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Category 3 are substances that were nominated but lack supporting information for the FDA to evaluate

Scientifically Validated Certificates of Analysis (COA) & HPLC Verified for Superior Quality Assurance

These GI effects typically peak during weeks 4 to 8 and resolve by week 12 for most users

Your body produces higher levels of red blood cells and you get more PRP from your blood

Patients should have routine complete blood counts (CBCs), vitamin B12 level checks, and neurological evaluations to facilitate early detection of potential complications and ensure effective management

human evidence is still emerging.) Musculoskeletal injury or post-surgical recovery Chronic tendonitis, ligament sprains, or joint pain Athletes or active individuals with overuse injuries Patients with GI inflammation or ulcerative symptoms Individuals seeking regenerative or anti-inflammatory support Generally well-tolerated in available data, but may include: Mild redness or irritation at injection site Transient headache, nausea, or dizziness (rare) Potential for allergic reaction (rare) Not FDA-approved