What is semaglutide used for? In the U.S., its brand labels cover type 2 diabetes, reducing certain heart and kidney risks, chronic weight management, and one form of liver disease called MASH. The exact use depends on the product. Ozempic, Rybelsus, Ozempic tablets, and Wegovy aren't interchangeable names for every purpose. Compounded semaglutide is separate from those brands, and its use is a prescriber's decision.
Semaglutide is a GLP-1 receptor agonist, a medicine that copies a natural gut-hormone signal. It helps the body release insulin when blood sugar is high, slows food leaving the stomach, and changes appetite signals. How semaglutide works explains that part in more detail.
What is semaglutide used for? The plain list
An indication is simply the specific job listed on a medicine's reviewed label. Here is the current U.S. list by brand and form.
| Brand and form | Approved use | In plain English |
|---|---|---|
| Ozempic injection | Type 2 diabetes; cardiovascular risk reduction in adults with type 2 diabetes and established cardiovascular disease; kidney and cardiovascular risk reduction in adults with type 2 diabetes and chronic kidney disease | Blood sugar control, plus protection from certain major heart and kidney outcomes in specific higher-risk groups |
| Rybelsus and Ozempic tablets | Type 2 diabetes; cardiovascular risk reduction in adults with type 2 diabetes who are at high risk | Oral semaglutide for blood sugar, with a heart-risk use for a defined higher-risk group |
| Wegovy injection | Long-term weight management; cardiovascular risk reduction in adults with established cardiovascular disease and overweight or obesity; noncirrhotic MASH with moderate-to-advanced fibrosis in adults | Weight care, a specific heart-risk use, and a specific form of liver disease |
| Wegovy tablets | Long-term weight management in adults; the same cardiovascular risk use listed for Wegovy injection | An oral option for the two adult uses; its label does not include pediatric weight management or MASH |
MASH means metabolic dysfunction-associated steatohepatitis: fat buildup has led to liver inflammation and scarring. Wegovy's MASH use is limited to adults without cirrhosis who have moderate-to-advanced scarring. It received accelerated approval, meaning FDA accepted an earlier measure while a longer study continues to test outcomes that matter to patients.
For a fuller name-and-form map, see semaglutide brand names.
Why the approved uses are so specific
The labels follow the people and outcomes actually studied. They don't mean every form was tested for every goal.
For weight management, a 2021 trial of 1,961 adults called STEP 1 found average weight change of 14.9% with semaglutide and lifestyle support, versus 2.4% with placebo and the same support, after 68 weeks. Those are group averages, not a forecast for one person (New England Journal of Medicine, 2021).
For heart risk, the 2023 SELECT trial enrolled 17,604 adults who already had cardiovascular disease and had overweight or obesity, but not diabetes. A major heart event occurred in 6.5% of the semaglutide group and 8.0% of the placebo group (New England Journal of Medicine, 2023). That narrow population is why the Wegovy heart indication isn't a general promise of heart protection.
For kidney risk, the 2024 FLOW trial followed 3,533 people with both type 2 diabetes and chronic kidney disease. Its combined major kidney outcome was 24% less frequent in the semaglutide group than with placebo (New England Journal of Medicine, 2024). Chronic kidney disease means kidney function or damage has stayed abnormal over time.
For MASH, the ongoing ESSENCE trial reported an interim look at 800 adults. At 72 weeks, MASH cleared without worse scarring in 62.9% of the semaglutide group and 34.3% of the placebo group; scarring improved without worse MASH in 36.8% and 22.4%, respectively (New England Journal of Medicine, 2025). The trial is still following people to learn whether those tissue changes lead to fewer serious liver outcomes.
What off-label use means
Off-label means a clinician prescribes an approved medicine for a use, age group, or form that isn't listed on that product's label. It can be a legitimate medical decision. It also means the evidence may be thinner, and the brand cannot be treated as if it carries an indication it does not.
Ozempic is the common example. Its injection label is for type 2 diabetes and certain heart and kidney risks, not weight management. A clinician may consider it off-label in another situation, while Wegovy has the weight-management label. The molecule is the same; the products, studied doses, and listed uses are not.
As of September 6, 2026, the day this article was written, a randomized trial in the American Journal of Psychiatry published online July 29 studied oral semaglutide for eight weeks in 50 adults with moderate or severe alcohol use disorder. A randomized trial assigns treatment by chance. Semaglutide did not significantly improve the study's main lab measure of craving or drinks per day, although it lowered heavy-drinking days and several secondary measures, the other outcomes researchers tracked. That is early research, not an approved alcohol-use treatment.
What compounded semaglutide is used for in practice
Compounded semaglutide is prepared by a licensed pharmacy for an individual patient from a clinician's prescription. In practice, a provider may consider it for a patient-specific weight-management or metabolic need. It does not inherit every Ozempic or Wegovy indication just because the active molecule has been studied under those brands.
Through Promise, semaglutide is dispensed as a compounded medication, which is different from an FDA-approved product: the formulation offered here is not FDA-approved. FDA explains that compounded drugs do not go through its premarket review for safety, effectiveness, or quality (FDA's GLP-1 compounding information).
That distinction is about the product, not a shortcut around medical judgment. A licensed provider reviews every request, not everyone qualifies, and a provider may still prescribe a compounded formulation when medically appropriate; that decision is between the patient and the doctor. Compounded semaglutide covers how the prescription and pharmacy route differs from a branded pen or tablet.
Why a provider may also discuss tirzepatide
Tirzepatide is a different molecule. It works through GLP-1 plus a second signal called GIP, a gut hormone involved in insulin and appetite. A provider may compare the two when the goal is weight or blood-sugar care, but they aren't two brands of one drug and shouldn't be combined. Semaglutide versus tirzepatide walks through that choice without turning it into a winner-take-all ranking.
What matters before a first visit
A first visit should match the goal to the right product and check the history that changes the risk. That includes pregnancy plans, prior pancreatitis or gallbladder trouble, diabetic eye disease, severe stomach-emptying problems, and all current medicines. Semaglutide labels also carry a boxed warning about thyroid C-cell tumors seen in rodents and rule out use with a personal or family history of medullary thyroid carcinoma, a rare thyroid cancer, or MEN 2, an inherited tumor syndrome.
The useful starting question isn't simply whether semaglutide can be used for something. It is which form has evidence for the goal, whether the label fits, and whether the reviewing clinician thinks the expected benefit is worth the risk for that person.