Treatment

How does my obesity medication work, and which side effects need a call?

Nausea is common and usually passes. The serious risks are rare, have names, and are worth knowing well enough to recognise, along with the plan for the day something feels wrong.

Most people start a new prescription with two stories already in their head. One is a friend who felt sick for a month and stopped. The other is a headline about eyesight, the thyroid or mood.

Neither is the whole picture. Both have numbers, and the numbers are calmer than the stories.

What does the medication do inside your body?

It copies a hormone your gut already makes. After a meal, the intestine releases GLP-1, a messenger that the brain, the stomach and the pancreas all listen for. Semaglutide and liraglutide mimic it; tirzepatide mimics it and a second gut hormone, GIP. A 2023 review in Diabetologia lays out where the signal lands:

  • The brain's appetite centres turn down. Hunger arrives later and food noise gets softer.
  • The stomach empties more slowly, so fullness lasts longer after a smaller meal.
  • The pancreas releases insulin mainly when blood sugar is high.

A slower stomach is part of how the drug works, and one reason for the queasiness. The medication eases the defence we described in why your body fights weight loss. It does not replace eating, sleeping or moving. Two older medications, naltrexone with bupropion and orlistat, work differently and have different side effects; this article is about the gut-hormone family.

Why does the dose start so low?

Because the gut needs weeks to adjust. Think of the dose as a dimmer rather than a switch: it comes up one notch at a time, and it can come back down a notch. Health Canada's product monograph for semaglutide climbs from 0.25 mg to 2.4 mg over sixteen weeks, one step every four weeks. Tirzepatide starts at 2.5 mg and rises by 2.5 mg no sooner than every four weeks. Your prescriber sets the pace.

In the pooled semaglutide trials, stomach effects bunched up around each step and then eased. So a step can wait. The Canadian semaglutide label even allows dropping back to 1.7 mg for up to four weeks. A paused climb is a normal adjustment, the same way a lapse is not a relapse.

The main idea

A side effect is information for the plan. Tell your prescriber early, and the dose can wait for your body.

Which side effects are common?

Nausea, diarrhoea, constipation and vomiting. In the Canadian semaglutide monograph, nearly half of people reported nausea, against about one in six on placebo. For tirzepatide it is roughly one in four to three in ten, against about one in twelve. In the pooled semaglutide trials, ninety-eight in a hundred stomach events were mild to moderate. About seven in a hundred people on semaglutide stopped because of side effects, against three on placebo.

Feeling sick is not what makes the weight come off. In the pooled semaglutide trials, people with and without stomach effects lost a similar amount. General habits that many people find help, and that your prescriber may tailor:

  • Smaller meals, and stopping at the first sign of fullness.
  • Sipping fluids through the day.
  • Eating protein first, as we covered in losing weight without losing strength.
  • Staying upright for a while after eating.

Which symptoms mean call today?

Most people never meet any of these. They're listed so you'd recognise one:

  • Severe belly pain that won't settle, sometimes through to the back, with or without vomiting. This can be pancreatitis. In the semaglutide weight trials it came to about two cases per thousand people a year, against fewer than one on placebo. In people with type 2 diabetes, a 2020 analysis of the large heart-outcome trials found no significant increase.
  • Pain under the right ribs, fever, or yellowing skin or eyes. This can be gallstones: about three in two hundred on semaglutide, against fewer than one in a hundred on placebo. A 2022 analysis of seventy-six trials found the risk higher in weight-loss trials, at higher doses and with longer use.
  • Not keeping fluids down. Dehydration can strain the kidneys.
  • Sudden loss or blurring of vision in one eye, even partial. That needs an urgent eye assessment.
  • New or worsening low mood, or thoughts of self-harm. In Canada you can call or text 9-8-8 at any hour.
  • A lump in the neck, hoarseness or trouble swallowing.
  • Swelling of the face or throat, or trouble breathing. Call 911.

And before any procedure with sedation or a general anaesthetic, tell the surgical team and your prescriber. A slow stomach may still hold food, and both Canadian weight-management monographs warn about it.

What about the headlines?

Each one is rare. None is ignored.

Eyesight. NAION is a sudden loss of blood flow to the front of the optic nerve. A 2024 study from a single eye clinic raised the alarm. A 2025 study across fourteen databases and thirty-seven million people with type 2 diabetes found a modest increase, smaller than first reported. The European Medicines Agency concluded in June 2025 that it is very rare with semaglutide, up to one person in ten thousand. In Canada, Health Canada's tirzepatide monograph has carried a warning since June 2026; the semaglutide monograph had not added one when we checked in September 2026.

The thyroid. The warning comes from rodent studies, and a 2023 French study raised a signal. A 2024 Scandinavian registry study of nearly a hundred and fifty thousand people with type 2 diabetes found no increase in thyroid cancer.

Mood. A 2024 study of almost a quarter of a million people with overweight or obesity found no increase in suicidal thoughts on semaglutide, compared with other obesity medications. The Canadian monographs still advise against these medications after a suicide attempt or with active suicidal thoughts.

