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10.1002/jso.24969 2 AkitaS.MitsukawaN.KuriyamaM.KubotaY.HasegawaM.TokumotoH.et al (2015)
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In the 12 mg dose group, 16% of subjects discontinued due to adverse events (AEs), but the overall incidence of severe adverse events (SAEs) was low, about 6%-8%
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Alternately, incensing number of evidences have confirmed or validated the formation of selenylsulfide (-Se-S-) intermediate and the involvement of thioldisulfide exchange during the GPx cycle [17,18,19]
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