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However, further research and clinical trials are necessary to determine its suitability for human use [7]

Theoretical and route-specific risks FDA's 2024 review specifically flagged that no published human exposure data exists for the subcutaneous, transdermal, or intranasal routes that compounding pharmacies have offered

The substance is given directly by subcutaneous (sub-Q), intramuscular (IM), or intra-arterial (IA) routes, as opposed to an intravenous (IV) injection/push that requires a commitment of time

Additionally, injecting water too quickly into the vial causes the powder to clump and dissolve unevenly, leading to inconsistent doses