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The search details are shown in Supplementary Table 1, meantime the inclusion criteria were as follows: (i) patients with PCOS, (ii) patients with the treatment of carnitine supplementation, (iii) patients with body weight information, (iv) patients with exact doses and durations of carnitine supplementation, and (v) patients with the control group

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[8] [9] The FDA Adverse Event Reporting System (FAERS) has received reports of acute kidney injury associated with these medications, but these reports do not establish causation and often involve patients with multiple risk factors or concurrent illnesses

While these complications are relatively rare, its important to know the warning signs