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In regulatory speak, this means: significant safety concerns. Compounding pharmacies can no longer legally produce it for human use
(6.1) Most common adverse reactions (incidence 5% and at a rate at least twice placebo) in adults with BED were dry mouth, insomnia, decreased appetite, increased heart rate, constipation, feeling jittery, and anxiety
The lawsuit accuses the manufacturers of failing to adequately warn consumers about the risks associated with the drugs, fraudulent concealment, and negligent misrepresentation
Enteral vitamin B12 supplements reverse postgastrectomy B12 deficiency
2014;2014:249810 Minich DM, Bland JS
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