Patient Medication Information: uses, side effects, how to take - Rybelsus
What RYBELSUS® is used for:
RYBELSUS® contains the active substance semaglutide. It is used to lower blood sugar (glucose) in adults with type 2 diabetes.
- RYBELSUS® is used on its own if your blood sugar level is not properly controlled by diet and exercise alone and you cannot use metformin.
- RYBELSUS® is used in combination with one or more other medicines for diabetes when they are not enough to control your blood sugar levels.
- RYBELSUS® is used to reduce the risk of serious heart issues (heart-related death, heart attacks, strokes) in adults with type 2 diabetes mellitus and established cardiovascular disease or are at high risk for those.
How RYBELSUS® works:
RYBELSUS® belongs to a class of medicines called GLP-1 receptor agonists (glucagon-like peptide-1 receptor agonists). RYBELSUS® helps your body make more insulin when your blood sugar is high.
The ingredients in RYBELSUS® are:
Medicinal ingredients: semaglutide
Non-medicinal ingredients for the initial formulation of RYBELSUS® tablets (3 mg, 7 mg and 14 mg).: magnesium stearate, microcrystalline cellulose, povidone K 90, salcaprozate sodium (SNAC)
Non-medicinal ingredients for the optimized formulation of RYBELSUS® tablets (1.5 mg, 4 mg and 9 mg).: magnesium stearate, salcaprozate sodium (SNAC).
RYBELSUS® comes in the following dosage forms:
Initial formulation of RYBELSUS® 3 mg, 7 mg and 14 mg tablets
3 mg tablets are white to light yellow, oval shaped debossed with “3” on one side and “novo” on the other side. The tablets are supplied in green coloured cartons and blister packaging.
7 mg tablets are white to light yellow, oval shaped debossed with “7” on one side and “novo” on the other side. The tablets are supplied in red coloured cartons and blister packaging.
14 mg tablets are white to light yellow, oval shaped debossed with “14” on one side and “novo” on the other side. The tablets are supplied in blue coloured cartons and blister packaging.
Optimized formulation of RYBELSUS® 1.5 mg, 4 mg and 9 mg tablets
1.5 mg tablets are white to light yellow, round shaped debossed with “1.5” on one side and “novo” on the other side. The tablets are supplied in green coloured cartons and blister packaging.
4 mg tablets are white to light yellow, round shaped debossed with “4” on one side and “novo” on the other side. The tablets are supplied in red coloured cartons and blister packaging.
9 mg tablets are white to light yellow, round shaped debossed with “9” on one side and “novo” on the other side. The tablets are supplied in blue coloured cartons and blister packaging.
Do not use RYBELSUS® if:
- you are allergic to semaglutide or any of the other ingredients in this medication;
- you or a member of your family has ever had medullary thyroid cancer (MTC);
- you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2);
you are pregnant or breastfeeding.
To help avoid side effects and ensure proper use, talk to your healthcare professional before you take RYBELSUS®. Talk about any health conditions or problems you may have, including if you:
- or a member of your family has or has had medullary thyroid carcinoma (MTC), or if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2);
- have type 1 diabetes – a condition where your body does not produce any insulin;
- you develop diabetic ketoacidosis (increased ketones in the blood or urine);
- have ever had an allergic reaction to RYBELSUS®;
- have a high heart rate (fast pulse);
- have ever had pancreatitis;
- are breastfeeding or plan to breastfeed;
- are pregnant or plan to become pregnant;
- have end stage renal disease;
- have gastrointestinal (digestive) problems, including severe vomiting, diarrhea and/or dehydration;
- have liver or gall bladder problems;
- have diabetic retinopathy;
- you take blood thinners (ex. Warfarin/Coumadin).
Other warnings you should know about:
Cardiovascular
RYBELSUS® may increase heart rate and could cause changes known as PR prolongation, which are detected by electrocardiogram (ECG) tracings. Increased heart rate is the same as a faster pulse. These heart rhythm changes are more likely if you have heart disease, or if you are taking certain other drugs. It is important to follow your doctor's advice about the dose of RYBELSUS® or about any special tests that you may need. See ‘What are possible side effects from using RYBELSUS®?’
Children and adolescents
RYBELSUS® is not recommended in children and adolescents under 18 years as the safety and efficacy in this age group have not yet been studied.
Pregnancy and Breastfeeding
Tell your doctor if you are pregnant, think you might be pregnant, or are planning to become pregnant. RYBELSUS® should not be used during pregnancy and for at least two months before a planned pregnancy because it is not known if it may affect your unborn child.
If you could become pregnant while using RYBELSUS®, it is recommended to use contraception.
Do not use RYBELSUS® if you are breastfeeding. RYBELSUS® passes into breast milk, and it is not known how it affects your baby.
Driving and Using Machines
If you use RYBELSUS® in combination with a sulfonylurea or insulin, low blood sugar (hypoglycemia) may occur which may reduce your ability to concentrate. Avoid driving or using machines if you get any signs of low blood sugar. Talk to your doctor for further information. You may feel dizzy when taking RYBELSUS®, especially if your dose is being increased. If you feel dizzy, avoid driving or using machines. Talk to your doctor for further information.
