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Dont reuse needles between access events as needle contamination bypasses the benzyl alcohol preservative at the vial entry point
The statements and the products of this company are not intended to diagnose, treat, cure, or prevent any disease
[6] Premarketing surveillance of parenteral arginine formulations identified nausea, vomiting, headache, flushing, numbness, and local venous irritation in approximately three per cent of infusions
No, it is not FDA-approved, and much of the evidence is preclinical
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