What eye problems can Ozempic (semaglutide) cause?

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Last updated: December 18, 2025View editorial policy

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Eye Problems Associated with Ozempic (Semaglutide)

Ozempic primarily causes worsening of diabetic retinopathy complications, particularly in patients with pre-existing retinopathy, and requires baseline eye examination before initiation. 1

Primary Ocular Risk: Diabetic Retinopathy Complications

Risk Profile and Mechanism

  • Semaglutide increases the risk of diabetic retinopathy complications, with 3.0% of treated patients experiencing events compared to 1.8% on placebo in a 2-year cardiovascular outcomes trial 1
  • The absolute risk is substantially higher in patients with pre-existing diabetic retinopathy (8.2% with semaglutide vs 5.2% placebo) compared to those without known retinopathy history (0.7% vs 0.4%) 1
  • The worsening appears related to rapid A1C reduction rather than direct drug toxicity, a phenomenon observed with other intensive glucose-lowering treatments 2, 3

Specific Retinopathy Complications

  • Progression to proliferative diabetic retinopathy (PDR) has been documented, though recent large-scale observational data suggests the risk may be similar to other GLP-1 receptor agonists 4
  • Treatment-requiring diabetic macular edema (DME) can occur, with some evidence suggesting lower risk compared to certain other diabetes medications 4
  • Visual acuity loss, eye pain, and photophobia require same-day ophthalmologic assessment 2

Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION)

  • Emerging case reports link semaglutide to NAION, a rare but serious cause of vision loss from compromised optic nerve blood flow 5
  • The temporal relationship between semaglutide initiation and NAION onset suggests potential causality, particularly in patients with pre-existing vascular risk factors 5
  • This represents a potentially severe complication requiring immediate ophthalmologic evaluation if suspected 5

Mandatory Pre-Treatment Assessment

Required Baseline Evaluation

  • All patients must undergo dilated eye examination before starting semaglutide, as recommended by the American Diabetes Association 2, 3
  • Assess retinopathy status specifically when intensifying glucose-lowering therapy with GLP-1 receptor agonists 2, 3
  • Document presence and severity of any diabetic retinopathy, as this stratifies risk 1

High-Risk Patient Identification

  • Patients with proliferative retinopathy require particular caution and closer monitoring 3, 6
  • Those with poor baseline glycemic control (high A1C) face increased vulnerability to retinopathy worsening 7
  • Patients currently using insulin are at higher risk for complications 7

Monitoring Protocol During Treatment

Frequency of Eye Examinations

  • If any level of diabetic retinopathy is present at baseline, repeat dilated retinal examinations at least annually 3
  • If no retinopathy is present and glycemia is well controlled, screening every 1-2 years may be considered 3
  • If retinopathy is progressing or sight-threatening, more frequent examinations by an ophthalmologist are required 3

Risk Mitigation Strategy

  • Consider more gradual improvement in glycemic control in patients with established retinopathy to minimize worsening risk 3
  • Optimize blood pressure and serum lipid control concurrently to reduce retinopathy progression risk 3
  • Monitor patients with history of diabetic retinopathy specifically for progression 1

Critical Clinical Pitfalls to Avoid

  • Do not attribute all eye problems in semaglutide users to the medication without proper ophthalmologic evaluation 2
  • Do not assume the retinopathy worsening is permanent—it may represent temporary deterioration associated with rapid glycemic improvement 2
  • Current pretreatment assessment in clinical practice is inadequate, with studies showing only 1.8% of patients receive appropriate disease history screening despite 98.6% having relevant conditions 8
  • Never share Ozempic pens between patients due to blood-borne pathogen transmission risk 1

Additional Ocular Considerations

  • The FDA label does not establish causality between semaglutide and medullary thyroid carcinoma, but patients should be counseled about neck mass symptoms (dysphagia, dyspnea, persistent hoarseness) 1
  • Long-term effects of semaglutide on diabetic retinopathy complications have not been fully studied 1
  • Patients with severe gastrointestinal reactions (nausea, vomiting, diarrhea) may develop acute kidney injury, which can indirectly affect ocular health 1

References

Guideline

Ozempic and Diabetic Retinopathy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

GLP-1 Receptor Agonists and Diabetic Retinopathy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Semaglutide and diabetic retinopathy: an OHDSI network study.

BMJ open diabetes research & care, 2025

Guideline

Semaglutide Safety and Efficacy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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