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Patients should exercise caution regarding unregulated or unlicensed sources offering investigational compounds outside of clinical trial settings, as these carry significant safety risks
The coordination of oncologists and endocrinologists becomes an essential factor in the management of superimposed toxicities
In addition, the FDA maintains a system of postmarketing surveillance and risk assessment programs to identify and evaluate adverse events that did not appear during the drug development process," the agency told CNN on Wednesday
These technologies are trickling down from pharmaceutical applications to cosmetic products
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