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The ChEMBL drug registry records tirzepatide at maximum phase 4 (approved), first approval 2022, parenteral, with a first-in-class GIP-agonist designation and a boxed-warning flag
While oral glutathione bioavailability has historically been debated, liposomal and acetylated forms improve uptake
The FDA's adverse event reporting system depends on voluntary paperwork
Once absorbed and inside the cells it is removed, thus leaving the glutathione molecule intact
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