Who will launch public awareness campaigns about Ozempic by end of 2025?
By Novo Nordisk • 25%
By health organizations • 25%
By both • 25%
No campaigns • 25%
Reports from health organizations or Novo Nordisk announcements
Novo Nordisk's Ozempic Linked to Rare Vision Loss in Denmark and Norway Study
Dec 13, 2024, 05:18 PM
A study has linked the use of Ozempic, a diabetes medication produced by Novo Nordisk A/S, to an increased risk of developing a rare form of vision loss known as non-arteritic anterior ischemic optic neuropathy (NAION). The research, which analyzed patient records from Denmark and Norway, found that diabetes patients using Ozempic were more than twice as likely to be diagnosed with NAION compared to those taking other diabetes medications. The condition, which can lead to irreversible vision loss, is associated with a loss of blood flow to the optic nerve and is more common in individuals over 50. Despite the low overall incidence rate, with only 1.4 additional cases per 10,000 years of patient observation, the study highlights the need for patient awareness of this potential risk. Novo Nordisk has stated that the risk-benefit profile of Ozempic remains unchanged, citing very few cases of NAION in its own trials. The study's findings were published on medRxiv, a pre-print server, and have not yet undergone peer review.
View original story
Somewhat positive • 25%
Highly positive • 25%
Negative • 25%
Neutral • 25%
No distribution approved • 25%
Approve distribution city-wide • 25%
No decision made • 25%
Approve limited distribution • 25%
Discontinue development • 25%
Partner with another company • 25%
Seek further trials • 25%
Submit for regulatory approval • 25%
70% or more reduction • 25%
Less than 25% reduction • 25%
50-69% reduction • 25%
25-49% reduction • 25%
Other • 25%
Pfizer • 25%
Novo Nordisk • 25%
Eli Lilly • 25%
Moderately effective • 25%
Highly effective • 25%
Not effective • 25%
Slightly effective • 25%
FDA approved and in market • 25%
Pending approval • 25%
Withdrawn by manufacturer • 25%
Rejected by FDA • 25%
Other • 25%
Addiction Treatment • 25%
Diabetic Macular Edema • 25%
Metabolic Liver Dysfunction • 25%
Product recall • 25%
Other regulatory actions • 25%
No action taken • 25%
Safety label update • 25%