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The FDA recommends using a non-oral contraceptive method or adding a backup method for 4 weeks after starting Zepbound and for 4 weeks after each dose increase
This is a critical issue in the lawsuit because the plaintiffs claim that Mounjaro and other GLP-1s are the primary reason the plaintiffs developed it
And if so, how do we make sure if these claimed impurities are not coming out of the instability of the patent formulation itself due to dilution by generic methods not due to the addition of B12 itself
Tirzepatide is not designed to be frozen at any point in its life cycle
"BSH Cobalamin and Folate guidelines" published 2014 NICE published a new B12 deficiency guideline in 2024 I have some doubts about this guideline but I think it's worth reading
Turner, J
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