GLP-1s and diabetic retinopathy: what the labels say

Short answer: six of the eight US labels covered here (Ozempic, Rybelsus, Wegovy, Trulicity, Mounjaro and Zepbound) warn that diabetic retinopathy can temporarily worsen when blood sugar improves quickly, and say people with a history of retinopathy should be monitored. In the trials they quote, the extra risk was concentrated in people who already had retinopathy: for Ozempic, 8.2% vs 5.2% on placebo, compared with 0.7% vs 0.4% in people without a known history. Saxenda and Victoza have no such warning, and the Canadian Trulicity monograph doesn't either.

On this page: US label rates · Canadian monographs · Why it happens · NAION is different · What to log

US labels: the retinopathy warning, drug by drug

Each figure below is from section 5 (Warnings and Precautions) of the current US prescribing information on DailyMed, checked November 4, 2026. "History" means people who had diabetic retinopathy when the trial started. The trials differ in length and population, so compare each drug with its own placebo, not across rows.

MedicationUS sectionOverall rateWith a history of retinopathyWithout a known history
Ozempic (semaglutide injection)5.3SUSTAIN 6, 2 years: 3.0% vs 1.8% placebo8.2% vs 5.2%0.7% vs 0.4%
Rybelsus / Ozempic tablets5.3Pooled glycemic trials: 4.2% vs 3.8% comparator; also quotes SUSTAIN 68.2% vs 5.2% (SUSTAIN 6)0.7% vs 0.4% (SUSTAIN 6)
Wegovy (semaglutide)5.8 (type 2 diabetes)SUSTAIN 6: 3% vs 1.8%; weight trial in type 2 diabetes: 4% vs 2.7%8.2% vs 5.2% (SUSTAIN 6)0.7% vs 0.4% (SUSTAIN 6)
Trulicity (dulaglutide)5.7REWIND, median 5.4 years: 1.9% (1.5 mg) vs 1.5% placebo8.5% vs 6.2%1% vs 1%
Mounjaro (tirzepatide)5.7No trial rate givenNot givenNot given
Zepbound (tirzepatide)5.8 (type 2 diabetes)No trial rate givenNot givenNot given
Saxenda (liraglutide)NoneNo retinopathy warning
Victoza (liraglutide)NoneNo retinopathy warning

Two more details from the US labels:

Canada: what the product monographs add

The Health Canada product monographs put the warning under "Ophthalmologic" in section 7. They mostly match the US text, with a few differences worth knowing.

MonographRetinopathy warningRates reportedExtra wordingMonograph date
OzempicYes (Ophthalmologic)SUSTAIN 6 (3,297 patients): 3.0% vs 1.8%; over 80% of events were in people with a documented history; trials up to 1 year (4,807 patients): 1.7% vs 2.0% comparatorsLong-term glycemic control "may decrease" retinopathy risk2026-07-13
RybelsusYes (Ophthalmologic)Pooled: 4.2% vs 3.8%; placebo-controlled table: 3.7% (7 mg), 2.8% (14 mg), 2.8% placeboMonitor for worsening and treat according to clinical guidelines2026-07-13
WegovyYes (retinal disorders, type 2 diabetes)Retinal disorders 6.9% Wegovy, 6.2% semaglutide 1 mg, 4.2% placebo; diabetic retinopathy 4.0%, 2.7%, 2.7%Too few teens with type 2 diabetes to assess2025-12-10
MounjaroYes (Ophthalmologic)No rate givenNot studied in NPDR needing acute therapy, PDR or macular edema; use with caution2026-06-23
ZepboundYes (type 2 diabetes)No rate givenSame not-studied list as Mounjaro2026-06-11
TrulicityNoNot in the monograph checkedUS label has a warning; Canadian monograph does not2024-07-05 (revision)
VictozaNoListed only in trial adverse-event tables2022-12-09 (revision)
SaxendaNoNot mentioned2022-12-09 (revision)

The reason the labels give

All six warnings use the same sentence: rapid improvement in glucose control has been associated with a temporary worsening of diabetic retinopathy. The labels do not say the drug damages the retina directly. The Mounjaro patient information in Canada puts it plainly: fast improvements in blood sugar may lead to a temporary worsening of diabetic eye disease, which may require treatment or lead to a loss of vision. None of the labels set a specific eye exam schedule; they say people with a history of retinopathy should be monitored for progression.

