Semaglutide: uses, dosing, side effects & brands
Semaglutide is a glp-1 receptor agonist sold in the U.S. under 4 brand and generic names, for type 2 diabetes mellitus. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
Key facts
- Drug class
- Glp-1 Receptor Agonist
- Treats (across its forms)
- Type 2 Diabetes Mellitus
- Available as
- Injectable · Tablet
- Sold as
- 4 products — Ozempic, Rybelsus and Wegovy, and others
- Prescription?
- Prescription only
- Generic available?
- Not in our catalog
- Half-life
- about 1 week (roughly 7 days)
- Boxed warning
- Boxed warning
How semaglutide is dosed
From the FDA label for Ozempic (application NDA209637). Other semaglutide products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
Administer once weekly at any time of day, with or without meals. ( 2.1 ) • Start at 0.25 mg once weekly. After 4 weeks, increase the dosage to 0.5 mg once weekly. ( 2.2 ) • If additional glycemic control is needed, increase the dosage to 1 mg once weekly after at least 4 weeks on the 0.5 mg dose. ( 2.2 ) • If additional glycemic control is needed, increase the dosage to 2 mg once weekly after at least 4 weeks on the 1 mg dosage. ( 2.2 ) • To reduce the risk of sustained eGFR decline, end-stage kidney disease and cardiovascular death, increase the dosage to 1 mg once weekly after at least 4 weeks on the 0.5 mg dosage. ( 1 , 2.2 ) • If a dose is missed, administer within 5 days of missed dose. ( 2.1 ) • Inject subcutaneously in the abdomen, thigh, or upper arm. ( 2.1 ) 2.1 Important Administration Instructions • Inspect OZEMPIC visually before use. It should appear clear and colorless. Do not use OZEMPIC if particulate matter and coloration is seen. • Administer OZEMPIC once weekly, on the same day each week, at any time of the day, with or without meals. • Inject OZEMPIC subcutaneously in the abdomen, thigh, or upper arm. Instruct patients to use a different injection site each week when injecting in the same body region. • When using OZEMPIC with insulin, instruct patients to administer as separate injections and to never mix the products. It is acceptable to inject OZEMPIC…
Semaglutide side effects
The following serious adverse reactions are described below or elsewhere in the prescribing information: • Risk of Thyroid C-cell Tumors [see Warnings and Precautions ( 5.1 )] • Acute Pancreatitis [see Warnings and Precautions ( 5.2) ] • Diabetic Retinopathy Complications [see Warnings and Precautions ( 5.3 )] • Hypoglycemia with Concomitant Use of Insulin Secretagogues or Insulin [see Warnings and Precautions ( 5.5 )] • Acute Kidney Injury Due to Volume Depletion [see Warnings and Precautions ( 5.6 )] • Severe Gastrointestinal Adverse Reactions [see Warnings and Precautions ( 5.7 )] • Hypersensitivity Reactions [see Warnings and Precautions ( 5.8 )] • Acute Gallbladder Disease [see Warnings and Precautions ( 5.9 )] • Pulmonary Aspiration During General Anesthesia or Deep Sedation [see Warnings and Precautions ( 5.10 )] The most common adverse reactions reported in ≥5% of patients treated with OZEMPIC are: nausea, vomiting, diarrhea, abdominal pain and constipation. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Novo Nordisk Inc., at 1-888-693-6742 or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the…
Who shouldn’t take semaglutide
OZEMPIC is contraindicated in patients with: • A personal or family history of MTC or in patients with MEN 2 [see Warnings and Precautions ( 5.1 )] . • A serious hypersensitivity reaction to semaglutide or to any of the excipients in OZEMPIC. Serious hypersensitivity reactions including anaphylaxis and angioedema have been reported with OZEMPIC [see Warnings and Precautions ( 5.8 )] . • Personal or family history of MTC or in patients with MEN 2. ( 4 ) • Serious hypersensitivity reaction to semaglutide or any of the excipients in OZEMPIC. ( 4 )
