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Large-scale pharmacovigilance analyses, such as those of the WHO VigiBase and Food and Drug Administration Adverse Event Reporting System, demonstrate that certain SSRIs carry disproportionate reporting signals, underscoring the need for individualized prescribing and long-term monitoring

Finally, although most of the included studies were of high quality, some trials had a potential risk of bias, such as open label design and pharmaceutical industry funding

The FDA does not review compounded drugs for safety, effectiveness, or quality before marketing

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, Grimes, J

Pratley R, Nauck M, Bailey T, Montanya E, Cuddihy R, Filetti S, et al