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CagriSema and Retatrutide are investigational compounds and are not FDA-approved for human treatment as described here
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The concerns include: Counterfeit or fraudulent labeling (e.g., fake pharmacies on the label or real pharmacies listed that didnt actually make the product) Potential quality problems (including improper storage/shipping) Dosing errors and adverse events, including cases requiring hospitalization Patients being prescribed doses that exceed FDA-approved labeling , with severe gastrointestinal side effects reported The agency also warns consumers about illegal sellers that market these drugs as for research purposes or not for human consumptionand emphasizes using legitimate, state-licensed pharmacies and prescriptions from licensed clinicians (FDA guidance for patients and providers)
Separating vision loss claims into their own MDL is an important step toward advancing these cases forward with the attention they deserve, said Motley Rice attorney and GLP-1 RA MDL co-lead counsel Jonathan Orent
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