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Research shows that BPC counteracts the deleterious effects of L-NAME, which has been known to cause ulceration in the GI tract
It has no FDA approval for any indication and carries significant side effects requiring careful management
Clinical trial data extend to 2-3 years of continuous use with no significant safety concerns emerging
The quality of evidence varies because PRP preparation methods differ between providers, making it hard to compare studies directly
Children This medicine should be used in children only under medical supervision
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