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Data exclusivity prevents applicants for authorization of generics or biosimilars of these innovative products from referencing the innovators preclinical and clinical trial data contained in the dossier of the reference product when applying for a generic or biosimilar (abbreviated) marketing authorization, for a period of eight years from the date on which the reference product was first authorized in the EU

[16] Reported rates from trials include: Nausea: ~44% Vomiting: ~25% Diarrhea: ~31% Constipation: ~23% Dyspepsia: ~10% These effects reflect slowed gastric motility and are usually mild, but can lead to clinical implications: Dehydration Electrolyte abnormalities ED presentations for poor oral intake

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This potent blend combines IV fluids, high-dose vitamin C, magnesium, zinc, and biotin to help your body combat active illness and oxidative stress