Fig. 3.

Adverse events. Most patients did not have AE 55.88% (19/34). The majority of adverse events were with capsule 29.41% (10/34) resulted more AE compared with tablets. No patient of sequence B had AE using UDCA tablets while sequence A had adverse event in UDCA tablets and capsules 5.88% (2/34). The discontinuation due to adverse event occurred in 5.88% (2/34) of patients in the sequence B. Legend: AE = adverse events