Semaglutide drug interactions
Oral Medications : OZEMPIC delays gastric emptying. May impact absorption of concomitantly administered oral medications. Use with caution. ( 7.2 ) 7.1 Concomitant Use with an Insulin Secretagogue (e.g., Sulfonylurea) or with Insulin OZEMPIC stimulates insulin release in the presence of elevated blood glucose concentrations. Patients receiving OZEMPIC in combination with an insulin secretagogue (e.g., sulfonylurea) or insulin may have an increased risk of hypoglycemia, including severe hypoglycemia. When initiating OZEMPIC, consider reducing the dose of concomitantly administered insulin secretagogue (such as sulfonylureas) or insulin to reduce the risk of hypoglycemia [see Warnings and Precautions ( 5.5 ), Adverse Reactions ( 6 )] . 7.2 Oral Medications OZEMPIC causes a delay of gastric emptying, and thereby has the potential to impact the absorption of concomitantly administered oral medications. In clinical pharmacology trials, semaglutide did not affect the absorption of orally administered medications to any clinically relevant degree [see Clinical Pharmacology ( 12.3 )] . Nonetheless, caution should be exercised when oral medications are concomitantly administered with OZEMPIC. 7.1 Concomitant Use with an Insulin Secretagogue (e.g., Sulfonylurea) or with Insulin OZEMPIC stimulates insulin release in the presence of elevated blood glucose concentrations. Patients receiving OZEMPIC in combination with an insulin secretagogue (e.g., sulfonylurea) or insulin may have an increased risk of hypoglycemia, including severe hypoglycemia. When initiating OZEMPIC, consider reducing the dose of concomitantly administered insulin secretagogue (such as sulfonylureas) or insulin to reduce the risk of hypoglycemia [see Warnings and Precautions ( 5.5 ), Adverse Reactions ( 6 )] . 7.2 Oral Medications OZEMPIC causes a delay of gastric emptying, and thereby has the potential to impact the absorption of concomitantly administered oral medications. In clinical pharmacology trials, semaglutide did not affect the absorption of orally administered medications to any clinically relevant degree [see Clinical Pharmacology ( 12.3 )] . Nonetheless, caution should be exercised when oral medications are concomitantly administered with OZEMPIC.
Every semaglutide product we track (4)
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
| # | Drug | Rating | Type | Form | Generic? | Pharmacy pays | |
|---|---|---|---|---|---|---|---|
| 1 | 70/100 | Prescription | Injectable | No data | — | View → | |
| 2 | 70/100 | Prescription | Tablet | No data | — | View → | |
| 3 | 70/100 | Prescription | Injectable | No data | — | View → | |
| 4 | 70/100 | Prescription | Injectable | No data | — | View → |
Semaglutide is one of the FDA-approved weight-loss medications — see every option compared (injections and pills, with each trial’s average weight loss).
What semaglutide pills look like
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
| Imprint | Strength | Colour | Shape | Maker |
|---|---|---|---|---|
| 4;novo | 4 mg | white | round | — |
| 1;5;novo | 1.5 mg | white | round | — |
| 9;novo | 9 mg | white | round | — |
| 25;novo | 25 mg | white | oval | — |
| 1;5;on;one;side;and;novo;on;other;side | 1.5 mg | white | round | — |
| 4;on;one;side;and;novo;on;other;side | 4 mg | white | round | — |
| 9;on;one;side;and;novo;on;other;side | 9 mg | white | round | — |
| 3;on;one;side;and;novo;on;other;side | 3 mg | white | oval | — |
| 7;on;one;side;and;novo;on;the;other;side | 7 mg | white | oval | — |
| 14;on;one;side;and;novo;on;the;other;side | 14 mg | white | oval | — |
| 1;5;on;one;side;and;novo;on;other;side | 1.5 mg | white | round | — |
| 9;on;one;side;and;novo;on;other;side | 9 mg | white | round | — |
Semaglutide recalls
From the FDA Enforcement database. A recall covers specific lots — not the drug as a whole.