Severe and on-going stomach pain which could be due to acute pancreatitis or gallbladder disease
If you have severe and on-going pain in the stomach area or experience jaundice (yellowing of your skin, eyes or mucous membranes) while taking RYBELSUS® – see a doctor straight away as this could be a sign of acute pancreatitis (inflamed pancreas) or gallbladder disease.
Effects on the digestive system, including dehydration
During treatment with RYBELSUS®, you may feel sick (nausea) or be sick (vomiting), or have diarrhea. These side effects can cause dehydration (loss of fluids). It is important that you drink plenty of fluids to prevent dehydration. This is especially important if you have kidney problems. Talk to your doctor if you have any questions or concerns.
Patients with delayed stomach emptying (gastroparesis)
If you have slow (delayed) stomach emptying (called gastroparesis), use of RYBELSUS® may lead to serious or severe gastrointestinal adverse events. RYBELSUS® is not recommended if you have severe gastroparesis.
Diabetic eye disease (retinopathy)
Fast improvements in blood sugar control may lead to a temporary worsening of diabetic eye disease. If you have diabetic eye disease and experience eye problems while taking RYBELSUS®, talk to your doctor.
Sudden changes to your eyesight
If you notice a sudden loss of vision or rapidly worsening eyesight during treatment with RYBELSUS®, urgently contact your doctor. This may be caused by a very rare side effect called non-arteritic anterior ischaemic optic neuropathy (NAION). Your doctor will refer you for an eye examination by an ophthalmologist and you may have to stop treatment with RYBELSUS®.
Low blood sugar (hypoglycemia)
Taking a sulfonylurea medicine or insulin with RYBELSUS® might increase the risk of getting low blood sugar levels (hypoglycemia). Your doctor may ask you to test your blood sugar levels. This will help your doctor decide if the dose of the sulfonylurea or insulin needs to be changed to reduce the risk of low blood sugar.
General Anesthesia or Deep Sedation
RYBELSUS® may delay how long your stomach takes to empty its contents. This may increase the risk of problems with food or liquid from the stomach getting into the lungs while under general anaesthesia or sedation. If you are about to have a procedure that requires you to be unconscious, tell your healthcare professional that you are taking RYBELSUS®.
Sodium Content RYBELSUS® contains 23 mg of sodium per tablet. This is equivalent to 1% of the maximum daily intake of sodium per day for adults recommended by the World Health Organization.
Tell your healthcare professional about all the medicines you take, including any drugs, vitamins, minerals, natural supplements or alternative medicines.
In particular, tell your doctor, pharmacist or nurse if you are using medicines containing any of the following:
- sulfonylurea;
- insulin;
- levothyroxine – this is because your doctor may need to check your thyroid levels if you are taking RYBELSUS® together with levothyroxine.
The following may interact with RYBELSUS®:
The following list includes some, but not all, of the drugs that may increase your heart rate. You should check with your doctor or pharmacist before taking any other medication with RYBELSUS®:
- drugs to treat hypertension;
- drugs to treat heart failure;
- drugs to treat HIV infection;
- drugs to treat attention deficit-hyperactivity disorder;
- drugs to suppress appetite/cause weight loss;
- decongestants;
- drugs to treat asthma.
How to take RYBELSUS®:
Always take this medicine exactly as your doctor has told you. Check with your doctor, pharmacist or nurse if you are not sure.
Follow these instructions carefully:
- Take your RYBELSUS® tablet on an empty stomach.
- Swallow your RYBELSUS® tablet whole with a sip of water (up to 120 ml). Do not split, crush or chew the tablet.
- After taking your RYBELSUS® tablet wait at least 30 minutes before you have your first meal or drink of the day or taking other oral medicines.
Usual dose:
Initial Formulation of RYBELSUS® 3 mg, 7 mg and 14 mg tablets
- The starting dose is one 3 mg tablet once a day for 30 days.
- After 30 days of 3 mg once a day, your doctor will increase your dose to 7 mg once a day.
- Your doctor may increase your dose to 14 mg once a day if your blood sugar is not controlled well enough with a dose of 7 mg once a day.
Optimized Formulation of RYBELSUS® 1.5 mg, 4 mg and 9 mg tablets:
- The starting dose is one 1.5 mg tablet once a day for 30 days.
- After 30 days of 1.5 mg once a day, your doctor will increase your dose to 4 mg once a day.
- Your doctor may increase your dose to 9 mg once a day if your blood sugar is not controlled well enough with a dose of 4 mg once a day.
Your doctor will prescribe the strength that is right for you. Do not change your dose unless your doctor has told you so. Do not take more than one tablet of RYBELSUS® daily. Do not take two tablets of RYBELSUS® to obtain a higher dose.
Do not stop this medicine without talking to your doctor. If you stop taking it, your blood sugar levels may increase.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.
Overdose:
If you take more RYBELSUS® than you should, talk to your doctor straight away. You may get more side effects such as feeling sick (nausea).
