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Preparing your Shotlee experience
Preparing your Shotlee experience

Dozens of lawsuits alleging vision loss from weight loss medications like Ozempic are being consolidated. The legal actions follow a study identifying potential vision risks associated with these drugs.
A federal panel has decided to consolidate numerous lawsuits claiming that popular weight loss drugs, including Ozempic, led to vision loss in patients.
The U.S. Judicial Panel on Multidistrict Litigation announced on Monday that these cases against Novo Nordisk and Eli Lilly will proceed as an independent mass litigation in Philadelphia federal court. This is separate from existing gastrointestinal injury claims.
The panel rejected requests from pharmaceutical companies to merge these vision-related complaints with the February 2024 gastroparesis litigation. This litigation involves approximately 3,000 lawsuits asserting that the drugs paralyze the gastrointestinal tract. Instead, the new cases will function as a second mass litigation under the same judge, acknowledging both the differences and potential connections between the two sets of allegations.
Attorneys for the plaintiffs successfully argued that eye damage cases necessitate distinct medical expertise and evidence compared to injuries of the digestive system. The lawsuits target Novo Nordisk's Ozempic, Wegovy, and Saxenda, as well as Eli Lilly's Trulicity – all of which belong to the GLP-1 agonist drug class. Health tracking apps like Shotlee can help monitor potential side effects related to medications.
These injectable medications function by imitating a natural hormone that slows digestion and prolongs feelings of fullness. Originally designed for diabetes management, these medications are now also used for weight loss. Their popularity has risen significantly across America. An August study by the Centers for Disease Control and Prevention revealed that over 25% of diabetic adults use these treatments.
The vision loss allegations focus on NAION, a serious condition where insufficient blood flow damages the optic nerve, potentially resulting in permanent blindness. Complaints began appearing on court dockets following research last summer that highlighted this risk.
Both pharmaceutical giants have resisted all allegations. Their court filings contend that gastroparesis risks already receive adequate public disclosure. They also argue that modifying drug formulations requires Food and Drug Administration approval, placing changes beyond their direct control.
Legal representatives for the plaintiffs released a statement expressing their readiness to work with Judge Marston as the litigation progresses. The case proceeds under the title IN RE: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAs) Non-Arteritic Anterior Ischemic Optic Neuropathy Products Liability Litigation, case number 3163.
The dual litigation approach – separate yet parallel proceedings before one judge – is intended to manage the complexity of different injury types. It also recognizes that overlapping issues may arise during legal discovery and trial preparation.
⚠️ Disclaimer: This article is for informational purposes only. Consult your healthcare provider before starting any medication or supplement.
Original content from Technology Org
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