SEMAGLUTIDE 7.5mg (5mg/mL)
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care, LLC · Jul 29, 2026
SEMAGLUTIDE 12.5MG (2.5MG/mL)
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care, LLC · Jul 29, 2026
SEMAGLUTIDE 2.25MG (0.9 mg/mL)
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care, LLC · Jul 29, 2026
SEMAGLUTIDE 2.5mg (1mg/mL)
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care, LLC · Jul 29, 2026
SEMAGLUTIDE 6.75mg (4.5 mg/mL)
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care, LLC · Jul 29, 2026
How long semaglutide keeps
No semaglutide label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.
Does semaglutide expire? The in-use limits and storage rules from its labelsSemaglutide and breastfeeding
From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.
Full LactMed record for semaglutide: levels in milk, effects in breastfed infants, and the drugs it would consider insteadSemaglutide was not detectable in the milk of mothers taking the drug subcutaneously. Their breastfed infants experienced no adverse effects. Some brands of oral semaglutide, such as Rybelsus, contain the absorption enhancer salcaprozate sodium, which may enter milk and accumulate in infants. Only injectable forms of semaglutide should be used during breastfeeding.
National Institute of Child Health and Human Development, record revised May 15, 2026. LactMed states its information is not a substitute for professional judgement.
What people report to the FDA about semaglutide
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 7,580 reports naming semaglutide, and the FDA flagged 76% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- nausea1,075 reports
- vomiting940 reports
- diarrhoea646 reports
- fatigue457 reports
- weight decreased425 reports
- dyspnoea401 reports
- dizziness359 reports
- weight increased353 reports
Read these as a signal, not a rate. A report does not mean semaglutide caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.
Source: openFDA drug/event (FAERS), retrieved August 26, 2026.
How long semaglutide stays in your system
The elimination half-life of semaglutide is about 1 week (roughly 7 days). This is the elimination half-life of semaglutide itself (the injectable, Ozempic/Wegovy); because it is so long, the drug stays in the body for about 5 weeks after the last dose. No active metabolite with a longer half-life is described.
OZEMPIC- semaglutide injection, solution (FDA prescribing information, DailyMed), Section 12.3 Elimination ↗Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.
Related calculators
Frequently asked questions
What is semaglutide?
Ozempic (Semaglutide) is a GLP-1 receptor agonist used to treat Type 2 Diabetes Mellitus.
What kind of drug is semaglutide?
The FDA classifies semaglutide as a glp-1 receptor agonist. GLP-1 receptor agonists mimic the gut hormone GLP-1: they prompt the pancreas to release insulin when blood sugar is high, curb the release of glucagon, and slow stomach emptying, which lowers blood sugar and reduces appetite. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.
How long does semaglutide stay in your system?
The elimination half-life of semaglutide is about 1 week (roughly 7 days) — that is how long the body takes to clear half of a dose. This is the elimination half-life of semaglutide itself (the injectable, Ozempic/Wegovy); because it is so long, the drug stays in the body for about 5 weeks after the last dose. No active metabolite with a longer half-life is described. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.
Can you take semaglutide with other medicines?
It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run semaglutide against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.
What brand names is semaglutide sold under?
We track 4 semaglutide-containing products in the U.S.: Ozempic, Rybelsus, Wegovy and Wegovy Hd. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.
What forms does semaglutide come in?
Across the brands we track, semaglutide is currently marketed as injectable and tablet, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.
Is there a generic semaglutide?
We do not currently list a generic-labelled semaglutide product. That does not always mean none exists — it means none appears under a generic name in the FDA data we track. Ask your pharmacist.
Has semaglutide been recalled?
The FDA's Enforcement database lists at least 5 recall records whose product description mentions semaglutide. The most recent: SEMAGLUTIDE 7.5mg (5mg/mL) (Jul 29, 2026). A recall applies to specific lots, not to the drug as a whole — check the record for the affected lot numbers.
What are the common side effects of Ozempic and Wegovy (semaglutide)?
