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See our BPC-157 storage guide for a concrete example of how this works in a multi-vial protocol
Adverse Reactions Nausea, vomiting, abdominal cramps, diarrhea, and a "fishy" body odor can occur with doses of about 3 g/day
These reports are submitted through the FDA Adverse Event Reporting System (FAERS) by healthcare professionals, patients, and manufacturers to document any potential safety concerns that arise during the use of these treatments after they have been approved
(This might relate to propofols inhibition of NMDA receptors, which blocks tolerance and withdrawal.) Propofol suppresses respiration, which can be helpful among ventilated patients to reduce ventilator dyssynchrony
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