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Faster absorption might result in higher peak plasma concentrations than intended, potentially increasing the risk or severity of dose-dependent adverse effects, particularly gastrointestinal symptoms such as nausea, vomiting, and diarrhea
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The phosphokinase activity of IRE1 prevents the oxidative stress injury through miR-25/Nox4 pathway after ICH
Being me (sciencey minded) I've done my own trials on myself with in-date and out-of-date ampoules and found no difference
The patients included in those studies had liver cirrhosis but had no overt HE compared to patients with liver cirrhosis and only minimal HE
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