How we approach this at GOALS

GOALS is the obesity and lifestyle medicine program at Guelph Internal Medicine Clinic, and the medical care is covered by OHIP, by referral from your family doctor or nurse practitioner. Your physician works out with you whether a medication belongs in your plan, which one, how fast to climb and when to hold, and you revisit it together at follow-up. A side effect is something to raise with your physician, not something to sit through alone.

Before your first dose or your next step, write down the one symptom you'd want to ask about. That note is where the next adjustment starts.

Common questions

Is nausea a sign the medication is working?

No. In the pooled trials of semaglutide for weight management, people with and without stomach side effects lost a similar amount, and stomach effects explained less than one percentage point of the difference from placebo. Feeling sick is not the price of results. If it isn't settling, tell your prescriber.

How long does the nausea last?

For most people, not long. In the trials it clustered around the start and each dose increase, and nearly all of it was mild to moderate and temporary. If it lingers, the next step can wait, or the dose can come back down for a while. That's a normal adjustment, not a setback.

Who shouldn't take these medications?

The Canadian product monographs rule them out for anyone with a personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type 2, and in pregnancy. They also advise against them after a suicide attempt or with active suicidal thoughts. Your physician will go through your own history before anything is prescribed.

Is a compounded or online version the same thing?

No. The 2025 Canadian guideline says compounded versions are not approved by Health Canada and should not be used, and Health Canada has warned about fake and unauthorized products. Fill a prescription only at a licensed pharmacy, and check the eight-digit DIN on the box.

What should I ask before I start?

Ask which side effects to expect in your first month, how to reach your prescriber between visits, and what to do if you can't keep fluids down. If you haven't been assessed yet, ask your family doctor or nurse practitioner about an OHIP-covered obesity medicine consultation.

Marcello Schmidt, MD, MSc, FRCPC, DABOM

Dr. Schmidt is an internal medicine physician and the founder and medical director of Guelph Internal Medicine Clinic, where he leads GOALS, the clinic’s obesity and lifestyle medicine program. He holds Royal College certifications in Internal Medicine and Adult Critical Care and is a Diplomate of the American Board of Obesity Medicine.

Sources & further reading

  1. Pedersen SD, Manjoo P, Dash S, et al. CMAJ (2025). Pharmacotherapy for obesity management in adults: 2025 clinical practice guideline update. PubMed 40789597
  2. Drucker DJ, Holst JJ. Diabetologia (2023). The expanding incretin universe: from basic biology to clinical translation. PubMed 36976349
  3. Wharton S, et al. Diabetes, Obesity and Metabolism (2022). Gastrointestinal tolerability of once-weekly semaglutide 2.4 mg in adults with overweight or obesity, and the relationship between gastrointestinal adverse events and weight loss. Pooled analysis of three trials. PubMed 34514682
  4. Health Canada. Product monograph, semaglutide injection 2.4 mg for chronic weight management. Date of authorization 2025-12-10 (control no. 296143). pdf.hres.ca
  5. Health Canada. Product monograph, tirzepatide injection for chronic weight management. Date of authorization 2026-06-11 (control no. 299409). pdf.hres.ca
  6. He L, et al. JAMA Internal Medicine (2022). Association of glucagon-like peptide-1 receptor agonist use with risk of gallbladder and biliary diseases: a systematic review and meta-analysis of randomized clinical trials. Seventy-six trials. PubMed 35344001
  7. Abd El Aziz M, et al. Diabetes, Obesity and Metabolism (2020). Incretin-based glucose-lowering medications and the risk of acute pancreatitis and malignancies: a meta-analysis based on cardiovascular outcomes trials. People with type 2 diabetes. PubMed 31750601
  8. Hathaway JT, et al. JAMA Ophthalmology (2024). Risk of nonarteritic anterior ischemic optic neuropathy in patients prescribed semaglutide. A single neuro-ophthalmology referral practice. PubMed 38958939
  9. Cai CX, et al. JAMA Ophthalmology (2025). Semaglutide and nonarteritic anterior ischemic optic neuropathy. Fourteen databases, 37.1 million people with type 2 diabetes. PubMed 39976940
  10. European Medicines Agency, Pharmacovigilance Risk Assessment Committee (June 2025). PRAC concludes eye condition NAION is a very rare side effect of semaglutide medicines. A European regulator, not a Canadian one. ema.europa.eu
  11. Bezin J, et al. Diabetes Care (2023). GLP-1 receptor agonists and the risk of thyroid cancer. French health insurance data, people with type 2 diabetes. PubMed 36356111
  12. Pasternak B, et al. BMJ (2024). Glucagon-like peptide 1 receptor agonist use and risk of thyroid cancer: Scandinavian cohort study. 145,410 people with type 2 diabetes in Denmark, Norway and Sweden. PubMed 38683947
  13. Wang W, et al. Nature Medicine (2024). Association of semaglutide with risk of suicidal ideation in a real-world cohort. 240,618 people with overweight or obesity. PubMed 38182782
  14. Health Canada. Thinking about buying GLP-1 drugs? Beware of fake or unauthorized products. Public advisory, updated 2026-01-21. recalls-rappels.canada.ca

This article is general health information, not personal medical advice. Do not change, hold or stop a dose on the strength of it: call your prescriber, and for severe symptoms go to emergency. Ask your family doctor or nurse practitioner about an OHIP-covered obesity medicine consultation.

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