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Ozempic, European Union
Health Officials Investigating Possible Link Between Ozempic and Eye-Rotting Condition
Ozempic manufacturer Novo Nordisk said patient safety is a priority and “the benefit-risk profile of semaglutide remains unchanged”
EU Drug Regulator to Review Ozempic’s Possible Link to Eye Condition
The European Union’s drug regulator said it would review two studies that linked Novo Nordisk’s blockbuster diabetes drug Ozempic to a rare eye condition.
Novo Nordisk's Ozempic faces EU review for potential eye disease connection
The European Union's drug regulator said it would assess two new Danish studies that link Novo Nordisk's popular diabetes drug Ozempic to a rare eye disease.
EU reportedly reviewing link between Ozempic, rare eye disease
With U.S. headquarters in Plainsboro, Novo Nordisk told NJBIZ, "NAION is a very rare eye disease, and it is not an adverse drug reaction for the marketed formulations of semaglutide (Ozempic, Rybelsus and Wegovy) as per the approved labels.
EMA to Investigate Eye Risk for Novo’s Ozempic: Reuters
Following an appeal by the Danish Medicines Agency, the European Union’s drug regulator will review two new studies that have strengthened the link between Novo Nordisk’s blockbuster GLP-1 and a rare eye disease.
Novo Nordisk's Ozempic potentially investigated for rare eye condition
Denmark's drug regulator has asked the European Medicine Agency's safety committee to evaluate two studies that found a potential link between Novo Nordisk's (NVO) type 2 diabetes drug Ozempic (semaglutide) and a rare eye condition.
EURACTIV
8h
Poland develops its first national critical medicines list
The Polish initiative establishes a proactive strategy for securing access to essential medicines and maintaining ...
17h
Plasma biomarkers offer new clues in Alzheimer's detection
How are emerging plasma biomarkers related to the diagnostic tests currently used in clinical routines? And does the earlier ...
3d
on MSN
GSK’s Cancer Drug Jemperli Moves a Step Closer to European Marketing Permission
In one of the final steps before a marketing authorization decision by the European Medicines Agency, it recommended ...
3d
Danish agency seeks probe as Ozempic study shows link to vision loss
The Danish Medicines Agency said it would ask European authorities to review two new studies that point to a link between ...
PharmiWeb
1d
Johnson & Johnson submits application to the European Medicines Agency seeking approval of a new indication for IMBRUVICA® (ibrutinib)
The European MCL Network Phase 3 TRIANGLE study, evaluated ibrutinib in combination with induction immunochemotherapy, both with and without an autologous stem cell transplant, followed by 24 months f ...
3d
on MSN
European agency endorses approval of Biocon Biologics’ biosimilar Ustekinumab
BENGALURU: Biocon Biologics, a biosimilars company and subsidiary of Biocon, has announced that the European Medicines Agency ...
FiercePharma
6d
EMA backs Merck's Welireg, Bayer's ATTR med and Gilead's liver drug from $4.3B deal
Merck & Co.’s kidney cancer drug Welireg, Bayer and BridgeBio’s transthyretin amyloid cardiomyopathy (ATTR-CM) therapy, and ...
3d
GSK announces EMA granted PRIME Designation for GSK5764227
GSK (GSK) announced that the European Medicines Agency, EMA, has granted Priority Medicines, PRIME, Designation for GSK5764227, its ...
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Ozempic
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