If you think you, or a person you are caring for, have taken too much RYBELSUS®, contact a healthcare professional, hospital emergency department, regional poison control centre or Health Canada’s toll-free number, 1-844 POISON-X (1-844-764-7669) immediately, even if there are no signs or symptoms.
Missed dose:
If you forget to take a dose, just take one tablet on the morning after.
Possible side effects from using RYBELSUS®:
These are not all the possible side effects you may feel when taking RYBELSUS®. If you experience any side effects not listed here, contact your healthcare professional.
Very common: may affect more than 1 in 10 people
- feeling sick (nausea) – this usually goes away over time;
- diarrhea – this usually goes away over time;
- low blood sugar (hypoglycemia) when this medicine is used with insulin or sulfonylureas.
The warning signs of low blood sugar may come on suddenly. They can include: cold sweat, cool pale skin, headache, fast heartbeat, feeling sick (nausea) or very hungry, changes in vision, feeling sleepy or weak, feeling nervous, anxious or confused, difficulty concentrating or shaking.
Your doctor will tell you how to treat low blood sugar and what to do if you notice these warning signs.
Low blood sugar is more likely to happen if you also take a sulfonylurea or insulin. Your doctor may reduce your dose of these medicines before you start using this medicine.
Common: may affect up to 1 in 10 people
- being sick (vomiting);
- upset stomach or indigestion;
- inflamed stomach (‘gastritis’) – the signs include stomachache, feeling sick (nausea) or being sick (vomiting);
- reflux or heartburn – also called ‘gastro-esophageal reflux disease’ (GERD);
- stomach pain;
- bloating of the stomach;
- constipation;
- change in the way food or drink tastes;
- tiredness;
- less appetite;
- gas (flatulence);
- increase of pancreatic enzymes (such as lipase and amylase);
- feeling dizzy;
- headache.
- changed skin sensation
Uncommon: may affect up to 1 in 100 people
- weight loss;
- gallstones;
- burping;
- fast pulse;
- allergic reactions like rash, itching or hives;
- a delay in the emptying of the stomach.
Unknown:
- Intestinal obstruction including ileus: a condition where your intestine can’t push food and waste out of your body (can cause bowel obstruction, a severe form of constipation with additional symptoms such as stomach ache, bloating, vomiting etc).
Rare: may affect up to 1 in 1,000 people
serious allergic reactions (anaphylactic reactions). You should seek immediate medical help and inform your doctor straight away if you get symptoms such as breathing problems,
- swelling of face and throat, wheezing, fast heartbeat, pale and cold skin, feeling dizzy or weak.
Serious side effects and what to do about them
| Frequency/Side Effect/Symptom | Talk to your healthcare professional | Stop taking drug and get immediate medical help | |
|---|---|---|---|
| Only if severe | In all cases | ||
| Common | |||
| Diabetic retinopathy complications – complications of diabetic eye disease/diabetic eye problems | ✓ | ||
| Gallbladder disease symptoms: severe or constant pain in your stomach area, fever or jaundice (yellowing of your skin, eyes or mucous membranes) | ✓ | ||
| Uncommon | |||
| Pancreatitis (severe and ongoing pain in the stomach area which could be a sign of inflamed pancreas) | ✓ | ✓ | |
| Severe hypoglycemia* (low blood sugar) symptoms: feeling confused, fits and passing out. | ✓ | ||
| Rare | |||
| Severe allergic reaction (anaphylactic reaction) symptoms: breathing problems, swelling of face and throat and a fast heartbeat. | ✓ | ✓ | |
| Very rare | |||
| Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) symptoms: a sudden loss of vision or rapidly worsening eyesight | ✓ | ✓ | |
*The risk of severe hypoglycemia is higher depending on the other diabetes medications.
If you have a troublesome symptom or side effect that is not listed here or becomes bad enough to interfere with your daily activities, talk to your healthcare professional.
Reporting side effects
You can report any suspected side effects associated with the use of health products to Health Canada by:
- Visiting the Web page on Adverse Reaction Reporting (canada.ca/drug-device-reporting) for information on how to report online, by mail or by fax; or
- Calling toll-free at 1-866-234-2345.
NOTE: Contact your healthcare professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.
Storage:
Do not use this medicine after the expiry date which is stated on the blister and carton after EXP. The expiry date refers to the last day of that month.
Store RYBELSUS® at room temperature (15 ºC to 30 ºC). RYBELSUS® must be stored in the original blister package to protect from moisture and light. Keep the tablet in the blister until you are ready to take it. Removing it too soon can prevent it from working as planned.
Do not use this medicine if you notice that the package is damaged or shows signs of tampering.
Keep this medicine out of the sight and reach of children.
If you want more information about RYBELSUS®:
- Talk to your healthcare professional
- Find the full product monograph that is prepared for healthcare professionals and includes the Patient Medication Information by visiting the Health Canada Drug Product Database website (Drug Product Database: Access the database); the manufacturer’s website www.novonordisk.ca, or by calling 1-800-465-4334.
Date of Authorization: 2026-07-13
© 2026
Novo Nordisk Canada Inc.
