Type 2 & other diabetes

Optic Ischaemic Neuropathy in Incretin‐Based Therapy: A Comparative Analysis of Real‐World Safety Data

Diabetes Obes MetabPublished Pharmacovigilance disproportionality analysis

Authors' conclusion

Significant post-marketing safety signals for optic ischaemic neuropathy were identified for semaglutide, tirzepatide, and liraglutide. The absence of signals with other glucagon-like peptide-1 receptor agonists argues against a uniform class effect.

Study context

Population
FDA Adverse Event Reporting System reports from each drug's approval date through Q3 2025
Comparison
Six incretin-based therapies: signals for optic ischaemic neuropathy
Outcome
Optic ischaemic neuropathy (MedDRA term): reporting odds ratio (ROR) and proportional reporting ratio (PRR)
Methodological detailsFDA Adverse Event Reporting System, OpenVigil 2.1, primary suspect drug reports only, Evans' criteria
  • FDA Adverse Event Reporting System
  • OpenVigil 2.1
  • Primary suspect drug reports only
  • Evans' criteria

Main finding

As reported in the abstract

Optic ischaemic neuropathy reporting signal
GroupValueReporting odds ratio (ROR) (95% CI)Proportional reporting ratio (PRR) (95% CI)
Semaglutide355 events94.45 (83.02-107.45)93.77 (82.48-106.61)
Tirzepatide49 events2.94 (2.20-3.93)2.94 (2.20-3.93)
Liraglutide13 events4.58 (2.65-7.91)4.58 (2.65-7.91)

Value

Semaglutide355 events
Tirzepatide49 events
Liraglutide13 events

Reporting odds ratio (ROR) (95% CI)

Semaglutide94.45 (83.02-107.45)
Tirzepatide2.94 (2.20-3.93)
Liraglutide4.58 (2.65-7.91)

Proportional reporting ratio (PRR) (95% CI)

Semaglutide93.77 (82.48-106.61)
Tirzepatide2.94 (2.20-3.93)
Liraglutide4.58 (2.65-7.91)

Further findings

OutcomeValues
Characteristics of semaglutide-associated reportsValue = mean ageSemaglutide mean 59 years · disability documented 18% · hospitalization 11%

Original publication

Optic Ischaemic Neuropathy in Incretin‐Based Therapy: A Comparative Analysis of Real‐World Safety Data. Diabetes Obes Metab. Published 8 June 2026. doi:10.1111/dom.70952

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