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Ravichandran S, Jegathaprathaban R, Radhakrishnan J, Usha R, Vijayan V, Teklemariam A
FDA Adverse Event Reporting System (FAERS)
Clinical trials may differ in patient population, baseline weight and BMI, diabetes status, medication dose, treatment duration, nutrition and lifestyle support, dropout rates, side-effect profiles, study design, and whether the data are published, peer-reviewed, or topline results
The authors of this study propose that both are possible and utilize a biopsychosocial model to explain how one drug can both enhance and impair sexual function
As interest continues to rise, many users still struggle with correct dosing
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