the weekly drugs.
- Appetite and digestion
- Shorter-acting, so appetite suppression is flatter across the day but fades faster if a dose is missed. Its effect on stomach emptying is the best studied, and in many people it wanes over the first few months rather than persisting.
What it means for how you eat
- Daily dosing means fewer peaks and troughs than a weekly injection, so eating patterns tend to be steadier week to week.
- If the early fullness eases after a few months, that is expected physiology, not the drug failing. Keep the protein-first habit anyway.
- Missing doses reintroduces appetite quickly, which is worth planning meals around rather than being caught out by.
Dulaglutide
Trulicity
Licensed in the UK
- What it acts on
- GLP-1 receptor agonist
- How it is taken
- Weekly injection
- Where it stands
- Licensed in the UK for type 2 diabetes only, not for weight management. Widely prescribed, so plenty of people are on a GLP-1 without ever having been given weight-loss dietary advice with it.
- What the trials found
- Weight change is modest, typically a few kilograms across the AWARD trial programme, because it is dosed for blood-sugar control rather than weight.
- Appetite and digestion
- The same family of effects at a gentler intensity: nausea, reduced appetite and some gut upset, usually worst in the first days and easing over a couple of weeks.
What it means for how you eat
- Because it is prescribed for diabetes, meal regularity matters more here than on the weight-management drugs, particularly if you also take insulin or a sulfonylurea.
- Milder appetite suppression means less risk of under-eating protein, but the protein-first habit still costs nothing.
- Carbohydrate timing and blood-sugar targets come from your diabetes team, not from a food page.
Exenatide
Byetta, Bydureon
Discontinued in the UK
- What it acts on
- GLP-1 receptor agonist (the original one)
- How it is taken
- Twice-daily or weekly injection
- Where it stands
- Discontinued in the UK: Byetta went in March 2024 and Bydureon supplies were exhausted after an October 2025 supply notification. It is here because people still search for it and because anyone moved off it has been switched to one of the drugs above.
- What the trials found
- Smaller weight effects than any current option, which is part of why it was superseded.
- Appetite and digestion
- Shorter-acting than everything else here, with nausea concentrated around each injection rather than spread across a week.
What it means for how you eat
- If you have been switched from exenatide to semaglutide or tirzepatide, expect a considerably stronger appetite effect and plan protein accordingly rather than assuming your old eating pattern transfers.
- A switch between drugs restarts the escalation-linked side effects, so the small-meals, low-fat approach is worth reinstating for the first few weeks.
Orforglipron
Foundayo
Licensed elsewhere, not yet routine in the UK
- What it acts on
- Non-peptide GLP-1 receptor agonist (a small molecule, not an injectable peptide)
- How it is taken
- Daily tablet
- Where it stands
- Approved in the United States in April 2026 for chronic weight management. UK licensing and NHS availability were still catching up at the time of review, so treat availability here as a question for your prescriber.
- What the trials found
- About 12% average body-weight reduction at the highest dose in its phase 3 programme, less than the weekly injections.
- Appetite and digestion
- The same family of appetite and digestion effects as the injectables, at a generally smaller magnitude in line with its smaller weight effect.
What it means for how you eat
- Unlike oral semaglutide, it does not require an empty stomach or a food-and-water gap, which removes the most disruptive scheduling constraint of the tablet route.
- Smaller average weight loss means a smaller lean-mass loss to defend against, but the protein and training principles are unchanged.
Cagrilintide with semaglutide (CagriSema)
Not approved anywhere
- What it acts on
- Amylin analogue combined with a GLP-1 receptor agonist
- How it is taken
- Weekly injection
- Where it stands
- Filed with the US regulator in December 2025, with a decision expected around late 2026. Not licensed in the UK at the time of review.
- What the trials found
- About 20% average body-weight reduction at 68 weeks in REDEFINE 1; a head-to-head trial against tirzepatide did not show it to be better.
- Appetite and digestion
- Adds amylin signalling, which independently slows gastric emptying and increases fullness, on top of the GLP-1 effect. Early fullness and nausea are correspondingly prominent.
What it means for how you eat
- Two fullness mechanisms stacked together makes the small-meals, protein-first, fluid-between-meals approach more important, not less.
- Nothing about a combination product changes the rule that eating too much fat in one sitting is the reliable way to feel unwell.
Retatrutide
Not approved anywhere
- What it acts on
- Triple GIP, GLP-1 and glucagon receptor agonist
- How it is taken
- Weekly injection
- Where it stands
- Not approved by any regulator anywhere at the time of review; still in phase 3, with a first regulatory submission expected no earlier than late 2026. It is nonetheless sold widely as a grey-market research peptide, which is a genuinely different risk from anything else on this page: unverified purity, unverified dose, no sterility guarantee and no clinician involved.
- What the trials found
- About 25% average body-weight reduction at 80 weeks on the 12 mg dose in the phase 3 TRIUMPH-1 trial, against 3.9% on placebo, with up to roughly 30% reported at the top of the programme.
- Appetite and digestion
- The strongest appetite suppression of the group, and gastrointestinal side effects to match: nausea was reported by up to around 60% of people at the highest dose in phase 2, again worst during dose escalation.
What it means for how you eat
- At this scale of weight loss the muscle question stops being theoretical. Protein at the top of the range and genuine resistance training are the difference between losing fat and losing your physique.
- Under-eating is the practical risk rather than over-eating. Liquid protein, small frequent meals and a fixed eating schedule are what keep intake adequate.
- Micronutrients matter when total intake is very low for months; this is worth an actual conversation with a dietitian.
- None of this is an endorsement of buying it. An unlicensed vial has no quality guarantee, and nothing in a nutrition plan compensates for that.
Sources
- Wilding JPH, et al. Once-weekly semaglutide in adults with overweight or obesity (STEP 1). NEJM 2021
- Jastreboff AM, et al. Tirzepatide once weekly for the treatment of obesity (SURMOUNT-1). NEJM 2022
- Wharton S, et al. Gastrointestinal tolerability of once-weekly semaglutide 2.4 mg in adults with overweight or obesity. Diabetes Obes Metab 2022
- Camilleri M, et al. Clinical consequences of delayed gastric emptying with GLP-1 receptor agonists and tirzepatide. J Clin Endocrinol Metab 2025
- NHS. Semaglutide: a medicine to manage type 2 diabetes or treat obesity
Work out your numbers
Frequently asked questions
- Which GLP-1 causes the least nausea?
- Nausea is common to all of them and is driven more by how fast the dose goes up than by which drug it is. Broadly, the drugs producing the largest weight loss also produce the most gastrointestinal symptoms, and every one of them is worst around a dose increase and settles afterwards.
- Is retatrutide approved?
- No. At the time of review it was not approved by any regulator anywhere, and was still in phase 3 trials, despite being sold widely as a research peptide. An unlicensed vial carries no guarantee of purity, dose accuracy or sterility, and no clinician is watching what it does to you.
- Does the tablet form change how I should eat?
- Oral semaglutide does: it has to be taken on an empty stomach with a small sip of water, with nothing else for at least 30 minutes afterwards, or absorption drops sharply. Orforglipron, the newer non-peptide tablet, has no such food or water restriction.
- Does a stronger drug mean I need to eat differently?
- Not differently, but more deliberately. The bigger the weight loss, the more lean tissue is in play and the smaller the margin for under-eating protein, so the protein target and the resistance training matter more, not less.
Related
Written and reviewed by Mathew Beale, MSc Biotechnology, University of Reading.
Last reviewed: