Wegovy tablets: side effects, contraindications and when to see a doctor
The side effects of Wegovy tablets according to the Summary of Product Characteristics and the OASIS 4 trial: when they appear and why they tend to ease off, who shouldn't take it and which warning signs mean you should see a doctor straight away.

Short answer
Wegovy tablets (oral semaglutide) mainly cause digestive side effects. In the OASIS 4 trial, 74.0% of people taking them had at least one, compared with 42.2% on placebo, although only 3.4% stopped treatment because of them. According to the Summary of Product Characteristics published by AEMPS, the Spanish medicines agency, these effects are concentrated in the weeks when the dose is being increased. The only contraindication is allergy to its ingredients, and it should not be used during pregnancy or breastfeeding.
Key points
- According to the Summary of Product Characteristics on CIMA, the very common reactions (more than 1 in 10 people) are nausea, vomiting, diarrhoea, constipation, dyspepsia, abdominal pain, headache and fatigue.
- In OASIS 4, hair loss affected 6.4% compared with 2.0% on placebo. It was always mild or moderate and had cleared up in about half of cases by the end of the trial.
- The Summary of Product Characteristics says to stop treatment if pancreatitis is suspected and not to restart it if it is confirmed. In OASIS 4, the rate was 0% on the tablet and 1.0% on placebo.
- Because of its long half-life, the Summary of Product Characteristics says semaglutide should be stopped at least 2 months before a planned pregnancy.
- Serious adverse events occurred in 3.9% on oral semaglutide and 8.8% on placebo, according to the OASIS 4 results posted on ClinicalTrials.gov.
Adverse effects in OASIS 4: oral semaglutide 25 mg vs placebo (64 weeks)
Percentage of patients with each effect over the course of the trial, based on the Summary of Product Characteristics for Wegovy tablets on CIMA (section 4.8) and, for the total gastrointestinal figure, the OASIS 4 paper published in NEJM.
| Effect | Oral semaglutide (% of patients) | Placebo (% of patients) |
|---|---|---|
| Any gastrointestinal effect | 74.0% | 42.2% |
| Nausea | 46.6% | 18.6% |
| Vomiting | 30.9% | 5.9% |
| Constipation | 20.1% | 9.8% |
| Dyspepsia | 18.1% | 8.8% |
| Diarrhoea | 17.6% | 8.8% |
| Abdominal pain | 16.7% | 7.8% |
| Hair loss | 6.4% | 2.0% |
| Altered skin sensation (dysaesthesia) | 4.9% | 0% |
| Gallstones (cholelithiasis) | 2.5% | 1% |
| Acute pancreatitis | 0% | 1.0% |
| Permanent discontinuation for any reason | 18% | 25.5% |
The most common side effects of Wegovy tablets are digestive. In the OASIS 4 trial, 46.6% of people taking oral semaglutide had nausea (18.6% on placebo) and 30.9% had vomiting (5.9%). These effects mostly appear while the dose is being increased, and most were mild or moderate and short-lived. The Summary of Product Characteristics (SmPC) lists only one contraindication: allergy to any of its ingredients. However, it does not recommend the tablets during pregnancy or breastfeeding, for under-18s, or for people with severe kidney or liver impairment.
Wegovy tablets are oral semaglutide made by Novo Nordisk. They are authorised in Spain for weight management in adults and are available on prescription. This article covers what the SmPC and patient information leaflet on CIMA (the database of AEMPS, the Spanish medicines agency) say, along with the main clinical trial. Prices for each pack are covered in Wegovy tablets in Spain: price, prescription and how to get started.
What are the side effects of Wegovy tablets?
The SmPC groups adverse reactions by frequency, using data from the STEP 1-4 trials of the injectable version (2,650 adults over 68 weeks). In OASIS 4, where 204 adults took the tablet for 64 weeks, the side effects were similar. The one exception was dyspepsia, which moved into a higher frequency category.
- Very common (more than 1 in 10 people): nausea, vomiting, diarrhoea, constipation, dyspepsia or indigestion, abdominal pain, headache and fatigue.
- Common (up to 1 in 10): dizziness, taste disturbance, altered skin sensation (dysaesthesia), gastritis, gastro-oesophageal reflux, belching, flatulence, abdominal distension, gallstones (cholelithiasis) and hair loss. People with type 2 diabetes may also have hypoglycaemia and complications of diabetic retinopathy.
- Uncommon (up to 1 in 100): increased heart rate, low blood pressure, acute pancreatitis, delayed gastric emptying and raised amylase and lipase on blood tests.
- Rare and very rare: anaphylactic reaction and angioedema (rare), and non-arteritic anterior ischaemic optic neuropathy, or NAION (very rare). Intestinal obstruction is listed with an unknown frequency, based on reports received after the medicine went on the market.
How many people get nausea and other side effects? What OASIS 4 found
The rates of digestive side effects are high, and that is worth saying plainly. OASIS 4 was a double-blind trial in adults without diabetes who had obesity, or overweight with complications. Of those taking 25 mg oral semaglutide, 74.0% had some kind of gastrointestinal effect, compared with 42.2% on placebo. Looking at each effect, nausea affected 46.6%, vomiting 30.9% and constipation 20.1%. Dyspepsia, diarrhoea and abdominal pain each affected between 16.7% and 18.1%, roughly double the placebo rates.
Most of these episodes were mild or moderate and short-lived, with constipation lasting longest. Although almost half had nausea, only 3.4% stopped treatment permanently because of a digestive problem. Counting every reason, 18% stopped taking the tablet, compared with 25.5% on placebo. Serious adverse events, according to the results posted on ClinicalTrials.gov, occurred in 3.9% on oral semaglutide and 8.8% on placebo.
Outside the digestive system, OASIS 4 recorded hair loss in 6.4% (2.0% on placebo). It was always mild or moderate, was more common in people who lost 20% or more of their body weight, and had cleared up in about half of cases by the end of the trial. Gallstones occurred in 2.5% (1% on placebo), with no cases of cholecystitis. Altered skin sensation, such as burning or tingling, affected 4.9%, against none on placebo, and most people recovered without stopping treatment. Heart rate rose by an average of 2 beats per minute. Acute pancreatitis occurred in 0% on the tablet and 1.0% on placebo.
When do side effects appear, and why do they tend to ease off?
The SmPC is clear that digestive effects were seen mainly while the dose was being increased. Treatment doesn't start at the final dose. It begins at 1.5 mg a day and then goes up to 4, 9 and 25 mg, with at least four weeks at each step, so it takes at least 12 weeks to reach the maintenance dose. The SmPC also allows the dose to stay at the previous level if needed. Your doctor decides the pace.
The patient leaflet puts it simply: these effects are seen mainly while the dose is being increased and usually go away over time. Dizziness, if it happens, mostly occurs in the first four months. The fact that side effects tend to ease off doesn't mean you should put up with them in silence. Talk to your doctor about them. For practical tips on handling the digestive side effects of these treatments day to day, see Ozempic and Mounjaro side effects: what to expect and how to manage them.
Who shouldn't take Wegovy tablets?
The only formal contraindication in the SmPC is hypersensitivity to semaglutide or to either of its excipients, salcaprozate sodium and magnesium stearate. But there are quite a few situations where the SmPC doesn't recommend it or advises caution:
- Pregnancy: it should not be used. Treatment is stopped if you become pregnant or want to become pregnant. Because semaglutide has a long half-life, it should be stopped at least 2 months before a planned pregnancy.
- Breastfeeding: it should not be used. No semaglutide was found in breast milk, but salcaprozate sodium and some of its metabolites were, and a risk to the baby cannot be ruled out.
- Under-18s: there are no data for the tablets (the pen is approved from age 12).
- Severe renal impairment (eGFR below 30 ml/min/1.73 m²) and severe hepatic impairment: not recommended. No dose adjustment is needed for mild or moderate impairment, although caution is advised for liver impairment. People with moderate renal impairment may have more digestive side effects.
- Type 1 diabetes, class IV heart failure, use of other weight-loss products, severe gastroparesis, and uncontrolled or unstable diabetic retinopathy: not recommended.
- Another GLP-1 receptor agonist at the same time: the two should not be combined.
- Use with caution, because experience is limited: people aged 85 or over, people with mild or moderate hepatic impairment, and people with inflammatory bowel disease.
Who can be prescribed it, based on BMI, is explained in BMI requirements and steps to get a prescription for oral Wegovy. Your doctor also needs to know about everything you take, because the SmPC describes interactions that need monitoring, such as with levothyroxine or warfarin.
What precautions does the SmPC list?
Anaesthesia and sedation. Cases of pulmonary aspiration have been reported in people on GLP-1 agonists who had a general anaesthetic or deep sedation. This happens because the stomach empties more slowly and may still contain food. If you are due to have an operation or a procedure under general anaesthetic or deep sedation, the patient leaflet asks you to tell the doctor that you take Wegovy.
Dehydration and the kidneys. Nausea, vomiting and diarrhoea can lead to dehydration and, in rare cases, worsening kidney function. The SmPC advises taking steps to avoid fluid loss, with extra care if your kidneys already don't work as well as they should.
Pancreatitis. It is uncommon, but the SmPC asks patients to know the symptoms. If pancreatitis is suspected, treatment is stopped, and if it is confirmed, treatment is not restarted. Extra caution is needed if you have had pancreatitis before. In the STEP programme for the injectable version, it occurred in 0.2% of people, compared with less than 0.1% on placebo.
Eyesight. Epidemiological studies link semaglutide with a higher risk of NAION, damage to the optic nerve that can cause painless loss of vision in one eye. In adults with type 2 diabetes, the relative risk is roughly double, which works out at about one extra case per 10,000 person-years. AEMPS issued a safety notice about this in 2025. Sudden loss of vision needs an eye examination.
When should you see a doctor?
The patient leaflet separates what can wait until your next appointment from what can't. It says to get medical help without delay if you have:
- Severe, persistent stomach pain, which may spread to your back. This could be pancreatitis.
- Difficulty breathing, rapid swelling of the face, throat, arms or legs, light-headedness, a fast heartbeat or loss of consciousness. These could be signs of a severe allergic reaction.
- Sudden loss of vision or vision that gets worse quickly.
- Severe constipation with stomach pain, bloating or vomiting, which the leaflet describes as a possible intestinal obstruction.
- A pregnancy during treatment, or having taken more tablets than prescribed.
You should also check in with your doctor, not as an emergency but without letting it slide, if nausea, vomiting or diarrhoea make it hard to stay hydrated (especially if you have kidney problems), if you have diabetes and notice changes in your vision, or if digestive symptoms don't settle over the weeks. You can report any suspected side effect to your doctor or pharmacist, even if it isn't listed in the leaflet.
Key points to remember
Digestive side effects are common with Wegovy tablets, especially while the dose is going up, and most are mild and temporary. The warning signs are few and specific, and they are worth knowing. Whether the treatment is right for you is a decision for a doctor who has reviewed your medical history.
What is available in Spain today for medically supported weight loss is a medical weight-loss treatment. It includes an initial assessment, a prescription from a registered doctor where appropriate, and ongoing follow-up with someone who checks in with you on how you're getting on. You can:
Sources
- Ficha técnica de Wegovy comprimidos (CIMA, AEMPS)
- Prospecto de Wegovy comprimidos (CIMA, AEMPS)
- Oral Semaglutide at a Dose of 25 mg in Adults with Overweight or Obesity (N Engl J Med 2025)
- Efficacy and Safety of Oral Semaglutide 25 mg Once Daily in Adults With Overweight or Obesity (OASIS 4, ClinicalTrials.gov NCT05564117)
- La AEMPS informa de una reacción adversa ocular muy infrecuente en pacientes tratados con semaglutida
It's time to reach your goal.
Online medical assessment, prescription when appropriate and 1:1 follow-up with this team.
Frequently asked questions
- Do Wegovy tablets cause more side effects than the injections?
Generally, no. The Summary of Product Characteristics says the safety profile of oral semaglutide was consistent with that of the injectable form, and that efficacy and safety were similar between OASIS 4 (25 mg tablet) and STEP 1 (2.4 mg pen). The exception was dyspepsia, which moved into a higher frequency category with the tablet. Bear in mind that this comparison comes from separate trials, not from a single trial testing the two forms against each other.
- If I don't get nausea, does that mean Wegovy tablets aren't working?
Not necessarily. The Summary of Product Characteristics notes that weight loss happened with or without gastrointestinal symptoms, so not having nausea doesn't mean the treatment is failing. What does matter is absorption. The Summary of Product Characteristics warns that it varies a lot and asks you to follow the instructions for taking it: on an empty stomach, with a sip of water, and waiting at least 30 minutes before eating or drinking.
- What happens if I stop taking Wegovy tablets because of side effects?
The patient leaflet says not to stop without talking to your doctor first, who will look at whether there are other options. Semaglutide has a half-life of about one week and stays in the body for around 7 weeks after the last dose, so its effects don't disappear overnight. If pancreatitis is suspected, however, the Summary of Product Characteristics says to stop treatment.
- Can I drive while taking Wegovy tablets?
Yes. According to the Summary of Product Characteristics, it has no or negligible effect on driving. It can cause dizziness, especially while the dose is being increased, and the patient leaflet says this happens mainly in the first 4 months. If you feel dizzy, drive with caution. People with type 2 diabetes who also take a sulphonylurea or insulin need to take more care behind the wheel because of the risk of hypoglycaemia.
Keep reading
Oral semaglutide and levothyroxine: taking Wegovy tablets with Eutirox, metformin and alcohol
What the Spanish summary of product characteristics for Wegovy tablets says about levothyroxine, metformin, anticoagulants and other morning medicines. It also covers why the half-hour wait and taking the tablet on its own matter, what is known about alcohol, and what happens in pregnancy and breastfeeding.
ReadTreatments and medicinesSwitching from Wegovy injections to tablets: what the product information says and who decides
The summary of product characteristics describes only one switch: from the 2.4 mg pen to the 25 mg tablet, one week after the last injection. This piece covers switching from other doses, from Ozempic or from Mounjaro, what you gain and lose, and what each form costs in Spain.
ReadTreatments and medicinesIs there a Mounjaro pill? What's available in Spain and what's happening with Lilly's pill
Tirzepatide doesn't come as a tablet. Mounjaro is only sold as an injection. Lilly's pill is a different molecule, orforglipron (Foundayo), and it's still waiting for a decision from the European Commission. We explain what still has to happen before it reaches Spain, what its trial found and which tablets you can get in Spain today.
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