The most common side effects are gastrointestinal: nausea, vomiting, diarrhea, constipation, and stomach (abdominal) pain. In Ozempic's diabetes-dose (0.5-1 mg) trials, nausea affected roughly 16-20% of people, diarrhea about 9%, vomiting 5-9%, abdominal pain about 7%, and constipation about 5%. At Wegovy's higher weight-loss dose (2.4 mg) these are markedly more common — nausea in roughly 44% in the STEP trials — so expect more GI upset on Wegovy than these Ozempic figures show. MedlinePlus also lists heartburn, burping, headache, and cold-like symptoms. These effects are dose-related: they are usually worst right after a dose increase and tend to ease over days to weeks as your body adjusts, which is exactly why prescribers start low and step the dose up slowly. Tell your doctor if nausea or vomiting is severe or keeps you from drinking fluids.
What are the serious side effects of Ozempic/Wegovy (semaglutide) — when should I call a doctor or go to the ER?
Get medical help right away for these. Pancreatitis: MedlinePlus describes "ongoing pain that begins in the upper left or middle of the stomach but may spread to the back, with or without vomiting." Gallbladder disease: "pain in upper stomach; yellowing of skin or eyes; fever; or clay-colored stools." Kidney injury from dehydration: "decreased urination; or swelling of legs, ankles, or feet." Severe stomach or intestinal problems (which can include a rare bowel blockage/ileus) and vision changes are also listed as reasons to call your doctor. Call 911 for a serious allergic reaction: "rash; itching; fainting or dizziness; swelling of the eyes, face, mouth, tongue, or throat; or difficulty breathing or swallowing." This is not a complete list — check the FDA label and your pharmacist's leaflet.
Does Ozempic/Wegovy (semaglutide) have a boxed warning about thyroid cancer?
Yes. Semaglutide carries the FDA's most serious "boxed" warning. Per the label: "In rodents, semaglutide causes thyroid C-cell tumors... It is unknown whether OZEMPIC causes thyroid C-cell tumors, including medullary thyroid carcinoma (MTC), in humans." Because of this, Ozempic and Wegovy are contraindicated (should not be used) in anyone with a personal or family history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia syndrome type 2 (MEN 2). MedlinePlus says to tell your doctor immediately if you notice "a lump or swelling in the neck; hoarseness; difficulty swallowing; or shortness of breath." Discuss your family history with your prescriber before starting.
Can Ozempic or Wegovy (semaglutide) cause sudden vision loss (NAION)?
This is an emerging but rare signal. Semaglutide has been linked to NAION (non-arteritic anterior ischemic optic neuropathy), a sudden, usually painless loss of vision in one eye caused by reduced blood flow to the optic nerve. Regulators have moved to add NAION as a rare labeled side effect after safety reviews. NAION can cause permanent, irreversible vision loss, and there is no proven treatment to reverse it. Sudden vision changes are already listed in the drug information as a reason to call your doctor promptly. If you notice sudden blurring or loss of vision in one eye, seek care right away. Also note the label warns semaglutide can worsen diabetic retinopathy in people with diabetes.
When do Ozempic/Wegovy side effects start, how long do they last, and can I just stop the drug?
Stomach-related side effects typically start within the first days after your first dose or after each dose increase, and for most people they ease over the following weeks as the body adapts. They often flare again at the next higher dose, which is why the schedule steps up gradually. Serious problems like pancreatitis, gallbladder disease, or NAION can appear at any point in treatment, not just at the start. Do not stop semaglutide on your own if it was prescribed for you — dosing and any decision to pause or stop is managed by your prescriber, who may adjust your dose to control side effects. If you are also taking insulin or a sulfonylurea, semaglutide raises the risk of low blood sugar (hypoglycemia), and your doctor may need to lower those medications; watch for shakiness, sweating, confusion, or dizziness.
Cite this page
- APA
- pharmaranks. (2026, July 24). Semaglutide: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/semaglutide
- MLA
- “Semaglutide: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/semaglutide.
We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.
Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.
Read the full FDA label for semaglutide on DailyMed (NIH) ↗ — including its boxed warning in full.