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a TUE is highly unlikely to be approved per USADA Known side effects: The most commonly reported adverse effects are transient injection site reactions (redness, itching, swelling), along with occasional headache, flushing, dizziness, or nausea, particularly early in therapy
about 98% in CAP and HCAP)
The reconstituted solution must be inspected for clarity and absence of particulates before use
[16] [18] Animal studies have not demonstrated teratogenicity, but high doses in pregnancy may theoretically increase the risk of fetal oxalate nephropathy or other metabolic disturbances
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