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The most commonly reported effects are mild and transient: slight redness at the injection site, occasional mild fatigue in the first few days of a protocol reflecting the circadian recalibration effect, and in some patients a temporary increase in dream vividness associated with improved REM architecture
up to 1,000 mg for therapeutic needs
Their true frequency and cause are unknown
In February 2023, the FDA gave Priority Review to Regenerons investigational antibody, which works by binding to the C5 complement factor, thereby disrupting the complement cascade and preventing associated diseases
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