Wegovy weight loss jab ‘may carry higher risk of sudden sight loss’ as new warning issued
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Weight-loss jab Wegovy may pose the highest risk of sudden sight loss when compared to other jabs of a similar nature, such as Ozempic, according to a new analysis.
The study also revealed that men were three times more likely than women to experience a so-called “eye stroke”.
Researchers, whose findings were published in the British Journal of Ophthalmology, stated that the results “highlight a potential dose-dependent safety concern” for semaglutide.
Wegovy, Ozempic, and Rybelsus – all produced by Novo Nordisk – share the same active ingredient but differ in their dosage and intended use.
Wegovy is approved on the NHS for weight management, utilising higher doses.
In contrast, Ozempic and Rybelsus, the latter being an oral medication, employ lower doses to treat type 2 diabetes.
For the study, experts examined the link between semaglutide and ischaemic optic neuropathy (Ion) – often called an eye stroke – which causes a sudden loss of vision due to reduced blood flow to the optic nerve.
Researchers analysed side-effect alerts submitted to the US Food and Drug Administration (FDA) Adverse Event Reporting System between December 2017 and December 2024.
Of more than 30 million alerts, some 31,774 involved semaglutide.
Researchers found Wegovy was most strongly linked with Ion compared to Ozempic (PA)
Some 3,070 were attributed to Wegovy, which launched in 2021, while 20,608 were linked to Ozempic, which was approved by the FDA in 2017.
Despite this, researchers found Wegovy was most strongly linked with Ion compared to Ozempic.
“Overall, Ion risk appears dose and formulation dependent, and highest with Wegovy,” they said.
“Ozempic’s earlier approval resulted in more reports than Wegovy, yet Wegovy showed the stronger signal.”
Further analysis suggested the odds of Ion were almost five times higher with Wegovy than Ozempic, and more than three times higher in men than in women.
Researchers said: “These findings highlight a potential dose-dependent safety concern that warrants urgent prospective evaluation to guide prescribing and regulatory policy.”
Meanwhile, Ion was not reported in association with Rybelsus, the study found.
Experts said this difference may be down to “the limited absorption and slower uptake of Rybelsus”.
A Novo Nordisk spokesperson said: “Patient safety is our top priority, and we take any reports about adverse events from the use of our medicines very seriously.
“We work closely with authorities and regulatory bodies from around the world to continuously monitor the safety profile of our products.”
They added that EU patient leaflets for Wegovy, Ozempic and Rybelsus have been updated to include non-arteritic anterior ischemic optic neuropathy (NAION).
However, the company has concluded that data “did not suggest a reasonable possibility of a causal relationship between semaglutide and NAION and Novo Nordisk believes that the benefit-risk profile of semaglutide remains favourable”.
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