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With side effects not usually a problem at low doses and improvements often seen, Dr

Jastreboff et al., 2022)

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The general drug development process is laboratory research preclinical research, including animal testing and basic safety tests clinical research, also known as human trials review, in which the FDA decides whether to approve the new drug post-marketing safety monitoring Using the information gathered from this process, the FDA will decide whether a drug requires a boxed warning
