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Description
48 WHO (2021b)
Option (Evidence Strength: Grade C) One randomized trial with an oral PPS group for comparison reported that CyA (3 mg/ kg/day divided into two doses) resulted in 75% of patients experiencing clinically significant improvement compared to 19% of a PPS comparison group after six months of treatment
cerevisiae BY4741
Important note: STTM is an information-only site based on what many patients have reported in their treatment
For maximum purity, we recommend using a reconstituted vial within 28-30 days
