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The incidence of SJS is estimated to be between 1.1 and 7.1 cases per million person-years.1 SJS is currently considered to be a part of bullous disease syndromes [SJS, SJS- toxic epidermal necrolysis (TEN) overlap syndrome, and TEN] in which keratinocyte cell death results in subepidermal separation

The conclusions of these studies were also consistent with the statistical results of our article

Others have promising animal data

The familiar supplement format integrates seamlessly into existing routines, while the extended duration of action supports sustained recovery processes