NAION is a separate warning

NAION (non-arteritic anterior ischemic optic neuropathy) affects the optic nerve rather than the retina. The Canadian Ozempic, Rybelsus, Mounjaro and Zepbound monographs say patients reporting a sudden loss of vision, including partial loss, should be urgently referred for an eye exam and the drug discontinued if NAION is confirmed. The semaglutide monographs describe the risk as very rare, based on epidemiological studies. More detail is in our thyroid warning and contraindications guide.

What to log and tell your prescriber

Sudden loss of vision, even in part of one eye, is a reason to get urgent care right away.

For the other class warnings, see GLP-1 pancreatitis and gallbladder warnings and GLP-1 side effects: rates and tracking.

Sources

This page summarizes official product labels as general information. It is not medical advice. Do not start, stop or change any medication without talking to your prescriber. Labels are updated; check the current version for your product.

Frequently asked questions

Can Ozempic make diabetic retinopathy worse?

The US Ozempic label reports that in a 2-year trial of people with type 2 diabetes and high cardiovascular risk (SUSTAIN 6), diabetic retinopathy complications occurred in 3.0% on Ozempic vs 1.8% on placebo. The gap was larger in people who already had retinopathy (8.2% vs 5.2%) than in those without a known history (0.7% vs 0.4%). The label links this to rapid improvement in blood sugar, which has been associated with a temporary worsening of retinopathy.

What counts as a "diabetic retinopathy complication" in these trials?

In SUSTAIN 6 it was an adjudicated composite endpoint. The Canadian Ozempic monograph lists its four parts: need for retinal photocoagulation (laser), need for treatment with intravitreal agents (eye injections), vitreous hemorrhage, and diabetes-related blindness.

Does Mounjaro or Zepbound have a retinopathy warning?

Yes. Both US labels say temporary worsening of diabetic retinopathy has been reported with rapid improvement in glucose control and that people with a history of retinopathy should be monitored. The labels give no trial rate. The Canadian monographs add that tirzepatide has not been studied in non-proliferative retinopathy needing acute therapy, proliferative retinopathy or diabetic macular edema, and should be used with caution, with appropriate monitoring.

Do Saxenda and Victoza carry a retinopathy warning?

Not in the labels we checked on November 4, 2026. The US Saxenda and Victoza labels have no diabetic retinopathy section in Warnings and Precautions, and neither do the Saxenda and Victoza Canadian monographs (revised December 9, 2022). The Victoza monograph lists diabetic retinopathy only as an adverse event in its trial tables.

Is the Trulicity warning the same in Canada and the US?

No. The US Trulicity label (section 5.7) reports REWIND results: 1.9% on Trulicity 1.5 mg vs 1.5% on placebo over a median 5.4 years, and 8.5% vs 6.2% in people with a history of retinopathy. The Canadian Trulicity monograph we checked (revised July 5, 2024) does not contain a diabetic retinopathy warning.

Does Wegovy affect the eyes in people without diabetes?

The Wegovy warning is written for people with type 2 diabetes. In the US label, the weight-loss trial of adults with type 2 diabetes and a BMI of 27 or more reported diabetic retinopathy in 4% on Wegovy vs 2.7% on placebo. The Canadian monograph reports retinal disorders overall in 6.9% on Wegovy, 6.2% on semaglutide 1 mg and 4.2% on placebo in that trial.

What is NAION and is it the same as retinopathy?

No. NAION (non-arteritic anterior ischemic optic neuropathy) is damage to the optic nerve, not the retina. The Canadian Ozempic, Rybelsus, Mounjaro and Zepbound monographs say a person reporting sudden loss of vision, including partial loss, should be urgently referred for an eye exam and the drug stopped if NAION is confirmed. See our thyroid and contraindications guide for how this compares with the US labels.

Should I get an eye exam before starting a GLP-1?

The labels do not set an exam schedule. They say people with a history of diabetic retinopathy should be monitored for progression, and the Rybelsus monograph adds that they should be treated according to clinical guidelines. Ask your prescriber or eye doctor what monitoring makes sense for you, and tell them if you have retinopathy before you start.

What should I log if I notice vision changes?

The date, which eye, what changed (blurring, dark spots or floaters, a shadow, partial loss), whether it came on suddenly, and your recent doses and blood sugar readings. A GLP-1 tracker such as Glidedose keeps doses and symptoms on one timeline you can show your prescriber. Sudden loss of vision needs urgent care, not a log entry.